Gambro Ak 200 S - Service Manual 5g3l4j

AK 200 S - Operator’s manual Program version 8.xx 1. Before you get started - general information 2. Description - the machine and its components 3. Controlling the machine - general guidelines 4. Hemodialysis, double needle treatment 5. Hemodialysis, single needle treatment 6. Isolated UF 7. Profiling 8. Hemodiafiltration, low volume 9. BVS - Blood Volume Sensor 10. BPM - Blood Pressure Monitor (option) 11. Diascan 12. Hygiene and maintenance 13. Technical data and specifications 14. Alarm list, Attention alarm list and Technical alarm list 15. Major changes in operator’s manual 16. Index

HCEN9751 Revision.12.2005 Program version 8.xx

Contents 1. Before you get started - general information How to use this manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Definitions of expressions used in this manual . . . . . . . . . . . . . . . . . . General precautions before use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Safety philosophy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The preparation of dialysis fluid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Inlet water requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Preparation of the dialysis fluid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . UFD- Ultrafiltered Dialysis Fluid (option) . . . . . . . . . . . . . . . . . . . . . . Ultrafilters; frequency of change . . . . . . . . . . . . . . . . . . . . . . . . . . . . . List of concentrates, accessories and disposables, for use with the AK 200 S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Concentrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Lines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Dialyzers/Ultrafilter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Infusion fluid for low volume HDF . . . . . . . . . . . . . . . . . . . . . . . . Blood pressure measurement accessories . . . . . . . . . . . . . . . . . . . . List of symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CE-marking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Copyright . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

1:2 1:4 1:5 1:8 1:9 1:12 1:12 1:12 1:12 1:12 1:13 1:13 1:14 1:14 1:15 1:15 1:16 1:18 1:18 1:18

2. Description - the machine and its components Blood monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:2 BM 200 - Single Pump, BM 202 - Double Pump . . . . . . . . . . . . . . . . . 2:2 Fluid monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:4 FM 202 - Acetate and Bicarbonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:4 Rear of the machine - without options . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:6 Rear of the machine - options included . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:8 Monitor stand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:10 MS 200: Adjustable height: five fixed positions . . . . . . . . . . . . . . . . . . 2:10 MS 202: Electrically adjustable height . . . . . . . . . . . . . . . . . . . . . . . . . 2:12

3. Controlling the machine - general guidelines Operator’s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hygiene group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Mode group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Concentrate stand-by mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Procedure for manual activation . . . . . . . . . . . . . . . . . . . . . . . . . . . Resume fluid preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Therapy group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Treatment overview group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Bargraph display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Flow diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Time display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Parameter buttons and their displays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Reset possibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarm indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3:2 3:4 3:5 3:6 3:7 3:7 3:9 3:10 3:10 3:10 3:11 3:12 3:16 3:17 3:17 HCEN9751 Revision.12.2005 Program version 8.xx

Alarm function of the parameter buttons . . . . . . . . . . . . . . . . . . . . . . . Override possibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Stand-by group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Display and setting group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Information display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Treatment overview screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Parameters shown on Treatment overview screen . . . . . . . . . . . . . . . . Function check overview screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Tests shown on Function check overview screen . . . . . . . . . . . . . . . . . The eight commandments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Setting of parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ing treatment parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The ultrafiltration control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Protective system for ultrafiltration . . . . . . . . . . . . . . . . . . . . . . . . . . . Power failure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Returning the blood during a power failure . . . . . . . . . . . . . . . . . . . . . Battery back-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Recovery from a short power failure . . . . . . . . . . . . . . . . . . . . . . . . . . Recirculation during treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Reconnection of the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Change of blood pump segment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BiCart/SelectCart change during treatment . . . . . . . . . . . . . . . . . . . . . . . .

3:18 3:20 3:22 3:23 3:23 3:24 3:25 3:26 3:27 3:28 3:29 3:32 3:33 3:34 3:35 3:38 3:38 3:38 3:39 3:40 3:40 3:42 3:43

4. Hemodialysis, double needle treatment Double needle treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Check before starting the machine . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the machine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Function check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Select concentrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect concentrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . SelectCart and SelectBag together with BiCart . . . . . . . . . . . . . Acidic concentrate and BiCart . . . . . . . . . . . . . . . . . . . . . . . . . . Acidic concentrate and liquid bicarbonate concentrate . . . . . . . Acetate concentrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the machine - continued . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Attaching the dialyzer and the blood lines . . . . . . . . . . . . . . . . . . . . . . Dialyzer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Arterial blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Preparations if the heparin pump is to be used . . . . . . . . . . . . . Venous blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming and rinsing the extracorporeal circuit . . . . . . . . . . . . . . . . Initiating . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Set the treatment parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pressure alarm limits setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Venous/Arterial pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Automatic emptying of BiCart, SelectCart and SelectBag . . . . . . . . Discontinuing procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .


4:2 4:2 4:2 4:3 4:4 4:6 4:7 4:8 4:8 4:8 4:9 4:11 4:11 4:12 4:14 4:16 4:17 4:17 4:19 4:19 4:20 4:21 4:22 4:22 4:22 4:24 4:24 4:25

Confirm treatment end . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . If desired, start emptying BiCart or BiCart, SelectCart and SelectBag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Return the blood . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . After-treatment handling of the machine . . . . . . . . . . . . . . . . . .

4:25 4:25 4:25 4:26

5. Hemodialysis, single needle treatment Single needle treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Glossary of single needle parameters and key . . . . . . . . . . . . Single needle treatment with two blood pumps - BM 202 only . . . . . . . . . Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Arterial blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Venous blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming and rinsing the extracorporeal circuit . . . . . . . . . . . . . . . . Priming and rinsing procedure in double needle mode, finishing in single needle/double pump mode . . . . . . . . . . . . . . . . . . . . . Priming and rinsing procedure in single needle/double pump mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Initiating . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Set the treatment parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Always check/adjust . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pressure alarm limits setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Venous/Arterial pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Single needle treatment with one blood pump . . . . . . . . . . . . . . . . . . . . . Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Single needle / single pump settings . . . . . . . . . . . . . . . . . . . . . . . . Connect the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . For both pressure- and time-controlled phases . . . . . . . . . . . . . Start the treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . For both pressure- and time-controlled phases . . . . . . . . . . . . . Only for pressure-controlled phases . . . . . . . . . . . . . . . . . . . . . Only for time-controlled phases . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Double needle to single needle treatment - change during treatment . . Resume treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Single needle / single pump settings . . . . . . . . . . . . . . . . . . . . . . . . Only for pressure-controlled phases . . . . . . . . . . . . . . . . . . . . . Only for time-controlled phases . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

5:2 5:2 5:3 5:4 5:4 5:4 5:5 5:6 5:6 5:6 5:9 5:11 5:11 5:11 5:12 5:13 5:15 5:15 5:15 5:17 5:18 5:18 5:19 5:19 5:19 5:21 5:21 5:21 5:22 5:23 5:24 5:24 5:24 5:25 5:26 5:27

6. Isolated UF 7. Profiling Profiling of Na+ and HCO3- dialysis fluid concentration . . . . . . . . . . . . . Profiling of ultrafiltration rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

7:2 7:4 HCEN9751 Revision.12.2005 Program version 8.xx

Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Curve Setting/Change/Cancellation: . . . . . . . . . . . . . . . . . . . . . Activation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Activation of profiling with already preset models . . . . . . . . . . . . . . . . Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

7:5 7:5 7:5 7:5 7:7 7:7

8. Hemodiafiltration, low volume General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Protective system for low volume HDF . . . . . . . . . . . . . . . . . . . . . . . . The following conditions have to be met in order to fulfil the accuracy of the measuring system . . . . . . . . . . . . . . . . . . . . . . . . . . Start up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming and rinsing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Initiating and starting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Bolus infusion possibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hemodiafiltration, low volume, single needle, single pump . . . . . . . . .

8:2 8:2 8:3 8:4 8:6 8:7 8:8 8:8

9. BVS - Blood Volume Sensor General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ∆BV text information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Graphs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BVS ON/OFF . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BVS Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BVS On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

9:2 9:3 9:4 9:5 9:6 9:6 9:7

10.BPM - Blood Pressure Monitor (option) General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:2 Patient factors which affect readings . . . . . . . . . . . . . . . . . . . . . . . . . . 10:3 Handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:5 The BPM screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:6 BPM button pressed once . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:6 BPM button pressed twice . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:7 Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:8 Alarm limits setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:8 Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:9 Start/Stop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:10 Start . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:10 Stop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:10

11.Diascan General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . How the measuring process is performed by the machine . . . . . . . . . . Glossary of Diascan parameters and key . . . . . . . . . . . . . . . . . . Precautions before use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The first screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . HCEN9751 Revision.12.2005 Program version 8.xx

11:2 11:2 11:2 11:3 11:4 11:5 11:5 11:6

Measurement mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:6 Alarm limit for clearance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:6 Measurement result values . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:7 The second screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:8 Distribution volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:8 Distribution volume calculation using the Watson formula . . . . 11:9 Forecast . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:10 Target . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:10 Alarm limit for Kt/V . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:10 Measurement result values when distribution volume has not been set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:11 Second screen symbol . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:11 Measurement result values when distribution volume has been set . 11:12 The third screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Latest measured values . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Accumulated and forecast values . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Time to target . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:14 Third screen symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:14 Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:15 Clearance alarm limit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:15 Kt/V alarm limit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:15 Step-by-step instructions for measuring clearance and Kt/V . . . . . . . . . . 11:16 Single clearance measurement check . . . . . . . . . . . . . . . . . . . . . . . . . . 11:16 Continuous measuring of clearance . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:18 Single Kt/V and clearance measurement check . . . . . . . . . . . . . . . . . . 11:20 Continuous measuring of Kt/V and clearance . . . . . . . . . . . . . . . . . . . 11:22

12.Hygiene and maintenance General hygiene and maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:2 Glossary of disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:3 Disinfection history . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:4 List of disinfection screen symbols . . . . . . . . . . . . . . . . . . . . . . . . . 12:4 Schedule for hygiene and maintenance . . . . . . . . . . . . . . . . . . . . . . . . . 12:6 When the machine is planned not to be in use . . . . . . . . . . . . . . . . 12:7 Characteristics of different disinfection, decalcification and cleaning agents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:8 Hygiene - Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:9 General - Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:9 Performing Heat disinfection program . . . . . . . . . . . . . . . . . . . . . . . . 12:11 Performing Heat disinfection program with CleanCart . . . . . . . . . . . . 12:12 Performing Heat disinfection program with liquid citric acid . . . . . . . 12:13 Performing integrated Heat disinfection program with WRO 300 H . . 12:14 Automatic start of Heat disinfection program . . . . . . . . . . . . . . . . . . . 12:16 Automatic switch off after Heat disinfection program . . . . . . . . . . . . . 12:17 Integrated Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:17 Hygiene - Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:18 General - Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:18 Chemical disinfectants . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:19 Performing Chemical disinfection program . . . . . . . . . . . . . . . . . . . . . 12:20 Filling the machine with chemical disinfectant . . . . . . . . . . . . . . . . 12:21 Residual test after Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . 12:23 Central Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:24 Performing central Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . 12:24


Hygiene - Rinse/Drain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:25 Performing Rinse/Drain program . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:25 Performing Rinse/Drain program with CleanCart . . . . . . . . . . . . . . . . 12:26 Automatic start of Rinse/Drain program . . . . . . . . . . . . . . . . . . . . . . . 12:28 Automatic switch off after Rinse/Drain program . . . . . . . . . . . . . . . . 12:29 Maintenance - the flow path . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 The flow path . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 Decalcification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 Ultrafilter; how to change . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:31 Ultrafilter replacement reminder . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:32 Maintenance - the exterior of the machine . . . . . . . . . . . . . . . . . . . . . . . . 12:33 The outside . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 Top tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 Blood pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 Blood leak detector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 BPM cuff . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:34

13.Technical data and specifications Performance and specification - Control System . . . . . . . . . . . . . . . . . . . . 13:2 Blood Flow Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:2 Air Detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Heparin istration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Blood Volume Sensor (BVS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Blood Pressure Monitor (BPM) . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Dialysis fluid preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:4 Dialysis fluid preparation (BiCart Select mode only) . . . . . . . . . . . . 13:5 Ultrafiltration control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:5 Substitution fluid (Low volume HDF) . . . . . . . . . . . . . . . . . . . . . . 13:5 Profiling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:5 Diascan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:6 Disinfection and Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:6 Water supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:9 Drain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:10 Power supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:10 Connection of external equipment . . . . . . . . . . . . . . . . . . . . . . . . . 13:10 Battery Back-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:12 Performance and specification - Supervisory system . . . . . . . . . . . . . . . . . 13:13 Blood Pressure Supervision . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:13 Air Detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:14 Heparin istration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:14 Dialysis fluid preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:14 Dialysis fluid preparation (BiCart Select mode only) . . . . . . . . . . . . 13:14 Ultrafiltration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:15 Substitution fluid (Low volume HDF) . . . . . . . . . . . . . . . . . . . . . . 13:15 Blood leak detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:15 Physical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:16 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:16 Materials in with water, concentrates and dialysis fluid . . . . . . . . . 13:17 Polymers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:17 Metals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:17 Others . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:17 Environmental data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18


Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Transportation and storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Electromagnetic environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:22

14.Alarm list, Attention alarm list and Technical alarm list Alarm list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14:2 Attention alarm list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14:9 Technical alarm list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14:45

15.Major changes in operator’s manual 16.Index


Figures 2. Description - the machine and its components Figure 2:1 Figure 2:2 Figure 2:3 Figure 2:4 Figure 2:5 Figure 2:6

Blood monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:2 Fluid monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:4 Rear of the machine - without options . . . . . . . . . . . . . . . . . 2:6 Rear of the machine, options included . . . . . . . . . . . . . . . . . 2:8 Monitor stand, five fixed positions . . . . . . . . . . . . . . . . . . . . 2:10 Monitor stand, electrically adjustable . . . . . . . . . . . . . . . . . . 2:12

3. Controlling the machine - general guidelines Figure 3:1 Figure 3:2 Figure 3:3 Figure 3:4 Figure 3:10 Figure 3:11 Figure 3:13 Figure 3:14

Operator’s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Concentrate stand-by mode, activation . . . . . . . . . . . . . . . . . Flow diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Treatment overview screen . . . . . . . . . . . . . . . . . . . . . . . . . . Function check overview screen . . . . . . . . . . . . . . . . . . . . . Temp button and the information display . . . . . . . . . . . . . Temp button and the information display . . . . . . . . . . . . . ing treatment parameters . . . . . . . . . . . . . . . . . .

3:3 3:7 3:10 3:24 3:26 3:28 3:29 3:32

4. Hemodialysis, double needle treatment Figure 4:1 Figure 4:2 Figure 4:3 Figure 4:4 Figure 4:5 Figure 4:6 Figure 4:7

Select Bicarbonate and type of concentrate . . . . . . . . . . . . . Select SelectBag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect the SelectCart cartridge and the SelectBag . . . . . . . Arterial blood line in HD, set-up . . . . . . . . . . . . . . . . . . . . . Change position of the heparin pump holder . . . . . . . . . . . . Syringe attached to heparin pump . . . . . . . . . . . . . . . . . . . . Venous blood line in HD, set-up . . . . . . . . . . . . . . . . . . . . .

4:4 4:5 4:7 4:13 4:14 4:14 4:16

5. Hemodialysis, single needle treatment Figure 5:1 Figure 5:2 Figure 5:5

Arterial blood line with expansion chamber in HD, single needle/double pump, set-up . . . . . . . . . . . . . . . . . . . . . . . . 5:4 Venous blood line with expansion chamber in HD, single needle/double pump, set-up . . . . . . . . . . . . . . . . . . . . . . . . 5:5 Venous blood line with attached expansion chamber in HD, single needle/single pump, set-up . . . . . . . . . . . . . . . . . . . . 5:18

7. Profiling Figure 7:1 Figure 7:2 Figure 7:3 Figure 7:4

3 different graphs for profiling sodium and bicarbonate . . . Profiling, Degressive graph . . . . . . . . . . . . . . . . . . . . . . . . . Profiling, Progressive graph . . . . . . . . . . . . . . . . . . . . . . . . . Linear graph for UF rate profiling . . . . . . . . . . . . . . . . . . . .

7:2 7:3 7:3 7:4

8. Hemodiafiltration, low volume Figure 8:1

Infusion line in HDF low volume, set-up . . . . . . . . . . . . . . .

9. BVS - Blood Volume Sensor HCEN9751 Revision.12.2005 Program version 8.xx

8:5

Figure 9:1 Figure 9:2 Figure 9:3 Figure 9:4 Figure 9:5 Figure 9:6 Figure 9:7

BVS, relative blood volume graph . . . . . . . . . . . . . . . . . . . . BVS, relative blood volume graph . . . . . . . . . . . . . . . . . . . . BVS, combination of graphs . . . . . . . . . . . . . . . . . . . . . . . . BVS, graphs without relative blood volume graph . . . . . . . . BVS turned on before the reference value has been acquired BVS, the reference value not related to the treatment start . BVS, interrupted relative blood volume graph . . . . . . . . . . .

9:3 9:4 9:5 9:6 9:7 9:7 9:8

10.BPM - Blood Pressure Monitor (option) Figure 10:1 Figure 10:2 Figure 10:3 Figure 10:4

BPM, screen with latest measured values and graph . . . . . . 10:6 BPM, screen with the 8 latest measured values . . . . . . . . . . 10:7 BPM, setting the alarm limits . . . . . . . . . . . . . . . . . . . . . . . 10:8 BPM, measurement check in progress . . . . . . . . . . . . . . . . 10:10

11.Diascan Figure 11:1 Figure 11:2 Figure 11:3 Figure 11:4 Figure 11:5 Figure 11:6 Figure 11:7 Figure 11:8 Figure 11:9 Figure 11:10 Figure 11:11 Figure 11:12 Figure 11:13 Figure 11:14 Figure 11:15 Figure 11:16

Diascan screens, without set distribution volume . . . . . . . . 11:5 Diascan screens, set distribution volume . . . . . . . . . . . . . . 11:5 First Diascan screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:6 First Diascan screen with measurement result values . . . . . 11:7 Second Diascan screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:8 The Watson screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:9 Second Diascan screen with set distribution volume . . . . . 11:10 Second Diascan screen with measurement result values, distribution volume not set . . . . . . . . . . . . . . . . . . . . . . . . . 11:11 Second Diascan screen with measurement result values, set distribution volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:12 Third Diascan screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Diascan, activated single measurement check . . . . . . . . . . 11:16 Diascan, activated continuous measuring . . . . . . . . . . . . . 11:18 Diascan, activated single measurement check . . . . . . . . . . 11:20 Diascan, distribution volume set . . . . . . . . . . . . . . . . . . . . 11:21 Diascan, activated continuous measuring . . . . . . . . . . . . . 11:22 Diascan, distribution volume, Kt/V target and alarm limit set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:23

12.Hygiene and maintenance Figure 12:1 Figure 12:2 Figure 12:3 Figure 12:4 Figure 12:5 Figure 12:6 Figure 12:7

Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:11 Auto Heat . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:16 Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:20 Rinse/Drain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:25 Auto Rinse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:28 Ultrafilter replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:32 BPM cuff, removal procedure of rubber bladder from cloth bag 1. Small hole 2. Large hole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:34


Chapter 1 Before you get started - general information How to use this manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Definitions of expressions used in this manual . . . . . . . . . . . . . . . . . . General precautions before use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Safety philosophy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The preparation of dialysis fluid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Inlet water requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Preparation of the dialysis fluid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . UFD- Ultrafiltered Dialysis Fluid (option) . . . . . . . . . . . . . . . . . . . . . . Ultrafilters; frequency of change . . . . . . . . . . . . . . . . . . . . . . . . . . . . . List of concentrates, accessories and disposables, for use with the AK 200 S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Concentrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Lines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Dialyzers/Ultrafilter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Infusion fluid for low volume HDF . . . . . . . . . . . . . . . . . . . . . . . . Blood pressure measurement accessories . . . . . . . . . . . . . . . . . . . . List of symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CE-marking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Copyright . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .


AK 200 S Operator’s manual - Definitions

1:2 1:4 1:5 1:8 1:9 1:12 1:12 1:12 1:12 1:12 1:13 1:13 1:14 1:14 1:15 1:15 1:16 1:18 1:18 1:18

1:1

How to use this manual Below is a brief explanation of how the chapters in this manual are structured and are intended to be used. Chapter 1; Before you get started - general information

This chapter contains information to be read before using the AK 200 S machine. Chapter 2; Description - the machine and its components

This chapter contains component descriptions of the blood monitor, the fluid monitor, the rear of the machine and the monitor stands. Chapter 3; Controlling the machine - general guidelines

This chapter contains explanations of how the machine is to be controlled. This is, for example, how to use the buttons of the Operator’s , their alarms functions, how parameters are to be set and how to use the concentrate stand-by mode. The Treatment- and Function check overview screens are explained as well as the ultrafiltration control, and information is provided on what to do if a power failure occurs. Chapter 4; Hemodialysis, double needle treatment

This chapter contains instructions on how to perform hemodialysis with two needles, using the AK 200 S machine. The chapter begins with how to start the machine and continues with how to attach the dialyzer and the blood lines, the priming procedure, starting the treatment, setting of parameters, and finishes with the discontinuing procedure. Chapter 5; Hemodialysis, single needle treatment

This chapter contains instructions on how to perform hemodialysis with one needle, either using the double pump (if BM 202) or single pump function. The chapter is based on chapter 4 with added specific instructions for single needle treatment. Chapter 6; Isolated UF

This chapter contains instructions on how to perform isolated ultrafiltration. Chapter 7; Profiling

This chapter contains instructions on how to use the profiling function for ultrafiltration, as well as for the dialysis fluid concentration of sodium and bicarbonate. Chapter 8; Hemodiafiltration, low volume

This chapter contains instructions on how to perform low volume hemodiafiltration using the AK 200 S machine. The chapter is based on chapter 4 with added specific instructions for low volume HDF treatment. There is a general section describing the protective system for low volume HDF, instructions for the bolus infusion possibility is also included.

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Chapter 9; BVS - Blood Volume Sensor

This chapter contains instructions on how to use the BVS, which measures changes in the blood volume of the patient continuously during treatment. The chapter begins with a general section where handling, alarm function and graphs are explained, and finishes with On and Off instructions. Chapter 10; BPM - Blood Pressure Monitor

This chapter contains instructions on how to use the BPM (if installed), which measures blood pressure and pulse rate. A particular blood pressure measurement cuff and a cuff hose are to be used. The chapter includes explanations of how the BPM is handled using the BPM button and the BPM screens, and also describes the alarm function. The BPM can be used manually if only one measurement check is to be done, or at set intervals during treatment. Chapter 11; Diascan

This chapter contains instructions on how to use the Diascan function, which measures clearance (K) and dialysis dose (Kt or Kt/V). The chapter is divided into two parts where the first section includes general information about the Diascan function, handling using the Kt/V button, explanation of the Diascan screens, and alarm functions. The second section includes step-by-step instructions for measuring clearance and Kt/V, single or continuous measuring. Chapter 12; Hygiene and maintenance

This chapter contains information and instructions concerning the hygiene and maintenance of the AK 200 S that should be carried out by the operator of the machine. The chapter begins with a general section where a schedule for hygiene and maintenance is included. The Hygiene sections contain general information and instructions on how to perform the disinfection programs. The Maintenance sections include instructions on the maintenance of the flow path and the exterior of the machine. Chapter 13; Technical data and specifications

This chapter contains technical specifications of the control- and supervisory systems of the machine. It also includes physical data; materials which come into with water, concentrates and dialysis fluid; environmental data; and a list of standards which the machine complies with. Chapter 14; Alarm list, Attention alarm list and Technical alarm list

This chapter contains lists of alarms, attention alarms and technical alarms. The alarm list includes additional information and possible causes of parameter button alarms. The attention- and technical alarm lists include additional information concerning the alarms, describing the alarm text more in detail and giving suggestions about measures to take. The attention- and technical alarm lists are shown in alphabetical order.



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Chapter 15; Major changes in operator’s manual

This chapter includes brief information about major changes between the current and previous program versions of the machine that have been made in the manual. The changes mentioned are mostly information concerning the operation of the machine and are specifically addressed to the operator. Note • A small reference number beside the figures in this manual has been added to simplify manual production. Note

Definitions of expressions used in this manual WARNING Is used to alert the /operator not to take a certain action, which if taken can cause a potential hazard and result in a serious adverse reaction, injury or death. A warning may also be used to alert the /operator to take a certain action to avoid the potential hazard as above. WARNING CAUTION Is used to alert the /operator to take a certain action to protect against a potential hazard which, if ignored, could have an adverse effect on the patient or the device. A caution may also be used to alert the /operator not to take a certain action to avoid the potential hazard as above. CAUTION Note • A reminder to the /operator on normal treatment activity and on what is a suitable action in a particular situation. Note

This symbol indicates that it is possible to preset the value of a parameter. This can be done to adapt the settings of the machine to correspond with the routines of the /clinic. It has to be done in service mode by an authorized service technician. All values mentioned in this manual are default values set in the machine when it was manufactured. It is important to check with the service technician if values have been changed, and if so, which ones. For instance, it is possible to preset the machine for which mode to start up in, some alarm limits, some functions and options.

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General precautions before use WARNING Unauthorized modifications, alterations or repair and lack of maintenance or calibration of the AK 200 S may result in malfunctioning or have other serious consequences for the safe operation of the equipment. WARNING CAUTION The AK 200 S may only be operated by persons trained in hemodialysis and who have studied the instructions in this manual. The /operator should draw special attention towards the text valid for the Safety philosophy of the machine. See section "Safety philosophy" in chapter 1. that the first digit of the program version of both the machine and the manual is the same. If the AK 200 S does not perform as described in this manual, it should not be used until the condition is rectified.

When unpacking, check the equipment for any signs of damage. If the equipment is in any way damaged, proper operation can not be assured. Patients connected to the AK 200 S should be monitored by competent medical personnel, learned intermediaries or the like, since life threatening circumstances sometime arise that may not activate alarms. The operator should pay attention to all appropriate alarms and follow the instructions, warnings, cautions, and notes given in this manual. It is imperative that the machine has ed the function check before connecting a patient. During installation all calibration checks must be completed before the machine is used to dialyze a patient. The AK 200 S needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the "Technical data and specifications" chapter in this manual. The use of mobile telephones or communication equipment in the vicinity of the AK 200 S could adversely influence the performance of the machine. For further information, see the "Technical data and specifications" chapter in this manual. The AK 200 S will perform as designed only if it is used and maintained in accordance with Gambro’s instructions. Any warranties made by Gambro with respect to the AK 200 S are void if the equipment is not used in accordance with the instructions provided. Gambro will not accept responsibility for any damage or injury resulting from improper use or maintenance or unauthorized repair. CAUTION → → →



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→ → → CAUTION Preventive inspection, maintenance and calibration of the AK 200 S shall be performed by a fully trained service technician according to the Maintenance Manual in the AK 200 S Service Manual which can be ordered from your Gambro representative. It is mandatory for preventive maintenance to be performed at least every other year. Yearly maintenance is recommended. The interval between preventive maintenance procedures might differ due to operating environment variations.

The AK 200 S dialysis machine is in compliance with certain requirements concerning patient leakage current from the dialysis fluid in accordance with international standards and regulations. When a central venous catheter is used, and the tip of the catheter is close to the heart, it is however necessary to take extra precautions to minimize the risk for arrythmia due to leakage currents. For these treatments it is necessary to connect the potential equalization conductor between the AK 200 S and the potential equalization bus bar in the electrical installation. To minimize the leakage currents from other electrical equipment it is recommended to place such equipment outside the patient area. Any equipment within the patient area shall fulfil the IEC 60601-1 and IEC 60601-1-1 standards and be a part of the potential equalization. One way to minimize the leakage currents from equipment within the patient area is to electrically isolate it. Make sure leakage current values are below respective limit required by CF type applied parts. Check with service technician. If your clinic/hospital use a central venous catheter during treatments please make sure your machine is equipped with a potential equalization connection. If not please your local Gambro Service Technician for further assistance. CAUTION

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Note • This operator’s manual provides instructions necessary for the proper operation of the AK 200 S. It is not a guide for the istration of hemodialysis.

• Machines are not disinfected before delivery. Always perform a chemical disinfection after installation, before initial use.

• When accuracy ranges are written as e.g. ”(±1 ml/min or ±1%)” the widest range is valid.

• During transportation and storage the equipment has to be kept in its original packing. If transportation or storage time is more than 15 weeks the environmental data relating to the operation has to be followed.

• For the qualified technician the AK 200 S Service Manual is available. The Service Manual provides all of the necessary information for installation and safe and required maintenance of the machine.

• It is important that the protective earth in the installation is of high quality.

• For the purpose of protecting the environment the AK 200 S must not be disposed with general domestic waste, but shall be separately collected for dismantling and recovery. Where applicable national regulations shall be applied. Consult your local Gambro distributor for information. Note



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Intended use The Gambro AK 200 S System is designed to be used as a single patient machine to perform hemodialysis treatments upon prescription by a physician. Patient counselling and teaching of treatment techniques are directly under the supervision and discretion of the physician. The AK 200 S System comprises of two monitors; one blood monitor (BM 200 or BM 202) and one fluid monitor (FM 202). The monitors are placed on a mobile stand (MS 200 or MS 202). The blood monitor is designed to control and supervise the extracorporeal blood circuit. Single needle treatment can be performed with one pump (double clamp function) or with two pumps (BM 202 only). To prevent coagulation, anticoagulantia may be istered by means of a heparin pump. The fluid monitor is designed to produce the dialysis fluid at a desired temperature, conductivity and pressure within given specifications, and to supervise the dialysis fluid. Both acetate and bicarbonate treatments can be performed. CAUTION Patient education, counselling, home care follow-up and medical maintenance must be performed under the direction of and supervision by the physician prescribing the treatment. Gambro specifically denies any responsibility for patient education, counselling or home care and medical maintenance.

When AK 200 S is used to produce bicarbonate containing dialysis fluid originating from non-liquid concentrates, the AK 200 S is designed and validated for use with the Gambro BiCart® system. When AK 200 S is used to produce sodium chloride containing dialysis fluid originating from non-liquid concentrates, the AK 200 S is designed and validated for use with the Gambro BiCart Select® system, i.e. the SelectCart® cartridge and SelectBag® concentrate. Gambro does not accept responsibility for use of other non-liquid concentrate containers. CAUTION

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Safety philosophy The AK 200 S is designed according to the current standards for hemodialysis equipment, IEC 60601-2-16. This means that safety under so-called Single Fault Conditions is granted. In practice this means that controllable treatment parameters (i.e. conductivity, temperature and ultrafiltration) are controlled by one system, the control system, and monitored by another completely separate protective system, utilizing its own sensors, electrical circuits and microprocessors. The functionality of the protective system is checked by the AK 200 S before each treatment. A fault detection during the pre-treatment tests will make it impossible to start the treatment. In order to that the corresponding control and protective systems are operating with the correct input values, the is instructed to compare the readings of the current bargraph display and the information display, before connecting the patient. The bargraph displays show the set value, the actual value and the alarm limits for the control system, while the information display shows the corresponding values from the protective system. If these comparisons are not satisfactory, call your service technician. The protective system will, when a parameter (measured by the protective system) is outside the alarm limits, put the AK 200 S into a patient-safe condition. This means that the protective system can stop the blood pump, close the venous clamp, prevent the dialysis fluid from reaching the dialyzer and alert the operator with sound and light. The ultrafiltration control system, the UF-cell, control the ultrafiltration volume with an accuracy corresponding to ± 50 ml x ed treatment time (h) or ±2,5%. If the accumulated UF volume, measured by the UF-cell, differs more than 200 ml from the expected volume the machine issues an attention. In addition to this system there are independent ultrafiltration measuring systems, protective systems, as described below. In AK 200 S an independent ultrafiltration measuring system based on restrictor flow measurement (FRN) is used as protective system for the UF-volume. For further description, see chapter 3. It is automatically checked before each treatment and a failure will make it impossible to start the treatment. The default alarm limit is set to 800 ml. The accuracy of the system is ±120 ml/h. This means that for a four hour treatment the maximum weight deviation without any alarm issued is less than 1280 g (800 + 4 x 120). As an additional precaution it is recommended that competent personnel supervise the patient and that the blood pressure is checked regularly. This protective system can be disabled via a preset. If this is done the remaining supervision is based on the transmembrane pressure, see further below for description of this system.



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As an extra precaution there is also a system for supervision of the UF-rate. This system is available on condition that the FRN system is not disabled. The UF rate supervision is using the FRN system and the measured UF rate is supervised against a limit. This limit constitutes the maximum allowed deviation between the UF rate measured by FRN and the UF rate measured by the UF cell over a period of 2 minutes. The default limit is set to 5 ml/min. The accuracy of the system is ± 2 ml/min. If this limit, i.e. 5 ml/min, is violated the system initiates a taration of the UF measuring system. If the limit is violated more than four times during 30 minutes, the machine terminates the treatment and a technical error is issued. In addition, an independent ultrafiltration measuring system based on the transmembrane pressure is used as protective system. Alarm limits for TMP related to the dialyzer UF coefficient and the expected UF rate, are to be set around the actual TMP value when starting treatment. The TMP alarm limit correspond to a UF-deviation limit described by TMPAlarm limit x UFcoefficient. Example: If the alarm window is set to ±50 mmHg and the UF-coefficient is 10 ml/mmHg x h the maximum weight deviations without any alarm is ±500 g/h. Default the alarm window is set to ±100 mmHg. It is essential to ensure that the alarm window is set as close as possible to the working TMP. As an additional precaution it is recommended that competent personnel supervise the patient and that the blood pressure is checked regularly. The composition of the dialysis fluid is supervised by the protective system using an independent conductivity measuring system. The dialysis fluid conductivity and temperature systems are automatically checked before each treatment. A failure will make it impossible to start the treatment. To protect the patient against a hazardous blood loss to the environment the AK 200 S incorporates a venous pressure monitoring system. This system will react upon a change in the venous pressure, i.e when the pressure falls below the low alarm limit. It must be observed that under certain pressure/flow conditions a blood loss to the environment may not be able to cause the venous pressure to fall below the low alarm limit. To avoid blood loss to the environment it is essential to ensure that all connections in the extracorporeal blood circuit are tight and secured, that the fistula needle is correctly positioned and secured and that the low alarm limit is set as close as possible to the working venous pressure. A visual monitoring by the /operator is recommended. The venous, arterial and system pressure measuring system is checked automatically at positive, atmospheric and negative pressure before each treatment. A failure will make it impossible to start the treatment. The supervision of the stop time of the blood pump is the protection system against patient blood loss due to coagulation during treatment. The operator will be notified via an attention alarm that the blood pump stop time has been exceeded.

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The blood leak detector system, which utilizes an optical sensor, is automatically tested before each treatment for being able to detect transparency (no blood) and non-transparency (blood). If the system cannot detect these states, it is impossible to start the treatment. Furthermore, the system is checked every 5 minutes to ensure that it is able to detect non-transparency. If not, the system will act as if a blood leak alarm has occurred and enter a patient safe condition. The air detector utilizes an ultrasonic sensing system in which the transmitter is handled by one microprocessor and the receiver by another. The system is continuously tested for being able to detect an air leakage condition. If this test is not successful the system will act as if an air detection has occurred and the machine will enter a patient safe condition. If the AK 200 S is used to perform Hemodiafiltration, low volume, an independent substitution flow supervision system is used as protective system. It is based on restrictor measuring as well as pump speed measuring. For the restrictor measuring it is essential that a correct infusion line is used to obtain specified level of safety. For a more detailed information, please refer to the AK 200 S Service Manual.



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The preparation of dialysis fluid Inlet water requirements The chemical and microbiological quality of the water used to prepare fluids for dialysis is an important factor for achieving and maintaining the proper quality of the dialysis fluid. The quality of the water depends on the technical equipment for water treatment. Further, proper maintenance of the water treatment system and of the water distribution loop is essential. The inlet water must comply with valid standards for water for dialysis; see chapter “Technical data and specifications/Water supply” in this manual for more details.

Preparation of the dialysis fluid The AK 200 S prepares dialysis fluid from inlet water and concentrates. The dialysis fluid should be made from dry concentrates (such as the BiCart Select® products) or from an acidic (A) concentrate and a dry bicarbonate concentrate (such as the BiCart® cartridge). It can also be made from an acidic (A) concentrate and a liquid bicarbonate (B) concentrate or from an acetate concentrate. See “List of concentrates” in this chapter.

UFD- Ultrafiltered Dialysis Fluid (option) The AK 200 S can be equipped with a holder in which an ultrafilter can be mounted. The ultrafilter purifies the dialysis fluid from possible contamination by bacteria and endotoxins.

Ultrafilters; frequency of change The ultrafilter used in Ultrafiltered Dialysis Fluid kit is to be changed regularly depending on the primary fluid quality and the desired final fluid quality. The results from microbiological controls have to determine the frequency of change. A frequency between once a month and once every three months can be expected. For instructions on how to change the ultrafilter, see "Ultrafilter; how to change" in chapter 12.

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List of concentrates, accessories and disposables, for use with the AK 200 S This manual contains a number of references to concentrates, accessories and disposables for use with the AK 200 S. For ease of reference, set out below is a comprehensive listing of such concentrates, accessories and disposables as follows:

Concentrates Liquid concentrates

Area of use

001-099 series 6xx series

Liquid acetate concentrates for preparation of acetate dialysis fluid.

2xx series 7xx series 8xx series

Liquid A-concentrate for preparation of bicarbonate dialysis fluid together with BiCart or with bicarbonate hemodialysis concentrate D 200 (Sodium bicarbonate 8,4 %).

3xx series

Liquid A and B concentrates for preparation of bicarbonate dialysis fluid.

SelectBag® series

Liquid A-concentrate for preparation of bicarbonate dialysis fluid together with SelectCart and BiCart.

Non-liquid concentrates

Area of use

BiCart®

Dry bicarbonate concentrate for preparation of bicarbonate dialysis fluid together with proper liquid A-concentrate or SelectCart and SelectBag.

SelectCart ®

Dry sodium chloride concentrate for preparation of bicarbonate dialysis fluid together with SelectBag and BiCart.

CAUTION Incorrect choice of dialysis fluid concentrate may cause incorrect composition of the dialysis fluid. CAUTION



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Lines Line number

Area of use

Gambro Medical Line (PVC+DOP/ EtO sterilized) BL 10 series BL 100 series AV 100 series A 5000 series V 5000 series

Arterial and venous blood line set. Arterial and venous blood line set. Arterial and venous blood line set. Arterial blood lines. Venous blood lines.

When performing low volume HDF, the venous blood line has to be equipped with a T/Y-connector.

Gambro Blood Tubing System (PVC+DOA/Beta sterilized) BL 200 series

Arterial and venous blood line set. The arterial blood line has a cuvette when BVS is to be used.

When performing low volume HDF, the venous blood line has to be equipped with a T/Y-connector.

Gambro Accessories C series

Hemodialysis accessories.

C 705

A connection line with an expansion chamber. Used in single needle/single pump mode.

C 200 HDF+EC

Infusion line used in low volume HDF.

Dialyzers/Ultrafilter

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Dialyzer/Ultrafilter

Area of use

U 8000 S

Ultrafilter used in Ultra Filtered Dialysis Fluid kit.

Dialyzers

Most types of dialyzers, except plate dialyzers, can be used. However, it is essential to that the specifications and instructions for use of the dialyzers are not in discrepancy with those given for AK 200 S, with regards to e.g. the recommended priming procedure. The connectors and the ports of the dialyzer must comply with ISO 8637 and EN 1283.



Infusion fluid for low volume HDF Infusion solution

Area of use

Hemofiltrasol 2x serie

Infusion fluid used for low volume hemodiafiltration.

Blood pressure measurement accessories Gambro Cuff

Area of use

Standard No. Standard No. Standard No. Standard No.

for 12 - 18 cm arm circumference. for 17 - 23 cm arm circumference. for 23 - 33 cm arm circumference. for 31 - 40 cm arm circumference.

1 (7 cm) 2 (9 cm) 3 (12 cm) 4 (14 cm)

Latex free Child Latex free Adult Latex free Large

for 18 - 26 cm arm circumference. for 25 - 35 cm arm circumference. for 33 - 47 cm arm circumference.

Single hand Child Single hand Adult Single hand Large

for 17 - 22 cm arm circumference. for 22 - 32 cm arm circumference. for 32 - 42 cm arm circumference.

Gambro Cuff hose 3,5 m

Cuff hose used for measuring blood pressure together with the AK 200 S.

CAUTION The AK 200 S has been tested and validated for use with the concentrates, accessories and disposables specified above.

Gambro does not accept any responsibility or liability for use of concentrates, accessories or disposables other than those specified above. Depending on the circumstances, use of concentrates, accessories or disposables other than those specified above may also reduce Gambro’s warranties for the AK 200 S. CAUTION Note • The should make sure to have a current listing of concentrates, accessories and disposables available.

• The should follow the facility procedures for proper disposal of used blood lines, dialyzers and other disposables per local regulations. Note



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List of symbols Note • All symbols in this list may not be represented on this product. Note

Symbol

Description

Alternating current

Protective earth (ground)

Warning, consult accompanying documents

Off (power, disconnection from the mains)

On (power, connection to the mains)

Type B, applied part

Handle with care

This way up

Keep dry

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Symbol

Description

Input /Output

Year of manufacturing

Heater power supply outlet

Conforms to requirements in EC Council Directive 93/42/EEC concerning medical devices. 0086 identifies BSI, British Standards Institution, as Notified Body.

CSA approved for Canada

CSA approved for Canada and USA

CSA-listed label manufacturer

Prohibited behaviour

Equipotentiality

Separate collection for electrical and electronic equipment



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CE-marking This product is CE-marked in accordance with the requirements in EC Council Directive 93/42/EEC of 14 June 1993 concerning medical devices and is classified as IIb equipment. Notified body is: British Standards Institution (BSI) with the notified body number 0086. The CE-marking of this manual is only valid if the device which it describes is CE-marked.

Manufacturer Gambro Lundia AB, Monitor Division, Box 10101, SE-220 10 LUND, Sweden. Phone +46 46 169000. Copyright

© 2001-2003, 2005 Gambro Lundia AB

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Chapter 2 Description - the machine and its components Blood monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:2 BM 200 - Single Pump, BM 202 - Double Pump . . . . . . . . . . . . . . . . . 2:2 Fluid monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:4 FM 202 - Acetate and Bicarbonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:4 Rear of the machine - without options . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:6 Rear of the machine - options included . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:8 Monitor stand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2:10 MS 200: Adjustable height: five fixed positions . . . . . . . . . . . . . . . . . . 2:10 MS 202: Electrically adjustable height . . . . . . . . . . . . . . . . . . . . . . . . . 2:12


AK 200 S Operator’s manual - Description

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Blood monitor BM 200 - Single Pump, BM 202 - Double Pump

Figure 2:1

Blood monitor

1. Top tray To protect the machine against leakage the top tray must always be placed on top of the machine. 2. Air detector The air detector head is designed for a drip chamber with a diameter of 22 mm. The ultrasonic air detector will detect air or foam in the venous drip chamber. 3. Venous pressure transducer connector 4. Arterial pressure transducer connector 5. BVS - Blood Volume Sensor An arterial blood line with a cuvette is required. 6. Arterial blood pump The blood pump will stop if the pump cover is opened. During a power failure the pump can be manually operated by use of the pump handle. It is only possible to turn the arterial blood pump in an anticlockwise direction. 2:2



7. Heparin pump The heparin pump can be programmed for different syringe sizes . Syringes shall comply with ISO 7886 - 2. Upon delivery the machine is programmed for a 30 ml Becton Dickinson syringe with a length of 81,0 mm . Syringes of other volumes and brands can be programmed. 8. Arterial line guide 9. Priming detector The priming detector detects if there is blood in the venous blood line. Before the priming detector detects blood certain alarms are suppressed to facilitate the priming. Treatment time and accumulation of values will start when blood has been detected. The treatment time will continue to count down as long as blood is detected. 10. Arterial and venous line clamps The clamps close the arterial and venous lines in certain alarm situations. The clamps are also used when performing single needle dialysis. 11. Level adjustment buttons The level in the venous drip chamber is adjusted by pressing ↑ or ↓ in the right (blue) area. The level in the expansion chamber connected to the system pressure transducer connector may be adjusted by pressing ↑or ↓ in the left (gray) area. When pressed and hold, the level adjustment buttons are active for maximum 6 seconds at a time. After this, the buttons need to be pressed again to further adjust the level. 12. System pressure transducer connector The system pressure transducer can be used for: - Predialyzer (post pump) pressure - System pressure in Single needle double pump - Flow supervision in HDF treatment 13. Venous blood pump/infusion pump (BM 202 only) The pump can be used as venous blood pump in hemodialysis single needle double pump. In low volume hemodiafiltration the pump is used as infusion pump for substitution fluid. The pump will stop if the pump cover is opened. During a power failure the pump can be manually operated by use of the pump handle. It is only possible to turn the venous blood pump/infusion pump in a clockwise direction. 14. Expansion chamber holder 15. Operator’s



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Fluid monitor FM 202 - Acetate and Bicarbonate

Figure 2:2

Fluid monitor

1. Disinfection ports for concentrate pick-up tubes 2. B pick-up tube marked blue-white The B pick-up tube is used for intake of: - Bicarbonate concentrate - Acetate concentrate - Concentrated or diluted disinfectants 3. A pick-up tube marked red The A pick-up tube is used for intake of acidic concentrate. 4. Dialysis fluid outlet (to dialyzer) 5. Dialysis fluid inlet (from dialyzer) 6. Safety coupling 7. Turnable dialyzer holder arm 8. Blood leak detector

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9. SelectBag holder The machine is designed for use with the Gambro SelectBag®, a bag containing electrolytes (except sodium chloride). 10. SelectCart holder The machine is designed for use with the Gambro SelectCart®, a cartridge containing dry sodium chloride. 11. BiCart holder The machine is designed to be used with Gambro’s BiCart® System, a cartridge containing dry bicarbonate powder. During disinfection mode, also used as a holder for CleanCart-C or CleanCart-A, cartridges containing a cleaning agent.



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Rear of the machine - without options

Figure 2:3

Rear of the machine - without options

1. BPM (Blood Pressure Monitor) connection The line to the optional blood pressure cuff is connected to the nipple. 2. Potential equalization connection This connection is used for the potential equalization conductor. When a central venous catheter is used, the conductor must be connected to minimize the risk of electric shock. The connection is marked with the symbol for equipotentiality (see “List of symbols” in this manual). 3. Relay interface connection, marked yellow 4. GSS / PC connection, marked black 5. Optional connection, marked grey 2:6



6. UF calibration unit connection, marked blue 7. Mains supply inlet 8. Main switch 9. Fuses 10. Power supply unit 11. Halt button When the button is pressed the power supply to the AK 200 S is interrupted. As soon as the button is released the power returns and the machine performs a recovery. 12. Charging indicator 13. Drain outlet - from the machine 14. Water inlet 15. Heating vessel overflow



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Rear of the machine - options included

Figure 2:4

Rear of the machine, options included

1. BPM (Blood Pressure Monitor) connection The line to the optional blood pressure cuff is connected to the nipple. 2. Potential equalization connection This connection is used for the potential equalization conductor. When a central venous catheter is used, the conductor must be connected to minimize the risk of electric shock. The connection is marked with the symbol for equipotentiality (see “List of symbols” in this manual). 3. Relay interface connection, marked yellow 4. GSS / PC connection, marked black 5. Optional connection, marked grey 2:8



6. UF calibration unit connection, marked blue 7. Mains supply inlet 8. Main switch 9. Fuses 10. Power supply unit 11. Halt button When the button is pressed the power supply to the AK 200 S is interrupted. As soon as the button is released the power returns and the machine performs a recovery. 12. Dialysis fluid filter (option) 13. Latch for filter change (option) 14. Drain air gap (option) 15. Charging indicator 16. Water inlet 17. Heating vessel overflow 18. Drain outlet - from the machine 19. Air gap (option) 20. Holder for the blood pressure measurement cuff (option)



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Monitor stand MS 200: Adjustable height: five fixed positions

Figure 2:5

Monitor stand, five fixed positions

1. Infusion pole The maximum allowed load is 10 kg. 2. Height adjustment for infusion pole 3. Rear handle 4. Bars, lifting positions Positions where the AK 200 S is safely lifted, both on the right and left hand side of the machine. 2:10



5. Screws For locking the handle (service frame). 6. Screws (rear side) For height adjustment in five fixed positions. 7. Tray for concentrate containers 8. Lockable wheels The wheels must be locked during treatment. During internal transportation the AK 200 S must be in upright position.



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MS 202: Electrically adjustable height

Figure 2:6

Monitor stand, electrically adjustable

1. Infusion pole The maximum allowed load is 10 kg. 2. Height adjustment for infusion pole 3. Rear handle 4. Bars, lifting positions Positions where the AK 200 S is safely lifted, both on the right and left hand side of the machine. 5. Screws For locking the handle (service frame). 2:12



6. Control for height adjustment 7. Power supply cord For height adjustable stand only. 8. Tray for concentrate containers 9. Lockable wheels The wheels must be locked during treatment. During internal transportation the AK 200 S must be in upright position.



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Chapter 3 Controlling the machine - general guidelines Operator’s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hygiene group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Mode group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Concentrate stand-by mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Procedure for manual activation . . . . . . . . . . . . . . . . . . . . . . . . . . . Resume fluid preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Therapy group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Treatment overview group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Bargraph display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Flow diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Time display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Parameter buttons and their displays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Reset possibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarm indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarm function of the parameter buttons . . . . . . . . . . . . . . . . . . . . . . . Override possibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Stand-by group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Display and setting group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Information display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Treatment overview screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Parameters shown on Treatment overview screen . . . . . . . . . . . . . . . . Function check overview screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Tests shown on Function check overview screen . . . . . . . . . . . . . . . . . The eight commandments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Setting of parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ing treatment parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The ultrafiltration control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Protective system for ultrafiltration . . . . . . . . . . . . . . . . . . . . . . . . . . . Power failure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Returning the blood during a power failure . . . . . . . . . . . . . . . . . . . . . Battery back-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Recovery from a short power failure . . . . . . . . . . . . . . . . . . . . . . . . . . Recirculation during treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Reconnection of the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Change of blood pump segment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BiCart/SelectCart change during treatment . . . . . . . . . . . . . . . . . . . . . . . .


AK 200 S Operator’s manual - Controlling

3:2 3:4 3:5 3:6 3:7 3:7 3:9 3:10 3:10 3:10 3:11 3:12 3:16 3:17 3:17 3:18 3:20 3:22 3:23 3:23 3:24 3:25 3:26 3:27 3:28 3:29 3:32 3:33 3:34 3:35 3:38 3:38 3:38 3:39 3:40 3:40 3:42 3:43

3:1

Operator’s Both the blood monitor and the fluid monitor are controlled and supervised from the operator’s . The consists of a number of buttons, bargraph displays, flow paths, a time display, an information display, a blood flow knob and one set knob. The is divided into six logical groups: 1. Hygiene group

These buttons are used to select machine modes mainly related to disinfection, rinsing and draining of the fluid monitor. 2. Mode group

The buttons in this group are used to select different treatment modes. 3. Therapy group

These buttons are used to initiate priming, select heparin data and special treatment therapies. 4. Treatment overview group

This group graphically shows the status of the treatment and allows for a complete overview of all important treatment parameters. 4.1. Bargraph display 4.2. Flow diagram 4.3. Time display 5. Stand-by group

These buttons can be used for direct control and stand-by of certain functions. 6. Display and setting group

The four buttons and the set knob are used for setting of all parameters except the blood flow. The flow is always directly controlled with the blood flow knob. The information is shown on the information display. 6.1. Information display 6.2. Blood flow knob 6.3. Set knob

3:2



6.3 6.2

6

6.1

5

4.3

4

4.2

3 HCEN9751 Revision.12.2005 Program version 8.xx

EN1034

2

AK 200 S

4

4.1

1 Figure 3:1

Operator’s AK 200 S Operator’s manual - Controlling

3:3

Hygiene group The ON/OFF button is used to switch the machine on and off. (The main switch on the back of the machine should always be in the ON position even when the machine is not in use). It is only possible to turn the machine off when time is 0.00 and no blood is detected by the priming detector. The Chem disinf button is used to select chemical disinfection mode. The AK 200 S can be turned off by pressing the ON/OFF button, as soon as the fill phase is completed. The Heat disinf button is used to select heat disinfection mode (heat disinfection alone or in combination with a citric acid or CleanCart disinfection). The Rinse/Drain button is used to select rinsing (rinsing alone or in combination with CleanCart) and draining mode. Rinse/drain, heat disinfection and chemical disinfection cannot be selected during treatment. The Auto Heat button is used to activate the possibility to start a Heat disinfection program at a predetermined time. See "Automatic start of Heat disinfection program" in chapter 12. The Auto Rinse button is used to activate the possibility to start a Rinse/Drain program at a predetermined time. See "Automatic start of Rinse/Drain program" in chapter 12. Note • The above mentioned buttons must be pressed for at least 3 seconds in order to activate/deactivate the functions. Note

3:4



Mode group The Isol UF button is used to select isolated ultrafiltration (sequential dialysis).

The SN button is used to select single needle treatment. Single needle treatment can be performed with one blood pump or with two blood pumps (BM 202 only). Function not available.

The Acetate button is used to select acetate treatment and type of concentrate . The lit Acetate button can be pressed twice in order to activate Concentrate stand-by mode after the machine has ed the function check and the by path on the flow diagram has lit up green (this cannot be done if blood has been detected). This means that the machine enters a stand-by mode where the consumption of concentrates will be stopped. For further information see “Concentrate stand-by mode” further on in this section. The Volume control button lights up to show that the machine runs with controlled ultrafiltration.

The Bicarbonate button is used to select bicarbonate treatment and type of concentrate . The lit Bicarbonate button can be pressed twice in order to activate Concentrate stand-by mode after the machine has ed the function check and the by path on the flow diagram has lit up green (this cannot be done if blood has been detected). This means that the machine enters a stand-by mode where the consumption of concentrates will be stopped. For further information see “Concentrate stand-by mode” further on in this section. The lit Bicarbonate button is also to be pressed twice in order to drain remaining fluid from the SelectBag, the SelectCart cartridge and the BiCart cartridge when treatment has been discontinued. See “Discontinuing” in corresponding chapter for the treatment mode performed. Note • The above mentioned buttons must be pressed for at least 3 seconds in order to activate/deactivate the functions. Note



3:5

Concentrate stand-by mode When the machine has been switched on, has ed the function check with proper concentrates connected, and the by path on the flow diagram lights up green, it is possible for the machine to enter a stand-by mode where the consumption of concentrates will be stopped. This stand-by mode, called Concentrate stand-by mode, can be activated before or after the flashing Fluid by button has been pressed during priming i.e. before or after the priming of the fluid compartment of the dialyzer has been performed. (It cannot be activated if blood has been detected.) Concentrate stand-by mode can be manually activated by twice pressing the Bicarbonate or Acetate button (default function) or automatically be activated by preset. On request from the clinic, an authorized technician can preset the type of presets for Concentrate stand-by mode that best suits the routine procedures of the specific clinic. There are two presets that can be used, separately or in combination: 1. Automatic activation of Concentrate stand-by mode when time is shown on the time display and the by path of the flow diagram lights up green. The time for activation may be straight away when the by path lights up green, or for a preset amount of time after. 2. The time for automatic activation can also be preset to be when the attention alarm PRIMING VOLUME ACHIEVED Check line in priming detector appears during priming. When the Concentrate stand-by mode is active, the Bicarbonate or Acetate button will be flashing and there will be a conductivity alarm without buzzer to indicate this. When Concentrate stand-by mode is active, the fluid flow is automatically decreased to 100 ml/min to minimize the water consumption.

3:6



Procedure for manual activation Press the lit Bicarbonate (or Acetate button) twice and this screen will be shown on the information display:

Figure 3:2

Concentrate stand-by mode, activation

Press the lit Arrow button to activate Concentrate stand-by mode. When the mode has been activated, the text will change and be replaced by CONCENTRATE STANDBY MODE ACTIVE. At the same time the Bicarbonate or Acetate button will start to flash and there will be a conductivity alarm without buzzer. This will continue during the period of time when the Concentrate stand-by mode is active.

Resume fluid preparation The dialysis fluid preparation will resume (Concentrate stand-by mode deactivated) when the flashing Bicarbonateor Acetate button is pressed once. The dialysis fluid will be ready within approximately 3 minutes. If dialysis fluid preparation has not been resumed during priming, it will automatically be resumed when blood is detected in the priming detector after treatment start. Dialysis fluid preparation will also automatically be resumed when Concentrate stand-by mode has been active for more than one hour.



3:7


3:8



Therapy group The Priming button is used to activate priming mode.

The Heparin button is used to select heparinization with the heparin pump.

The Profiling button is used to select automatic variation of sodium, bicarbonate and ultrafiltration rate.

The HDF button is used to select low volume hemodiafiltration mode and set infusion parameters. Note • The above mentioned buttons must be pressed for at least 3 seconds in order to activate/deactivate the functions. Note

The Fluid flow button is used to select dialysis fluid flow.



3:9

Treatment overview group Bargraph display The bargraph displays shows values from the control system in the machine. There are bargraphs attached to values for venous pressure, arterial pressure, blood flow, temperature, conductivity, TMP, UF volume and UF rate. For further information, see corresponding button below “Parameter buttons and their displays” in this chapter. The viewing angle of the bargraph displays can be adjusted as follows: Press the middle Arrow button below the unlit information display and keep pressed down while adjusting the viewing angle using the Set knob. When the angle has been adjusted, release the Arrow button.

Flow diagram The flow diagram shows the status of the blood flow and the dialysis fluid flow. 1-2 Blood path The blood path lights up when the priming detector detects blood. When blood has been detected for 20 seconds the blood path will remain lit until the treatment is discontinued. 3-4-6-7 Dialyzer path The dialyzer path is lit when dialysis fluid es through the dialyzer. 3-5-7 By path The by path is lit when the dialysis fluid manually or automatically by the dialyzer. The machine will automatically by the dialyzer during certain alarm conditions and during self-calibration. 6 Ultrafiltration path The ultrafiltration path is lit during isolated UF and during fluid by.

Figure 3:3

3:10

Flow diagram



The flow diagram can be lit in different colours: 1-2 lights off during priming. 1-2 is red when the priming detector detects blood. 3-4-6-7 is green when dialysis fluid is correct and es through the dialyzer. 3-5-7 is green when dialysis fluid is correct but the machine performs a self-calibration. 3-5-7 is green and 6 is yellow during isolated UF or when the dialysis fluid is byed manually. 3-5-7 is orange and 6 is yellow when dialysis fluid is incorrect (could be wrong conductivity or temperature).

Time display During function check the time display shows FCH/Fch. During treatment it shows the remaining treatment time. During disinfection programs it shows estimated remaining time for the ongoing program.



3:11

Parameter buttons and their displays Bargraph display

Information display

Explanation

Yellow bar Red bars

VEN PRES LOW HIGH

Actual value Alarm limits

Double needle mode SET Green bar BL FLOW Yellow bar ACC VOL SEGMENT Single needle/single pump mode ART FL Green bar MEAN FL Yellow bar ACC VOL SEGMENT

Set value Actual value Accumulated volume Blood pump segment diameter

Set arterial blood flow Actual mean blood flow Accumulated volume of blood treated Blood pump segment diameter

Single needle/double pump mode (only valid for HD) MFL SET Green bar Set mean blood flow Yellow bar Actual mean blood MFL/ACC flow/Accumulated volume of blood treated Red bar Low alarm limit for actual blood flow VEN Venous blood flow ART Arterial blood flow Single needle/single pump mode STROKE VEN TME ART TME PRESSURE

Actual stroke volume Time for venous phase Time for arterial phase Actual system pressure

Single needle/double pump mode (only valid for HD) STROKE Actual stroke volume SET Set stroke volume PRESSURE Actual system pressure HIGH High limit for system pressure

3:12



Bargraph display

Information display

Explanation

Green bar Yellow bar Red bars

SET TEMP LOW HIGH

Set value Actual value Alarm limits

SET Na+ COND

Calculated conductivity value Set value Actual value Alarm limits Temporarily extended alarm limits Actual pH value (optional)

Acetate mode Green bar Yellow bar Red bars Flashing red bars

(pH) Bicarbonate mode Green bar

(pH)

Calculated conductivity value Set value Actual value Alarm limits Temporarily extended alarm limits Actual pH value (optional)

Yellow bar Red bars

ART PRES LOW HIGH


Yellow bar Red bars

TMP LOW HIGH


Yellow bar Red bars Flashing red bars

SET Na+ HCO3COND

Clinic automation See "ing treatment parameters" in this chapter for instructions.

..... ...... .......

Green bar Yellow bar

SET UF VOL CALC UFR


Set UF volume (patient weight loss) Accumulated UF volume (patient weight loss) Calculated UF rate


3:13

Bargraph display

Information display

Explanation

If pressed twice (not valid if the function is removed by preset) SUPERV UF supervision measured accumulated UF volume LOW Lower level for UF supervision alarm LIMIT Settable alarm limit for UF supervision HIGH Upper level for UF supervision alarm

Green bar

SET

Yellow bar

UF RATE PRIMING MIN UFR

Red bar Low volume HDF SET Green bar Yellow bar

UF RATE PRIMING TOTAL MIN UFR

Red bar

SET ACC STOP LIM

3:14

Calculated set UF rate (patient weight loss/h) Actual UF rate (patient weight loss/h) Priming UF rate (displayed during priming) Minimum UF rate during treatment UF rate limit

Calculated set UF rate (patient weight loss/h) Actual UF rate (patient weight loss/h) Priming UF rate (displayed during priming) Actual total UF rate (filtrate flow rate/h, displayed during treatment) Minimum UF rate during treatment UF rate limit

Heparin set value Accumulated volume Stop limit



Bargraph display

Information display

Explanation

No display. When the function check of the blood monitor is completed, the button is flashing. The button has to be pressed to activate priming mode, the button lights up. The light will go off when the priming detector has detected blood. NOTE: The dialysis fluid tubings must remain connected to the safety coupling during the complete function check. Profiling capability of Na+, HCO3and UF (see chapter 7).

Low volume HDF INFUSION PRIMING BOLUS SET PRIMING BOLUS

DIA FLOW ACC VOL SET HIGH

REMAIN ED NON DIFF


Accumulated infusion volume Accumulated priming volume (displayed during priming) Accumulated extra infusion volume (displayed during treatment) Set total infusion volume Set priming volume (displayed during priming) Set extra infusion volume (displayed during treatment)

Actual Dialysis fluid flow Accumulated Dialysis fluid flow Set value Max set value The TIME-display always shows the REMAINING time (h.min) Remaining treatment time ed treatment time ed treatment time without diffusion


3:15

Bargraph display

Information display

Explanation

The BPM measures blood pressure and pulse rate. See the BPM chapter for activation and settings.

The BVS measures relative blood volume. See the BVS chapter for activation and settings.

The Diascan measures clearance, Kt and Kt/V. See the Diascan chapter for activation and settings.

Reset possibilities The accumulated values for Blood flow, Time, UF volume, UF volume supervision, Dialysis fluid flow, Heparin as well as Infusion volume together with priming and bolus volumes can be reset to 0 by pressing the Time button for 15 seconds when no blood is detected. Note that the remaining time as well as the ed treatment time and treatment time without diffusion will be reset to 0.

3:16



Alarms Alarm indicators The alarm indicators will light up in certain alarm situations. The Mute button will flash and the buzzer will sound. By pressing a lit alarm indicator it is possible to obtain further information on the information display.

Air detector alarm Steady light indicates that air is detected in the venous drip chamber. A flashing button indicates that the fault has been rectified. In order to reset the alarm, the button must be pressed. See "Alarm list" in chapter 14 of this manual.

BVS Steady light indicates that the blood volume has decreased below the set alarm limit. Press the BVS button followed by the left Arrow button, turn the Set knob in order to change the alarm limit.

Attention alarm Steady light indicates that attention from the operator is required. The button has to be pressed in order to get further information or instructions on the information display. A small arrow in the right corner of the information display indicates more than one attention. The next attention will be displayed when the button is pressed again.

Technical alarm Flashing light indicates that there is a technical fault. Press the button for further information. If necessary call for your service technician. A small arrow in the right corner of the information display indicates more information. The next information will be displayed when the right Arrow button (HIGH) is pressed.

Blood leak alarm Steady light indicates that blood has been detected in the dialysis fluid after the dialyzer. A flashing button indicates that the fault has been rectified. In order to reset the alarm, the button must be pressed.

pH alarm (option) Steady light indicates that the pH of the dialysis fluid/substitution fluid is outside the limits. The alarm limits can be changed in alarm situations.



3:17

Alarm function of the parameter buttons Certain parameter buttons also serve as alarm indicators for the corresponding parameters. The parameter button/alarm indicator will light up in alarm situations. In addition, the Mute button blinks and the buzzer sounds.

Venous pressure alarm Steady light The venous pressure is outside the set limits.

Centralizing alarm Flashing light The venous pressure limits are too wide, or the low venous pressure alarm limit is below +10 mmHg.

Blood flow rate alarm (single needle/double pump mode only) Steady light The actual mean blood flow rate is too low, default: 70% of set value

.

Temperature alarm Steady light The temperature of the dialysis fluid is outside the set limits.

Conductivity alarm Steady light The conductivity of the dialysis fluid is outside the limits.

Arterial pressure alarm Steady light The arterial pressure is outside the set limits.

Centralizing alarm Flashing light The arterial pressure limits are too wide.

Transmembrane pressure alarm Steady light The transmembrane pressure is outside the set limits.

Centralizing alarm Flashing light The transmembrane pressure limits are too wide.

UF volume alarm Steady light The UF volume is outside its limits, see attention list chapter 14.

3:18



Time attention alarm Flashing light The treatment time has expired.

BPM attention alarm Flashing light. See attention message.

Diascan attention alarm Flashing light. See attention message.



3:19

Override possibilities It is possible to override (by) the alarm actions for low venous pressure, arterial pressure, air detector and blood leak alarms for a limited amount of time . The purpose of the override option is to facilitate the handling of the machine in alarm situations. Activate the override function by pressing the lit alarm indicator for 3 seconds. It is possible to override the alarm actions for more than one alarm at the same time, in this case, press each alarm indicator separately. The buzzer will still sound during the override time but can be silenced by the Mute button being pressed. If the cause of the alarm has not been corrected within the override time, the alarm actions will automatically recur. For information concerning machine alarm actions for each alarm, see Alarm list in chapter 14. Arterial pressure alarm override

Press the lit Arterial pressure button for 3 seconds; the blood pump will now run with the set blood flow rate and the venous clamp will be open. This will continue for 15 seconds . If necessary, it is always possible to stop the blood pump by pressing the Blood pump button. When the override time has ed and if the alarm is still active, the arterial pressure alarm actions will automatically recur. Low venous pressure alarm override

Press the lit Venous pressure button for 3 seconds; the blood pump will now run with the set blood flow rate and the venous clamp will be open. This will continue for 15 seconds . If necessary, it is always possible to stop the blood pump by pressing the Blood pump button. When the override time has ed and if the alarm is still active, the low venous pressure alarm actions will automatically recur. Air detector alarm override

Press the lit Air detect button for 3 seconds; the blood pump will now run at 100 ml/min (in single needle/double pump mode, the venous pump will run at approximately 100 ml/min) and the venous clamp will continue to be closed. Adjust the level in the venous drip chamber by using the level adjustment buttons while the blood pump is running. If a low venous pressure alarm is simultaneously present, the blood pump will still be running. The blood pump will run for 15 seconds . If necessary, it is always possible to stop the blood pump by pressing the Blood pump button. When the override time has ed, the air detector alarm actions will automatically recur. When the fault has been rectified, the flashing Air detect button must be pressed in order to reset the alarm. Note • The blood flow rate has automatically been decreased when the air detector alarm override was activated. to adjust this to the proper value for the ongoing treatment. Note

3:20



Blood leak alarm override

Press the lit Blood leak button for 3 seconds; the blood pump will now run with the set blood flow rate and the venous and arterial clamps will be open. The dialysis fluid will not be byed, the UF rate will be set to minimum UF rate. This will continue for 15 seconds . If necessary, it is always possible to stop the blood pump by pressing the Blood pump button. When the override time has ed, the blood leak alarm actions will automatically recur. When the fault has been rectified, the flashing Blood leak button must be pressed in order to reset the alarm. WARNING When entering an override mode it is essential to that the machine does not monitor that specific parameter. The operator is responsible for the monitoring during the override time. WARNING



3:21

Stand-by group The Blood pump button is used to start and stop the blood pump at the selected flow rate. The button can show a constant light, a flashing light or no light at all. Constant light - the blood pump is activated. Flashing light - the blood pump is stopped and the selected blood flow rate is more than 0 ml/min. Light off - the blood pump is stopped and the selected blood flow rate is 0 ml/min or priming has not been activated. When the blood pump is stopped the venous clamp automatically closes. Pressing the Blood pump button during treatment will automatically widen the venous pressure, arterial pressure and TMP alarm windows (flashing buttons). To centralize the alarm limits around the actual values, press the respective flashing button (see chapter 4). The maximum permitted stop time for the blood pump during treatment is 3 minutes . When this time has expired an attention alarm will be activated instructing the operator to restart the pump. Note • Emergency - Stop The blood pump can in all situations be manually stopped by pressing the Blood pump button and the venous clamp closes. Note

The Mute button is used to silence the buzzer for varying times depending on the alarm. The mute times for the different alarms are shown in the alarm and the attention lists (see chapter 14). There are two buzzer sounds: •

Soft: for attention alarms: – – – – – – – – – –

•

Continuous: for all other alarms: –––––––––––

The Fluid by button is used to manually by the dialysis fluid from the dialyzer. If the button is pressed when the dialysis fluid has the desired temperature and conductivity the button will flash. When the Fluid by button has flashed for 5 min. during treatment an attention alarm will be activated. The Start UF Stop button is used to start and stop ultrafiltration. When the priming detector has detected blood, the treatment time will start counting down and the following parameters will start to accumulate: treated blood volume, heparin volume, ed treatment time, and UF volume. The ultrafiltration will start when the Start UF Stop button is pressed. Pressing Start UF Stop button during treatment will decrease the ultrafiltration rate to the set minimum UF rate. The TMP alarm window will automatically widen and the TMP button starts to flash. To centralize the alarm limits around the actual value, press the flashing TMP button (see chapter 4 or 5). The permitted stop time is 5 min. When this time is expired, an attention alarm will be activated instructing the operator to restart the ultrafiltration.

3:22



Display and setting group Information display The information display, as the name implies, is used to give the operator further information. In order to obtain information on the display, an appropriate button has to be pressed. The information is then shown for 15 seconds . If the operator wishes to turn off the display earlier the Hold button can be pressed and then be pressed a second time to turn off the screen. The Arrow buttons below the information display light up in order to show which of the displayed values that are adjustable. If a lit Arrow button is pressed, the text above the value will flash and the value can be changed using the Set knob. It is sometimes possible to press two Arrow buttons at the same time, for example to move low and high alarm limits simultaneously. In some attention messages the operator is instructed to confirm an action by pressing a lit Arrow button. In these cases the Arrow buttons are referred to as: Left = LOW Middle = SET Right = HIGH The Hold button is used to hold the information on the information display. When the Hold button is lit, the Set knob is disconnected. If the lit Hold button is pressed a second time the display turns off. If a parameter button is pressed when the Hold button is lit the information display changes and the hold function disappears. The Set knob is used for setting of all parameters with one exception the blood flow.

The Blood flow knob is used to set the blood flow. The Blood flow knob is directly accessible, i.e. without first having to press a parameter button. As soon as the knob is turned the information display is lit.



3:23

Treatment overview screen When no other screen is displayed on the information display, the Treatment overview screen will be displayed at all times during treatment. On this screen, the operator can obtain an overall picture of parameter values, valid at that time, for the on-going treatment. All parameters are measured values except sodium and bicarbonate concentrations which are set values. If desired, the Treatment overview screen can be removed by preset and in that case the left Arrow button is to be pressed to display the screen when the information display is unlit. The picture below shows an example of the Treatment overview screen:

Figure 3:4

3:24

Treatment overview screen



Parameters shown on Treatment overview screen Qb

current blood flow rate

Pa

current arterial pressure

Pv Qbacc

current venous pressure

Ps

current system pressure

UFR

current ultrafiltration rate

UFV

accumulated ultrafiltration volume (patient weight loss)

accumulated blood volume

accumulated ultrafiltration volume (patient weight loss) as percentage of the set value TMP

current transmembrane pressure

Vinf

accumulated infusion volume

Rinf

current infusion rate

Na+

sodium concentration (set value)

HCO3

bicarbonate concentration (set value)

∆BV

relative blood volume from measurement start (BVS)

SYS

systolic blood pressure (BPM)

DIA

diastolic blood pressure (BPM) pulse rate (BPM) time of latest measurement check (BPM)

K

latest measured clearance value (Diascan)

Kt/V

latest measured Kt/V value (Diascan) time of latest measurement check (Diascan) time to target is estimated to be within the remaining treatment time set (Diascan)



3:25

Function check overview screen The Function check overview screen will be displayed on the information display during the function check of the machine. The screen gives the operator information about how long the function check has been in progress and also what is being tested at that moment. The ticks to the right of each test show that the test has been successfully performed. The green field on the progress bar shows the successfully performed part of the function check. The time in minutes at the bottom of the screen shows elapsed time of the function check. If desired, the Function check overview screen can be removed by preset and in that case the Technical alarm button is to be pressed to display the screen when the information display is unlit. The picture below shows an example of the Function check overview screen:

Figure 3:10

3:26

Function check overview screen



Tests shown on Function check overview screen


Fch_BM

function check of the blood monitor

Fch_FM

function check of the fluid monitor, this position is the main test, tests below are more detailed and included in this

↓mS/cm

test of the conductivity cell

↑mS/cm

test of the conductivity cell

↑°C

test of the temperature sensor

°C

test of the temperature sensor

mmHg

leakage test of the fluid monitor

↑FRN

test of UF supervision system

↓FRN

test of UF supervision system

BiCart

priming of the BiCart cartridge


3:27

The eight commandments 1. When a blue button is lit, it indicates an activated function.

2. When a red button is lit, it indicates an alarm.

3. When a button flashes, it is a request to press it.

4. The information display only shows information on request.

5. To request information in the display, the appropriate button has to be pressed.

Figure 3:11

Temp button and the information display

6. Values in the information display, which can be changed, are indicated by a lit arrow button.

7. When a lit arrow button is pressed, the indicated value can be changed with the set knob.

8. The blood flow rate is always changed directly with the blood flow knob.

3:28



Setting of parameters All treatment parameters are set in a similar way. To illustrate this, a detailed description follows showing how the values for the Temp (temperature) are changed. Press the Temp button. The information display and its buttons show:

Figure 3:13

Temp button and the information display

The set value for the temperature can be changed with the Set knob if the middle Arrow button is pressed. To indicate that the set value is possible to change, the text SET on the information display and the green bargraph on the temperature display will flash. The alarm limits can be changed either together or separately. If the low or high limit is to be changed, press the corresponding Arrow button. The limits are changed together by pressing both left and right Arrow buttons simultaneously. To indicate the limits that can be changed, the corresponding texts and bargraphs will flash. The light of the information display goes out 15 seconds after the Set knob or the buttons are touched. It is however, possible to select new information on the information display by pressing another button before the 15 seconds have ed. If the values need to be studied in digital form for more than 15 seconds the Hold button can be pressed. The Set knob is then disconnected. Pressing an Arrow button will again make a value changeable. It is always possible to exit the hold function by pressing another button or the Hold button again.



3:29

Note • The bargraphs displays show the set value, the actual value and the alarm limits for the control system, while the information display shows the corresponding values of the protective system (see chapter 1). In order to that the control and protective systems are operating with the correct input values, the is instructed to compare the readings of the current bargraph displays and the information display before connecting the patient. Note

Venous pressure

The low and high alarm limits can be changed with the Set knob either together or separately. Blood flow in single pump mode

The Blood flow knob is directly accessible i.e. without first having to press the parameter button. In double needle/single pump mode, the blood flow rate can be changed with the Blood flow knob. In single needle/single pump mode, the arterial blood flow rate, can be changed with the Blood flow knob. Blood flow in single needle/double pump mode

The mean blood flow rate can be changed with the Blood flow knob. The venous blood flow rate as well as the arterial blood flow rate can be changed separately, using the Set knob. In this mode the actual blood flow value is not compensated for as regards arterial pressure. Blood pump segment adjustment

Three different blood pump segment diameters can be selected by pressing the Blood flow button when the blood pump is stopped in double needle mode. The blood pump segment diameter is changed with the Set knob (see “Change of blood pump segments” in this chapter). SN data in single needle/single pump mode

The times for the venous and the arterial phases can be changed with the Set knob. SN data in single needle/double pump

The stroke volume and the high system pressure limit can be changed with the Set knob. Temperature

The set value, the low and high alarm limits for the temperature can be changed with the Set knob. When the set value is changed, the alarm limits will automatically follow. However, the alarm limits can also be changed separately. See previously in this chapter (Setting of parameters, Temperature example). Conductivity in acetate mode

The set value for sodium can be changed with the Set knob. When the set value is changed, the alarm limits will automatically follow, at 5% of the resulting set value of the conductivity.

3:30



Conductivity in bicarbonate mode

The set values for sodium and bicarbonate can be changed with the Set knob. When one or both set values are changed, the alarm limits will automatically follow, at 5% of the resulting set value of the conductivity. Arterial pressure

The low and high alarm limits can be changed with the Set knob either together or separately. TMP

The low and high alarm limits for the transmembrane pressure can be changed either together or separately using the Set knob. UF volume

The set value for the total ultrafiltration volume (patient weight loss) can be changed with the Set knob. UF rate

The priming UF rate and the minimum UF rate during treatment can be changed with the Set knob. Time

The remaining treatment time shown in the TIME-display, can be changed with the Set knob. Heparin

The set value for the heparin flow rate and the stop time for the heparinization (time before treatment ends) can be changed with the Set knob. Dialysis fluid flow

The set value for dialysis fluid flow can be changed between the low and high value, in steps of 25 ml/min, with the Set knob. BPM (option), BVS and Diascan

The parameter settings for the above mentioned functions are described in the corresponding chapter for each function.



3:31

ing treatment parameters It is possible to certain treatment parameters from an external computer system via a patient card or other external equipment. After the ON/OFF button has been pressed and the first part of the function check has been completed (“Fch” shown on the time display), it is possible to a list of treatment parameters and their values. The Clinic automation button can be pressed directly after ing to view the list, or if desired, reject it. Once the Priming button starts to flash, the complete list of treatment parameters can either be accepted (Accept) or rejected (Reject) by the operator. The list will be displayed on the information display when the flashing Clinic automation button has been pressed, see figure 3:14. Acceptance/rejection can be done at any time during treatment preparation until blood has been detected.

Figure 3:14

ing treatment parameters

All parameters in the list will be accepted or rejected at the same time, it is not possible to exclude or add separate parameters or change values in the list. When the list has been accepted, the values will automatically be set in the machine (any previously set values will be replaced). If the list is rejected it is possible to redo the ing. After the ed list of parameters are accepted or rejected, it is possible to set/adjust treatment parameters as usual. Concentrate parameters will be automatically set by the machine after ing (before acceptance). The reason for this is not to disturb or prolong the function check.

3:32



If the list of treatment parameters is rejected, the ed settings for concentrates will remain. An attention alarm will appear to remind the operator about this. CONC. SETTINGS NO LONGER DEFAULT Check settings, press LOW To continue, press the lit Arrow button to confirm the ed settings. Check if the ed concentrate settings are the desired ones, if not, select and connect new concentrates manually, as is the usual procedure. If any parameter or parameter value in the list is not accepted by the machine, an attention alarm will appear after ing. The complete list of parameters must be rejected. CAN NOT APPLY ED PARAM. All parameters must be rejected Press the Clinic automation button to check which parameter, shown in red, cannot be set. Redo the ing after changing the parameter or set all parameters manually. If this attention alarm occurs, it is important to note that the ed settings for concentrates have not been automatically set.

Procedure 1. Press the flashing Clinic automation button. A list of the ed treatment parameters will be shown on the information display. 2. Check all the parameter values displayed; scroll down through the complete list by using the Set knob; the green arrow to the left of the parameter indicates your current position in the list. All parameters in the list must be scrolled through. The parameters in the list must correspond with the prescription. Choose either to accept or reject the list, then continue to the appropriate point 3 in the instructions below. Accept

3. Press the Arrow button below Accept, see figure 3:14. At this moment, the complete list of treatment parameters will automatically be set in the machine (any previously set values will be replaced). During the setting time (about 15 seconds), only the Mute button and the Blood pump button are accessible. Note that it is not possible for the machine to display the list of ed parameters after the acceptance has been done. When checking parameters after this, each parameter must be checked separately by pressing the corresponding parameter button. Reject

3. Press the Arrow button below Reject, see figure 3:14. All treatment parameters shown in the list will now be rejected. Note that the ed concentrate settings will remain.



3:33

The ultrafiltration control During treatment the following equation is always applicable.

Ultrafiltration volume UF rate Treatment time Treatment time and UF volume can be set within certain limits. The machine will automatically calculate and show the UF rate. When treatment time or UF volume is changed the UF rate will also change and new TMP alarm limits have to be set. An example of how a UF setting is done is shown below. 1. Press the Time button and select the treatment time. 2. Press the UF volume button and select total UF volume. (As soon as the ”SET” Arrow button is pressed the bar on the UF rate display also starts to flash, showing the calculated UF rate). 3. When the flashing Start UF Stop button has been pressed (lit up), the TMP alarm limits must be centralized. Note that the alarm limits should be set in accordance with the UF rate and dialyzer UF coefficient. CAUTION When negative TMP alarm limits are set, no alarm that backfiltration may occur.

will indicate CAUTION

An attention alarm may appear if an incorrect combination of settings is made, e.g. the time is 0.00 and the UF volume is set. The alarm will disappear as soon as the time is increased sufficiently. A UF rate limit is automatically calculated and set. The limit is 20% above the calculated UF rate. This limit is the highest permitted UF rate during the treatment. If for any reason the UF rate has been too low during a period of time, the machine will try to compensate for this by increasing the UF rate up to the UF rate limit. If it is impossible for the AK 200 S to reach the set UF volume within the remaining time and current UF rate limit, an attention alarm will be given. The operator is instructed to change either time or UF volume.

3:34



Protective system for ultrafiltration Upon demands from the clinic the below described function in the machine can be removed. This preset (i.e. removal of function) is done by a qualified technician in the clinic. The operator is requested to read the corresponding information for the ultrafiltration system in section “Safety philosophy” in chapter 1 in this manual. The protective system for ultrafiltration, also called the UF supervision system, measures the accumulated ultrafiltration volume during treatment independent of the control system mentioned before in this chapter in section “The ultrafiltration control”. The protective system will estimate accumulated UF volume throughout the treatment based on treatment Time and UF volume set when the treatment is initiated. This estimated accumulated UF volume will not be shown on the information display. When the treatment is running the actual measured accumulated UF volume (SUPERV) will be compared with the estimated accumulated UF volume at all times during treatment. If the deviation between these values is more than a certain set limit (LIMIT) an attention alarm is generated to notify the operator of this, the ultrafiltration is stopped and the blood flow is decreased. The attention alarm is shown on the information display as below: UF VOLUME DEVIATION Check cause, press UF volume Check the machine for visual leakage. Check accumulated UF volume in both control and protective system. Check alarm limits for UF volume in protective system. Do customary patient checks as whenever the ultrafiltration volume is suspected to be incorrect. Evaluate if it is possible to continue the treatment. The attention alarm is confirmed by pressing the UF volume button for 3 seconds. If the attention alarm is confirmed, the machine will recalculate a new estimated accumulated UF volume, based on the remaining treatment Time and the remaining UF volume and the ultrafiltration will start again. Note that every time the attention alarm is confirmed, the deviation accepted will be added to the previous accepted deviation. Therefore it is not necessary to adjust LIMIT after an attention alarm. If problem remains call for technical service. CAUTION Incorrect weight loss may occur if confirmation is done without having corrected the technical cause for the attention alarm. CAUTION

LIMIT is the alarm limit for the deviation between the estimated accumulated UF volume and the actual measured accumulated UF volume (SUPERV). LIMIT is settable by the operator between 0.1 and 2.0 litres of accumulated ultrafiltration volume. The limit must be



3:35

set by the operator according to the patients needs and tolerance and according to the routines of the clinic. The alarm limits HIGH and LOW will automatically be set by the machine equally around the estimated accumulated UF volume, i.e. if LIMIT is set to 0.4 the deviation between HIGH and LOW will be 0.8. Note • The lower limit for LIMIT in the machine is 0.1 litre multiplied with treatment time. I.e. if LIMIT is set to 0.4 by the operator at the beginning of the treatment the machine will after 4 hours of treatment start to increase LIMIT with 0.1 litres per hour. Note

To view and set the parameters of protective system UF supervision: 1. Press the UF volume button, this will display the UF volume settings. 2. Press the UF volume button again while the UF settings display is active. The protective system UF supervision parameters are now displayed. SUPERV - UF supervision measured accumulated UF volume LOW - Lower level for UF supervision alarm LIMIT - Settable alarm limit for UF supervision HIGH - Upper level for UF supervision alarm 3. The settable part of the alarm limit (LIMIT) can be adjusted by pressing the lit Arrow button below LIMIT followed by turning the Set knob. This will affect the LOW and HIGH limits which are automatically set according to LIMIT.

3:36






3:37

Power failure Returning the blood during a power failure If the AK 200 S is not equipped with a battery back-up function, it is possible to manually return the blood to the patient during a power failure. 1. Clamp the arterial blood line and disconnect it from the patient. 2. Connect the arterial blood line to the rinse-back solution and unclamp it. 3. Open the cover of the blood pump and turn the blood pump manually in an anticlockwise direction. Be careful with the guiding pins so that they do not interfere with the pump segment. 4. When the required amount of blood has been returned to the patient, clamp the venous blood line and disconnect it from the patient. When the power returns, the treatment settings and accumulated values can be read off as usual. WARNING During manual procedure to return blood to patient in power failure, the operator assumes responsibility for visually monitoring all safety parameters which the machine can not monitor in a power failure (e.g. air detection). WARNING

Battery back-up The AK 200 S can be equipped with a battery back-up function. The battery acts as a power supply in the event of a power failure. If this happens, an attention alarm simultaneously appears: POWER FAILURE, BATTERY OPERATION Battery operated for X minutes The battery supplies the AK 200 S with power to all functions except for that of heating the dialysis fluid. This means that a low temperature alarm will occur within a minute after the power failure has occurred. When the power in the battery has been consumed, the machine acts in the same way as it would with no battery back-up function. All instructions for installation and replacement of the battery back-up are included in the AK 200 S Service Manual, Installation Guide.

3:38



Recovery from a short power failure In case of a power failure, settings and accumulated values are stored by the AK 200 S. The machine will perform a recovery when the power returns; ”rec” is shown on the time display and the buzzer sounds. The operator must check the extracorporeal circuit for possible blood clots and has to confirm continued treatment by pressing the Time button. It is also necessary to press the Blood leak and Air detector alarm indicators. 1. Press the Mute button to silence the buzzer when the power has returned. 2. Press the Attention button to read the messages. 3. Press the Time button to confirm the recovery. 4. Press the flashing Air detector button and the flashing Blood leak button. 5. If no heparin values were set, press the Heparin button to confirm no heparinization. The AK 200 S will continue the treatment from where it was interrupted. However, if the AK 200 S has made ten recoveries during the same working session, the eleventh power failure will result in a function check. CAUTION Check treatment parameters after a recovery. CAUTION Note • The recovery function will not store the new settings in case of a power failure during the function check.

• The AK 200 S is equipped with a battery to the buzzer during power failure. During power failures when the buzzer is muted, the current consumption from the battery is high. In order to avoid this high consumption, switch the machine off by pressing the ON/OFF button for 3 seconds instead of pressing the Mute button. When the power returns, switch it on again by using the ON/OFF button. A normal recovery (see above) will now follow. Note



3:39

Recirculation during treatment When the blood circuit is recirculated it is the operator’s responsibility to decide for how long a period it can be safely done. The operator should also to note the time for the recirculation in order to add it to the non-diffusion time at the end of the treatment. 1. Stop the ultrafiltration by pressing the Start UF Stop button. The button will start to flash and the ultrafiltration decreases to the minimum ultrafiltration rate. 2. Check that the minimum ultrafiltration rate is set according to the package insert for the dialyzer. 3. Set the blood flow to 100 ml/min. 4. Stop the blood pump. 5. Disconnect the arterial and venous blood line from the patient and connect them to a connection line. 6. Start the blood pump. 7. Connect a saline bag to the venous drip chamber with help of an infusion line. Raise the infusion pole to 0.5-1 meter above the venous drip chamber in order to keep the venous pressure above zero. Open the clamp on the infusion line from the saline bag. 8. Press the flashing Arterial pressure, Venous pressure and TMP buttons to set the alarm limits around current pressures. 9. After 5 minutes of by of the ultrafiltration an attention is given: TREATMENT STOP TIME EXPIRED Press START UF key Press the Start UF Stop button to restart the ultrafiltration. Press the Start UF Stop button a second time to stop the ultrafiltration again. 10. When the Start UF Stop button is pressed the TMP button starts to flash and the alarm limits widens. Press the flashing TMP button to set the alarm limits.

Reconnection of the patient 1. Close the clamp on the infusion line from the saline bag and stop the blood pump. 2. Check and remove any air bubbles from the blood lines. Disconnect the arterial and venous blood line from the connection line. 3. Reconnect the blood lines to the patient and start the blood pump. Set the required blood flow rate.

3:40



4. If required increase the minimum UF rate to the desired set value. 5. If required adjust the UF volume. 6. Press the flashing Start UF Stop button to restart ultrafiltration. Press the flashing Arterial pressure, Venous pressure and TMP buttons to set the alarm limits around current pressures.



3:41

Change of blood pump segment AK 200 S can be used with 3 presettable diameters of blood pump segments. Change of blood pump segment should be done before the patient is connected. CAUTION Make sure a correct blood pump rotor is used. The blood pump rotor has to be properly adjusted in order to correctly occlude the blood pump segment being used. This is important in order to achieve the correct blood flow. Check with the service technician responsible. CAUTION

AK 200 S has to be in double needle mode and the blood pump has to be stopped in order for the diameter of the blood pump segment to be changed. 1. Press the Blood flow button. 2. Press the Arrow button below SEGMENT. 3. Select the appropriate blood pump segment diameter by using the Set knob. 4. Make sure to use a correct blood pump rotor. The blood pump rotor has to be properly adjusted in order to correctly occlude the blood pump segment being used. 5. Confirm the attention: ADJUST PUMP HEAD TO TUBE x.xx Press BLOOD FLOW key to confirm by pressing the Blood flow button.

3:42



BiCart/SelectCart change during treatment If the BiCart and/or the SelectCart cartridge needs to be replaced by new ones during treatment, do as follows: 1. Remove the cartridge that is to be changed and close both the latches of the cartridge holder properly (vertical position) for at least 2 seconds. (To close the lower latch; pull out and close.) 2. Open the upper latch of the holder, pull out the latch and lift upwards to its uppermost position. 3. Open the lower latch of the holder. 4. Place the bottom port of the cartridge into the hole of the lower latch. Bring down the upper latch and place the top port of the cartridge into the hole of the upper latch. Press down the upper latch to puncture the cartridge. 5. The cartridge will now be primed automatically. When the cartridge has been attached correctly, the priming process is indicated by a cartridge symbol in the upper right corner of the information display. The S or the B before the symbol indicates SelectCart or BiCart cartridge. Figures or letters (0,1,2....A,B,C....) are shown on the cartridge symbol during the priming process to show the progress of the process. The cartridge symbol disappears when the priming process is complete.



3:43


3:44



Chapter 4 Hemodialysis, double needle treatment Double needle treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Check before starting the machine . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the machine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Function check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Select concentrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect concentrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . SelectCart and SelectBag together with BiCart . . . . . . . . . . . . . Acidic concentrate and BiCart . . . . . . . . . . . . . . . . . . . . . . . . . . Acidic concentrate and liquid bicarbonate concentrate . . . . . . . Acetate concentrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the machine - continued . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Attaching the dialyzer and the blood lines . . . . . . . . . . . . . . . . . . . . . . Dialyzer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Arterial blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Preparations if the heparin pump is to be used . . . . . . . . . . . . . Venous blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming and rinsing the extracorporeal circuit . . . . . . . . . . . . . . . . Initiating . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Set the treatment parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pressure alarm limits setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Venous/Arterial pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Automatic emptying of BiCart, SelectCart and SelectBag . . . . . . . . Discontinuing procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Confirm treatment end . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . If desired, start emptying BiCart or BiCart, SelectCart and SelectBag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Return the blood . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . After-treatment handling of the machine . . . . . . . . . . . . . . . . . .


AK 200 S Operator’s manual - Double needle

4:2 4:2 4:2 4:3 4:4 4:6 4:7 4:8 4:8 4:8 4:9 4:11 4:11 4:12 4:14 4:16 4:17 4:17 4:19 4:19 4:20 4:21 4:22 4:22 4:22 4:24 4:24 4:25 4:25 4:25 4:25 4:26

4:1

Double needle treatment Check before starting the machine •

That the mains cable is connected to a mains supply with protective earth.

•

That the main switch on the rear of the machine is turned on.

•

That the water supply is turned on.

•

That the dialysis fluid tubes are connected to the safety couplings.

•

That the drain tube is properly placed with an air gap between the machine and the drain/sewer system.

CAUTION In order to protect the operator’s fingers, keep the blood pump and the clamp covers shut during the function check for the blood monitor, since the pump(s) as well as the clamps will be tested during the check. CAUTION Note • If the machine has been stored with chemical disinfectant, this solution must be rinsed out of the system before any treatment can be initiated. Note

Start the machine The dialyzer and the blood lines may be attached before power on or when the Priming button is flashing. Follow the instructions further on in this chapter ”Attaching the dialyzer and the blood lines”. Follow the six consequent steps below to start the machine. 1. Press the ON/OFF button for 3 seconds. All the buttons and bargraphs on the operator’s are illuminated simultaneously and the operator is requested to check their functionality by visual inspection. If the machine has been filled with a chemical disinfectant the Chem disinf button will be lit at this moment as well as the Rinse/Drain button. For further information see “Filling the machine with chemical disinfectant” in chapter 12. CAUTION After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION

4:2



Function check When the machine starts up it always carries out checks on internal safety and calibrations; the function check. FCH/Fch is shown on the time display. These checks require that the dialysis fluid tubes are connected to the safety couplings during the entire function check. The dialysis fluid tubes can be moved from the safety couplings when the time appears on the time display instead of ”Fch” and the by path lights up on the flow diagram. These checks also require that no buttons are touched before the first part of the function check is completed, i.e. when ”FCH” on the time display has been replaced by ”Fch”. The Function check overview screen will be displayed on the information display during this function check. The screen gives the operator information about how long the function check has been in progress and also what is being tested at that moment. See “Function check overview screen” in the “Controlling the machine - general guidelines” chapter for details. Note • If the buzzer sounds continuously and the Attention alarm button lights up, press the button for information. One of the points below ”Check before starting the machine” has normally been forgotten.

• If the Technical alarm button lights up, there is a technical error. Press the button for further information. If the information display says:

ERROR! RESTART OR CALL SERVICE

start a new function check, using the ON/OFF button. If the technical error reoccurs, call your service technician.

• The dialysis fluid tubes must remain connected to the safety coupling during the complete function check (until preset time is shown in the TIME display and the dialysis fluid flow path is lit). Note



4:3

Select concentrates 2. Check that the correct treatment mode has been selected; the corresponding button for Bicarbonate mode or Acetate mode will be lit. Press the lit button briefly in order to select/check that the proper concentrate has been selected on the information display and is in accordance with the prescribed concentrates that will be connected to the machine during treatment. The selected alternative will be flashing.

Figure 4:1

Select Bicarbonate and type of concentrate

The picture above shows the information display when the Bicarbonate button has been pressed. The concentrate combinations may vary from clinic to clinic according to patient needs and the routines of the clinic. The information display above shows the default values the machine has been delivered with. It is possible to choose between three combinations on the information display, preset by the authorised technician in the clinic. The selected concentrates are flashing and the corresponding Arrow button below will not be lit. When SelectBag is to be used, and is preset as the first alternative on the information display, it is possible to choose between different SelectBag concentrations . The Arrow button below SelectBag will then still be lit indicating that it is possible to choose different SelectBags. Press the lit Arrow button.

4:4



Figure 4:2

Select SelectBag

The picture above shows the information display when the lit Arrow button below SelectBag is pressed. SelectBag will flash and the concentrate below will be lit. Turn the Set knob until the desired SelectBag is shown. Press the Arrow button again to confirm the chosen concentrate, both BiCart and SelectBag will be flashing. CAUTION The operator must make sure that the chosen concentrates on the information display correspond with the connected concentrates during function check and during treatment. CAUTION



4:5

Connect concentrates There are four different alternatives for concentrate combinations described below. Choose the alternative that is to be used. •

SelectCart and SelectBag together with BiCart: Follow step 3 and 4 in corresponding instruction.

•

Acidic concentrate and BiCart: Follow step 3 and 4 in corresponding instruction.

•

Acidic concentrate and liquid bicarbonate concentrate: Follow step 3 in corresponding instruction. (Step 4 is not valid)

•

Acetate concentrate: Follow step 3 in corresponding instruction. (Step 4 is not valid)

CAUTION that the correct prescribed concentrate(s) for the specific treatment is (are) used. Avoid changing concentrate containers during treatments. CAUTION Note • The concentrate pick-up tubes must be placed in the corresponding concentrate containers or in the disinfection ports on the machine, according to table below, otherwise function check will not be completed. Placement of pick-up tubes in different treatment modes: A pick-up tube

A pick-up tube in

B pick-up tube

B pick-up tube in

in concentrate

disinfection port

in concentrate

disinfection port

x

BiCart Select:

x

Acidic concentrate and

x

x

BiCart: Acidic concentrate and liquid

x

x

bicarbonate Acetate

x

x Note

4:6



SelectCart and SelectBag together with BiCart

Handling procedure: 3. SelectCart: Open the upper latch of the SelectCart holder, pull out the latch and lift upwards to its uppermost position. Open the lower latch. Place the bottom port of the SelectCart cartridge into the hole of the lower latch. Bring down the upper latch and place the top port of the cartridge into the hole of the upper latch. Press down the upper latch to puncture the cartridge. The SelectCart cartridge will be primed automatically. SelectBag: Remove the protective foil from the connector port of the SelectBag. Open and hold the latch of the SelectBag holder in its uppermost position while hanging the SelectBag into the holder with the connector port upwards. Press down the latch to a horizontal position, whereby the membrane of the SelectBag is punctured by the spike. Tap lightly on the SelectBag so that any air bubbles gather at the top.

Figure 4:3

Connect the SelectCart cartridge and the SelectBag

WARNING Avoid touching the plastic spike.

Be careful to avoid fluid from the SelectBag splashing into your eyes. WARNING Note • Follow the instructions for use of the SelectCart cartridge and the SelectBag.

• The SelectCart and SelectBag can be attached before or during the function check. They must have been attached for the function check to be completed.

• Both concentrate pick-up tubes must be placed in the disinfection ports of the machine. Note



4:7

4. BiCart: Open the upper latch of the BiCart holder, pull out the latch and lift upwards to its uppermost position. Open the lower latch. Place the bottom port of the BiCart cartridge into the hole of the lower latch. Bring down the upper latch and place the top port of the cartridge into the hole of the upper latch. Press down the upper latch to puncture the cartridge. The BiCart cartridge will be primed automatically. Note • Follow the instructions for use of the BiCart cartridge.

• The BiCart cartridge can be attached before, during or after the function check. Note

Acidic concentrate and BiCart

Handling procedure: 3. Place the A pick-up tube (marked red) into an acidic container. The B pick-up tube (marked blue-white) must remain in the disinfection port. 4. BiCart: Open the upper latch of the BiCart holder, pull out the latch and lift upwards to its uppermost position. Open the lower latch. Place the bottom port of the BiCart cartridge into the hole of the lower latch. Bring down the upper latch and place the top port of the cartridge into the hole of the upper latch. Press down the upper latch to puncture the cartridge. The BiCart cartridge will be primed automatically. Note • Follow the instructions for use of the BiCart cartridge.

• The BiCart cartridge can be attached before, during or after the function check. Note

Acidic concentrate and liquid bicarbonate concentrate

Handling procedure: 3. Place the A pick-up tube (marked red) into an acidic concentrate container and the B pick-up tube (marked blue-white) in a liquid bicarbonate concentrate container. Acetate concentrate

Handling procedure: 3. Place the B pick-up tube (marked blue-white) into an acetate concentrate container.

4:8



Start the machine - continued 5. Check all set values and alarm limits. Adjust if necessary. Press the respective button and check/adjust the values on the information display by using the Arrow buttons and the Set knob. 6. Turn the BVS off if it is not to be used. Press the BVS button followed by the right Arrow button and turn the Set knob until BVS OFF is shown on the information display. Note • After the machine has ed the function check and the by path on the flow diagram lights up green, it is possible to activate Concentrate stand-by mode in order to save concentrates before patient connection. See information in “Concentrate stand-by mode” in the “Controlling the machine” chapter. Note



4:9


4:10



Attaching the dialyzer and the blood lines When the Priming button is flashing, the dialyzer and the blood lines may be attached, if this has not been done before power on. WARNING The operator must take proper precaution in order to prevent coagulation in the extracorporeal circuit. Coagulation may lead to: • inadequate delivery of dialysis

• risks associated with propagation of blood clots to the patient • disabling of the air detector function if blood clots aggregate in the drip chamber WARNING CAUTION To avoid safety hazards, when attaching the blood lines, it is important to follow the instructions given in the package inserts for the blood lines and to ensure that the connections are secured tightly. CAUTION Note • Since tests of the blood pumps and the clamps are included in the function check, it is important that the blood lines are attached either before the function check or when the function check for the blood monitor has been completed (Priming button is flashing).

• The self test of the BVS has to be performed on an empty cuvette holder, therefore the cuvette has to be outside the holder until the function check for the blood monitor has been completed (Priming button is flashing).

• The dialysis fluid tubes must remain connected to the safety coupling during the complete function check (until preset time is shown in the TIME display and the dialysis fluid flow path is lit). Note

Dialyzer Set up the dialyzer according to the instructions for the specific dialyzer. Place the dialyzer in the holder.



4:11

Arterial blood line Follow the instructions for the use of the arterial blood line. Specifically observe the following items. 1. Arterial line clamp - place the patient end of the arterial line in the line clamp colour-coded with the red dot. 2. Arterial line guide- place the line in the guide. 3. Arterial pressure transducer connector - attach the transducer protector firmly to the pressure transducer connector. 4. Blood pump - open the cover of the blood pump and place the pump segment inside the pump housing. The pump segment can be threaded manually or automatically. 4.a. Manually: Turn the blood pump manually to thread the pump segment through it. When the pump segment is in place, close the blood pump cover. 4.b. Automatically: Place the pump segment over the blood pump rotor and close the blood pump cover. - If this is done before the machine is switched on, the blood pump segment will be threaded during function check. - If this is done during function check (i.e. when “FCH” on the time display has been replaced by “Fch”), the blood pump segment will be threaded automatically when Priming is activated and the Blood pump button has been pressed. 5. BVS - place the cuvette in the cuvette holder. Note • The BVS cuvette has to be outside the cuvette holder until the function check of the blood monitor has been completed (Priming button is flashing). Note

6. Dialyzer - attach the dialyzer end of the arterial line firmly to the dialyzer.

4:12



Figure 4:4

Arterial blood line in HD, set-up

7. Heparinization - using the heparin pump. See the following pages for instructions on how to attach the syringe to the heparin pump, and setting the heparin values in the machine. WARNING The operator must take proper precaution in order to prevent coagulation in the extracorporeal circuit. Coagulation may lead to: • inadequate delivery of dialysis

• risks associated with propagation of blood clots to the patient • disabling of the air detector function if blood clots aggregate in the drip chamber WARNING Note • Make sure that the heparin pump is adjusted for the syringe size that is being used. Note



4:13

Preparations if the heparin pump is to be used

If heparinization is desired by using the heparin pump the preparations are made in the two following steps: 1. Attach the syringe to the heparin pump: a.

Prepare a syringe with the desired amount of heparin solution (or other anticoagulantia).

b.

Attach the syringe to the heparin line on the arterial blood line.

c.

Prime the heparin line with the solution to the point where the heparin line ends in the arterial blood line.

d.

Pull out the piston on the heparin pump to end position.

Figure 4:5

Change position of the heparin pump holder

To change the position of the piston, press the end of the piston, hold it in and move the holder. When the piston is released the holder cannot move. e.

Insert the syringe in the pump; the plastic collar at the end of the syringe must fit in the groove of the pump.

f.

Push back the piston and insert the plastic plate on the plunger in the groove by the locking wheel.

g.

Turn the locking wheel upwards until resistance is felt. This is to lock the plastic plate of the plunger in the groove.

h.

Check that the syringe is properly secured by lightly pulling on the plunger.

Figure 4:6

4:14

Syringe attached to heparin pump



2. Set the heparin values in the machine: a.

Press the Heparin button briefly.

b.

Select the heparin flow rate (ml/h).

c.

Check/adjust the STOP TIME in minutes i.e. at which time the heparinization should stop before treatment ends.

As soon as the treatment starts (priming detector detects blood) the heparinization starts (the Heparin button: lights up). To start heparinization during priming, press the Heparin button for 3 seconds. If the set value is 0 when the priming detector detects blood, the Heparin button starts to flash and an attention is given. CAUTION To prevent the syringe from loosening from the heparin pump during treatment the syringe plunger has to be thoroughly secured. Check by lightly pulling on the plunger. When doing so, it must be impossible to pull the syringe out of the heparin pump. CAUTION



4:15

Venous blood line Follow the instructions for the use of the venous blood line. Specifically observe the following items. 1. Venous line clamp - place the patient end of the venous line in the line clamp colour-coded with the blue dot. CAUTION Check carefully that the venous blood line is correctly placed in the priming detector. CAUTION

2. Air detector - place the venous drip chamber in the air detector. The venous drip chamber should be placed as low as possible to prevent air from ing into the venous line. At the same time it should be possible to adjust the level well above the air detector head. Close the air detector cover. 3. Venous pressure transducer connector - attach the transducer protector firmly to the pressure transducer connector. 4. Dialyzer - attach the dialyzer end of the venous line firmly to the dialyzer.

Figure 4:7

4:16

Venous blood line in HD, set-up



Priming Priming and rinsing the extracorporeal circuit Before priming •

Connect the arterial line to the priming fluid.

•

Check that the venous line is correctly positioned in the priming detector.

•

Check all connections.

•

Check that the priming UF rate is correct by pressing the UF rate button, check PRIMING. Follow the instruction for use of the dialyzer.

Note • A flashing Bicarbonate or Acetate button indicates that Concentrate stand-by mode is active. Resume dialysis fluid preparation (deactivate concentrate stand-by mode) by pressing the flashing button once. The dialysis fluid will be ready within approximately 3 minutes. Note

Priming and rinsing procedure 1. Press the flashing Priming button for three seconds to activate priming (lights up). 2. Follow the manufacturer’s instructions for use of the dialyzer and the blood lines. WARNING Do not use the level adjustment buttons in combination with blood lines incorporating the ”balloon” type transducer protector, as the venous pressure reading might be adversely affected. WARNING

3. Press the flashing Blood pump button. The blood flow rate will automatically start at 100 ml/min. Adjust the blood flow. If the blood pump segment has been automatically threaded, check for possible kinks. Prime and de-air the blood lines and the dialyzer. 4. Adjust the level in the venous drip chamber, so the level is well above the air detector head. 5. Attach the dialysis fluid tubes to the dialyzer when the time appears on the time display instead of Fch and the by path lights up on the flow diagram. Press the flashing Fluid by button and the dialysis fluid will enter the dialyzer when the by path lights up green on the flow diagram. HCEN9751 Revision.12.2005 Program version 8.xx


4:17

6. When the level in the air detector is correct, the Air detect button will start flashing and an attention regarding the inactivated air detector will appear. The buzzer can be muted but the attention will remain until the air detector is activated (manually when desired/automatically if the PRIMING VOLUME ACHIEVED attention alarm appears or when blood has been detected). 7. When the priming volume has been achieved, the blood pump automatically stops and the attention PRIMING VOLUME ACHIEVED Check line in priming detector appears. Note • Always follow the manufacturer’s recommendations for the minimum rinsing volume (for the blood lines and the dialyzer). Note

8. If necessary, continue priming by pressing the flashing Blood pump button. When a certain amount of extra priming volume has been used this attention appears: EXTRA PRIMING VOLUME ACHIEVED Check line in priming detector Check priming fluid and waste bag. Stop the blood pump. If the operator wishes to restart priming, and at the same time set the priming volume value to zero, the Priming button has to be pressed for 3 seconds to exit priming mode. The Priming button starts to flash. After that, press the Priming button again to activate priming. The Priming button will light up and it is possible to repeat the priming procedure. Note • After the machine has ed the function check and the by path on the flow diagram lights up green, it is possible to activate Concentrate stand-by mode in order to save concentrates before patient connection. See information in “Concentrate stand-by mode” in the “Controlling the machine” chapter. Note

4:18



Initiating Set the treatment parameters CAUTION To avoid hazardous side effects during the treatment, parameters set should be suitable for the patient’s needs and tolerance.

The correct setting of the UF rate is important to avoid backfiltration. Set a minimum UF rate according to the instruction for the specific dialyzer. CAUTION Note • Negative pressure may cause generation of ”microbubbles”. Note

Always check/adjust •

Check the time on the Time display. Adjust if necessary; press the Time button, adjust REMAIN.

•

Check the required UF volume (patient weight loss). Press the UF volume button, check SET, adjust if necessary.

•

Check that the calculated UF rate (patient weight loss/h) is suitable. Press the UF volume button, check CALC UFR. Adjust time or UF volume if necessary.

•

Check that the minimum UF rate is set to the required value. Press the UF rate button, check MIN UFR, adjust if necessary.

•

Check that the dialysis fluid flow rate is set to the required value. Press the Fluid flow button, check SET, adjust if necessary.

CAUTION Once the treatment parameters are set the should that the control and protective systems (see chapter 1) for conductivity and temperature operate with the desired values and that they are in agreement. This verification is made by comparing the bargraph displays and the information display before connecting the patient. CAUTION



4:19

Connect the patient Note • A flashing Bicarbonate or Acetate button indicates that Concentrate stand-by mode is active. Resume dialysis fluid preparation (deactivate concentrate stand-by mode) by pressing the flashing button once. The dialysis fluid will be ready within approximately 3 minutes. Note

1. Check that there is no air in the blood lines and that the level in the venous drip chamber is well above the air detector head. If expansion chambers are used, check that they are filled to the correct levels (refer to the instructions for use of the individual blood line). 2. Activate the air detector by pressing the Air detect button if it has not previously been activated during priming. Note • If the air detector has not been previously activated, it will automatically be activated when the priming detector detects blood. Note

3. When the priming and rinsing procedure is complete, check that the blood pump has been stopped, if not, press the Blood pump button. Adjust the blood flow rate to the proper start value. Note • Always follow the manufacturer’s recommendations for the minimum rinsing volume (for the blood lines and the dialyzer). Note

4. Connect the blood lines to the patient. Note • The blood pump can automatically be stopped when the priming detector detects blood in the venous line and the blood path of the flow diagram lights up. Note

5. Remove any obstructing clamps. 6. Start the blood pump and set the required blood flow rate suitable for the patient. When the priming detector detects blood in the venous line, the blood path in the flow diagram will light up red. The Start UF Stop button, the Venous pressure button, the Arterial pressure button and the TMP button starts to flash. If no heparin value has been set, the Heparin button will also flash. The machine will start to count down the treatment time at the same time as blood is detected.

4:20



When blood has been detected for 20 seconds the blood path will remain lit until treatment has been discontinued. This is valid even if the venous blood line is removed from the priming detector.

Start the treatment CAUTION Make sure that the blood path of the flow diagram lights up, if it does not light up, check that the venous blood line is correctly placed in the priming detector. If the blood path does not light up, the machine considers the patient not connected and as a consequence the UF system is not controlling the patient ultrafiltration. If the air detector has not been activated during priming it will not be automatically activated until the priming detector detects blood. CAUTION

1. Press the flashing Start UF Stop button (steady light) to start ultrafiltration. (The machine will start to count down the treatment time at the same time as blood has been detected.) 2. Press the flashing Venous pressure, Arterial pressure and TMP buttons to set the alarm limits around the current pressures. To set the limits manually press the respective button and change the values on the information display by using the Arrow buttons and the Set knob. Note that the TMP alarm limits should be set in accordance with the UF rate and dialyzer UF coefficient. 3. If the Heparin button flashes, press the button to confirm no heparinization using the heparin pump, or set the values. See “Arterial blood line, Heparinization” in this chapter. 4. If the BPM, the BVS or the Diascan functions are going to be used during treatment, see the corresponding chapters for activation and settings. Note • When no other screen is displayed on the information display, the Treatment overview screen will be displayed at all times during treatment1. On this screen, the operator can obtain an overall picture of parameter values, valid at that time, for the on-going treatment. See “Treatment overview screen” in the “Controlling the machine general guidelines” chapter for details. Note

1 Can HCEN9751 Revision.12.2005 Program version 8.xx

be removed by preset AK 200 S Operator’s manual - Double needle

4:21

Pressure alarm limits setting The machine is equipped with a centralizing function to simplify the correct setting of the pressure alarm limits. If there is a choice not to use the centralizing function as a preset or wide alarm limits range are preset, it is the operator’s responsibility to check that the alarm limits are set around current pressure. When the alarm limits are outside the preset range, the respective button starts to flash. If 2.5 min. of the treatment have elapsed and the alarm limits are still outside the preset range, an attention alarm is activated. (The Attention alarm button can be pressed in order to read on the information display which pressure limits that need to be adjusted). When the respective button has been pressed the alarm limits will centralize around the current pressure. Venous/Arterial pressure

The alarm display automatically widens and the button starts to flash when the blood flow is changed or when the Blood pump button is pressed. The alarm display may also be widened temporarily: Press the Venous pressure button followed by the Arrow button beneath the required alarm limit and adjust that specific limit. (The Venous pressure button will start to flash as described above as soon as the alarm display is outside the preset range). TMP

The alarm display automatically widens and the button starts to flash when the blood flow is stopped. Also when the UF equation is changed or when the Start UF Stop button is pressed the button will start to flash. The alarm display may also be widened temporarily: Press the TMP button followed by the Arrow button beneath the required alarm limit and adjust that specific limit. (The button will start to flash as soon as the alarm display is outside the preset range). CAUTION When negative TMP alarm limits are set, no alarm that backfiltration may occur.


4:22



Low venous pressure alarm limit setting below +10 mmHg

During certain conditions a very low venous pressure can occur e.g. when a central venous catheter is being used. In order to perform a dialysis treatment under this condition it can be necessary to set the low alarm limit below the normal limit of +10 mmHg. To make this possible the AK 200 S can be preset upon request from the clinic. However, the following conditions have to be fulfilled: •

The function has to be ordered by the physician

•

The machine has to be identified/labelled

•

The preset has to be documented in the machine logbook

CAUTION If a venous pressure alarm limit below +10 mmHg is set, a disconnection of the venous blood line may not be detected through a venous pressure drop. Special attention from the operator is therefore mandatory. CAUTION

Operating and setting

1. Press the Venous pressure button. 2. Press the LOW and HIGH arrows simultaneously and move the alarm limit below +10 mmHg. The centralizing function will now work below +10 mmHg.



4:23

Discontinuing In order to maintain a high level of performance of the AK 200 S machine, it is recommended that the machine carries out a disinfection program after each treatment. When the treatment is finished certain conditions must have been fulfilled for the machine to be able to start a disinfection program; end of treatment must have been confirmed; the patient must be completely disconnected from the machine and the blood path on the flow diagram must be extinguished; the dialysis fluid tubes must be connected to the safety couplings on the machine; the used concentrates must be removed i.e. the concentrate pick-up tubes must be placed in the disinfection ports of the machine, and the latches of the SelectBag, SelectCart and the BiCart holders must be closed.

Automatic emptying of BiCart, SelectCart and SelectBag If the BiCart Select system or the BiCart cartridge has been used during treatment, it is possible for the machine to automatically empty the containers after use. This will take some minutes and will vary depending on how much concentrate remains in the containers. The emptying procedure of the containers can be started at any time during the discontinuing procedure after treatment end has been confirmed. This means that it can be done while the blood is being returned to the patient, or directly after, in order to shorten the time before the disinfection program can be started, see the conditions mentioned above. It can also be done when the blood has been returned to the patient and the blood path of the flow diagram has been extinguished (confirmed patient disconnection). Once the automatic emptying procedure of the containers has been started (Arrow button pressed), the fluid unit of the machine will automatically be disconnected and the dialysis fluid to the dialyzer will be byed. The blood alarms will remain active (if automatic emptying is started before the blood path of the flow diagram has been extinguished). The treatment time displayed on the time display will be set to zero and it will not be possible to return to treatment. It should be particularly noted that if the emptying procedure is started before the blood has been returned to the patient, the blood should be returned to the patient as soon as possible since diffusion is consequently disabled.

4:24



Discontinuing procedure Note • If the treatment is to be discontinued before the set treatment time is achieved, the remaining time should be changed to 0:00 (press Time button, change by using the Set knob). Note

Confirm treatment end

When the remaining treatment time shown on the Time display equals 0:00 an attention alarm appears: TREATMENT TIME EXPIRED Press TIME key to confirm At this moment the UF rate will be automatically reduced to minimum UF rate as the set UF volume is achieved; the Start UF Stop button will be extinguished to indicate this. The time shown on the time display will continue to count down but will show negative figures. 1. Confirm treatment end by pressing the flashing Time button. When this is done the TMP alarm limits will widen. If desired, start emptying BiCart or BiCart, SelectCart and SelectBag

2. If used and if desired, start emptying the SelectBag, the SelectCart cartridge and BiCart cartridge (All) or only the BiCart cartridge (BiCart) at this point. Once the emptying procedure has been started (Arrow button pressed), the fluid unit of the machine will automatically be disconnected and the dialysis fluid to the dialyzer will be byed. The blood alarms will remain active. The treatment time will be set to zero and it will not be possible to return to treatment. For further information, see in "Automatic emptying of BiCart, SelectCart and SelectBag" previously in this section. 2.a. Open the upper latch(es) of the cartridge holder(s), pull out the latch(es) and lift upwards to their uppermost positions. 2.b. Press the Bicarbonate button twice, select All or BiCart by pressing corresponding Arrow button. Once the Arrow button has been pressed, the emptying procedure will start (see in 2 above). The SelectBag will automatically be drained after the cartridges has been drained if All has been selected. Return the blood

3. Stop the blood pump. This will automatically widen the venous and arterial pressure alarm limits to their priming values without a subsequent centralizing alarm. The blood flow rate will now automatically be set to 100 ml/min. 4. Clamp the arterial blood line and disconnect it from the patient. 5. Connect the arterial blood line to the rinse-back solution and remove the clamp.



4:25

6. Start the blood pump, the rinse-back flow rate (blood flow rate) is set to 100 ml/min, adjust if required. CAUTION After having started the blood pump again, the operator is responsible for the monitoring of the venous pressure. CAUTION Note • The blood pump can automatically be stopped when the priming detector stops detecting blood in the venous line. Note

7. Stop the blood pump and clamp the venous blood line when the required amount of blood has been returned to the patient. 8. Disconnect the venous blood line from the patient. 9. Check that the patient is not connected to the machine in any way and that the blood pump has been stopped. 10. Remove the venous blood line from the priming detector. 11. Confirm patient disconnection; manually extinguish the blood path of the flow diagram by briefly pressing one of the Rinse/Drain, Heat disinf, or Chem disinf buttons. When this is done the machine does not detect blood anymore (the treatment time will be frozen, the air detector has now been byed and it is not possible to run the blood pump). After-treatment handling of the machine

12. If used and if not previously done, start emptying the SelectBag, the SelectCart cartridge and BiCart cartridge or only the BiCart cartridge. Once the emptying procedure has been started (Arrow button pressed), the fluid unit of the machine will automatically be disconnected and the dialysis fluid to the dialyzer will be byed. The treatment time will be set to zero and it will not be possible to return to treatment. 12.a. Open the upper latch(es) of the cartridge holder(s), pull out the latch(es) and lift upwards to their uppermost positions. 12.b. Press the Bicarbonate button twice, select All or BiCart by pressing corresponding Arrow button. Once the Arrow button has been pressed, the emptying procedure will start (see in 12 above). The SelectBag will automatically be drained after the cartridges has been drained if All has been selected. 13. If the pick-up tubes have been used for concentrates, place them in the disinfection ports of the machine. Once this is done, the fluid unit of the machine will automatically be disconnected and the dialysis fluid to the dialyzer will be byed. The treatment time will be set to zero and it will not be possible to return to treatment.

4:26



14. If used, remove the empty BiCart and SelectCart cartridge(s) after draining and close both the latches of the cartridge holder(s) properly (vertical position). (To close the lower latch; pull out and close.) If used, also remove the SelectBag when it is empty (or earlier if desired) by lifting the latch upwards. Then remove the SelectBag, pull out the latch and close it properly (vertical position). WARNING Avoid touching the plastic spike.

Be careful to avoid fluid from the SelectBag splashing into your eyes. WARNING

15. Invert the dialyzer. Disconnect the outlet dialysis fluid tube (to dialyzer) from the dialyzer and attach it to the safety coupling of the machine. The AK 200 S will now automatically create negative pressure in the fluid path, which empties the dialyzer of dialysis fluid. 16. When the dialyzer has been emptied, disconnect the inlet dialysis fluid tube from the dialyzer and attach it to the safety coupling of the machine as well. 17. Start a disinfection program, see handling instructions for each program in chapter 12, "Hygiene and maintenance", in this manual. 18. Open the door to the BVS cuvette holder. 19. Remove the dialyzer and the blood lines, dispose of according to local regulations. 20. Follow the instructions for hygiene and maintenance of the AK 200 S machine in chapter 12, "Hygiene and maintenance", in this manual. CAUTION If any of the pressure transducer protectors on the blood lines have been filled with blood and show signs of damage, i.e. blood has penetrated the disc filter, there is a risk of contamination of the machine. It is necessary to call an authorized technician who must replace and clean machine components that may have been contaminated. CAUTION



4:27


4:28



Chapter 5 Hemodialysis, single needle treatment Single needle treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Glossary of single needle parameters and key . . . . . . . . . . . . Single needle treatment with two blood pumps - BM 202 only . . . . . . . . . Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Arterial blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Venous blood line . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming and rinsing the extracorporeal circuit . . . . . . . . . . . . . . . . Priming and rinsing procedure in double needle mode, finishing in single needle/double pump mode . . . . . . . . . . . . . . . . . . . . . Priming and rinsing procedure in single needle/double pump mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Initiating . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Set the treatment parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Always check/adjust . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Connect the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Start the treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pressure alarm limits setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Venous/Arterial pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Single needle treatment with one blood pump . . . . . . . . . . . . . . . . . . . . . Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Single needle / single pump settings . . . . . . . . . . . . . . . . . . . . . . . . Connect the patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . For both pressure- and time-controlled phases . . . . . . . . . . . . . Start the treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . For both pressure- and time-controlled phases . . . . . . . . . . . . . Only for pressure-controlled phases . . . . . . . . . . . . . . . . . . . . . Only for time-controlled phases . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Double needle to single needle treatment - change during treatment . . Resume treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Single needle / single pump settings . . . . . . . . . . . . . . . . . . . . . . . . Only for pressure-controlled phases . . . . . . . . . . . . . . . . . . . . . Only for time-controlled phases . . . . . . . . . . . . . . . . . . . . . . . . Discontinuing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .


AK 200 S Operator’s manual - Single needle

5:2 5:2 5:3 5:4 5:4 5:4 5:5 5:6 5:6 5:6 5:9 5:11 5:11 5:11 5:12 5:13 5:15 5:15 5:15 5:17 5:18 5:18 5:19 5:19 5:19 5:21 5:21 5:21 5:22 5:23 5:24 5:24 5:24 5:25 5:26 5:27

5:1

Single needle treatment General The blood monitor offers a single needle facility using either one or two blood pumps (two blood pumps only possible with BM 202). Single needle treatment with two blood pumps is controlled by the stroke volume which gives an optimized accumulated blood volume for the treatment. Single needle treatment with one blood pump uses the arterial and venous clamps, which can be controlled and supervised by either time or pressure settings. Note • When performing single needle treatment there is always a certain amount of recirculation. The AK 200 S is equipped with a clamp on the arterial side in order to minimize recirculation. To further minimize recirculation the stroke volume should be maximized. To achieve this the following should be considered: - Make sure a correct blood pump rotor is used. There must be a correct adjustment of the occlusion of the blood pump segment being used. Check with the service technician responsible. - The volume of the expansion chamber(s) should be as big as possible. - The internal diameter of the needle should be as big as possible.

• Single needle treatment with two blood pumps cannot be selected if Low volume HDF mode is to be performed.

• Make sure that the venous blood pump is adjusted for the right pump segment diameter when single needle/double pump is performed. Note

5:2



Glossary of single needle parameters and key Single needle, double pump

The Arterial phase is when the arterial blood pump is running. The arterial blood pump runs until the system pressure high alarm limit has been reached. The Venous phase is when the venous blood pump is running. The venous blood pump runs until the stroke volume has been achieved. Cycle, together, an arterial phase and a venous phase are called a cycle. The Mean blood flow rate is the effective blood flow rate during the complete cycle, calculated from the venous blood flow rate. The mean blood flow rate can be adjusted by adjusting the blood flow rates for the arterial pump and the venous pump separately. The Stroke volume is the blood volume that es through the dialyzer during a cycle. The lower the stroke volume the greater the recirculation. The System pressure is measured after the dialyzer before the venous blood pump. The pressure fluctuates between the arterial phase and the venous phase, increasing during the arterial phase, decreasing during the venous phase. The machine uses the system pressure high alarm limit to control the arterial phase. Single needle, single pump

The Arterial phase is when the blood pump is running, the arterial line clamp is open and the venous line clamp is closed. The arterial phase can either be controlled by time or pressure settings. The Venous phase is when the blood pump is not running, the venous line clamp is open and the arterial line clamp is closed. The venous phase can either be controlled by time or pressure settings. Cycle, together, an arterial phase and a venous phase are called a cycle. The Mean blood flow rate is the effective blood flow rate during the complete cycle, calculated from the arterial blood flow rate. The Stroke volume is the blood volume that es through the dialyzer during a cycle. The lower the stroke volume the greater the recirculation.



5:3

Single needle treatment with two blood pumps - BM 202 only Preparations Follow the instructions in chapter 4 "Double needle treatment" beginning with "Check before starting the machine". Continue up to "Arterial blood line" in "Attaching the dialyzer and the blood lines".

Arterial blood line Continue to follow the instructions in chapter 4 in "Arterial blood line". Add the following item below, which refers to single needle/double pump treatments. 1. Arterial expansion chamber - place the expansion chamber in the holder (inlet and outlet facing downwards).

Figure 5:1

5:4

Arterial blood line with expansion chamber in HD, single needle/double pump, set-up



Venous blood line Continue to follow the instructions in chapter 4 in "Venous blood line". Add the following items below, which refer to single needle/double pump treatments. 1. Venous blood pump - leave the venous blood pump segment outside the pump housing as priming with one blood pump is recommended. See “Priming and rinsing procedure” further on in this chapter. 2. Venous expansion chamber - place the expansion chamber in the holder (inlet and outlet facing downwards). 3. System pressure transducer connector - attach the transducer protector firmly to the pressure transducer connector.

Figure 5:2


Venous blood line with expansion chamber in HD, single needle/double pump, set-up


5:5

Priming Priming and rinsing the extracorporeal circuit Before priming •

Connect the arterial line to the priming fluid.

•

Check that the venous line is correctly positioned in the priming detector.

•

Check all connections.

•

Check that the priming UF rate is correct by pressing the UF rate button, check PRIMING. Follow the instruction for use of the dialyzer.

Note • A flashing Bicarbonate or Acetate button indicates that Concentrate stand-by mode is active. Resume dialysis fluid preparation (deactivate concentrate stand-by mode) by pressing the flashing button once. The dialysis fluid will be ready within approximately 3 minutes. Note

Priming and rinsing procedure The priming and rinsing procedure can be performed either in double needle mode or in single needle/double pump mode. (The recommended procedure is in double needle mode as it is easier and less time-consuming.) The priming and rinsing procedure in double needle mode is described below as the first alternative. It is followed by the description of the procedure in single needle/double pump mode. Priming and rinsing procedure in double needle mode, finishing in single needle/double pump mode

1. Tilt the double chamber holder backwards until it clicks into position. By doing so the expansion chambers will be filled to a suitable level during priming. 2. Check that the venous blood line segment has not been inserted into the venous blood pump. 3. Press the flashing Priming button for three seconds to activate priming (lights up). 4. Follow the manufacturer’s instructions for use of the dialyzer and the blood lines.

5:6



WARNING Do not use the level adjustment buttons in combination with blood lines incorporating the ”balloon” type transducer protector, as the venous pressure reading might be adversely affected. WARNING

5. Press the flashing Blood pump button. The blood flow rate will automatically start at 100 ml/min. Adjust the blood flow. If the arterial blood pump segment has been automatically threaded, check for possible kinks. Prime and de-air the blood lines and the dialyzer. 6. Adjust the level in the venous drip chamber, so the level is well above the air detector head. 7. Attach the dialysis fluid tubes to the dialyzer when the time appears on the time display instead of Fch and the by path lights up on the flow diagram. Press the flashing Fluid by button and the dialysis fluid will enter the dialyzer when the by path lights up green on the flow diagram. 8. When the level in the air detector is correct, the Air detect button will start flashing and an attention regarding the inactivated air detector will appear. The buzzer can be muted but the attention will remain until the air detector is activated (manually when desired/automatically if the PRIMING VOLUME ACHIEVED attention alarm appears or when blood has been detected). 9. When the priming volume has been achieved, the blood pump automatically stops and the attention PRIMING VOLUME ACHIEVED Check line in priming detector appears. Note • Always follow the manufacturer’s recommendations for the minimum rinsing volume (for the blood lines and the dialyzer). Note

10. Place the double chamber holder back in its upright position. 11. Open the cover of the venous blood pump and place the venous pump segment inside the pump housing as in the figure below.

The pump segment can be threaded manually or automatically.



5:7

11.a. Manually: Turn the blood pump manually to thread the pump segment through it. When the pump segment is in place, close the blood pump cover. 11.b. Automatically: Place the pump segment over the blood pump rotor and close the blood pump cover, the blood pump segment will be threaded as soon as the flashing Blood pump button has been pressed. 12. Press the SN button briefly. Check that double pump mode has been selected, (DOUBLE PUMP will be flashing), or select DOUBLE PUMP by using the corresponding Arrow button. Activate the function by pressing the SN button for three seconds (lights up). 13. Press the flashing Blood pump button and let the machine go through a few cycles in double pump mode. At the same time, check that the arterial and venous blood pumps alternate sufficiently. If the venous blood pump segment has been automatically threaded, check for possible kinks. 14. Stop the blood pump or, if necessary, continue priming. When a certain amount of extra priming volume has been used this attention appears: EXTRA PRIMING VOLUME ACHIEVED Check line in priming detector Check priming fluid and waste bag. Stop the blood pump. If the operator wishes to restart priming, and at the same time set the priming volume value to zero, the Priming button has to be pressed for 3 seconds to exit priming mode. The Priming button starts to flash. After that, press the Priming button again to activate priming. The Priming button will light up and it is possible to repeat the priming procedure. If this is done, to remove the venous blood pump segment from the venous pump and deactivate the SN function to be able to repeat the priming procedure from the beginning. Note • After the machine has ed the function check and the by path on the flow diagram lights up green, it is possible to activate Concentrate stand-by mode in order to save concentrates before patient connection. See information in “Concentrate stand-by mode” in the “Controlling the machine” chapter. Note

5:8



Priming and rinsing procedure in single needle/double pump mode

1. Tilt the double chamber holder backwards until it clicks into position. By doing so the expansion chambers will be filled to a suitable level during priming. 2. Open the cover of the venous blood pump and place the venous pump segment inside the pump housing as in the figure below.

The pump segment can be threaded manually or automatically. 2.a. Manually: Turn the blood pump manually to thread the pump segment through it. When the pump segment is in place, close the blood pump cover. 2.b. Automatically: Place the pump segment over the blood pump rotor and close the blood pump cover, the blood pump segment will be threaded as soon as the flashing Blood pump button has been pressed. 3. Press the SN button briefly. Check that double pump mode has been selected, (DOUBLE PUMP will be flashing), or select DOUBLE PUMP by using the corresponding Arrow button. Activate the function by pressing the SN button for three seconds (lights up). 4. Press the flashing Priming button for three seconds to activate priming (lights up). 5. Follow the manufacturer’s instructions for use of the dialyzer and the blood lines. WARNING Do not use the level adjustment buttons in combination with blood lines incorporating the ”balloon” type transducer protector, as the venous pressure reading might be adversely affected. WARNING

6. Press the flashing Blood pump button. The mean blood flow rate will automatically start at 100 ml/min. Adjust the mean blood flow. If the blood pump segments has been automatically threaded, check for possible kinks. Prime and de-air the blood lines and the dialyzer. 7. Check that the arterial and venous blood pumps alternate sufficiently. 8. Adjust the level in the venous drip chamber, so the level is well above the air detector head.



5:9

9. Attach the dialysis fluid tubes to the dialyzer when the time appears on the time display instead of Fch and the by path lights up on the flow diagram. Press the flashing Fluid by button and the dialysis fluid will enter the dialyzer when the by path lights up green on the flow diagram. 10. When the level in the air detector is correct, the Air detect button will start flashing and an attention regarding the inactivated air detector will appear. The buzzer can be muted but the attention will remain until the air detector is activated (manually when desired/automatically if the PRIMING VOLUME ACHIEVED attention alarm appears or when blood has been detected). 11. When the priming volume has been achieved, the blood pumps automatically stops and the attention PRIMING VOLUME ACHIEVED Check line in priming detector appears. Note • Always follow the manufacturer’s recommendations for the minimum rinsing volume (for the blood lines and the dialyzer). Note

12. Place the double chamber holder back in its upright position. 13. If necessary, continue priming by pressing the flashing Blood pump button. When a certain amount of extra priming volume has been used this attention appears: EXTRA PRIMING VOLUME ACHIEVED Check line in priming detector Check priming fluid and waste bag. Stop the blood pump. If the operator wishes to restart priming, and at the same time set the priming volume value to zero, the Priming button has to be pressed for 3 seconds to exit priming mode. The Priming button starts to flash. After that, press the Priming button again to activate priming. The Priming button will light up and it is possible to repeat the priming procedure. Note • After the machine has ed the function check and the by path on the flow diagram lights up green, it is possible to activate Concentrate stand-by mode in order to save concentrates before patient connection. See information in “Concentrate stand-by mode” in the “Controlling the machine” chapter. Note

5:10



Initiating Set the treatment parameters CAUTION To avoid hazardous side effects during the treatment, parameters set should be suitable for the patient’s needs and tolerance.

The correct setting of the UF rate is important to avoid backfiltration. Set a minimum UF rate according to the instruction for the specific dialyzer. CAUTION Note • Negative pressure may cause generation of ”microbubbles”. Note

Always check/adjust •

Check the time on the Time display. Adjust if necessary; press the Time button, adjust REMAIN.

•

Check the required UF volume (patient weight loss). Press the UF volume button, check SET, adjust if necessary.

•

Check that the calculated UF rate (patient weight loss/h) is suitable. Press the UF volume button, check CALC UFR. Adjust time or UF volume if necessary.

•

Check that the minimum UF rate is set to the required value. Press the UF rate button, check MIN UFR, adjust if necessary.

•

Check that the dialysis fluid flow rate is set to the required value. Press the Fluid flow button, check SET, adjust if necessary.

CAUTION Once the treatment parameters are set the should that the control and protective systems (see chapter 1) for conductivity and temperature operate with the desired values and that they are in agreement. This verification is made by comparing the bargraph displays and the information display before connecting the patient. CAUTION



5:11


1. Check that single needle mode has been activated (lit SN button). Also check that double pump mode has been selected; DOUBLE PUMP will be flashing on the information display. 2. Check that the venous blood pump segment has been properly inserted into the venous blood pump. 3. Check that the expansion chambers are in an upright position and are filled to the correct levels (refer to the instructions for use of the individual blood line). 4. Check that there is no air in the blood lines and that the level in the venous drip chamber is well above the air detector head. 5. Activate the air detector by pressing the Air detect button if it has not previously been activated during priming. Note • If the air detector has not been previously activated, it will automatically be activated when the priming detector detects blood. Note

6. When the priming and rinsing procedure is complete, check that the blood pumps have been stopped, if not, press the Blood pump button. Adjust the mean blood flow rate to the proper start value. Note • Always follow the manufacturer’s recommendations for the minimum rinsing volume (for the blood lines and the dialyzer). Note

7. Connect the blood lines to the patient. Note • The blood pump can automatically be stopped when the priming detector detects blood in the venous line and the blood path of the flow diagram lights up. Note

8. Remove any obstructing clamps. 9. Start the blood pumps and set the required mean blood flow rate suitable for the patient.

5:12



When the priming detector detects blood in the venous line, the blood path in the flow diagram will light up red. The Start UF Stop button, the Venous pressure button (if the Venous pressure is below +10 mmHg) and the TMP button starts to flash. If no heparin value has been set, the Heparin button will also flash. The machine will start to count down the treatment time at the same time as blood is detected. When blood has been detected for 20 seconds the blood path will remain lit until treatment has been discontinued. This is valid even if the venous blood line is removed from the priming detector.


1. Press the flashing Start UF Stop button (steady light) to start ultrafiltration. (The machine will start to count down the treatment time at the same time as blood has been detected.) 2. Press the flashing TMP button to automatically set the alarm limits around the current pressure. Note that the TMP alarm limits should be set in accordance with the UF rate and dialyzer UF coefficient. 3. If the Venous pressure button is flashing, press the button to automatically set the low alarm limit to +10 mmHg. 4. Press the Venous pressure button to manually set the alarm limits around the current pressure. Change the limits on the information display by using the Arrow buttons and the Set knob. 5. Press the Arterial pressure button to manually set the alarm limits around the current pressure. As the arterial pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob. 6. If necessary, adjust the levels in the expansion chambers. The levels should be as low as possible (i.e. without air ing into the blood lines at the end of the venous phase), in order to best achieve the stroke volume (SET). 7. Press the SN data button. Check that the current stroke volume (STROKE) corresponds with the set value (SET). At the same time, read off the system pressure (PRESSURE). See "Glossary of single needle parameters and key " previously in this chapter for further information. HCEN9751 Revision.12.2005 Program version 8.xx


5:13

Note • It is possible to optimize the current mean blood flow rate by adjusting the blood flow rate for the venous pump or the arterial pump separately. This results in more cycles1 during treatment i.e. increased accumulated blood volume. Note that the arterial pump never runs faster than twice the speed, or more slowly than half the speed, of the venous pump and vice versa. If this optimization is desired: Press the Blood flow button, select VEN and/or ART by using the Arrow buttons. Adjust the blood flow rates, making sure that venous and arterial pressure remain within the limits recommended by the clinic for that particular patient’s blood access. Note

8. If the Heparin button flashes, press the button to confirm no heparinization using the heparin pump, or set the values. See “Arterial blood line, Heparinization” in chapter 4. 9. If the BPM, the BVS or the Diascan functions are going to be used during treatment, see the corresponding chapters for activation and settings. Note • When no other screen is displayed on the information display, the Treatment overview screen will be displayed at all times during treatment2. On this screen, the operator can obtain an overall picture of parameter values, valid at that time, for the on-going treatment. See “Treatment overview screen” in the “Controlling the machine general guidelines” chapter for details. Note

1 For

further information, see "Glossary of single needle parameters and key " previously in this chapter 2 Can be removed by preset 5:14



Pressure alarm limits setting TMP

The machine is equipped with a centralizing function to simplify the correct setting of the TMP alarm limits. If there is a choice not to use the centralizing function as a preset or wide alarm limits range are preset, it is the operator’s responsibility to check that the alarm limits are set around current pressure. When the alarm limits are outside the preset range, the TMP button starts to flash. If 2.5 min. of the treatment have elapsed and the alarm limits are still outside the preset range, an attention alarm is activated: TMP LIMITS ADJUST Press TMP key Press the TMP button to centralize the alarm limits around the current pressure. The alarm display automatically widens and the button starts to flash when the blood flow is stopped. Also when the UF equation is changed or when the Start UF Stop button is pressed the button will start to flash. The alarm display may also be widened temporarily: Press the TMP button followed by the Arrow button beneath the required alarm limit and adjust that specific limit. (The button will start to flash as soon as the alarm display is outside the preset range). CAUTION When negative TMP alarm limits are set, no alarm that backfiltration may occur.


Venous/Arterial pressure

There is no centralizing function for Arterial and Venous pressure when performing single needle treatments. The alarm limits has to be set manually. The Arterial pressure alarm limits may be widened temporarily when the blood flow rate has been changed, or when the blood pump(s) has been stopped. Press the Arterial pressure button followed by the Arrow button below the required alarm limit and adjust that specific limit. As soon as the Venous pressure low alarm limit is set below +10 mmHg the button starts to flash. Press the Venous pressure button and the low alarm limit will automatically be set to +10mmHg.



5:15

Low venous pressure alarm limit setting below +10 mmHg

During certain conditions a very low venous pressure can occur e.g. when a central venous catheter is being used. In order to perform a dialysis treatment under this condition it can be necessary to set the low alarm limit below the normal limit of +10 mmHg. To make this possible the AK 200 S can be preset upon request from the clinic. However, the following conditions have to be fulfilled: •

The function has to be ordered by the physician

•

The machine has to be identified/labelled

•

The preset has to be documented in the machine logbook

CAUTION If a venous pressure alarm limit below +10 mmHg is set, a disconnection of the venous blood line may not be detected through a venous pressure drop. Special attention from the operator is therefore mandatory. CAUTION

Operating and setting

1. Press the Venous pressure button. 2. Press the LOW and HIGH arrows simultaneously and move the alarm limit below +10 mmHg. The centralizing function will now work below +10 mmHg.

5:16



Discontinuing The discontinuing procedure can be performed either in double needle mode or in single needle/double pump mode. (The recommended procedure is in double needle mode as it is easier and less time-consuming.) Discontinuing in double needle mode after single needle/double pump treatment

Follow the instructions in chapter 4 "Discontinuing" and "Discontinuing procedure". Add the following instructions below, after point 3 (Stop the blood pump) in "Return the blood". 1. Press the lit SN button for 3 seconds to deactivate the single needle function. 2. Remove the venous pump segment from the venous blood pump. 3. Continue by following the instructions in "Return the blood" in chapter 4, starting with point 4. Discontinuing in single needle/double pump mode

Follow the instructions in chapter 4 "Discontinuing" and "Discontinuing procedure" without deactivating the single needle function.



5:17

Single needle treatment with one blood pump Preparations Follow the instructions in chapter 4 "Double needle treatment" beginning with "Check before starting the machine". Add the following below. Attach an expansion chamber, connecting it between the dialyzer and the venous blood line. This is in order to reduce the amount of recirculation in the system (i.e. to achieve a greater stroke volume). Follow the instructions in chapter 4, "Venous blood line" in "Attaching the dialyzer and the blood lines", and attach the expansion chamber as in the figure 5:5. 1. Venous expansion chamber - place the expansion chamber in the holder in an upright position (inlet and outlet facing downwards). 2. Connect the dialyzer end of the venous blood line to the blood line with the expansion chamber. 3. Connect the blood line with the expansion chamber to the dialyzer. Do not connect the line at the top of the expansion chamber to the system pressure transducer (the system pressure is not used when single needle/single pump treatment is performed).

Figure 5:5

5:18

Venous blood line with attached expansion chamber in HD, single needle/single pump, set-up



Prime and de-air the blood lines and the dialyzer as described in chapter 4. The venous expansion chamber should be filled to be level with the groove of the chamber. Close the clamp at the top of the expansion chamber.

Single needle / single pump settings The arterial and venous phases during a cycle can either be controlled by pressure or time settings. In practice this means that if the times for the phases are maximized to 20 seconds, the high and low venous pressure alarm limits set will control the phases. Pressure control settings usually imply more cycles and a greater accumulated blood volume for the treatment. The following pages include instructions for both the variants. Continue to follow the instructions in chapter 4 up to "Connect the patient" in "Initiating hemodialysis".


For both pressure- and time-controlled phases

1. Press the SN data button briefly and check/adjust the preset times for the arterial and venous phases; at this point they should be adjusted to suitable times to be used during patient connection and treatment start. Adjust the times below VEN TME and ART TME separately by using the Arrow buttons and the Set knob. 2. Check that the venous expansion chamber is in an upright position and is filled to a correct level (refer to the instructions for use of the individual blood line). 3. Check that there is no air in the blood lines and that the level in the venous drip chamber is well above the air detector head. 4. Activate the air detector by pressing the Air detect button if it has not previously been activated during priming. Note • If the air detector has not been previously activated, it will automatically be activated when the priming detector detects blood. Note

5. When the priming and rinsing procedure is complete, check that the blood pump has been stopped, if not, press the Blood pump button. Adjust the blood flow rate to the proper start value.



5:19

Note • Always follow the manufacturer’s recommendations for the minimum rinsing volume (for the blood lines and the dialyzer). Note

6. Press the SN button briefly and select SINGLE PUMP by using the corresponding Arrow button; SINGLE PUMP will be flashing. Activate the function by pressing the SN button for 3 seconds (lights up). 7. Connect the blood lines to the patient. Note • The blood pump can automatically be stopped when the priming detector detects blood in the venous line and the blood path of the flow diagram lights up. Note

8. Remove any obstructing clamps. 9. Start the blood pump and set the arterial blood flow rate (ART FL). Check that the resulting mean blood flow rate (MEAN FL) is the required flow, suitable for the patient. When the priming detector detects blood in the venous line, the blood path in the flow diagram will light up red. The Start UF Stop button, the Venous pressure button (if the Venous pressure is below +10 mmHg) and the TMP button starts to flash. If no heparin value has been set, the Heparin button will also flash. The machine will start to count down the treatment time at the same time as blood is detected. When blood has been detected for 20 seconds the blood path will remain lit until treatment has been discontinued. This is valid even if the venous blood line is removed from the priming detector.

5:20




For both pressure- and time-controlled phases

1. Press the flashing Start UF Stop button (steady light) to start ultrafiltration. (The machine will start to count down the treatment time at the same time as blood has been detected.) 2. Press the flashing TMP button to automatically set the alarm limits around the current pressure. Note that the TMP alarm limits should be set in accordance with the UF rate and dialyzer UF coefficient. 3. If the Venous pressure button is flashing, press the button to automatically set the low alarm limit to +10 mmHg. Depending on whether pressure- or time-controlled phases are to be used, continue by following the instructions starting with position 4 for each variant. Only for pressure-controlled phases

4. Press the SN data button briefly and maximize the preset times for the arterial and venous phases to 20 seconds . Set the times separately below VEN TME and ART TME by using the Arrow buttons and the Set knob. 5. Press the Venous pressure button. Set the high venous pressure alarm limit to, say, +400 mmHg. After this, during the arterial phase, gradually adjust the low venous pressure alarm limit to, say, +200 mmHg. Make sure that the venous pressure alarm limits remain within the limits recommended by the clinic for that particular patient’s blood access. See Note below for further information about this setting. 6. Press the Arterial pressure button to manually set the alarm limits around the current pressure. As the arterial pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob. 7. If necessary, adjust the level in the venous expansion chamber. The level should be as low as possible (i.e. without air ing into the blood lines at the end of the venous phase), in order to best achieve a proper stroke volume (STROKE).



5:21

8. Press the SN data button. Check that the current stroke volume (STROKE) shows a proper value. See "Glossary of single needle parameters and key " previously in this chapter for further information. Note • The achieved stroke volume is determined by the size and position of the venous pressure alarm window. The wider the window, the greater the stroke volume. The higher the position of the window, the higher the venous flow. Set the venous pressure alarm limits in such a way that a proper stroke volume is being achieved. Bear in mind that as the venous pressure alarm limits are used to control the arterial and venous phases the extracorporeal circuit must continuously be monitored by visual inspection. A decreasing stroke volume and/or a decreasing mean blood flow rate may indicate clotting or a kinked venous blood line. To optimize the treatment: - Check the stroke volume; press the SN data button, check STROKE. Optimize by adjusting the venous pressure alarm window and keeping the level in the venous expansion chamber as low as possible. - Maximize the arterial blood flow rate; turn the Blood flow knob, adjust ART FL. This will shorten the arterial phase, which results in more cycles3 during the treatment i.e. increased mean blood flow rate (MEAN FL) resulting in increased accumulated blood volume (ACC VOL). Note

9. If the Heparin button flashes, press the button to confirm no heparinization using the heparin pump, or set the values. See “Arterial blood line, Heparinization” in chapter 4. 10. If the BPM, the BVS or the Diascan functions are going to be used during treatment, see the corresponding chapters for activation and settings. Continue by following "Pressure alarm limits setting" instructions under "Single needle treatment with two blood pumps", in this chapter, as they are the same for single needle double pump and single needle single pump treatments. Only for time-controlled phases

4. Press the SN data button briefly and check/adjust the preset times for the arterial and venous phases. Adjust the times below VEN TME and ART TME separately by using the Arrow buttons and the Set knob. 5. Press the Venous pressure button to manually set the alarm limits around the current pressure. As the venous pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob.

3 For

further information, see "Glossary of single needle parameters and key " previously in this chapter 5:22



6. Press the Arterial pressure button to manually set the alarm limits around the current pressure. As the arterial pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob. 7. If necessary, adjust the level in the venous expansion chamber. The level should be as low as possible (i.e. without air ing into the blood lines at the end of the venous phase), in order to best achieve a proper stroke volume (STROKE). 8. Press the SN data button. Check that the current stroke volume (STROKE) shows a proper value. See "Glossary of single needle parameters and key " previously in this chapter for further information. 9. If the Heparin button flashes, press the button to confirm no heparinization using the heparin pump, or set the values. See “Arterial blood line, Heparinization” in chapter 4. 10. If the BPM, the BVS or the Diascan functions are going to be used during treatment, see the corresponding chapters for activation and settings. Continue by following "Pressure alarm limits setting" instructions under "Single needle treatment with two blood pumps", in this chapter, as they are the same for single needle double pump and single needle single pump treatments.

Discontinuing The discontinuing procedure can be performed either in double needle mode or in single needle/single pump mode. (The recommended procedure is in double needle mode as it is easier and less time-consuming.) Discontinuing in double needle mode after single needle/single pump treatment

Follow the instructions in chapter 4 "Discontinuing" and "Discontinuing procedure". Add the following instructions below, after point 3 (Stop the blood pump) in "Return the blood". 1. Press the lit SN button for 3 seconds to deactivate the single needle function. 2. Continue by following the instructions in "Return the blood" in chapter 4, starting with point 4. Discontinuing in single needle/single pump mode

Follow the instructions in chapter 4 "Discontinuing" and "Discontinuing procedure" without deactivating the single needle function.



5:23

Double needle to single needle treatment - change during treatment Attach an expansion chamber, connecting it between the dialyzer and the venous blood line. This is in order to reduce the amount of recirculation in the system (i.e. to achieve a greater stroke volume). Follow the instructions below. 1. Prime and de-air a blood line with an expansion chamber, the expansion chamber should be filled to be level with the groove of the chamber. Close the clamp at the top of the expansion chamber and clamp the ends of the line. 2. Stop the Blood pump and stop ultrafiltration by pressing the Start UF Stop button. 3. Clamp the venous blood line close to the dialyzer (it is recommended to add an extra clamp on the arterial blood line close to the dialyzer as well) and disconnect the venous blood line from the dialyzer. 4. Connect the line with an expansion chamber between the dialyzer and the venous blood line, see figure 5:5 in "Preparations" in "Single needle treatment with one blood pump" previously in this section. Place the expansion chamber in the holder in an upright position (inlet and outlet facing downwards). Do not connect the line at the top of the expansion chamber to the system pressure transducer (the system pressure is not used when single needle/single pump treatment is performed).

Resume treatment 5. Press the SN button briefly and select SINGLE PUMP by using the corresponding Arrow button; SINGLE PUMP will be flashing. Activate the function by pressing the SN button for 3 seconds (lights up). 6. Remove any obstructing clamps. 7. Start the blood pump and set the arterial blood flow rate (ART FL). Check that the resulting mean blood flow rate (MEAN FL) is the required flow, suitable for the patient. 8. Press the flashing Start UF Stop button to start ultrafiltration. Press the flashing TMP button to automatically set the alarm limits around the current pressure.

Single needle / single pump settings The arterial and venous phases during a cycle can either be controlled by pressure or time settings. In practice this means that if the times for the phases are maximized to 20 seconds, the high and low venous pressure alarm limits set will control the phases. Pressure control settings usually imply more cycles and a greater accumulated blood volume for the treatment.

5:24



Depending on whether pressure- or time-controlled phases are to be used, continue by following the instructions starting with position 9 for each variant. Only for pressure-controlled phases

9. Press the SN data button briefly and maximize the preset times for the arterial and venous phases to 20 seconds . Set the times separately below VEN TME and ART TME by using the Arrow buttons and the Set knob. 10. Press the Venous pressure button. Set the high venous pressure alarm limit to, say, +400 mmHg. After this, during the arterial phase, gradually adjust the low venous pressure alarm limit to, say, +200 mmHg. Make sure that the venous pressure alarm limits remain within the limits recommended by the clinic for that particular patient’s blood access. See Note below for further information about this setting. 11. Press the Arterial pressure button to manually set the alarm limits around the current pressure. As the arterial pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob. 12. If necessary, adjust the level in the venous expansion chamber. The level should be as low as possible (i.e. without air ing into the blood lines at the end of the venous phase), in order to best achieve a proper stroke volume (STROKE). 13. Press the SN data button. Check that the current stroke volume (STROKE) shows a proper value. See "Glossary of single needle parameters and key " previously in this chapter for further information.



5:25

Note • The achieved stroke volume is determined by the size and position of the venous pressure alarm window. The wider the window, the greater the stroke volume. The higher the position of the window, the higher the venous flow. Set the venous pressure alarm limits in such a way that a proper stroke volume is being achieved. Bear in mind that as the venous pressure alarm limits are used to control the arterial and venous phases the extracorporeal circuit must continuously be monitored by visual inspection. A decreasing stroke volume and/or a decreasing mean blood flow rate may indicate clotting or a kinked venous blood line. To optimize the treatment: - Check the stroke volume; press the SN data button, check STROKE. Optimize by adjusting the venous pressure alarm window and keeping the level in the venous expansion chamber as low as possible. - Maximize the arterial blood flow rate; turn the Blood flow knob, adjust ART FL. This will shorten the arterial phase, which results in more cycles4 during the treatment i.e. increased mean blood flow rate (MEAN FL) resulting in increased accumulated blood volume (ACC VOL). Note

Continue by following "Pressure alarm limits setting" instructions under "Single needle treatment with two blood pumps", in this chapter, as they are the same for single needle double pump and single needle single pump treatments. Only for time-controlled phases

9. Press the SN data button briefly and check/adjust the preset times for the arterial and venous phases. Adjust the times below VEN TME and ART TME separately by using the Arrow buttons and the Set knob. 10. Press the Venous pressure button to manually set the alarm limits around the current pressure. As the venous pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob. 11. Press the Arterial pressure button to manually set the alarm limits around the current pressure. As the arterial pressure fluctuates during the cycle the alarm window has to be set accordingly. Change the limits on the information display by using the Arrow buttons and the Set knob. 12. If necessary, adjust the level in the venous expansion chamber. The level should be as low as possible (i.e. without air ing into the blood lines at the end of the venous phase), in order to best achieve a proper stroke volume (STROKE). 13. Press the SN data button. Check that the current stroke volume (STROKE) shows a proper value. See "Glossary of single needle parameters and key " previously in this chapter for further information. 4 For

further information, see "Glossary of single needle parameters and key " previously in this chapter 5:26



Continue by following "Pressure alarm limits setting" instructions under "Single needle treatment with two blood pumps", in this chapter, as they are the same for single needle double pump and single needle single pump treatments.

Discontinuing Follow the instructions in "Single needle treatment with one blood pump", "Discontinuing" in this chapter.



5:27


5:28



Chapter 6 Isolated UF


AK 200 S Operator’s manual - Isolated UF

6:1

Follow the instructions in "Hemodialysis, double needle treatment" up to "Connect the patient" chapter 4, after that see below. Note • Isolated UF can only be run in hemodialysis mode.

• Isolated UF can be performed before, in the middle of, or after the "normal" dialysis treatment.

• Set the heparin stop limit to 0.00 if heparinization is desired during the complete ultrafiltration phase. Note

1. Press the Time button and set the time for the ultrafiltration phase. 2. Press the UF volume button and select the UF volume for the ultrafiltration phase. 3. Press the Heparin button and set the heparin stop limit to the required time. 4. Start the blood circulation according to the instructions in "Hemodialysis, double needle treatment, Connect the patient" see chapter 4. 5. Press the Isol UF button for 3 seconds (lights up). 6. Press the Start UF Stop button (lights up). 7. Press the flashing TMP button to set alarm limits around the current pressures.

6:2



When the time for the ultrafiltration phase is 0.00, an attention alarm appears and the Time button starts to flash. 1. Press the Isol UF button for 3 seconds (the light goes out). 2. Press the Time button and set the time for the diffusion phase. 3. Press the UF volume button and select the UF volume for the diffusion phase. 4. Press the Heparin button and set the heparin stop limit to the required value. 5. Press the Start UF Stop button (lights up). 6. Press the flashing TMP button to set alarm limits around the current pressures. Note • By pressing the Time button the information display shows ed treatment time (ED) and ed treatment time without diffusion (NON DIFF) and the time in isolated ultrafiltration mode is included in both of these. By pressing the UF volume button the information display shows accumulated volume (UF VOL) and the ultrafiltration volume achieved in isolated ultrafiltration mode is included in this. Note



6:3


6:4



Chapter 7 Profiling Profiling of Na+ and HCO3- dialysis fluid concentration . . . . . . . . . . . . . Profiling of ultrafiltration rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Curve Setting/Change/Cancellation: . . . . . . . . . . . . . . . . . . . . . Activation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Activation of profiling with already preset models . . . . . . . . . . . . . . . . Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .


AK 200 S Operator’s manual - Profiling

7:2 7:4 7:5 7:5 7:5 7:5 7:7 7:7

7:1

Profiling of Na+ and HCO3- dialysis fluid concentration In order to optimize the dialysis treatment, the dialysis fluid concentrations of sodium and bicarbonate can automatically follow a predetermined, continuous curve changing the concentrations in a linear, degressive or progressive graph. A linear graph gives a constant change of concentration. A progressive graph means that the change of concentration values accelerates and a degressive graph means that the change of concentration slows down during treatment time. There are three parameters which determine the shape of the respective profile: The start value, the stop value and the so called half-time. The half-time describes and determines the time interval to reach halfway between the start and stop concentration. Different profile combinations can be programmed into three memories (models ) The simplest type of profile is the linear one. It is determined by selecting the linear graph and by setting a start and a stop concentration. AK 200 S will then perform a smooth and constant adjustment during the treatment time.

Figure 7:1

7:2

3 different graphs for profiling sodium and bicarbonate



Setting individualized non-linear (exponential) profiles requires one figure more: half-time (set in hours and minutes). Half-time determines the time interval to reach halfway between start and stop concentration. The individual curves can easily be drawn into a diagram. To show a degressive graph, draw the start concentration value at time zero and stop concentration value at end of treatment.

Figure 7:2

Profiling, Degressive graph

The progressive graph is just a reversed degressive graph.

Figure 7:3


Profiling, Progressive graph


7:3

Profiling of ultrafiltration rate The UF rate can follow a predetermined decreasing or increasing linear graph. The UF profile is determined by the total UF volume, time and start UF rate.

Figure 7:4

Linear graph for UF rate profiling

When UF profiling is used TMP is also acting as protective system. The operator has to readjust the TMP alarm limits during treatment in accordance with the UF rate and the dialyzer UF coefficient. Note • The UF profile curve will perform a parallel shift if either time or volume are changed. Note

7:4



Operation Follow the instructions in "Hemodialysis, double needle treatment" up to "Pressure alarm limits setting" chapter 4 and add the following.

Curve Setting/Change/Cancellation:

The setting is guided by menu technique, stepping back with the Hold button. 1. Press the Profiling button briefly. 2. Select the MODEL (memory). 3. Select the parameters to be profiled. (Na+, HCO3- and UF). Note • The parameters that are not profiled are set by using the standard handling for each parameter. Note

4. Select, if an actual stored profile should be CHANGE or CANCEL. If UF is selected, set START value in l/h (STOP value is automatically adjusted so that the total UF volume which was previously set is maintained). 5. Select the graph: LINEAR, PROGRESS or DEGRESS. (If UF is selected only LINEAR can be selected.) 6. Set START value (in mmol/l), STOP value (in mmol/l), if a non linear graph is chosen also HALF TME (in h:min). Note • If the remaining time is changed in priming after a certain half-time is set, the half-time will automatically readjust, keeping the same percentage in relation to remaining time. Note

Activation

7. Activate the profiling mode by pressing the Profiling button for 3 seconds. As soon as blood is detected in the venous line the profiling mode starts. Verification

8. the sodium, bicarbonate and UF-rate settings: 8.a. Press the Profiling button. 8.b. Select the parameters to be verified and press the arrow below CHECK on the information display. The characteristic (L: linear, D: degressive, P: progressive) and the half time are alternatively shown on the time display.



7:5

8.c. Press the arrow below the START value and one flashing dot on the bargraph display for conductivity will indicate the start conductivity, if sodium and bicarbonate profiles are to be verified. One flashing dot on the bargraph display for UF-rate will indicate the start value for UF-rate, if UF-profile is to be verified. 8.d. Compare the conductivity value and/or UF-rate value on the bargraph display with the conductivity value and/or UF-rate value shown on the information display. 8.e. Press the arrow below the STOP value and two flashing dots are indicating the stop conductivity and/or stop UF-rate on the baragraph displays. 8.f. Compare and the conductivity value and/or UF-rate on the information display. 9. Readjust the TMP alarm limits during treatment in accordance with the UF rate and the dialyzer’s UF coefficient. When treatment time equals 0:00, the profiling automatically stops. CAUTION When the remaining time is changed after the activation, the profiles for Na+ and HCO3- will not change. The stop value will not be reached if the remaining treatment time is decreased. CAUTION Note • The profiling parameters preset in each MODEL remain stored in AK 200 S memory even when the machine is switched off. Any preset MODEL can be activated for any treatment. Note

7:6



Activation of profiling with already preset models 1. Press the Profiling button briefly. 2. Select the MODEL: 1, 2 or 3. 3. Activate the profiling mode by pressing the Profiling button for 3 seconds. As soon as blood is detected in the venous line the profiling mode starts. Note • The profiling mode can be switched off at any time during the treatment. If the mode is switched off, AK 200 S will continue with the actual values (where it was stopped). If the profiling mode is switched on again, without having changed parameters, the machine will continue at the point where it was switched off. If profiling is activated during treatment, the profile will follow the predetermined parameters within the remaining time. This is also valid if a profiling mode has been stopped and is going to be continued with changed or cancelled parameters. Note

When treatment time equals 0:00 the profiling function stops. Verification

4. the sodium, bicarbonate and UF-rate settings: 4.a. Press the Profiling button. 4.b. Select the parameters to be verified and press the arrow below CHECK on the information display. The characteristic (L: linear, D: degressive, P: progressive) and the half time are alternatively shown on the time display. 4.c. Press the arrow below the START value and one flashing dot on the bargraph display for conductivity will indicate the start conductivity, if sodium and bicarbonate profiles are to be verified. One flashing dot on the bargraph display for UF-rate will indicate the start value for UF-rate, if UF-profile is to be verified. 4.d. Compare the conductivity value and/or UF-rate value on the bargraph display with the conductivity value and/or UF-rate value shown on the information display. 4.e. Press the arrow below the STOP value and two flashing dots are indicating the stop conductivity and/or stop UF-rate on the baragraph displays. 4.f. Compare and the conductivity value and/or UF-rate on the information display.



7:7

5. Readjust the TMP alarm limits during treatment in accordance with the UF rate and the dialyzer’s UF coefficient. CAUTION The operator has to make sure that the profile chosen is suitable for the treated patient. The parameters have to be verified prior to the treatment. CAUTION

7:8



Chapter 8 Hemodiafiltration, low volume General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Protective system for low volume HDF . . . . . . . . . . . . . . . . . . . . . . . . The following conditions have to be met in order to fulfil the accuracy of the measuring system . . . . . . . . . . . . . . . . . . . . . . . . . . Start up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priming and rinsing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Initiating and starting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Bolus infusion possibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hemodiafiltration, low volume, single needle, single pump . . . . . . . . .


AK 200 S Operator’s manual - HDF, low volume

8:2 8:2 8:3 8:4 8:6 8:7 8:8 8:8

8:1

General The BM 202 offers the possibility to perform infusion of substitution fluid from external infusion bags using the venous/infusion pump. A special infusion line for low volume HDF is required in addition to normal arterial and venous blood lines. See “List of concentrates, accessories and disposables, for use with the AK 200 S, Gambro Accessories” in chapter 1.

Protective system for low volume HDF The system is based on pump speed measuring as well as restrictor measuring. If the measured infusion pump speed differs from the calculated speed an attention alarm is issued to make the operator attentive to the pump failure. For the restrictor measuring it is essential that a correct infusion line is used to obtain the specified level of safety. The pressure in the expansion chamber changes due to changes of the infusion flow. This pressure is measured by the system pressure transducer. The supervision system uses this pressure to calculate the actual infusion flow and thereby the accumulated infusion volume. This accumulated volume is compared to the infusion volume calculated from the set infusion volume and ed treatment time. If there is a difference there will be an attention alarm to make the operator attentive to e.g. an obstructed line or an empty infusion bag. The attention alarms that can occur are: INFUSION PUMP FAILURE Deactivate HDF to continue Or INFUSION VOLUME DEVIATION Check cause, press HDF key For more information about them, see the Attention list in chapter 14.

8:2



The following conditions have to be met in order to fulfil the accuracy of the measuring system 1. The correct infusion line has to be used. 2. The placement of the infusion bags has to be correct throughout the treatment. The lowest part of the bags should be placed 0.5-1 meter above the venous infusion pump before priming procedure starts. This is to obtain a correct pressure in the infusion line. The bags have to stay in this position throughout the treatment. If they are moved a measurement error will be present until the next taration in the machine is performed. 3. The bags should be at room temperature. This is important since the fluid temperature affects the pressure in the expansion chamber.



8:3

Start up Follow the instructions in chapter 4 “Hemodialysis, double needle” from the beginning to “Priming and rinsing the extracorporeal circuit”. Continue as follows: 1. Place the infusion bags on the infusion pole 0.5-1 meter above the venous/infusion pump. 2. Expansion chamber - place the expansion chamber in the expansion chamber holder. The inlet lines must be facing downwards and the groove on the expansion chamber must be turned towards the rear of the machine. Tilt the expansion chamber holder backwards until it clicks into it’s first position. The expansion chamber will then be filled to a suitable level during priming procedure. 3. Infusion pump - open the cover of the pump and place the pump segment inside the pump housing. Turn the pump manually to thread the pump segment through it. When the pump segment is in place, close the pump cover. 4. Attach the infusion line coming from the infusion pump, firmly to the T/Y-connector prior to the drip chamber (see that there are no closed clamps). 5. System pressure transducer protector - attach the pressure transducer protector to the system pressure transducer connector. 6. Infusion line clamps - attach the male connector on the infusion line to the infusion solution (if more than two bags, use a multiconnector/multidivider). Make sure that the clamps on the connected lines are open. (And see that the clamps on the lines not used are properly closed).

8:4



Figure 8:1


Infusion line in HDF low volume, set-up


8:5

Priming and rinsing Follow the instructions in chapter 4 “Priming and rinsing the extracorporeal circuit” Add the following: 1. Activate HDF by pressing the HDF button for 3 seconds (the button will light up). 2. Set the priming volume for the infusion line (PRIMING) to at least 200 ml. The priming will start as soon as the Blood pump button is pressed, or if this is already done, as soon as the value is selected. The infusion pump will run at the same rate as when bolus is given. 3. When the priming of the infusion line is complete, the venous/infusion pump stops automatically. Turn the expansion chamber to it’s upright position. It is not necessary to adjust the level in the expansion chamber. Check the infusion line for air. If air is present, prime the line extra until it is free of air. If the blood lines were primed/rinsed before the infusion line, readjust the level in the venous drip chamber if necessary (see position 4 and 5 in “Priming and rinsing procedure” in chapter 4 in this manual). Note • It is not possible to use the level adjustment buttons (left (gray) area) for adjusting the level in the expansion chamber. There will be an alarm for system pressure if this is done. The machine will automatically readjust the level in the expansion chamber during both priming and treatment. Note

8:6



Initiating and starting Continue to follow the instructions in chapter 4, “ Initiating dialysis” and “Start the treatment” and add the following: 1. Briefly press the HDF button and set the total infusion volume (SET). AK 200 S will now automatically calculate the “total” ultrafiltration volume, i.e. the infusion volume + patient weight loss. Note • The UF volume set via UF volume button gives the net fluid removal from the patient, i.e. total ultrafiltration - infusion volume. Note

2. When blood is detected and the Start UF Stop button is pressed, the HDF procedure starts. CAUTION Make sure that the blood path of the flow diagram lights up, if it does not light up, check that the venous blood line is correctly placed in the priming detector. If the blood path does not light up, the machine considers the patient not connected and as a consequence the UF system is not controlling the patient ultrafiltration. If the air detector has not been activated during priming it will not be automatically activated until the priming detector detects blood. CAUTION Note • The HDF procedure start is delayed approximately 15 seconds after blood is detected. It is also stopped during the automatic calibration of the UF system. Note

When the treatment time equals 0:00, the HDF procedure stops automatically.



8:7

Bolus infusion possibility The machine is equipped with a ”bolus infusion” function to simplify extra infusion, e.g. in case of a hypotension episode during treatment. 1. Press the HDF button briefly. 2. Select the extra infusion volume (BOLUS). As soon as the value is selected, the bolus infusion will start and automatically run with a rate of 50 ml/min until the set infusion volume is given. The UF rate is automatically decreased to minimum UF rate during the time when the bolus infusion is given. Note • The accumulated bolus infusion volume is displayed below BOLUS. This volume is not automatically compensated for, thus if the UF goal is to be achieved, the same amount has to be added to the UF volume. Note

Hemodiafiltration, low volume, single needle, single pump Follow the instructions for single needle with one blood pump in chapter 5 and the instructions for low volume HDF in chapter 8, in this manual.

8:8



Chapter 9 BVS - Blood Volume Sensor General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ∆BV text information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Graphs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BVS ON/OFF . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BVS Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . BVS On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .


AK 200 S Operator’s manual - BVS

9:2 9:3 9:4 9:5 9:6 9:6 9:7

9:1

General CAUTION Medical decisions must not be based only on information from BVS, as there are many other factors that should be taken into .

There is no direct, independent supervision of the BVS. CAUTION

The BVS measures changes in the blood volume of the patient continuously during the treatment. 5 minutes after the priming detector has detected blood the BVS will acquire a reference value, 0%. Blood volume changes (∆BV) during the treatment will be related to the reference value. If the patient’s blood volume decreases this will result in a negative percentage. Conversely an increased blood volume will show as a positive percentage. During the function check of the blood monitor the BVS performs an self test, provided the BVS is in its on-position. The self test has to be performed with an empty cuvette holder. Therefore, the cuvette must be outside the cuvette holder until the function check of the blood monitor has been completed (flashing Priming button). Note • The blood flow rate has to be above a certain rate and the Hemoglobin value of the patient has to be above a certain value in order for a correct BVS reference value to be obtained. If not, attention alarms will be generated 30 minutes after treatment start. See the “Technical data and specifications” chapter for further details. If the blood flow rate decreases below the specified value after the BVS reference value has been obtained, no ∆BV value will be displayed (--- will be shown).

• If the BVS is turned on when priming has started, no self test will take place. As a consequence the accuracy may be outside the specified range. Note

9:2



The BVS is handled through the information display. Press the BVS button and the information display will light up. Data and parameters are entered using the Set knob. The information display is capable to show the following graphs: •

relative blood volume (∆BV) from the start of the measurement

•

UF rate from the start of the measurement

•

conductivity of the dialysis fluid from the start of the measurement

•

systolic blood pressure (if BPM has been installed) from the start of the measurement, the latest measured value before treatment start will be shown at time 0

The ∆BV is also presented as text information on the information display (bottom, left).

Figure 9:1

BVS, relative blood volume graph

Note • If the BVS button is pressed when no BVS is installed, the information display will remain dark. Note

BV text information The actual value of the ∆BV is presented as text information in the lower left corner. The range is from -40% to +10%. If the value is below -40% this is shown as “- -“, over +10% is shown as “++“ and “currently no data“ is shown as “....“.



9:3

Alarm An alarm is issued when the relative blood volume is outside the set alarm limit. The alarm limit is adjustable at any time (default level presettable). The alarm function can be turned on or off (presettable).

Figure 9:2

BVS, relative blood volume graph

To set an alarm limit, press the left Arrow button and turn the Set knob. It is possible to set the alarm limit in the range from -40% to -1%. To turn the alarm off, turn the Set knob until OFF is shown on the information display. OFF are fixed end points at both ends of the alarm range (OFF, -40%, -39%,...-2%,- 1%, OFF) which cannot be ed by turning the Set knob further. When an alarm is being issued the BVS button will light up with steady light and the Mute button will flash. There will be a soft buzzer signal. The BVS button then has to be pressed to show the information display.

9:4



Graphs It is possible to choose which combination of graphs to be shown on the information display. In addition to the ∆BV graph, which is always shown, the graphs that can be selected are: •

UF rate

•

conductivity in dialysis fluid

•

systolic blood pressure (if BPM has been installed)

Figure 9:3

BVS, combination of graphs

To select which combination of graphs to show, press the middle Arrow button and turn the Set knob. The graphs text information will be: •

∆BV = relative blood volume

•

∆BV/UFr = relative blood volume and UF rate

•

∆BV/COND = relative blood volume and conductivity

•

∆BV/UF/C = relative blood volume, UF rate and conductivity

•

∆BV/Psys = relative blood volume and systolic blood pressure

•

∆BV/UF/P = relative blood volume, UF rate and systolic blood pressure

The current setup will remain throughout the treatment. If the same setup is to be used for more treatments, a setup can be preset.



9:5

BVS ON/OFF Pressing the right Arrow button, allows two options. These are BVS ON and BVS OFF. This can be performed any time during the treatment. By turning the Set knob it is possible to select the functions: •

OFF

•

ON

Note • The BV value is not available until the reference value has been acquired. Note

BVS Off

Figure 9:4

BVS, graphs without relative blood volume graph

Turning the BVS off will stop all measurements. If the BVS button is pressed while the BVS is turned off, the information display will show the selected number of graphs, except the ∆BV (see figure above).

9:6



BVS On The BVS is turned on by turning the Set knob to ON. The effect will depend on in which context this is done and on the previous history during treatment. If the BVS is turned on before the reference value has been acquired, the information display will change from the OFF display above to the following example. Reference value will be acquired as normal.

Figure 9:5

BVS turned on before the reference value has been acquired

If the BVS is turned on after the reference value would have been acquired in a normal treatment, the information display will change from the OFF display to an ON display. The reference value will be acquired as soon as possible. The information display will show the ∆BV graph but it will not be related to the treatment start.

Figure 9:6


BVS, the reference value not related to the treatment start


9:7

Note • If the BVS is turned on after the reference value would have been acquired in a normal treatment, the reference value will not be related to the treatment start. Note

If the BVS is turned on again in a treatment during which the reference value has been acquired before, the BVS display may look like this:

Figure 9:7

BVS, interrupted relative blood volume graph

The ∆BV data which have been acquired earlier in treatment have been stored for later display.

9:8



Chapter 10 BPM - Blood Pressure Monitor (option) General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:2 Patient factors which affect readings . . . . . . . . . . . . . . . . . . . . . . . . . . 10:3 Handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:5 The BPM screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:6 BPM button pressed once . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:6 BPM button pressed twice . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:7 Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:8 Alarm limits setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:8 Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:9 Start/Stop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:10 Start . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:10 Stop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10:10


AK 200 S Operator’s manual - BPM

10:1

General The Blood Pressure Monitor measures blood pressure and pulse rate. It is possible to use the BPM as soon as the machine is started. All measurements which are taken 30 minutes before the priming detector detects blood will be displayed as previously measured values on the information display. The BPM cuff and cuff hose are protected against the discharge from a defibrillator (Type BF, defibrillator proof). CAUTION Do not touch the BPM cuff or cuff hose when a defibrillator is being discharged, as doing so may cause electric shock.

In the event of accidental wetting of the BPM cuff or cuff hose connections, wipe immediately to prevent moisture from entering the machine. No protective means for burn of the patient are provided when the BPM is used together with high frequency (HF) surgical equipment. CAUTION

The line from the cuff (cuff hose) is attached to the back of the AK 200 S (see "Rear of the machine" in chapter 2). The cuff is available in different designs and sizes, see "List of concentrates, accessories and disposables, for use with the AK 200 S" in chapter 1. The cuff and the cuff hose can be ordered from your Gambro representative. It is important to use proper cuff size for accurate measurements. Use the circumference of the patient’s arm to determine cuff size. If the bladder is too wide, the blood pressure reading will be erroneously low; if it is too narrow, the reading will be erroneously high. Apply the cuff snugly so that one finger can fit between the cuff and the patient’s arm. More information about how to choose the right cuff size, how to connect the cuff to the cuff hose and the cuff hose to the machine can be read in the “package insert” leaflet which is enclosed to the cuff and cuff hose. The “package insert” leaflet also contains information about how to properly apply the cuff on the patients arm.

10:2



Patient factors which affect readings Excess patient movement can interfere with readings. Ensure that the patient is not moving during readings, just as one would with manual readings. Avoid applying external pressure to the cuff during readings. Some arrhythmias may cause pressure fluctuations that make obtaining readings more difficult. If difficulty obtaining readings occurs in the presence of arrhythmia, blood pressure should periodically be verified by another method. •

Do not apply a blood pressure cuff to a limb with an access, e.g. fistula or graft.

•

Do not apply a blood pressure cuff to a limb being monitored with a pulse oximetry sensor.

•

Do not apply a cuff to a limb that has restricted blood flow.

•

Avoid applying a cuff to a limb that has an intravenous line in place.

CAUTION Check that the blood circulation in the arm is not affected due to blood pressure measurements.

The Blood Pressure Monitor must be used only for adult patients or for children with a pediatric cuff and not for infant or neonatal patients. The manufacturer advises the that the information originating from the Blood Pressure Monitor cannot be used alone as unique source of information to induce any therapeutic or pharmacological actions. CAUTION



10:3


10:4



Handling The BPM is handled using the BPM button, the Arrow buttons and the Set knob, see “Operator’s ” in the “Controlling the machine - general guidelines” chapter. When the BPM button is pressed, once or twice, the BPM screens will be shown on the information display. BPM button, steady light; indicates that a measurement check is in progress. BPM button, flashing light; indicates that an attention alarm which needs confirmation has been generated. Confirm by pressing the flashing BPM button.

When a measurement check is in progress, the BPM button will light up (steady light) and the current pressure in the cuff will be displayed in the bottom left corner of the information display. At the top of the information display the measurement values will be presented as “---” instead of numbers (not valid for continuous mode). As soon as the measurement check is finished the values for blood pressure and pulse rate will be presented beside the clock symbol which indicates the time for when the measurement check was performed. The cuff pressure will be maximum 180 mmHg the first time the blood pressure is being measured when a blood pressure measurement check is carried out. If there are difficulties for the BPM to obtain the correct values there will be two re-measurements with higher cuff pressure. If the measurement check still fails there will be an attention alarm to guide the operator to take correct actions (see chapter 14). If the measurement check was successfully performed, the cuff pressure will be maximum 50 mmHg above the latest measured systolic blood pressure for the following measurement checks in the sequence. Note • If the BPM button is pressed when no BPM has been installed, the information display will remain dark. Note



10:5

The BPM screens BPM button pressed once When the BPM button is pressed once, the latest measured values for systolic, diastolic, mean blood pressure and pulse rate will be shown as numerical values at the top of the information display. The clock symbol indicates the time for when the measurement check was performed. Previously measured values for systolic, diastolic, mean blood pressure and pulse rate will be shown as lines in the graph. It is also possible to start and stop measurement checks, choose mode and set alarms on this screen, see information further on in this chapter for each activity. •

The numerical value for the latest systolic blood pressure is presented in white. A white point marks every measurement check and a white line connects the points.

•

The numerical value for the latest diastolic blood pressure is presented in yellow. A yellow point marks every measurement check and a yellow line connects the points.

•

The numerical value for the latest mean blood pressure is presented in green. A green point marks every measurement check and a green line connects the points.

•

The numerical value for the latest pulse rate is presented in red and is . A red point marks every measurement marked with this symbol check and a red line connects the points.

Figure 10:1

BPM, screen with latest measured values and graph

The horizontal axis shows the time. The length of the axis equals the treatment time +10 min rounded off to the next half hour. Minimum length of the axis is 3 hours and maximum 10 hours. The red line shows elapsed treatment time.

10:6



The vertical axis to the left will show mmHg for the blood pressure. The grading will be set to 25 - 250 mmHg, with a marker on every 25 mmHg. The vertical axis to the right will show beats/min for the pulse rate and is marked with this symbol . The grading will be set to 25 - 175 beats/min with a marker at every 25 beats/min. If a measurement check fails or is outside the set interval, there will be an interruption of the line in the graph. However, in the event that a measurement check is outside the set interval, the value will be shown as numerical information at the top of the information display. It is possible to move between the points on the lines in the graph by using the Set knob in order to read off previously measured values. Turn the Set knob anticlockwise and a light blue horizontal line will be shown, indicating which measurement check is shown. The numerical values for this measurement check will now be shown at the top of the information display. This can be done in any BPM mode, also when a measurement check is in progress.

BPM button pressed twice When the BPM button is pressed twice, the 8 latest measured values for systolic, diastolic, mean blood pressure and pulse rate will be shown as numerical values, starting with the latest values at the top of the screen. It is also possible to start and stop measurement checks, choose time intervals for automatic mode and set alarms on this screen, see indicates information further on in this chapter for each activity. pulse rate, indicates the time for when the measurement check was performed.

Figure 10:2


BPM, screen with the 8 latest measured values


10:7

Alarm The BPM alarm function can be set to on or off by pressing the lit Arrow button below ALARM. Choose ON or OFF by using the Set knob. When the alarm function has been set to ON, attention alarms are generated when a value is outside the set alarm limit. The BPM button will flash simultaneously. When the attention alarm message has been read, confirm by pressing the flashing BPM button and the BPM screen will be shown. The measured numerical values outside the set alarm limits will be flashing.

Alarm limits setting To set an alarm limit, press the BPM button once or twice. Press the lit Arrow button below ALARM and turn the alarm function to ON by using the Set knob. Press the Arrow button a second time and the alarm limits will now be shown at the top of the information display.

Figure 10:3

BPM, setting the alarm limits

A white marker will point at the alarm limit that can be adjusted, set the alarm limit by using the Set knob. Pressing the left Arrow button once more will move the marker to the next alarm limit, set the alarm limit by using the Set knob. Repeat the procedure until all alarm limits have been set. Alarm limits can be adjusted at any time during treatment. There is also the possibility to preset the alarm limits. The alarm ranges are:

10:8

Systolic

Diastolic

Mean

Pulse rate

Low alarm limit

60-250

40-200

45-235

40-180

High alarm limit

60-250

40-200

45-235

40-180



Mode When the lit Arrow button below MODE is pressed it is possible to choose BPM mode. Set the desired mode by using the Set knob. The possibilities are manual (MANUAL ), automatic (AUTO), continuous (CONT) or off (OFF ). •

Manual; in this mode a measurement check has to be started manually when desired. Press the lit Arrow button below START and a measurement check will start. START will now change to STOP, and consequently, the measurement check will stop if the Arrow button is pressed a second time. When a measurement check is started manually the Hold button will light up and the information display will remain lit.

•

Automatic; in this mode measurement checks will take place automatically at set time intervals. A measurement check can always be started manually between the set intervals for the measurement checks by using the lit Arrow button below START. To set the time intervals press the BPM button twice, then press the lit Arrow button below INTERVAL and set the time intervals by using the Set knob. It is possible to set the time intervals between 3 - 60 minutes. The time until the next measurement check in the sequence is going to be performed is shown below NEXT on the screens in this mode.

•

Continuous; in this mode measurement checks will take place continuously for 5 minutes. Start the measurement check sequence by pressing the lit Arrow button below START. START will now change to STOP, and consequently, the measurement checks will stop if the Arrow button is pressed a second time. As soon as continuous mode has been started, the second screen will automatically be displayed. Previously measurement values will be shown at that time and values measured for the continuous mode will be added as soon as a new measurement check has been performed. The second screen will be shown during the period of time for when the mode is active.

•

Off; the blood pressure monitor is turned off (OFF).

Note • It is always possible to stop a blood pressure measurement check in progress, in any mode, by using the lit Arrow button below STOP.

• After treatment, when the cuff is removed from the patient, the blood pressure measurement will continue as set when automatic or continuous mode is chosen. Manual mode (MANUAL) or off (OFF) has to be chosen to stop measurement. It is still possible to read off previously performed measurement check values by pressing the BPM button once or twice. Note



10:9

Start/Stop Press the BPM button once in order to light up the information display.

Start To start a measurement check manually press the lit Arrow button below START. When a measurement check is in progress the current pressure in the cuff will be displayed in the bottom left corner of the information display. At the top of the information display the values will be presented as "---" instead of numbers (not valid for continuous mode). As soon as the measurement check has finished the new values will be presented.

Figure 10:4

BPM, measurement check in progress

Stop To stop a measurement check in progress, press the lit Arrow button below STOP. The measurement check will be stopped and the cuff will be deflated.

10:10



Chapter 11 Diascan General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:2 Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:2 How the measuring process is performed by the machine . . . . . . . . . . 11:2 Glossary of Diascan parameters and key . . . . . . . . . . . . . . . . . . 11:3 Precautions before use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:4 Handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:5 Screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:5 The first screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:6 Measurement mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:6 Alarm limit for clearance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:6 Measurement result values . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:7 The second screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:8 Distribution volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:8 Distribution volume calculation using the Watson formula . . . . 11:9 Forecast . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:10 Target . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:10 Alarm limit for Kt/V . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:10 Measurement result values when distribution volume has not been set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:11 Second screen symbol . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:11 Measurement result values when distribution volume has been set . 11:12 The third screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Latest measured values . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Accumulated and forecast values . . . . . . . . . . . . . . . . . . . . . . . . . . 11:13 Time to target . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:14 Third screen symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:14 Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:15 Clearance alarm limit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:15 Kt/V alarm limit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:15 Step-by-step instructions for measuring clearance and Kt/V . . . . . . . . . . 11:16 Single clearance measurement check . . . . . . . . . . . . . . . . . . . . . . . . . . 11:16 Continuous measuring of clearance . . . . . . . . . . . . . . . . . . . . . . . . . . . 11:18 Single Kt/V and clearance measurement check . . . . . . . . . . . . . . . . . . 11:20 Continuous measuring of Kt/V and clearance . . . . . . . . . . . . . . . . . . . 11:22


AK 200 S Operator’s manual - Diascan

11:1

General Application The Diascan can be used for: •

Clearance measurement (K) in order to read off the current dialysis efficiency for the on going treatment.

•

Dialysis dose measurement (Kt or Kt/V) in order to check that the prescribed dialysis dose is being maintained, which provides quality assurance for the treatments.

•

Kt/V target supervision, which means that the machine constantly calculates if the desired and minimum values for Kt/V, set by the operator for each individual patient, can be reached at treatment end. If not, the operator will be immediately notified during treatment.

The measurement checks can be performed one at a time when required, or continuously at set intervals during treatment. If Kt/V measurement is required, a distribution volume (VOLUME) has to be set before the measurement check takes place. The distribution volume is patient-related (based on the patients dry weight) and has to be properly estimated and set by the operator of the machine in order to obtain a correct Kt/V value.

How the measuring process is performed by the machine With the use of a conductivity sensor, placed after the dialyzer in the fluid path, it is possible to measure clearance during treatment. A measurement check is performed in two phases. During the first measurement phase (base line phase) data from the sensor is collected for some minutes. The second phase (step phase) begins with an increase or a decrease in the conductivity level. This is followed by data collection for some minutes. If there will be an increase or a decrease is dependent on the relation of the conductivity levels in the dialysis fluid before and after the dialyzer in the first phase. This is to ensure that the patient’s sodium balance remains as neutral as possible. When the second phase is complete the conductivity level is returned to the set value and the clearance calculation is performed. The calculation is based on the measured difference between the conductivity levels in the first and second phases.

11:2



Glossary of Diascan parameters and key Parameters:

K is clearance. Clearance tells the operator how much blood, in ml/min, is cleaned of urea after it has ed the dialyzer. This value can be compared with the current blood flow rate at that time. Kt is clearance multiplied by elapsed treatment time. This value (in litres) can be compared with the accumulated blood volume (in litres) achieved since treatment start. Kt/V is a calculation done by the machine depending on the set distribution volume entered by the operator of the machine. Qb is blood flow rate in ml/min. Na+ is the estimated sodium concentration in serum calculated by the machine with respect to serum conductivity. Key :

Diascan is the commercial name for a clearance sensor. Distribution volume is the urea distribution volume in litres (water in the body), estimated for the individual patient, based on the patient’s dry weight. The estimation is based on certain formulae used for this purpose, chosen by the prescribing physician responsible for the patient. The distribution volume has to be set by the operator of the machine in order for a correct Kt/V value to be obtained. Forecast in this context, is a machine-calculated prediction of the Kt or/and Kt/V value to be achieved at treatment end. Target in this context, is the desired Kt/V value set by the operator that is to be achieved at treatment end.



11:3

Precautions before use CAUTION Medical decisions must not be based only on information from the Diascan, as there are many other factors that should be taken into . CAUTION

The Diascan function can be used in HD mode, double needle treatment. It can be used when performing single needle treatment but the accuracy of the machine measurement may be compromised. The same is valid for profiling of sodium and bicarbonate, whereas the measurement accuracy is not affected when using profiling of ultrafiltration rate. If profiling is active, the profiling values will be frozen during the Diascan step. If the Diascan is activated in Isolated UF mode, the machine will generate an attention alarm telling the operator that the Diascan function is not available. An attention alarm is generated if a treatment parameter (see below) is changed at the same time as a measurement check is in progress, and it will not be possible to change the parameter. The treatment parameters that cannot be changed during an ongoing measurement check are: - sodium and bicarbonate (conductivity) - temperature - dialysis fluid flow - UF volume - profiling settings - isolated UF activation If possible, wait until the check is complete or turn off the Diascan in order to change the parameter. Another attention alarm is generated when one of the following is done at the same time as a measurement check is in progress: - the blood flow rate is changed - the Blood pump button is pressed - the Start UF Stop button is pressed - the Fluid by button is pressed - a treatment alarm that produce dialysis fluid by or blood pump stop is generated. In this case the measurement check is interrupted. The attention alarm is to be confirmed by pressing the flashing Kt/V button and the machine will automatically reschedule measuring as soon as possible. Note • The blood flow rate and the dialysis fluid flow rate have to be set within certain ranges in order for correct Diascan measuring results to be obtained. See the “Technical data and specifications” chapter for further details. Note

11:4



Handling The Diascan is handled using the Kt/V button, the Arrow buttons and the Set knob, see “Operator’s ” in the “Controlling the machine - general guidelines” chapter. When the Kt/V button is pressed the Diascan screens will be shown on the information display. Kt/V button, steady light; indicates that a measurement check is in progress. Kt/V button, flashing light; indicates that an attention alarm which needs confirmation has been generated. Confirm by pressing the flashing Kt/V button.

Screens

EN1115

The Diascan shows three different screens on the information display depending on whether the Kt/V button is pressed once, twice or three times. The screens change in sequence every time the Kt/V button is pressed.

Figure 11:1

Diascan screens, without set distribution volume

EN1161

If the distribution volume (VOLUME) has been set by the operator, the second and third screen will change automatically and it will be possible to set a Kt/V target value (TARGET) and a Kt/V alarm limit (LIMIT).

Figure 11:2


Diascan screens, set distribution volume


11:5

The first screen The Diascan measurement mode is to be set on this screen and, if desired, an alarm limit for clearance. Measurement result values for K, Kt (or Kt/V), Na+, Qb and elapsed treatment time are displayed when measurement checks have been performed. Press the Kt/V button once and the first Diascan screen will be shown:

Figure 11:3

First Diascan screen

Measurement mode The Diascan is activated by pressing the lit Arrow button below Diascan. When Diascan is flashing, turn the Set knob clockwise to choose a single measurement check or continuous checks at intervals (the intervals are 15, 30 or 60 minutes). If desired, it is also possible to deactivate the Diascan by turning the Set knob anticlockwise to (OFF).

Alarm limit for clearance The alarm limit for minimum clearance is to be set by pressing the lit Arrow button below K LIMIT until the text is flashing. Set a proper alarm limit by turning the Set knob. For further information; see “Alarms, Clearance alarm limit” in this chapter.

11:6



Measurement result values

Figure 11:4

First Diascan screen with measurement result values

When a measurement check has been performed, measurement result values are shown as numerical values as well as graphs. •

Red graph on the base line of the diagram shows elapsed treatment time (t) in hours.

•

Green dots and graph in the diagram show all measured serum sodium (Na+) values in mmol/l during treatment.

•

Red graph in the diagram shows blood flow rate (Qb) in ml/min.

•

The numerical value below K shows the latest measured clearance value. White dots and graph in the diagram show all measured clearance (K) values in ml/min during treatment.

•

The numerical value below Kt (or Kt/V if distribution volume has been set in the second screen), shows the accumulated Kt (or Kt/V) value that has been achieved since treatment start.

Failed measurement checks are indicated by the symbol --- below K. Broken line graphs for clearance (K) and serum sodium (Na+) will also be displayed in this case.



11:7

The second screen On this screen the distribution volume is to be set if Kt/V measurement is desired. It is also possible to set a target value and an alarm limit for Kt/V. Forecast and measurement result values for accumulated Kt (or Kt/V if distribution volume has been set) will be displayed when measurement checks have been performed. The screen will automatically change when distribution volume has been set. Press the Kt/V button twice and the second Diascan screen will be shown:

Figure 11:5

Second Diascan screen

Distribution volume The operator is requested to set a distribution volume in litres, estimated for the individual patient, in order to obtain a correct Kt/V value from the Diascan. The distribution volume has to be properly estimated and set by the operator. The calculation of Kt/V done in the machine is entirely dependent on the value for the individual patient being the correct one. For further information; see “Glossary of Diascan parameters and key ” in this chapter. When the lit Arrow button below VOLUME is pressed the text will flash and --- (zero) will be shown on the information display. The volume is now to be set by using the Set knob, see below. If desired, it is possible for the machine to carry out a distribution volume calculation using the Watson formula, see next section for instructions. After the lit Arrow button has been pressed, once the Set knob is turned clockwise, 40 l is the default starting point value . Adjust the value as necessary. If desired, set the value to zero (---) by turning the Set knob anticlockwise, and the machine will consequently display only the Kt value. When a measurement check has been performed, the screen will show different measurement result values dependent on whether the distribution volume has been set or not. The screen will automatically change.

11:8



Distribution volume calculation using the Watson formula

It is possible for the machine to carry out a distribution volume calculation, displayed in litres, using the Watson formula. In order for the machine to provide a value, gender, weight, height and age (if male) of the particular patient must be entered into the machine. When the calculation has been done, a (W) will be displayed beside the distribution volume value provided, showing that the value has been calculated by the machine. After the lit Arrow button below VOLUME has been pressed, the text will flash and --- (zero) will be shown on the information display. Immediately turn directly the Set knob anticlockwise and the Watson screen will be displayed as below.

Figure 11:6

The Watson screen

Confirm entering the calculation procedure by pressing the Arrow button below Continue and the screen will change. Gender, Male or Female, is to be selected first by turning the Set knob. The selected alternative will flash; press the Arrow button below Continue to confirm selected alternative. The screen will then automatically change and patient weight is to be selected. Enter patient weight and height in a similar way, as above. If Male has been selected, patient age is to be entered in the same way too. If necessary, cancellation can be done by pressing the Hold button during the procedure. When all data have been entered, the screen will change and it will take a few seconds until it changes again and returns to the original screen. The distribution volume value, in litres, calculated by the machine according to the Watson formula, will be shown below VOLUME. A W in brackets is shown beside the value indicating that the value has been calculated by the machine. Note that if the distribution volume value (VOLUME) is changed, the (W) beside the value will disappear. If a new calculation is desired, turn the Set knob anticlockwise until --(zero) appears, and it will be possible to redo the procedure from the start.



11:9

Forecast The numerical value below FORECAST is a calculation of the Kt or Kt/V value that is estimated to be obtained when the treatment is complete. If a distribution volume (VOLUME) has been set, this Kt/V forecast value will be calculated by the machine and automatically be shown as soon as the first measurement check has been performed. If a distribution volume has not been set, the machine will only calculate and display the Kt forecast value. The calculated forecast value (Kt or Kt/V) is adjusted after every successfully performed measurement check throughout the treatment.

Figure 11:7

Second Diascan screen with set distribution volume

Target When the lit Arrow button below TARGET is pressed the text will flash and it is possible to set a desired dialysis dose target value (Kt/V) that is to be achieved at the end of treatment by using the Set knob. The target value for Kt/V can be set between OFF and 2.0. When the Kt/V target value has been set, the machine calculates the time needed to reach the target. This time to target is displayed on the third screen.

Alarm limit for Kt/V The alarm limit for minimum Kt/V is to be set by pressing the lit Arrow button below LIMIT until the text is flashing. Set a proper alarm limit by using the Set knob. For further information; see “Alarms, Kt/V alarm limit” in this chapter.

11:10



Measurement result values when distribution volume has not been set

Figure 11:8 Second Diascan screen with measurement result values, distribution volume not set •


•

Blue graph in the diagram shows the accumulated Kt value that has been achieved since treatment start. The graph continues as a dashed line until it reaches the goal flag indicating the forecast Kt value at treatment end.

•

The numerical value below FORECAST shows the Kt value that is estimated to be obtained when the treatment is complete.

Second screen symbol the goal flag indicates end of treatment.



11:11

Measurement result values when distribution volume has been set

Figure 11:9 volume

Second Diascan screen with measurement result values, set distribution

•


•

White graph in the diagram shows the accumulated Kt/V value that has been achieved since treatment start. The graph continues as a dashed line until it reaches the goal flag indicating the forecast Kt/V value at treatment end.

•

The numerical value below FORECAST shows the Kt/V value that is estimated to be obtained when the treatment is complete.

•

If the alarm limit for Kt/V has been set, it is indicated by a red dot in the vertical axis of the diagram and the axis will be red below the dot.

•

If a target value for Kt/V has been set, it is indicated in green in the vertical axis of the diagram.

•

If target value and alarm limit for Kt/V have been set, the difference between the two values is shown in yellow in the vertical axis of the diagram.

Second screen symbol the goal flag indicates end of treatment.

11:12



The third screen The third screen summarises measured and calculated parameters during treatment, shown as numerical values as soon as measurement checks have been performed. It is also possible to set or adjust the distribution volume and consequently the target value and the alarm limit for Kt/V, if this has not been done in the second screen. The screen will automatically change, as the second screen does, when distribution volume has been set. Press the Kt/V button three times and the third Diascan screen will be shown:

Figure 11:10

Third Diascan screen

Latest measured values The latest measured values for clearance (K) and serum sodium (Na+) are shown below date and time. The clock symbol indicates the time when the latest measurement check was performed.

Accumulated and forecast values The accumulated value for Kt, obtained since treatment start, is shown next. The small arrows indicate the calculated Kt forecast value that is estimated to be obtained when the treatment is complete. The same value is also shown below FORECAST as in the second screen. However, if distribution volume (VOLUME) has been set, the accumulated and forecast values for Kt/V are also shown directly underneath. In this case the value below FORECAST changes to the Kt/V forecast value.



11:13

Time to target When a target value for Kt/V (TARGET) has been set in the second screen (or in this screen), the machine will show an estimate of the treatment time needed in order to reach the desired Kt/V target value. Time to target will be calculated by the machine and automatically shown as soon as the first measurement check has been performed indicated by . this symbol If time to target is estimated to be within the remaining treatment time set, . the time will be displayed in green and a happy smiley symbol appears If not, the time will be displayed in red indicating that the treatment must be extended for the desired Kt/V target value to be reached. Note that an attention alarm will not be generated in this case.

Third screen symbols The happy smiley shows that the forecast remaining treatment time to reach the Kt/V target value is within the remaining set treatment time. The clock indicates time. This symbol indicates time to target, i.e. the time needed to reach the Kt/V target value set by the operator. The arrows indicates a forecast value. A dashed line; ---- indicates that there are no values measured or calculated to be displayed.

11:14



Alarms Clearance alarm limit The alarm limit for clearance is the lowest acceptable clearance value measured during treatment. When the lit Arrow button below K LIMIT (first screen) is pressed the text will flash. Set a proper alarm limit by using the Set knob. Once the Set knob is turned the starting point value is 50% of the current blood flow rate. Adjust the value as necessary. If desired, set the alarm limit to OFF by turning the Set knob anticlockwise. If the measured clearance value is below the alarm limit set, an attention alarm will be generated: CLEARANCE TOO LOW Check cause, adjust treatment parameters to increase clearance or adjust the alarm limit for clearance as above.

Kt/V alarm limit The alarm limit for Kt/V is the lowest acceptable Kt/V forecast value (calculated by the machine), that is to be accepted when the treatment is complete. The value that is to be set is the minimum Kt/V value that has to be achieved when the treatment has finished. When the lit Arrow button below LIMIT (second screen) is pressed the text will flash. Set a proper alarm limit by using the Set knob. If desired, set the alarm limit to OFF by turning the Set knob anticlockwise. If the Kt/V forecast value, estimated at that time to be obtained when the treatment is complete, is below the Kt/V alarm limit set, an attention alarm will be generated: Kt/V FORECAST TOO LOW Check cause, adjust treatment parameters or adjust the alarm limit for Kt/V as above.



11:15

Step-by-step instructions for measuring clearance and Kt/V Single clearance measurement check Procedure 1. Press the Kt/V button once and the first Diascan screen will be shown. 2. Press the lit Arrow button below Diascan; the text will flash. 3. Turn the Set knob clockwise one step and SINGLE A single measurement check is now activated.

Figure 11:11

will be shown.

Diascan, activated single measurement check

The single clearance measurement check will be performed on an appropriate occasion chosen by the machine. The occasion chosen is dependent on when the self-calibrations of the machine are to be performed. The Kt/V button will light up (steady light) during the period of time when the measurement check is being performed. When the measurement check has been performed the Diascan will automatically be turned to OFF. It is possible to repeat the procedure at any time during treatment.

11:16



Result The measurement result values are summarised and displayed as numerical values on the third Diascan screen. Read off the measurement result values there or, if further information is desired, on the corresponding Diascan screen, by pressing the Kt/V button once, twice or three times. Refer to information below “The first screen”, “The second screen” and “The third screen” in this chapter. Note • To ensure a correct result a single clearance measurement check should be activated no later than 30 minutes before discontinuing treatment. This is in order to have time to obtain a measurement result. Note



11:17

Continuous measuring of clearance Procedure 1. Press the Kt/V button once and the first Diascan screen will be shown. 2. Press the lit Arrow button below Diascan; the text will flash. 3. Turn the Set knob clockwise step by step until desired intervals for the measuring are shown (15, 30 or 60 minutes). Continuous measuring is now activated at set intervals. 4. If an alarm limit for clearance is required, press the lit Arrow button below K LIMIT; the text will flash. Turn the Set knob clockwise until a suitable value is shown and the alarm limit is set. For further information; see "Alarms, Clearance alarm limit", in this chapter.

Figure 11:12

Diascan, activated continuous measuring

The first clearance measurement check in the sequence will be performed on an appropriate occasion chosen by the machine. The occasions chosen are dependent on when the self-calibrations of the machine are to be performed. The Kt/V button will light up (steady light) during the period of time when the measurement checks are being performed.

11:18



Result The measurement result values are summarised and displayed as numerical values on the third Diascan screen. Read off the measurement result values there or, if further information is desired, on the corresponding Diascan screen, by pressing the Kt/V button once, twice or three times. Refer to information below “The first screen”, “The second screen” and “The third screen” in this chapter.



11:19

Single Kt/V and clearance measurement check Procedure 1. Press the Kt/V button once and the first Diascan screen will be shown. 2. Press the lit Arrow button below Diascan; the text will flash. 3. Turn the Set knob clockwise one step and SINGLE A single measurement check is now activated.

Figure 11:13

will be shown.

Diascan, activated single measurement check

4. Press the Kt/V button a second time and the second Diascan screen will be shown. 5. Press the lit Arrow button below VOLUME; the text will flash and --(zero) will be shown. The distribution volume is now to be set to a correct value for the individual patient, using the Set knob. If desired, it is possible for the machine to carry out a distribution volume calculation using the Watson formula, see "The second screen", "Distribution volume calculation using the Watson formula" in this chapter for instructions. If the value is to be set manually, once the Set knob is turned clockwise, 40 l is the default starting point value . Adjust the value as necessary. Note that the distribution volume has to be properly estimated for the individual patient. The calculation of Kt/V done in the machine is entirely dependent on the value for the individual patient being the correct one. For further information; see "Glossary of Diascan parameters and key " in this chapter.

11:20



Figure 11:14

Diascan, distribution volume set

The single Kt/V and clearance measurement check will be performed on an appropriate occasion chosen by the machine. The occasion chosen is dependent on when the self-calibrations of the machine are to be performed. The Kt/V button will light up (steady light) during the period of time when the measurement check is being performed. When the measurement check has been performed the Diascan will automatically be turned to OFF. It is possible to repeat the procedure at any time during treatment.

Result The measurement result values are summarised and displayed as numerical values on the third Diascan screen. Read off the measurement result values there or, if further information is desired, on the corresponding Diascan screen, by pressing the Kt/V button once, twice or three times. Refer to information below “The first screen”, “The second screen” and “The third screen” in this chapter. Note • Changes in treatment parameters (above all blood flow rate) affect measured clearance (K) values obtained during treatment and consequently the calculated Kt/V result. If the Kt/V calculation at treatment end is based on few clearance results, or only one, check that these results are relevant for the complete treatment. This is in order to ensure that the Kt/V value is a relevant one.

• To ensure a correct result a single Kt/V and clearance measurement check should be activated no later than 30 minutes before discontinuing treatment. This is in order to have time to obtain a measurement result. Note



11:21

Continuous measuring of Kt/V and clearance Procedure 1. Press the Kt/V button once and the first Diascan screen will be shown. 2. Press the lit Arrow button below Diascan; the text will flash. 3. Turn the Set knob clockwise step by step until desired intervals for the measuring are shown (15, 30 or 60 minutes). Continuous measuring is now activated at set intervals. 4. If an alarm limit for clearance is required, press the lit Arrow button below K LIMIT; the text will flash. Turn the Set knob clockwise until a suitable value is shown and the alarm limit is set. For further information; see "Alarms, Clearance alarm limit", in this chapter.

Figure 11:15

Diascan, activated continuous measuring

5. Press the Kt/V button a second time and the second Diascan screen will be shown.

11:22



6. Press the lit Arrow button below VOLUME; the text will flash and --(zero) will be shown. The distribution volume is now to be set to a correct value for the individual patient, using the Set knob. If desired, it is possible for the machine to carry out a distribution volume calculation using the Watson formula, see "The second screen", "Distribution volume calculation using the Watson formula" in this chapter for instructions. If the value is to be set manually, once the Set knob is turned clockwise, 40 l is the default starting point value . Adjust the value as necessary. Note that the distribution volume has to be properly estimated for the individual patient. The calculation of Kt/V done in the machine is entirely dependent on the value for the individual patient being the correct one. For further information; see "Glossary of Diascan parameters and key " in this chapter. 7. When the distribution volume (VOLUME) has been set the second screen will automatically change and it is possible to set a Kt/V target value that is to be achieved at treatment end, and an alarm limit for Kt/V. Press the lit Arrow button below TARGET; the text will flash. Turn the Set knob clockwise until a suitable value is shown. The machine uses the set target value to calculate the time needed to reach the target. For further information; see " The second screen", in this chapter. 8. If an alarm limit for Kt/V is required, press the lit Arrow button below LIMIT; the text will flash. Turn the Set knob clockwise until a suitable alarm limit value is shown. For further information; see "Alarms, Kt/V alarm limit", in this chapter.

Figure 11:16

Diascan, distribution volume, Kt/V target and alarm limit set

The first Kt/V and clearance measurement check in the sequence will be performed on an appropriate occasion chosen by the machine. The occasions chosen are dependent on when the self-calibrations of the machine are to be performed. The Kt/V button will light up (steady light) during the period of time when the measurement checks are being performed. HCEN9751 Revision.12.2005 Program version 8.xx


11:23

Result The measurement result values are summarised and displayed as numerical values on the third Diascan screen. Read off the measurement result values there or, if further information is desired, on the corresponding Diascan screen, by pressing the Kt/V button once, twice or three times. Refer to information below “The first screen”, “The second screen” and “The third screen” in this chapter. Note • Changes in treatment parameters (above all blood flow rate) affect measured clearance (K) values obtained during treatment and consequently the calculated Kt/V result. If the Kt/V calculation at treatment end is based on few clearance results, or only one, check that these results are relevant for the complete treatment. This is in order to ensure that the Kt/V value is a relevant one. Note

11:24



Chapter 12 Hygiene and maintenance General hygiene and maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:2 Glossary of disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:3 Disinfection history . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:4 List of disinfection screen symbols . . . . . . . . . . . . . . . . . . . . . . . . . 12:4 Schedule for hygiene and maintenance . . . . . . . . . . . . . . . . . . . . . . . . . 12:6 When the machine is planned not to be in use . . . . . . . . . . . . . . . . 12:7 Characteristics of different disinfection, decalcification and cleaning agents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:8 Hygiene - Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:9 General - Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:9 Performing Heat disinfection program . . . . . . . . . . . . . . . . . . . . . . . . 12:11 Performing Heat disinfection program with CleanCart . . . . . . . . . . . . 12:12 Performing Heat disinfection program with liquid citric acid . . . . . . . 12:13 Performing integrated Heat disinfection program with WRO 300 H . . 12:14 Automatic start of Heat disinfection program . . . . . . . . . . . . . . . . . . . 12:16 Automatic switch off after Heat disinfection program . . . . . . . . . . . . . 12:17 Integrated Heat disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:17 Hygiene - Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:18 General - Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:18 Chemical disinfectants . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:19 Performing Chemical disinfection program . . . . . . . . . . . . . . . . . . . . . 12:20 Filling the machine with chemical disinfectant . . . . . . . . . . . . . . . . 12:21 Residual test after Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . 12:23 Central Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:24 Performing central Chemical disinfection . . . . . . . . . . . . . . . . . . . . . . 12:24 Hygiene - Rinse/Drain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:25 Performing Rinse/Drain program . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:25 Performing Rinse/Drain program with CleanCart . . . . . . . . . . . . . . . . 12:26 Automatic start of Rinse/Drain program . . . . . . . . . . . . . . . . . . . . . . . 12:28 Automatic switch off after Rinse/Drain program . . . . . . . . . . . . . . . . 12:29 Maintenance - the flow path . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 The flow path . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 Decalcification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:30 Ultrafilter; how to change . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:31 Ultrafilter replacement reminder . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:32 Maintenance - the exterior of the machine . . . . . . . . . . . . . . . . . . . . . . . . 12:33 The outside . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 Top tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 Blood pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 Blood leak detector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:33 BPM cuff . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12:34


AK 200 S Operator’s manual - Hygiene and maintenance

12:1

General hygiene and maintenance The contents of this chapter concern the hygiene and maintenance of the AK 200 S that should be carried out by the operator of the machine. CAUTION No other maintenance than that mentioned in this chapter shall be performed by the operator/ of the machine. The casing must only be opened by a fully trained service technician, refer to the Service Manual.

Preventive maintenance shall be performed according to instructions in "General precautions before use" in chapter 1, in this manual. CAUTION

In order to maintain high microbiological quality of the dialysis fluid, it is important that the operator/ is attentive to hygiene and the maintenance of the machine. There are factors and procedures that affect the hygiene of the flow path and consequently the quality of the prepared dialysis fluid. The following must be considered: •

the disinfection, decalcification and cleaning must be performed according to instructions in this chapter

•

the frequency of disinfection, decalcification and cleaning of the machine should be carried out according to recommendations in this chapter

•

the quality of the inlet water entering the machine

•

the quality of the concentrates being used

•

the inlet water tube, which preferably should be disinfected by using integrated heat disinfection program

•

the arrangement of the drain connection from the machine, either using the integrated air-gap on the machine or via an arranged air-gap, to avoid back contamination from the drain system in both cases

Note • An attention alarm appears when the machine is started if more than 7 days1 have ed since the last complete disinfection. It is still possible to perform a treatment, and the attention light will switch off as soon as the priming button is lit (steady light). However, the attention alarm will appear again the next time the machine is turned on, if a disinfection program has not been completely carried out. Note

1 The

12:2

period of time can be preset AK 200 S Operator’s manual - Hygiene and maintenance


Glossary of disinfection Disinfection is removal or reduction of bacteria in the fluid path of the dialysis machine. Decalcification is removal of calcium and magnesium carbonate precipitates in the fluid path, originating from the bicarbonate dialysis fluid. Cleaning is removal of fats, proteins and organic material, originating from the patient and located mainly in the fluid path of the machine downstream the dialyzer.



12:3

Disinfection history When the Heat disinf or Chem disinf button is pressed a list of the most recently performed disinfection programs (both heat and chemical disinfection programs) will be displayed on the screen. The last performed disinfection program is shown at the top of the screen. The 50 most recently performed disinfection programs can be displayed, scroll up and down by using the Set knob. The symbols to the left on the screen show type of disinfection program. See list of disinfection symbols below. Date and time are shown next. If the disinfection program was successfully performed, the time for when the disinfection program was complete, in combination with a green tick, is shown. If the disinfection program was not successfully performed, the time for when the disinfection program was started, in combination with a red cross, is shown.

List of disinfection screen symbols indicates Heat disinfection program. C

indicates Heat disinfection program with CleanCart.

indicates Heat disinfection program with liquid Citric acid. indicates Chemical disinfection program with low concentration Peracetic acid. L

P

indicates Chemical disinfection program with Peracetic acid.

H

indicates Chemical disinfection program with Sodium hypochlorite.

F

indicates Chemical disinfection program with Formaldehyde.

indicates Chemical disinfection program with other chemical disinfectant. indicates Central chemical disinfection. C

12:4

indicates Chemical disinfection program with liquid Citric acid.






12:5

Schedule for hygiene and maintenance The schedule below is recommended for use by the operator/ of the AK 200 S. This recommendation is to keep a high level of performance of the machine. It is also a guideline for maintaining the hygiene of the fluid path and the outside of the machine to ensure the safety of the patient.

Frequency

Measures

After each treatment

1) Heat disinfection program. 2) Wipe down the outside of the machine with 70% ethanol or 60% isopropanol.

At least after every third treatment

Combine the Heat disinfection program with CleanCart C or liquid citric acid.

x

x

x

At least once every seventh treatment day

Heat disinfection program in combination with CleanCart A or a Chemical disinfection program with sodium hypochlorite. This should be performed directly after a Heat disinfection program in combination with CleanCart C or liquid citric acid.

x

x

x

When time after disinfection has exceeded seven days

Heat disinfection program before treatment.

Once every one to three months if UFD is installed2

Change of ultrafilter followed by a Heat disinfection program.

2 For

12:6

Cleaning

Decalcification

Disinfection

x

x

x

more information, see “Ultrafilters; frequency of change” in chapter 1 AK 200 S Operator’s manual - Hygiene and maintenance


Any Heat disinfection program can be exchanged to a Heat disinfection program in combination with CleanCart C or liquid citric acid. Heat disinfection can be replaced by Chemical disinfection but note that decalcification with CleanCart C or liquid citric acid has to be performed at least after every third treatment. An integrated Heat disinfection program is recommended when possible since it also includes the inlet water tube. In order to enable the cleaning agents to remove fats, proteins etc. efficiently, cleaning (CleanCart A or sodium hypochlorite) should be carried out after decalcification (CleanCart C or liquid citric acid). Note • An attention alarm appears when the machine is started if more than 7 days3 have ed since the last complete disinfection. It is still possible to perform a treatment, and the attention light will switch off as soon as the priming button is lit (steady light). However, the attention alarm will appear again the next time the machine is turned on, if a disinfection program has not been completely carried out. Note

When the machine is planned not to be in use If the machine is planned not to be in use for a period of time exceeding seven days the microbiological standard of the flow path can be maintained with one of the following alternatives: •

Perform a Heat disinfection program at least every seventh day and a Heat disinfection program before treatment.

•

Fill the machine with a proper chemical disinfectant in order to preserve it.

3 The HCEN9751 Revision.12.2005 Program version 8.xx

period of time can be preset AK 200 S Operator’s manual - Hygiene and maintenance

12:7

Characteristics of different disinfection, decalcification and cleaning agents The table below summarizes the characteristics of some generic substances used for internal disinfection, decalcification and cleaning of the AK 200 S. For more specific information about a certain commercial product, see manufacturer’s information. Disinfection, decalcification and cleaning Efficiency on inorganic precipitates

Efficiency on organic precipitates fats, proteins

Efficiency of disinfection

Calcium

Iron oxide

CleanCart-C and heat

High

Low

Medium

High

CleanCart-A and heat

None

None

High

High

Peracetic acid 0.01 to 0.15%

Low4

None

None

High

Citric acid liquid 2% and heat

High

Low

Medium

High

Sodium hypochlorite 0.5%

None

None

High

High

Formaldehyde 4%

None

None

None

High

Glutardialdehyde 2%

None

None

None

High

Decalcification and cleaning could also be performed at a lower temperature Acetic acid 2%

High

None

None

None

Oxalic acid 2%5

Low

High

None

None

CleanCart-C

High

Low

None

None

CleanCart-A

None

None

Low

None

4 The manufacturers of disinfectants based on peracetic acid claim that these agents can also be used for decalcification. However, experience has shown that peracetic acid is not reliable alone, use CleanCart-C, citric acid or acetic acid regularly. 5 Oxalic acid is recommended only when having problems with iron oxide precipitates (reddish-brown). Oxalic acid increases the wear of the machine.

12:8



Hygiene - Heat disinfection General - Heat disinfection During the Heat disinfection program (HEAT) the inlet water is heated up and flushed through the fluid monitor. The program begins with a rinse in order to rinse out possible residues from concentrates used in the preceding treatment. After this, the program consists of three consecutive phases; fill-up phase, circulation phase and drain phase. The actual disinfection takes place in the circulation phase. The circulation phase consists of a number of cycles where each cycle is a sequence where heated water is ed through all parts of the fluid path. The standard heat disinfection program consists of 15 such cycles. The AK 200 S fluid path is constructed in a way that prevents possible contaminants in the post-dialyzer fluid path from reaching the patient. The construction principle is called single , which means no recirculation in the fluid path, and a separation between the pre-dialyzer circuit and the post-dialyzer circuit. This is to ensure that no fluid from the downstream (post) dialyzer circuit comes into with the pre-dialyzer circuit. The construction principle is an effective obstacle to transmission of blood-borne viruses like Hepatitis B, from the fluid path to the patient, when a blood leak in the dialyzer has occurred. In addition the standard heat disinfection program has the capacity to make viruses inactive. The combination of the standard heat disinfection program process (15 cycles) and the safe hygienic construction of the fluid path (single ) described above provides high safety levels for the patient. The standard heat disinfection program is validated by using microbiological challenge tests according to NFS 90-304. The standard heat disinfection program fulfils the requirements in this standard. The heat disinfection program can be extended, and has been evaluated for 25 cycles. 25 cycles may be used in case of substantial contamination of the fluid path. This program provides different positions of the fluid path with at least 30% more heat. As a consequence, the duration of this heat disinfection program will be extended by approximately 10 minutes, compared to the standard program. It is possible to run a Heat disinfection program in combination with CleanCart: • Decalcification program with CleanCart-C •

Cleaning program with CleanCart-A

If Heat disinfection program with CleanCart is chosen, the contents of the CleanCart are dissolved and the solution is heated up and flushed through the fluid monitor during the heat disinfection program as described above. A rinse phase has been added at the end of the program, which leads to longer time for the program to be complete. The CleanCart-C can be replaced by liquid citric acid in order to perform a decalcification program; Heat disinfection program with liquid citric HCEN9751 Revision.12.2005 Program version 8.xx


12:9

acid. The program is performed in a similar way as Heat disinfection program with CleanCart. Note • In order to enable the cleaning agents to remove fats, proteins etc. efficiently, cleaning should be carried out after decalcification. Note

For further details; see “Data and specifications/Disinfection and Cleaning”. Handling instructions of above mentioned heat disinfection programs are described further on in this chapter.

12:10



Performing Heat disinfection program Note • The Heat disinfection program can be interrupted at any time by pressing the Rinse/Drain button for 3 seconds. The machine will then interrupt the procedure and finish off with a rinse and drain sequence. Note

Before starting Heat disinfection program •

Check that the dialysis fluid tubes are connected to the safety couplings

Procedure 1. Press the Heat disinf button briefly and check that HEAT is flashing on the information display.

Figure 12:1

Heat disinfection

The flashing text indicates that the Heat disinfection program, which is the default procedure, has been selected. If HEAT is not flashing, press the corresponding Arrow button below HEAT, the text will flash. 2. Confirm the choice by pressing the Heat disinf button for 3 seconds (the button lights up) and the Heat disinfection program starts. 3. If an automatic switch off is required, press the ON/OFF button for 3 seconds. 4. When the program is complete, rinse and drain sequence included, the Rinse/Drain button starts to flash.



12:11

5. Switch off the machine by pressing the ON/OFF button for 3 seconds. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine.

Performing Heat disinfection program with CleanCart Note • The Heat disinfection program with CleanCart can be interrupted at any time by pressing the Rinse/Drain button for 3 seconds. The machine will then interrupt the procedure and finish off with a rinse and drain sequence. Note

Before starting Heat disinfection program with CleanCart •


Procedure 1. Press the Heat disinf button briefly and select CleanCart by using the corresponding Arrow button below CleanCart on the information display. The text will flash indicating that the Heat disinfection program with CleanCart has been selected. 2. Confirm the choice by pressing the Heat disinf button for 3 seconds (the button lights up). 3. When the attention alarm CleanCart NOT ATTACHED TO HOLDER Attach or check Clean Cart appears, open the latches of the BiCart holder and place the CleanCart cartridge into the holder. Both pick-up tubes must remain in the disinfection ports of the machine. 3.a. If the attention alarm EMPTY AND REMOVE CleanCart Close holder appears, open the upper latch. The CleanCart cartridge will now be emptied. When the CleanCart is empty, remove it and close the latches. 3.b. Leave the cartridge in the holder during the entire program will automatically be emptied.

, it

4. The Heat disinfection program with CleanCart is now performed.

12:12



5. If an automatic switch off is required, press the ON/OFF button for 3 seconds. If preset, the CleanCart cartridge can be left in the holder until next function check is started. 6. When the program is complete and the machine has been drained, the Rinse/Drain button starts to flash. 7. Switch off the machine by pressing the ON/OFF button for 3 seconds. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine.

Performing Heat disinfection program with liquid citric acid Note • The Heat disinfection program with liquid citric acid can be interrupted at any time by pressing the Rinse/Drain button for 3 seconds. The machine will then interrupt the procedure and finish off with a rinse and drain sequence. Note

Before starting Heat disinfection program with liquid citric acid •


Procedure 1. Press the Heat disinf button briefly and select CITRIC by using the corresponding Arrow button below CITRIC on the information display. The text will flash indicating that the Heat disinfection program with liquid citric acid has been selected. 2. Confirm the choice by pressing the Heat disinf button for 3 seconds (the button lights up). 3. Place the B pick-up tube marked blue-white into the container with citric acid solution. (The A pick-up tube marked red must remain in the disinfection port of the machine). 4. When the machine is filled with citric acid solution an attention alarm appears: CHEM DIS FILLUP PHASE COMPLETED Place pick up tube in machine Put the B pick-up tube back into the disinfection port of machine. 5. The Heat disinfection program with liquid citric acid is now performed.



12:13

6. If an automatic switch off is required, press the ON/OFF button for 3 seconds. 7. When the program is complete and the machine has been drained, the Rinse/Drain button starts to flash. 8. Switch off the machine by pressing the ON/OFF button for 3 seconds. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine.

Performing integrated Heat disinfection program with WRO 300 H By an authorized technician, the AK 200 S can be preset to perform integrated Heat disinfection program ed by WRO 300 H. This program is recommended when possible since it includes heating of the inlet water tube. The program starts with a Heat disinfection program of the AK 200 S. When the circulation phase (see "General - Heat disinfection" in this chapter) has finished a Low Flow Heat phase automatically starts. In this phase, the machine will receive hot water from the WRO 300 H, at a low flow rate, for 15 minutes. When this phase is complete, the machine finishes the program off as usual, with a drain phase. Note • The integrated Heat disinfection program with WRO 300 H can be interrupted at any time by pressing the Rinse/Drain button for 3 seconds. The machine will then interrupt the procedure and when the WRO 300 H has cooled down, finish off with a rinse and drain sequence. Note

Before starting integrated Heat disinfection program with WRO 300 H •


•

Make sure that the WRO 300 H is switched on.

Procedure 1. Press the Heat disinf button briefly and select HEAT+ WRO 300H by using the corresponding Arrow button below HEAT+ WRO 300H on the information display. The text will flash indicating that the integrated Heat disinfection program with WRO 300 H has been selected.

12:14



2. Confirm the choice by pressing the Heat disinf button for 3 seconds (the button lights up). The integrated Heat disinfection program with WRO 300 H will now be performed. For information about the program, see in the introductory part in these instructions. 3. If an automatic switch off is required, press the ON/OFF button for 3 seconds. 4. When the integrated Heat disinfection program with WRO 300 H is complete, rinse and drain sequence included, the Rinse/Drain button starts to flash. 5. Switch off the machine by pressing the ON/OFF button for 3 seconds. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine.



12:15

Automatic start of Heat disinfection program The machine is equipped with an automatic start function for the Heat disinfection program. Whenever this is activated, and the machine has been turned off, the Heat disinfection program will be started at the programmed time (see below).

Before automatic start of Heat disinfection program •


Procedure 1. Press the Auto Heat button briefly. 2. Set the desired ready day (RDY DAY) and ready time (RDY TME) by using corresponding Arrow buttons and the Set knob. 3. Activate the function by pressing the Auto Heat button for 3 seconds (the button lights up).

Figure 12:2

Auto Heat

If a weekly program is to be selected: 1. Press the Auto Heat button briefly. 2. Set the desired ready day (RDY DAY) and ready time (RDY TME) by using corresponding Arrow buttons and the Set knob. The automatic function can be switched off for the selected day by setting the ready time (RDY TME) to OFF (i.e. setting the time between 23:59 h and 0:00 h). 3. Select the next day (RDY DAY) by using the corresponding Arrow button and the Set knob. 12:16



4. Select the ready time (RDY TME) or the OFF function (see above) for that day by using the corresponding Arrow button and the Set knob. Proceed according to the above until a complete weekly program has been set. 5. Activate the function by pressing the Auto Heat button for 3 seconds (the button lights up). Note • The lit Auto Heat button must be pressed for 3 seconds (the button is extinguished) for the function to be deactivated. Note

In combination with CleanCart If a Heat disinfection program with CleanCart is desired, place a CleanCart cartridge into the BiCart holder before the automatic start of the Heat disinfection program is set to be started.

Automatic switch off after Heat disinfection program The machine can be preset to switch itself off after a complete Heat disinfection program, i.e. when the Rinse/Drain button is flashing, by a qualified technician in the clinic. It can also be switched off during the Heat disinfection program by manually pressing the ON/OFF button while the program is running. This will make all of the operator lights go out, except for the Heat disinf button and the time display. When the final drain starts the Rinse/Drain button lights up while the Heat disinf button is extinguished. When the program is complete the Rinse/Drain button flashes three times, the time display lights go out, the inlet valve closes and the machine is automatically switched off.

Integrated Heat disinfection The AK 200 S can be programmed to perform integrated Heat disinfection. In this mode, the machine receives hot water from the central water supply system when performing Heat disinfection. The Heat disinfection can be started manually or preferably be programmed to start automatically, during heating of the central water supply system. The advantage with integrated Heat disinfection is that the tube between the central water supply system (inlet water tube) and the machine is also disinfected.



12:17

Hygiene - Chemical disinfection General - Chemical disinfection CAUTION Disinfectants may be toxic. The must therefore take note of necessary precautions before use. The manufacturer’s instructions and recommendations have to be followed. Local regulations regarding the utilization of the different chemicals must be followed.

After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION

During Chemical disinfection program the machine is filled with disinfectant. The disinfectant could be concentrated or already diluted. If it is concentrated it is mixed with water to the correct concentration in the machine. The solution is then filled in all parts of the fluid path. After the Dwell time (the time when the fluid path is filled with correct concentration of the disinfectant) the machine is rinsed and drained. If the machine is not to be used for a long period of time it is possible to turn it off during the dwell time and then it stays filled until it is started again. For further details; see “Data and specifications/Disinfection and Cleaning”.

12:18



Chemical disinfectants Chemical disinfectants may be harmful to the materials used in the fluid path of dialysis machines. Disinfectants may also contain additives that cause foaming or are difficult to rinse out. The disinfectants listed below are examples of chemicals recommended for use in the AK 200 S, i.e. they are compatible with the materials in the machine, provided that they are used in accordance with the recommendations in chapter “Technical data and specifications/Disinfection and Cleaning”. It is essential that the chemical disinfection program is adapted to the disinfectant used regarding dilution and dwell time. The machine has to be properly preset by a qualified technician. CAUTION Local regulations have to be followed regarding approved levels of disinfectant residues.

After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION

Solutions based on peracetic acid:

Active ingredients: Trade names: Test for residues:

Peracetic acid and hydrogen peroxide. Dialox, Renalin, Actril, Acetoper, Puristeril 340, Peresal Iodine starch test strips (e.g. Merckoquant 10011). Follow the manufacturers recommendations.

Sodium hypochlorite:

Active ingredient: Test for residues:

Sodium hypochlorite Chlorine test kit (e.g. Hach or Merck)

Other disinfectants based on sodium hypochlorite:

Active ingredient: Trade names: Test for residues:

Sodium hypochlorite Maranon H and Amuchina Follow the manufacturers instructions

Formaldehyde:

Active ingredient: Trade name: Test for residues:

Formaldehyde Rectapur Formalert or Aquamerck 8028. Note that the ultrafilter used in UFD kit must be changed prior to the following treatment. Alternatively perform additional rinse/drain procedures according to section “Residual test after Chemical disinfection” in this chapter.

For further information about the disinfectants, such as dwell times, concentrations, consumption and mixing instructions, see “Technical data and specifications/Disinfection and Cleaning”. HCEN9751 Revision.12.2005 Program version 8.xx


12:19

Performing Chemical disinfection program Before starting Chemical disinfection program •


Procedure 1. Press the Chem disinf button briefly and select the desired program/chemical by using the corresponding Arrow button below the desired alternative on the information display. The text will flash indicating that the desired alternative has been selected.

Figure 12:3

Chemical disinfection

PER-LOW is the default program which will be performed if nothing else is selected. The text will flash indicating that PER-LOW has been selected. 2. Confirm the choice by pressing the Chem disinf button for 3 seconds (the button lights up). 3. Place the B pick-up tube marked blue-white into a container with the appropriate disinfectant. (The A pick-up tube marked red must remain in the disinfection port of the machine). 4. When the machine is filled with disinfectant an attention alarm appears: CHEM DIS FILLUP PHASE COMPLETED Place pick up tube in machine Put the B pick-up tube back into the disinfection port of machine. 5. The Chemical disinfection program is now performed. The Chem disinf button will remain lit until the final rinse starts. 12:20



6. Do not switch the machine off until the Rinse/Drain procedure has started i.e. the Rinse/Drain button lights up. (See “Filling the machine with chemical disinfectant” below.) 7. When the program is complete and the machine has been drained, the Rinse/Drain button starts to flash. 8. Switch off the machine by pressing the ON/OFF button for 3 seconds. 9. If FORMAL program has been performed, the ultrafilter used in UFD kit must be changed prior to the following treatment. Alternatively perform additional rinse/drain procedures according to section “Residual test after Chemical disinfection” in this chapter. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine. The machine can be preset to switch itself off after a complete Chemical disinfection program, i.e. when the Rinse/Drain button is flashing, by a qualified technician in the clinic. CAUTION After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION

Filling the machine with chemical disinfectant There may be a need to fill the machine with a chemical disinfectant during storage or when the AK 200 S is planned to be left unused for a long period of time. The chemical disinfectant should preferably be peracetic acid. In order to perform a filling of the machine with chemical disinfectant follow the instructions below “Performing Chemical disinfection program” in this chapter - points 1, 2, 3 and 4. Continue as follows: 5. Press the ON/OFF button as soon as the B pick-up tube has been put back into the disinfection port of machine. The machine will continue to run the program for some minutes after the ON/OFF button has been pressed. This is to fill up all the tubes and to even out the concentration of the disinfectant. Now the machine is filled with disinfectant. 6. When the machine is to be used again and the ON/OFF button is pressed, the machine will start up with a Rinse/Drain program as soon as it is switched on. The Chem disinf button will be lit at this moment as well as the Rinse/Drain button. The remaining time will be shown on the time display. The Chem disinf button will remain lit until the final rinse starts and during this sequence only the Rinse/Drain button will be lit. 7. When the program is complete and the machine has been drained, the Rinse/Drain button starts to flash.



12:21

8. Switch off the machine by pressing the ON/OFF button for 3 seconds. 9. If FORMAL program has been performed, the ultrafilter used in UFD kit must be changed prior to the following treatment. Alternatively perform additional rinse/drain procedures according to section “Residual test after Chemical disinfection” in this chapter. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine. The machine can be preset to switch itself off after a complete Chemical disinfection program, i.e. when the Rinse/Drain button is flashing, by a qualified technician in the clinic. CAUTION After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION

12:22



Residual test after Chemical disinfection Before connecting a patient a residual test must be done on the prepared dialysis fluid. This is to make sure that the patient will not be exposed to chemical residuals after a chemical disinfection program. The residual concentration in the dialysis fluid must be below levels specified by the clinic or by national standards. It is essential to use an appropriate test method, either with proven sensitivity for the chemical or recommended by the manufacturer of the chemical disinfectant. 1. Switch the machine on and let it function check (Fch) with the proper concentrates attached. 2. When the green fluid path lights up, press the flashing Fluid by button in order to let fresh dialysis fluid flow through the dialysis fluid tubes. 3. Take the residual test sample from the flowing fluid on the dialysis fluid outlet tube (to dialyzer). If the tests shows disinfectant residues: •

DO NOT use connected BiCart and SelectCart.

•

Press the Rinse/Drain button for 3 seconds (the button lights up) and start a new rinse/drain procedure. When this is finished, repeat the handling procedure described above.

If the machine still shows disinfectant residues, service technician. CAUTION After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION



12:23

Central Chemical disinfection The AK 200 S can be programmed to perform Central Chemical disinfection . In this mode, the machine receives disinfection solution through the central water supply system. The Central disinfection program in AK 200 S performs a drain and then a fill with disinfection solution. During the dwell time the pumps are turned off. It is advisable to turn the AK 200 S off if it is not supposed to be disinfected; this is to make sure that no disinfection solution will enter the machine when not desired.

Performing central Chemical disinfection Before starting central Chemical disinfection program •


Procedure 1. Press the Chem disinf button briefly. 2. Select CENTRAL DISINF. by using the corresponding Arrow button below CENTRAL DISINF. on the information display. The text will flash indicating that Central Chemical disinfection program has been selected. 3. Confirm the choice by pressing the Chem disinf button for 3 seconds (the button lights up). 4. When the preset dwell time has ed, an attention is given to indicate that the Rinse/Drain sequence can be started. When no more chemicals are left in the central water supply system: 5. Start the Rinse/Drain program by pressing the Rinse/Drain button for 3 seconds (the button lights up). 6. When the Rinse/Drain program is complete and the machine has been drained, the Rinse/Drain button starts to flash. CAUTION After Chemical disinfection procedure a test for residues must have been performed prior to connecting a patient. CAUTION

12:24



Hygiene - Rinse/Drain Performing Rinse/Drain program Note • The Rinse/Drain program can be interrupted at any time by pressing the Rinse/Drain button for 3 seconds. The machine will then interrupt the procedure and finish off with drain sequence. Note

Before starting Rinse/Drain program •


Procedure 1. Press the Rinse/Drain button briefly and check that RINSE is flashing on the information display.

Figure 12:4

Rinse/Drain

The flashing text indicates that the Rinse/Drain program, which is the default procedure, has been selected. If RINSE is not flashing, press the corresponding Arrow button below RINSE, the text will flash. 2. Confirm the choice by pressing the Rinse/Drain button for 3 seconds (the button lights up) and the Rinse/Drain program starts. If the button is pressed a second time for 3 seconds an immediate drain starts. 3. If an automatic switch off is required, press the ON/OFF button for 3 seconds. 4. When the program is complete, the Rinse/Drain button starts to flash. HCEN9751 Revision.12.2005 Program version 8.xx


12:25

5. Switch off the machine by pressing the ON/OFF button for 3 seconds. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine.

Performing Rinse/Drain program with CleanCart Note • The Rinse/Drain program with CleanCart can be interrupted at any time by pressing the Rinse/Drain button for 3 seconds. The machine will then interrupt the procedure and finish off with a rinse and drain sequence. Note

Before starting Rinse/Drain program with CleanCart •


Procedure 1. Press the Rinse/Drain button briefly and select CleanCart by using the corresponding Arrow button below CleanCart on the information display. The text will flash indicating that the Rinse/Drain program with CleanCart has been selected. 2. Confirm the choice by pressing the Rinse/Drain button for 3 seconds (the button lights up). 3. When the attention alarm CleanCart NOT ATTACHED TO HOLDER Attach or check Clean Cart appears, open the latches of the BiCart holder and place the CleanCart cartridge into the holder. Both pick-up tubes must remain in the disinfection ports of the machine. 3.a. If the attention alarm EMPTY AND REMOVE CleanCart Close holder appears, open the upper latch. The CleanCart cartridge will now be emptied. When the CleanCart is empty, remove it and close the latches. 3.b. Leave the cartridge in the holder during the entire program will automatically be emptied.

, it

4. The Rinse/Drain program with CleanCart is now performed.

12:26



5. If an automatic switch off is required, press the ON/OFF button for 3 seconds. If preset, the CleanCart cartridge can be left in the holder until next function check is started. 6. When the program is complete and the machine has been drained, the Rinse/Drain button starts to flash. 7. Switch off the machine by pressing the ON/OFF button for 3 seconds. If a new treatment is to be started, press the flashing Rinse/Drain button to start a new function check instead of switching off the machine.



12:27

Automatic start of Rinse/Drain program The machine is equipped with an automatic start function for the Rinse/Drain program. Whenever this is activated, and the machine has been turned off, the Rinse/Drain program will be started at the programmed time (see below).

Before automatic start of Rinse/Drain program •


Procedure 1. Press the Auto Rinse button briefly. 2. Set the desired ready day (RDY DAY) and ready time (RDY TME) by using corresponding Arrow buttons and the Set knob. 3. Activate the function by pressing the Auto Rinse button for 3 seconds (the button lights up).

Figure 12:5

Auto Rinse

If a weekly program is to be selected: 1. Press the Auto Rinse button briefly. 2. Set the desired ready day (RDY DAY) and ready time (RDY TME) by using corresponding Arrow buttons and the Set knob. The automatic function can be switched off for the selected day by setting the ready time (RDY TME) to OFF (i.e. setting the time between 23:59 h and 0:00 h). 3. Select the next day (RDY DAY) by using the corresponding Arrow button and the Set knob. 12:28



4. Select the ready time (RDY TME) or the OFF function (see above) for that day by using the corresponding Arrow button and the Set knob. Proceed according to the above until a complete weekly program has been set. 5. Activate the function by pressing Auto Rinse button for 3 seconds (the button lights up). Note • The lit Auto Rinse button must be pressed for 3 seconds (the button is extinguished) for the function to be deactivated. Note

In combination with CleanCart If a Rinse/Drain program with CleanCart is desired, place a CleanCart cartridge into the BiCart holder before the automatic start of the Rinse/Drain program is set to be started.

Automatic switch off after Rinse/Drain program The machine can be preset to switch itself off after a complete Rinse/Drain program, i.e. when the Rinse/Drain button is flashing, by a qualified technician in the clinic. It can also be switched off during the Rinse/Drain program by manually pressing the ON/OFF button while the program is running. This will make all of the operator lights go out, except for the Rinse/Drain button and the time display. When the program is complete the Rinse/Drain button flashes three times, the time display lights go out, the inlet valve closes and the machine is automatically switched off.



12:29

Maintenance - the flow path The flow path The maintenance of the flow path with aspect to cleaning and decalcification is important in order to maintain the specified performance of the machine.

Cleaning Fats, proteins and organic material originating from the patient may deposit down stream the dialyzer. The requirements for cleaning vary depending on the use of convective therapies (Low volume HDF) and the permeability properties of the used dialyzer membranes. The number of treatments and the setting of parameters will also influence the amount of deposits downstream the dialyzer. A general guideline for the frequency of cleaning with CleanCart-C and sodium hypochlorite (alternatively CleanCart-A) is described in the introductory part of this chapter. An increased cleaning may be necessary but, depending on the conditions described above, also a lower frequency may be sufficient to maintain the system.

Decalcification Calcium carbonate may deposit in the flow path. The requirements for decalcification vary depending on elements as water quality, type of concentrate and Bicarbonate settings. A general guideline for the frequency of decalcification with CleanCart-C or liquid citric acid is described in the introductory part of this chapter. An increased decalcification may be necessary but, depending on the conditions described above, also a lower frequency may be sufficient to maintain the system. Note • Incorrect cleaning of the UF cell may be a contributing factor for increased inaccuracy of the UF system. If any deviations in UF accuracy should occur, it is recommended to use sodium hypochlorite weekly.

• In order to enable the cleaning agents to remove fats, proteins etc. efficiently, cleaning should be carried out after decalcification. Note

12:30



Ultrafilter; how to change Note • Make sure that the ultrafilter is changed in an aseptic way. Note

1. Release the lower part of the ultrafilter holder by pulling the handle and pressing the latch downwards. 2. Remove the ultrafilter by pulling it gently downwards. 3. Insert the new ultrafilter into the holder and push it gently upwards. 4. Close the holder by pushing the lower latch into position. 5. Label the ultrafilter with date for change. 6. Perform a Heat disinfection program before the AK 200 S is used for treatment after the ultrafilter has been changed.



12:31

Ultrafilter replacement reminder By preset, an attention alarm can be generated when it is time for the ultrafilter to be changed. The reminder can appear when a preset number of days have ed or when a preset number of heat disinfection programs have been performed (or a combination of both) since the last change of ultrafilter. When the preset is active, and it is time for the ultrafilter to be changed, this attention appears when the machine has been started: NEW ULTRA FILTERS REQUIRED Replace ULTRA filters The attention alarm will disappear as soon as priming is activated. When the ultrafilter has been changed, press the Heat disinf or the Chem disinf button twice and this screen will appear on the information display:

Figure 12:6

Ultrafilter replacement

Confirm the ultrafilter change by pressing the lit Arrow button for three seconds. The text on the screen will change to: ULTRA FILTER REPLACEMENT New filter confirmed! and the counting of number of days and/or heat disinfection programs will be set to zero. The calendar symbol on the screen indicates the date of the latest ultrafilter change. The thermometer symbol indicates number of heat disinfection programs performed and the hourglass indicates number of days since the latest change of ultrafilter.

12:32



Maintenance - the exterior of the machine The outside Wipe the outside of the machine with a cloth moistened with ethanol (70%) or isopropanol (60%) in order to clean and disinfect it. Note • Do not use tenside-containing or iodine-based disinfectants. These solutions may crack or discolour most polymers. Note

Top tray The top tray may be cleaned and disinfected with ethanol (70%) or isopropanol (60%). CAUTION In order to protect the internal parts of the AK 200 S against spillage, the top tray must always be placed on top of the machine, except during technical service. CAUTION

Blood pump To remove the blood pump rotor; pull out the handle. Turn until the blood pump rotor loosens from the pump shaft. The blood pump rotor can be cleaned and disinfected in ethanol (70%) or isopropanol (60%). To attach the blood pump rotor; place it on the pump shaft. Move your fingers from the handle and place them on the rotor. Turn the rotor slowly and push slightly until it reaches the bottom position. Continue turning until the blood pump handle clicks in.

Blood leak detector The blood leak detector shall only be cleaned when a suspected false blood leak alarm has occurred and not as a preventive action, as the risk of contaminating the blood leak detector is large when opening it. Unscrew the blood leak detector cover and clean the lenses with a soft non-fluffy cloth, moistened with disinfectant solution. Note • Make sure that the sealing ring on the inside of the cover is securely in place when replacing the cover. Note



12:33

BPM cuff The instructions below concerns only the standard cuffs; No. 1 to No. 4. Use a damp cloth with 70% ethyl alcohol or 30 to 50% isopropyl alcohol for cleaning the surface of the cuff. Never put any solutions inside the cuff. If this occurs, dry the inside of cuff before use. The cloth covering of the cuff is removable and washable. The following procedure shown below is the procedure for taking the rubber bladder out of the cloth bag. In the cloth bag are holes for the rubber bladder and the rubber hose. The large hole is used to put the rubber bladder through and the small hole is used to put the rubber hose through. Figure A. Put the rubber hose inside and pull out the inside cloth to make the hole larger. Figure B and C. Take the rubber bag out of the larger hole. Figure D.

Figure 12:7 BPM cuff, removal procedure of rubber bladder from cloth bag 1. Small hole 2. Large hole Reverse the order when putting the rubber bladder in the cloth bag. When the cloth bag of the cuff is removed, pay attention to the hole through which the rubber hose of the rubber bladder goes. Unless the hole is used, the rubber bag gets out of the cloth bag, leading to blow out.

12:34



Chapter 13 Technical data and specifications Performance and specification - Control System . . . . . . . . . . . . . . . . . . . . 13:2 Blood Flow Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:2 Air Detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Heparin istration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Blood Volume Sensor (BVS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Blood Pressure Monitor (BPM) . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:3 Dialysis fluid preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:4 Dialysis fluid preparation (BiCart Select mode only) . . . . . . . . . . . . 13:5 Ultrafiltration control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:5 Substitution fluid (Low volume HDF) . . . . . . . . . . . . . . . . . . . . . . 13:5 Profiling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:5 Diascan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:6 Disinfection and Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:6 Water supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:9 Drain . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:10 Power supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:10 Connection of external equipment . . . . . . . . . . . . . . . . . . . . . . . . . 13:10 Battery Back-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:12 Performance and specification - Supervisory system . . . . . . . . . . . . . . . . . 13:13 Blood Pressure Supervision . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:13 Air Detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:14 Heparin istration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:14 Dialysis fluid preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:14 Dialysis fluid preparation (BiCart Select mode only) . . . . . . . . . . . . 13:14 Ultrafiltration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:15 Substitution fluid (Low volume HDF) . . . . . . . . . . . . . . . . . . . . . . 13:15 Blood leak detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:15 Physical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:16 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:16 Materials in with water, concentrates and dialysis fluid . . . . . . . . . 13:17 Polymers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:17 Metals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:17 Others . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:17 Environmental data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Transportation and storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Electromagnetic environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:18 Standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13:22


AK 200 S Operator’s manual - Technical data and specifications

13:1

Performance and specification - Control System Note • When accuracy ranges are written as e.g. “(±1 ml/min or ±1%)” the widest range is valid.

• For the qualified technician the AK 200 S Service Manual is available. The Service Manual provides all the necessary information for the safe and required maintenance of the machine. Note

Blood Flow Control Values for the blood pump(s) are based on the arterial blood pump with a pump segment of 7.9 mm and 2.0 mm wall thickness. It is possible to preset the machine so the blood flow values are based only on the blood pump rotations. For paediatric blood tubes with pump segment of 4.0 mm it is also possible to set blood flow to 10 or 15 ml/min. Accuracy is then ±5 ml/min. Double Needle Blood Flows in HD, single 20 to 500 ml/min (±10 ml/min or ±15%) pump: Blood Flows in Low volume 20 to 500 ml/min (±10 ml/min or ±15%) HDF: Accumulated blood volume: 0 to 327 litres (±0.6 l * treatment time (h) or ±15%) Single Needle Single Pump Arterial flow: Time control:

20 to 500 ml/min (±10 ml/min or ±18%) 2 to 20 sec (±1 sec), Arterial and venous time. The actual clamp opening time is depending on blood flow rate, size of expansion chamber and pressure limits. Pressure control: 10 to 600 mmHg (±50 mmHg), venous pressure control Accumulated blood volume: 0 to 327 litres (±0.6 l * treatment time (h) or ±18%) Single Needle Double Pump (HD only) Double pump-A Double pump-V Mean Flow-SN/DP Accumulated blood volume Stroke Volume-SN/DP

13:2

20 to 800 ml/min 20 to 800 ml/min 10 to 400 ml/min (±10 ml or ±15%) 0 to 99.9 litres (±0.6 l * treatment time (h) or ±15%) 20 to 60 ml/stroke (±15%) at a cycle time < 20 s



Air Detection Sensitivity

Venous drip chamber size (diameter)

Bubbles larger than 1 µl will be trapped by the drip chamber. An alarm will be issued if the blood level falls below the middle of the air detector. 22 mm

Heparin istration Heparinization Stop time, can be preset (Default) Syringe size, can be preset (Default) Maximum counter pressure

0/0.5 to 10 ml/h (±1 ml or 0.2 ml * heparinization time (h) or ±5%) 0 to 4.00 h.min (±1 min) (20 min) 6 to 30 ml (30 ml) +650 mmHg

The accuracy is based on tests with 20 ml and 30 ml syringes

Blood Volume Sensor (BVS) Relative blood volume ∆BV

- 40% to + 10% from reference value (Standard deviation ±3%) Sensor active for Hb ≥ 80 g/l and blood flow ≥180 ml/min

Blood Pressure Monitor (BPM) The alarm limits below can be preset. The value put in brackets and in italics is the default value. Systolic pressure range1 Low alarm limit High alarm limit

60 - 250 mmHg 60 - 250 mmHg (100 mmHg) 60 - 250 mmHg (150 mmHg)

Diastolic pressure range1 Low alarm limit High alarm limit


Mean pressure range1 Low alarm limit High alarm limit


Pulse rate range Low alarm limit High alarm limit

40 - 200 bpm (±2 bpm or ±2 % of reading) 40 - 180 bpm (40 bpm) 40 - 180 bpm (150 bpm)

1 Meets

ANSI/AAMI SP-10 (1992). Mean error ±5 mmHg. Standard deviation 8 mmHg HCEN9751 Revision.12.2005 Program version 8.xx


13:3

Dialysis fluid preparation Temperature Dialysis Fluid Temperature

30-39 °C (+0,5/-1,5 °C) (+0,5/-2,0 °C) with UFD-kit at fluid flow < 500 ml/min. Accuracy is valid only if dialysis fluid temperature is greater or equal to ambient temperature. Temperature low alarm, can 28 to 40 °C (35°) be preset (Default) Temperature high alarm, can 28 to 40 °C (39°) be preset (Default) Fluid flow Dialysis Fluid Flow Rate

300 to 700 ml/min (±10 ml/min)

Conductivity Conductivity measuring Alarm limits in Acetate mode Alarm limit in Bicarbonate mode, A-step Alarm Limit in Bicarbonate mode, B-step

0.1 - 20 mS/cm (±0.1 mS/cm) ±5 % of set value ±5% of set value for A-step conductivity ±5% of set value for B-step conductivity

Alarm limits are extended to 10% for maximum 2 minutes of 10 minutes Concentration Na+, Acetate mode Na+, Bicarbonate mode HCO3-, Bicarbonate mode

115 to 160 mmol/l (±4 mmol/l) 130 to 150 mmol/l (±6 mmol/l) 20 to 40 mmol/l (±6 mmol/l)

Concentrates Max. pressure for concentrates

+50 kPa

pH supervision pH measurement of Dialysis Fluid pH low alarm, can be preset (Default) pH high alarm, can be preset (Default)

13:4

1 to 9.9 pH units (±0,2 pH units) 1 to 15 pH units (6 Acetate mode, 6.5 Bicarb mode) 1 to 15 pH units (8 Acetate mode, 7.8 Bicarb mode)



Degassing Degassing pressure in Acetate mode, can be preset (Default) Degassing pressure in Bicarbonate mode, can be preset (Default)

-700 to -500 mmHg (±30 mmHg) (-630 mmHg) Minimum 75 mmHg absolute pressure -700 to -500 mmHg (±30 mmHg) (-580 mmHg) Minimum 75 mmHg absolute pressure

Dialysis fluid preparation (BiCart Select mode only) Fluid flow SelectBag Proportioning Ratio

1:400 (±3%) SelectBag Proportioning Ratio is defined as the quotient SelectBag flow/dialysis fluid flow

Ultrafiltration control UF volume UF-rate Treatment Time

max. 30 litres (±50 ml or ±50 ml * ed treatment time (h) or ±2.5%) 0.0 to 4.0 l/h 0.05 to 9.59 hour.minute (±1 minute)

Substitution fluid (Low volume HDF) Substitution fluid flow rate

1.0 to 2.0 l/h (±10%)

Profiling UF-rate Na+, Acetate mode Na+, Bicarbonate mode HCO3-, Bicarbonate mode

0 to 4 l/h 115 to 160 mmol/l 130 to 150 mmol/l 20 to 40 mmol/l

Half-times: Degressive Progressive


Set in h.min, 10 to 25% of remaining treatment time Set in h.min, 75 to 90% of remaining treatment time


13:5

Diascan Accuracy is valid in HD double needle and on-line HDF postdilution, for blood flows 200 to 500 ml/min and fluid flows 500 to 700 ml/min, UF profiling is allowed. Clearance, K Cumulated water volume cleared of urea, Kt Dialysis dose, Kt/V Plasma sodium, Na+

0 to 350 ml/min (±10%) 0 to 100 l (±10%) 0 to 3 (±10%) 130 to 160 mmol/l

Disinfection and Cleaning Temperature and time in different phases and concentration of disinfectant are possible to preset. The values in this specification are the default values and what the machine has been validated against. Follow the instructions from the manufacturer of the disinfectant, to set the correct dilution and dwell time. All disinfection programs in the AK 200 S are tested in accordance with the French standard NFS 90-304 and established to fulfil the requirements expressed in the same standard. Time for disinfection programs is estimated and may vary. Heat disinfection Program Temperature Fill up phase Circulation phase Drain phase Total time

93 °C 10 minutes (13 minutes with UFD-kit, (optional)) 15 minutes 4 minutes 29 minutes (32 minutes with UFD-kit, (optional))

Heat disinfection Program with CleanCart Decalcification Cleaning Temperature Fill up and mixing phase Circulation phase Rinse/Drain phase Total time

13:6

CleanCart-C CleanCart-A 93 °C 12 minutes (13 minutes with UFD-kit, (optional)) 15 minutes 5 minutes (15 minutes with UFD-kit, (optional)) 32 minutes (43 minutes with UFD-kit, (optional))



Heat disinfection Program with liquid citric acid Temperature Concentration Concentration in machine Consumption Fill up and mixing phase Circulation phase Rinse/Drain phase Total time

93 °C 20 % citric acid 2 % citric acid; i.e. diluted 1 + 9 Approx. 200 ml (Approx. 230 ml with UFD-kit, (optional)) 15 minutes (18 minutes with UFD-kit, (optional)) 15 minutes 13 minutes (14 minutes with UFD-kit, (optional)) 43 minutes (47 minutes with UFD-kit, (optional))

Heat disinfection Program with WRO 300 H Temperature Fill up phase Circulation phase Low flow heat phase Drain phase Total time

93 °C 10 minutes (13 minutes with UFD-kit, (optional)) 15 minutes 20 minutes 4 minutes 49 minutes (52 minutes with UFD-kit, (optional))

Peracetic Acid Program Concentration of disinfectant Concentration in machine Consumption Fill up and mixing phase Dwell time Rinse/Drain phase Total time


3.5 % peracetic acid 0.1 %; i.e. diluted 1 + 34 Approx. 65 ml (Approx. 75 ml with UFD-kit, (optional)) 12 minutes (17 minutes with UFD-kit, (optional)) 10 minutes 26 minutes (46 minutes with UFD-kit, (optional)) 48 minutes including 10 min dwell time (73 minutes including 10 min dwell time with UFD-kit, (optional))


13:7

Low concentration Peracetic Acid Program Concentration of disinfectant Concentration in machine Consumption Fill up and mixing phase Dwell time Rinse/Drain phase Total time

0.35 % peracetic acid (0.35 % peracetic acid with UFD-kit, (optional)) 0.01 % ; i.e. diluted 1 + 34 (0.01 % ; i.e. diluted 1 + 34 with UFD-kit, (optional)) approx. 65 ml (approx. 75 ml with UFD-kit, (optional)) 12 minutes (17 minutes with UFD-kit, (optional)) 10 minutes 19 minutes (31 minutes with UFD-kit, (optional)) 41 minutes including 10 min dwell time (58 minutes including 10 min dwell time with UFD-kit, (optional))

Hypochlorite Program Concentration of disinfectant Concentration in machine Consumption Fill up and mixing phase Dwell time Rinse/Drain phase Total time

0.5% available chlorine (approximately 70% of sodium hypochlorite concentration) 0.5% ; i.e. not diluted Approx. 2000 ml (Approx. 2500 ml with UFD-kit, (optional)) 12 minutes (25 minutes with UFD-kit, (optional)) 10 minutes, Maximum 20 min 26 minutes (42 minutes with UFD-kit, (optional)) 48 minutes including 10 min dwell time (77 minutes including 10 min dwell time with UFD-kit, (optional))

Formaldehyde Program Concentration of disinfectant Concentration in machine Consumption Fill up and mixing phase Dwell time Rinse/Drain phase Total time

13:8

4% formaldehyde 4% ; i.e. not diluted Approx. 2000 ml (Approx. 2500 ml with UFD-kit, (optional)) 12 minutes (25 minutes with UFD-kit, (optional)) 20 minutes 45 minutes (67 minutes with UFD-kit, (optional)) 77 minutes including 20 min dwell time (112 minutes including 20 min dwell time with UFD-kit, (optional))



Central Disinfection Program Concentration of disinfectant Concentration in machine Consumption Dwell time Total time

0.1% peracetic acid or 0.5% available chlorine Not diluted Approx. 3100 ml (Approx. 3600 ml with UFD-kit, (optional)) Must be preset, maximum 20 min. for hypochlorite 35 minutes (dwell time not included) (66 minutes (dwell time not included) with UFD-kit, (optional))

Other programs, total time Rinse/Drain with CleanCart 31 min (32 min with UFD-kit, (optional)) 12 min (13 min with UFD-kit, (optional)) Rinse/Drain Drain 4 min External Cleaning

70% ethanol or 60% Isopropanol

Water supply


Water Supply Flow Rate Treatment Disinfection

300 to 750 ml/min 0 to 1150 ml/min

Inlet Water Pressure to regulator to machine

120 to 800 kPa 85 to 120 kPa

Inlet Water Temperature Treatment Disinfection

+5 to +30 °C +5 to +90 °C

Inlet Water Quality

Inlet water quality must comply with local regulations and if no such regulation is available follow ISO 13959. Level for conductivity shall not exceed 0.1 mS/cm. It is possible to use water with higher conductivity if it consists mainly of sodium salts. This may however affect the accuracy of the fluid composition.

Inlet tube length

Maximum 5 m or the specially designed spiral PEX tubing


13:9

Drain Drain (length of tube) Drain capacity Drain outlet

Maximum 5 m Minimum 1.0 l/min Maximum 1.2 m above floor

If the optional air-gap on the machine is used the distance between the air-gap and the drain must not be less than 0.3 m. For an electrically adjustable stand in its lowest position this means that the drain must not be higher than 580 mm. For a mechanically adjustable stand in its lowest position the drain must not be higher than 550 mm.

Power supply Mains Voltage Frequency Power Consumption Cable: Connector: Mains plug: Earth Leakage Current Patient Leakage Current Fuses

115; 230 V AC (±10%) 50 to 60 Hz (±5 Hz) Max. 2250 W at 230 V Max. 1650 W at 115 V 3 conductor cable, Length max. 3 m rating 250 V 10 A Certified to IEC 320/C13. Earthed plug, 250 V AC / 10 -16 A, approved or Hospital grade, earthed plug, 125 V AC / 15 A, approved. max 500 µA, typical <100 µA (115 V), max 500 µA, typical <145 µA (230 V) max 100 µA, typical <10 µA (115 V), max 100 µA, typical <10 µA (230 V) 2 x T 12 A

All leakage currents are specified without external equipment connected to the machine.

Connection of external equipment External equipment intended for connection to signal input, signal output or other connectors, shall comply with relevant IEC standard (e.g. IEC 60950 for IT equipment and the IEC 60601 series for medical electrical equipment). In addition, all such combinations - systems shall comply with the standard IEC 60601-1-1, Safety requirements for medical electrical systems. Equipment not complying to IEC 60601 shall be kept outside the patient environment, as defined in the standard. (The normal distance can be mentioned i.e. at least 1.5 m from the patient or the patient .) Any person who connects external equipment to signal input, signal output or other connectors has formed a system and is therefore responsible for the system to comply with the requirements of IEC 60601-1-1. If in doubt, qualified technician or your local representative. Use of other cables may result in increased emissions or decreased immunity for the equipment or system. Protective caps shall be attached when the connectors are not in use.

13:10



External serial interface: External connector P 63 :

External equipment:

8 pin REDEL , black. RS-232 or RS-422 compatible connection. Opto insulated fulfilling IEC 60601-1-1. Attached cable length 2.5 m unshielded. Serial port for connection to PC used for logging and preset.

RS-232 Max input voltage: High level min output voltage: Low level max output voltage: Max output current:

± 15 V DC + 5 V DC - 5 V DC ± 5 mA

RS-422 Max input voltage: Diff. input threshold voltage: Diff. max. output voltage: Diff. min. output voltage: Short circuit output current:

± 7 V DC ± 0.2 V DC 5 V DC 2 V DC 100 mA

External interface: External connector P 79 : External equipment: ratings: Max voltage: Max current:

8 pin REDEL, yellow, configured as 1 make- and 2 change over- relay s. Attached cable length 2.9 m unshielded. Port for connection to central alarm system and remote control of water system. 24 V AC or DC 100 mA AC or DC

External I/O Interface External connector P 76: External equipment:

8 pin REDEL blue. Opto insulated fulfilling IEC 60601-1-1. Attached cable length 1,5 m unshielded. Connection to Gambro UF Calibration Unit. Service purpose only.

External interface: External connector P 64: External equipment:


8 pin REDEL, grey. Attached cable length 2.0 m unshielded. Service purpose only.


13:11

Battery Back-up Battery back-up of power supply Running time Fuse

13:12

24 volt, 6.5 Ah >15 minutes T 15 A



Performance and specification - Supervisory system Note • When accuracy ranges are written as e.g. “(±1 ml/min or ±1%)” the widest range is valid. Note

Blood Pressure Supervision The alarm limits below can be preset. The value put in brackets and in italics is the default value. Venous Pressure Operating range

Alarm limit HIGH max Alarm limit LOW min

-700 to +750 mmHg (±10% at -700 to -500 mmHg) (±5 mmHg or 3% at -500 to +500 mmHg) (±10% at +500 to +750 mmHg) +600 mmHg (+300 mmHg) -50 mmHg (-50 mmHg) When blood is detected the operator is requested to centralize the alarm limits and the low limit is by default set to +10 mmHg

Arterial Pressure Operating range

Alarm limit HIGH max Alarm limit LOW min.

-700 to +750 mmHg (±10% at -700 to -500 mmHg) (±5 mmHg or 3% at -500 to +500 mmHg) (±10% at +500 to +750 mmHg) +750 mmHg (+250 mmHg) -700 mmHg (-250 mmHg)

System Pressure Operating range

Alarm limit SN/DP HIGH max Alarm limit SN/DP LOW min. Alarm limit SP HIGH max Alarm limit SP LOW min. Alarm limit Low-Volume HDF HIGH max Alarm limit Low-Volume HDF LOW min


-700 to +750 mmHg (±10% at -700 to -500 mmHg) (±5 mmHg or 3% at -500 to +500 mmHg) (±10% at +500 to +750 mmHg) +300 mmHg (+175 mmHg) -200 mmHg (+10 mmHg) +750 mmHg (+150 mmHg) +750 mmHg (+150 mmHg) -300 mmHg (+100 mmHg)


13:13

Air Detection Sensitivity

Venous drip chamber size (diameter)

Bubbles larger than 1 µl will be trapped by the drip chamber. An alarm will be issued if the blood level falls below the middle of the air detector. 22 mm

Heparin istration Heparinization volume alarm limit

±0.3 ml of set value (±1 ml or 0.2 ml * heparinization time (h) or ±5%)

The accuracy is based on tests with 20 ml and 30 ml syringes

Dialysis fluid preparation Temperature Temperature alarm (fixed)

40 °C (±1 °C)

Conductivity Alarm limits in Acetate mode Alarm Limit in Bicarbonate mode, A-step Alarm Limit in Bicarbonate mode, B-step

±5% of set value ±5% of set value for A-step conductivity ±5% of set value for B-step conductivity

Alarm limits are temporarily extended to 10%. Maximum mean deviation for a 5 hour treatment is 0.2 mS/cm.

Dialysis fluid preparation (BiCart Select mode only) Dialysis Fluid Flow Rate Dialysis Fluid Flow Rate alarm limit SelectBag Proportioning Ratio alarm limit

13:14

300 - 700 ml/min (±9 ml/min) ±5% 1:400 ±12%, alarm given within 20 minutes. For larger errors the alarm time is shorter. SelectBag Proportioning Ratio is defined as the quotient SelectBag flow/dialysis fluid flow



Ultrafiltration Dialysis fluid flow operating 300 - 700 ml/min range UF rate supervision -4.0 to +4.0 l/h (±2 ml/min) Accuracy ±5 ml/min verified at start-up. UF rate supervision, max ±1-10 ml/min, (±5 ml/min) allowed difference between control and protective system, can be preset (Default) Accumulated UF volume ±0.10 - 2.0 l (±0.80 l) or ±0.10 l/h * ed alarm limit, can be preset treatment time (h) (Default) Treatment Time Control 0.05 to 9.59 hour.minute (±1 minute) TMP supervision alarm -200 to +550 mmHg (±15 mmHg) For AK 200 S, TMP is defined as the difference, Pb out - Pd out, where Pb out is the venous drip chamber pressure and Pd out is the pressure measured in the dialysis fluid, where it enters the machine after the dialyzer.

Substitution fluid (Low volume HDF) Infusion volume supervision ±15% of calculated volume (±10%) alarm

Blood leak detection Sensitivity Alarm response time (diffusion mode)


≥0.35 ml blood/min, haematocrit 32% ±2%, at 700 ml/min dialysis fluid flow rate 7 seconds


13:15

Physical data Depth Width Total Height Floor Area Weight Blood Monitor Weight Fluid Monitor Weight Stand Infusion Stand Height Transportation

Approx. 610 mm Approx. 570 mm Adjustable heights 1175-1340 mm Five position stand 1152 - 1382 mm 573 x 753 mm Approx. 17 kg Approx. 40 kg Approx. 24 to 31 kg 1300 to 2150 mm Max. load 10 kg One man installation Fitting into a normal Estate car

References Assembly Drawing: K22100

13:16



Materials in with water, concentrates and dialysis fluid Polymers Silicon rubber Santroprene PVC (Polyvinylchloride) PEEK (Polyetherketone) PEX (Polyethylene) PP (Polypropylene) PP (Polypropylene reinforced with talcum) PSU (Polysulphone) PVDF (Polyvinylidene fluoride) PTFE (Polytetrafluoro ethylene)

Metals Stainless steel SS2343 Stainless steel SS2353 Stainless steel SS2562 Titanium Platinum

Others Carbon Ceramic, Steatite 221 Ceramic, Aluminium oxide (Al2O3) Ceramic, Zirconium oxide (ZrO2) Glass Ferrite (Barium-Strontium- Ferrit)



13:17

Environmental data Operation If condensation occur when moving the equipment between locations with different temperatures and high relative humidity (e.g. outdoor and indoor locations), the inside of the equipment shall be allowed to dry before switching on the equipment. Ambient Temperature range Relative Humidity range Air Pressure range (atm. pressure) Maximum altitude

+18 to +35 °C 15 to 85% RH 700 to 1060 hPa ≈ 2000 m above see level

Transportation and storage During transportation and storage the equipment has to be kept in its original packing. If transportation or storage time is more than 15 weeks, the environmental data relating to the operation has to be followed. The maximum ambient temperature for transportation and storage in 96% Relative humidity is +40 °C. Ambient Temperature range -20 to +70 °C 10 to 96% RH Relative Humidity range 500 to 1060 hPa Air Pressure range (atm. pressure)

Electromagnetic environment The AK 200 S is intended for use in the electromagnetic environment specified below. The customer or the of the AK 200 S should assure that it is used in such an environment.

13:18

Emissions test

Compliance

Electromagnetic environment – guidance

RF emissions CISPR 11

Group 1

The AK 200 S uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment

RF emissions CISPR 11

Class B

The AK 200 S is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes

Harmonic emissions IEC 61000-3-2

Class A (Not applicable for 115 V version)

Voltage fluctuations /flicker emissions IEC 61000-3-3

Complies (Not applicable for 115 V version)



Immunity test

IEC 60601 test level

Compliance level

Electromagnetic enviroment-guidance

Electrostatic discharge (ESD), IEC 61000-4-2

±6 kV ±8 kV Air

±6 kV ±8 kV Air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.

Electrical fast transisent/burst, IEC 61000-4-4

±2 kV for power lines ±1kV for input/output lines

±2 kV for power lines ±1kV for input/output lines

Mains power quality should be that of a typical commercial or hospital environment.

Surge IEC 61000-4-5

±1KV for differential mode ±2kV for common mode

±1KV for differential mode ±2kV for common mode

Mains power quality should be that of a typical commercial or hospital environment

Voltage dips, short interruptions and voltage variations from power supply input lines. IEC 61000-4-11

<5 % UT (>95 % dip in UT) for 0,5 cycle 40 % UT (60 % dip in UT) for 5 cycles 70 % UT (30 % dip in UT) for 25 cycles <5 % UT (>95 % dip in UT) for 5 sec

<5 % UT (>95 % dip in UT) for 0,5 cycle 40 % UT (60 % dip in UT) for 5 cycles 70 % UT (30 % dip in UT) for 25 cycles <5 % UT (>95 % dip in UT) for 5 sec

Mains power quality should be that of a typical commercial or hospital environment. If the of the AK 200 S requires continued operation during power mains interruptions, it is recommended that the AK 200 S be powered from an uninterruptible power supply or a battery.

Power frequency (50/60 Hz) magnetic field IEC 61000-4-8

3 A/m

3 A/m

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

Note • UT is the a.c. mains voltage prior to application of the test level. Note



13:19

Portable and mobile RF communications equipment should be used no closer to any part of the AK 200 S, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance Conducted RF IEC 61000-4-6

3 Vrms 150 kHz to 80 MHz

3V

d = 1.2 P

Radiated RF IEC 61000-4-3

3 V/m 80 MHz to 2,5 GHz

3 V/m

d = 1.2 P 80 MHz to 800 d = 2.3 P 800 MHz to 2,5 GHz

Radiated RF mobile phones

-

30V/m

where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey2, should be less than the compliance level in each frequency range3. Interference may occur in the vicinity of equipment marked with the following symbol:

Note • At 80 MHz and 800 MHz, the higher frequency range applies.

• These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. Note

2 Field

strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the AK 200 S is used exceeds the applicable RF compliance level above, the AK 200 S should be observed to normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the AK 200 S. 3 Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. 13:20



Recommended separation distances between portable and mobile RF communications equipment and the AK 200 S The AK 200 S is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the of the AK 200 S can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the AK 200 S as recommended below, according to the maximum output power of the communications equipment. Rated maximum output power of transmitter W

Separation distance according to frequency of transmitter (m)

150kHz - 80MHz

80MHz - 800MHz

800MHz - 2500MHz

0,01

0.11

0.11

0.23

0,1

0.37

0.37

0.74

1

1.2

1.2

2.3

10

3.7

3.7

7.4

100

12

12

23

Rated maximum output power of mobile phone

-

-

7 d=  P  30 

2W GSM/3G

-

-

0.33

 3,5  d =  P  3

 3,5  d =  P  3

7 d=  P  3

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. Note • At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

• These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. Note



13:21

Standards The machine complies with the following standards: IEC 60601-1 General requirements for safety, Class I, type B IEC 60601-2-16 Particular requirements for safety of haemodialysis, haemodiafiltration and haemofiltration equipment IEC 60601-2-30 Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment IEC 60601-1-2 Electromagnetic compatibility EN 1060-1 Non-invasive sphygmomanometers Part 1: General requirements EN 1060-3 Non-invasive sphygmomanometers Part 3: Supplementary requirements for electromechanical blood pressure measuring systems NFS 90-304 Medico-surgical equipment Hemodialysis equipment

13:22



Chapter 14 Alarm list, Attention alarm list and Technical alarm list Alarm list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14:2 Attention alarm list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14:9 Technical alarm list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14:45


AK 200 S Operator’s manual - Alarm

14:1

Alarm list Light: Steady Mute time: 2 min Additional information: Low limit: blood pump stopped, venous clamp closed (only when blood is detected). High limit: blood pump stopped, in SN mode arterial clamp closed. Buzzer only when blood is detected. If necessary, it is possible to override the alarm actions, see "Override possibilities" in chapter 3 of this manual. Possible cause: Low alarm: The blood line has separated from the dialyzer. The blood line has separated at the arterial or venous side of the access. The position of the venous needle has changed. Clotting before or in the dialyzer. The blood flow rate has been reduced. High alarm: The venous blood line is kinked or clamped. The position of the venous needle has changed. Clotting has occurred after the venous pressure measurement e.g. in the blood line, in the venous drip chamber or in the needle. Light: Flashing Mute time: 2 min Additional information: Alarm limits are too wide. After 2.5 min an attention also appears. Will only appear when blood is detected. Possible cause: The alarm limits have been widened due to a started or stopped blood pump or a change in the set blood flow.

14:2



Light: Steady Mute time: 2 min Additional information: Temperature alarm. Dialysis Fluid byed. Buzzer only when blood is detected Possible cause: Low alarm: The machine has not yet stabilized the temperature after an interruption of the water supply. No power supply to the heating elements. High alarm: The temperature of the incoming water is too high. The machine has not yet stabilized the temperature after the function check. Light: Steady Mute time: 2 min Additional information: Dialysis fluid flow byed. Buzzer only when blood is detected. If conductivity is below 9 mS/cm the UF rate will automatically be set to zero. Possible cause: Low alarm: The concentrate container/BiCart cartridge is empty. The concentrate has not been connected. Incorrect concentrate has been connected. The proper concentrate has not been selected on the display. There is an interruption in the concentrate istration to the machine e.g. the connector is not properly connected to the pick-up tube, the concentrate line is kinked or occluded. Air is drawn into the machine instead of concentrate. The filter(s) of the concentrate(s) is/are clogged. The content of the concentrate container does not correspond to the specifications given. High alarm: Incorrect concentrate has been connected. The proper concentrate has not been selected on the display. The content of the concentrate container does not correspond to the specifications given.



14:3

Light: Steady Mute time: 2 min Additional information: Blood pump stopped, venous clamp closed. Buzzer only when blood is detected. If necessary, it is possible to override the alarm actions, see "Override possibilities" in chapter 3 of this manual. Possible cause: Low alarm: The arterial blood line is kinked or clotted between the arterial access and the arterial pressure measurement. The set blood flow rate exceeds the blood flow that the arterial access has possibility to deliver. The position of the arterial needle has changed. High alarm: The blood line has separated at the arterial side of the access. The position of the arterial needle has changed. Air or infusion enters the arterial line between the arterial access and the blood pump e.g. when a pre blood pump infusion is connected. Light: Flashing Mute time: 2 min Additional information: Alarm limits are too wide. After 2.5 min an attention also appears. Will only appear when blood is detected. Possible cause: The alarm limits have been widened due to a started or stopped blood pump or a change in the set blood flow.

14:4



Light: Steady Mute time: 1 min Additional information: Buzzer only when blood is detected Possible cause: The TMP during treatment depends mainly on five parameters: - UF-coefficient of the dialyzer - treatment time - UF-volume - blood flow - if HDF, infusion volume Changes in TMP during treatment depends on several different things: - changed UF value - changed treatment time - the condition of the dialyzer - the substitution fluid volume during HDF treatment - changes in the UF-control system that can cause reduced accuracy in the weight loss of the patient - change of blood flow The changes can cause both high- and low TMP alarms. Low alarm: - the set value for the treatment time has been increased - the set value for the UF volume has been decreased - decreasing venous pressure - decreased substitution fluid volume, during HDF - changes in the UF-control system that can cause reduced accuracy in the weight loss of the patient. High alarm: - the set value for the treatment time has been decreased - the set value for the UF volume has been increased - increasing venous pressure - partly or complete clogged dialyzer - increased substitution fluid volume, during HDF, can lead to a UF-rate that is too high in proportion to the blood pump flow - changes in the UF-control system that can cause reduced accuracy in the weight loss of the patient.



14:5

Light: Flashing Mute time: 2 min Additional information: Alarm limits are too wide. After 2.5 min an attention also appears. Will only appear when blood is detected. Possible cause: The alarm limits have been widened due to - a started or stopped blood pump - changed treatment time - changed UF volume - started or stopped ultrafiltration Light: Steady Mute time: 2 min Additional information: Blood pump stopped, venous and arterial clamps closed. Buzzer only when blood is detected. Adjust the level in the venous drip chamber by using the level adjustment buttons. If necessary (particularly when performing single needle/double pump), it is possible to override the alarm actions, see “Override possibilities” in chapter 3 of this manual. Possible cause: Blood line(s) not properly connected at e.g. the arterial needle connection, the dialyzer connection(s), the infusion port(s). Blood line(s) or the dialyzer not properly de-aired during priming. An empty infusion container with air inlet is connected to the blood line(s). The arterial needle is dislocated. Light: Flashing Mute time: 2 min Additional information: Air has been detected. The fault has been rectified, but the Air detect button must be pressed in order to reset the alarm and to continue the treatment. Possible cause: -

14:6



Light: Steady Mute time: 2 min Additional information: The ∆BV is below the set alarm limit. Possible cause: The ultrafiltration rate or the accumulated ultrafiltration volume, tolerated by the patient, has been exceeded. Light: Steady Mute time: 2 min Additional information: Dialysis fluid flow byed. Buzzer only when blood is detected Possible cause: The content of the concentrate container does not correspond to the specifications given. Incorrect concentrate has been connected. Either the acid container or the bicarbonate container/BiCart cartridge has been emptied during bicarbonate treatment. Light: Steady Mute time: 2 min Additional information: Blood pump stopped, arterial and venous clamps closed. Dialysis fluid flow byed, UF rate is automatically set to zero (only when blood is detected). If necessary, it is possible to override the alarm actions, see "Override possibilities" in chapter 3 of this manual. Possible cause: A leakage, which allows blood to flow from the blood compartment to the dialysis fluid compartment, has occurred in the dialyzer. Air bubbles or particles, which can cause a false blood leak alarm, have entered the blood leak detector.



14:7

Light: Flashing Mute time: 2 min Additional information: A blood leak has been detected. The fault has been rectified, but the Blood leak button must be pressed in order to reset the alarm and to continue the treatment. Possible cause: Light: Steady Mute time: 2 min Additional information: The treatment time has expired. An attention appears simultaneously. Possible cause: Treatment time has expired. Light: Steady Mute time: 2 min Additional information: System pressure too high or system pressure too low. See attention message Possible cause: Light: Steady Mute time: 2 min Additional information: UF volume too high. See attention message. Possible cause: -

14:8



Attention alarm list The attentions are described in alphabetical order.

A-PICK UP TUBE IMPROPER POSITION Mute time: 2 min Additional information: Buzzer is delayed 2 min. Check pick-up tube and mode.

ABSENT HEATER SUPPLY VOLTAGE Check fuses and connector Mute time: 2 min Additional information: Will only appear during disinfection a) Check cable between fluid monitor and power supply unit b) Check fuses in power supply unit

ADJUST PUMP HEAD TO TUBE 0.00 Press BLOOD FLOW key to confirm Mute time: Infinite Additional information: After the diameter of the blood pump segment has been changed, this attention alarm will occur when the blood pump is started again.

AIR DETECTOR NOT ACTIVATED Press AIR DETECTOR key Mute time: Infinite Additional information: Will only appear during priming.



14:9

ARTERIAL PRESSURE LIMITS ADJUST Press ARTERIAL key Mute time: 2 min Additional information: Alarm limits are too wide: will only appear when blood is detected.

ARTERIAL PUMP COVER NOT CLOSED Close cover Mute time: 2 min Additional information: Blood pump stopped. Venous clamp closed.

ARTERIAL PUMP OVERLOAD Press BLOODPUMP key Mute time: 2 min Additional information: Blood pump stopped. Venous clamp closed.

ARTERIAL PUMP REVOLUTION HIGH Check cause, press BLOOD PUMP key Mute time: 2 min Additional information: Blood pump stopped, venous clamp closed. Check for kinks on arterial blood line a) Check arterial blood flow, when necessary decrease b) Decrease high system pressure limit c) Decrease stroke volume

14:10



B/ACETATE - PICK UP TUBE IMPROPER POSITION Mute time: 2 min Additional information: Buzzer is delayed 2 min. Check pick-up tube and mode

BATTERY FAILURE Press LOW to confirm further use Mute time: Infinite Additional information: A reminder to change or recharge the battery. Must be confirmed in order to disappear. If the attention is confirmed without change or recharge of the battery, note that there is no battery backup in case of a power failure during treatment. This means that the machine will not be able to alarm or restart in case of a power failure.

BLOOD LEAK DETECTOR FAILURE Clean and press BLOODLEAK key Mute time: Infinite Additional information: Will only appear during Fch. For cleaning instructions, see "Maintenance - the exterior of the machine", "Blood leak detector", chapter 12, in this manual.

BLOOD MONITOR TEMPERATURE ALARM Insufficient internal cooling Mute time: 2 min Additional information: Check FAN filter on left hand side



14:11

BLOOD PUMP(S) STOP TIME EXPIRED Press BLOODPUMP key Mute time: 2 min Additional information: Appears after 1 min: will only appear when blood is detected

BPM FAILURE Turn off BPM Mute time: Infinite Additional information: An error is detected by the BPM. Turn the BPM off and then on again.

BPM PRESS. OUTSIDE ALARM LIMITS Check patient and press BPM key Mute time: Infinite Additional information: Blood pressure measurement values is outside the set alarm limits. Check patient. Confirm by pressing the flashing BPM button. The BPM screen will then be shown and the measured numerical values outside the set alarm limits will be flashing.

BVS DOOR OPEN Close door Mute time: 2 min Additional information: Buzzer delayed 2 min. The BVS door has to be closed during self test, priming and treatment. Close the BVS door.

14:12



BVS FAILURE Switch off BVS Mute time: 2 min Additional information: An error has been detected by the BVS. Turn the BVS off to continue the treatment. The cause of the attention alarm can either be that the patient’s Hemoglobin value is outside the specified range for the BVS to be active or a technical BVS error. If a technical error is suspected, note the two-figure number to the right of the attention text before turning off the BVS. Inform the technician responsible for the machine.

BVS LOW BLOOD FLOW Increase blood flow Mute time: 2 min Additional information: If possible, increase the blood flow rate. If this is not possible, turn the BVS off to continue the treatment.

BVS SELF TEST Remove cuvette Mute time: 2 min Additional information: Buzzer delayed 2 min. Appears during the function check of the blood monitor. The BVS self test is to be performed with an empty holder. Remove the BVS cuvette from the holder.

BiCart EMPTY Check or replace BiCart Mute time: 2 min Additional information: If BiCart is to be replaced close both latches, open and attach new BiCart. Priming will then be done automatically.



14:13

BiCart HOLDER NOT CLOSED Close or check BiCart holder Mute time: 2 min Additional information: Buzzer is delayed 2 min.

BiCart NOT ATTACHED TO HOLDER Attach or check BiCart Mute time: Infinite Additional information: Buzzer is delayed 2 min. Check if BiCart cartridge is empty. Check that the BiCart cartridge is properly primed by the machine, if not, remove the cartridge, close the latches and attach the cartridge again. If the BiCart cartridge is properly primed and there are no visual leakage, press the Arrow button below HIGH to continue.

BiCart NOT ATTACHED TO HOLDER Attach/check BiCart, press HIGH Mute time: 2 min Additional information: Appears only in function check. Check that the BiCart cartridge is properly primed by the machine, if not, remove the cartridge, close the latches and attach the cartridge again.

CAN NOT APPLY ED PARAM. All parameters must be rejected Mute time: Infinite Additional information: Appears if any treatment parameter or value in the ed list is not accepted by the machine. The complete list of parameters must be rejected. Press the Clinic automation button to check which parameter, shown in red, cannot be set. Redo the ing after changing the parameter or set all parameters manually. It is important to note that the ed settings for concentrates have not been automatically set.

14:14



CENTRAL CHEM DISINF. COMPLETED Press Rinse/Drain key Mute time: Infinite Additional information: Will appear when the preset dwell time in central disinfection has ed.

CHANGE OF TREATMENT MODE FAILED Check settings, press LOW Mute time: Infinite Additional information: Appears when the machine was not able to automatically set treatment mode after acceptance of ed treatment parameters. Check treatment mode, activate manually if necessary.

CHECK FLUID TUBES FOR LEAKAGE Press LOW to confirm Mute time: 2 min Additional information: Appears only in function check. Check that the dialysis fluid tubes are properly attached to the machine.

CHEM DIS FILLUP PHASE COMPLETED Place pick up tube in machine Mute time: 2 min Additional information: -



14:15

CLEARANCE TOO LOW Mute time: Infinite Additional information: The measured clearance value is below the alarm limit set. Check cause, adjust treatment parameters to increase clearance or adjust alarm limit for clearance. The alarm limit for clearance is changed by pressing the Kt/V button once (to reach the first Diascan screen). Then press the lit Arrow button below K LIMIT and adjust by using the Set knob.

CONC. SETTINGS NO LONGER DEFAULT Check settings, press LOW Mute time: Infinite Additional information: Appears after rejection of the ed treatment parameter list, when the ed concentrate settings differ from the settings which the machine started up with. The machine has automatically set the ed concentrate settings. To continue, press the lit Arrow button to confirm the ed settings. Select and connect new concentrates manually as is the usual procedure.

CONDUCTIVITY MEASURED Check concentrate supply Mute time: 2 min Additional information: Appears when performing disinfection program, it is not possible for the machine to rinse out remaining concentrates. Check concentrate connections. If function check has not been performed prior to the disinfection program, and the inlet water conductivity is higher than 0.5mS/cm, the machine must be restarted. After restart, the function check must continue until an attention alarm appears indicating high inlet water conductivity. After confirmation of this attention alarm, restart the disinfection program.

14:16



CleanCart NOT ATTACHED TO HOLDER Attach or check CleanCart Mute time: 2 min Additional information: -

DECALCIFICATION REQUIRED XX hours since last decalc Mute time: Infinite Additional information: Buzzer is delayed 2 min. Will disappear as soon as priming is activated. The period of time between the last performed decalcification and the appearance of the attention alarm can be preset.

DIALYSER UF-COEFF TOO SMALL Decrease infusion SET value Mute time: Infinite Additional information: The "total" UF value cannot be achieved due to e.g. a) Too small dialyzer b) Clotted dialyzer

DISCONNECT ARTERIAL PRESSURE Press ART PRES key to confirm Mute time: 2 min Additional information: Further function check stopped. May appear during function check when blood lines are attached.



14:17

DISCONNECT SYSTEM PRESSURE ress SN DATA key to confirm Mute time: 2 min Additional information: Further function check stopped. May appear during function check when blood lines are attached.

DISCONNECT VENOUS PRESSURE Press VENOUS key to confirm Mute time: 2 min Additional information: Further function check stopped. May appear during function check when blood lines are attached.

DISINFECTION REQUIRED XX days since last disinfection Mute time: Infinite Additional information: Buzzer is delayed 2 min. Will disappear as soon as priming is activated. The period of time between the last performed disinfection and the appearance of the attention alarm can be preset.

14:18



Diascan FAILURE Turn OFF Diascan Mute time: Infinite Additional information: During function check: Appears when there is a technical error of the Diascan function; it is not possible to use the Diascan. Turn the Diascan off by pressing the Kt/V button once (to reach the first Diascan screen). Then press the lit Arrow button below Diascan and turn the Set knob anticlockwise until OFF appears. an authorized service technician. During treatment: Appears when too many Diascan steps have been done during that particular treatment. Performing further Diascan steps may lead to an imbalance in the sodium level of the patient. The Diascan function is not permitted to perform any more measurement checks. Turn the Diascan off by pressing the Kt/V button once (to reach the first Diascan screen). Then press the lit Arrow button below Diascan and turn the Set knob anticlockwise until OFF appears. If this attention appears frequently, discuss preset limits with an authorized service technician.

Diascan IN PROGRESS To change param, cancel Diascan Mute time: 1 min Additional information: Appears when one of the following treatment parameters are changed at the same time as a measurement check is in progress: - sodium and bicarbonate (conductivity) - temperature - dialysis fluid flow - UF volume - profiling settings - isolated UF activation It is not possible to change the treatment parameter. If possible, leave the attention without immediate action (i.e. just silence the buzzer by using the Mute button), the attention will disappear automatically within 30 seconds. Change the parameter when the measurement check is complete. If the treatment parameter must be changed immediately, turn the Diascan off by pressing the Kt/V button once (to reach the first Diascan screen). Then press the lit Arrow button below Diascan and turn the Set knob anticlockwise until OFF appears. It is possible to activate the Diascan again when the treatment parameter has been changed. The Diascan will then be rescheduled.



14:19

Diascan MEASUREMENT FAILED Press Kt/V to confirm Mute time: Infinite Additional information: The machine was not able to perform the measurement check. Confirm by pressing the flashing Kt/V button. If desired, reactivate the measurement check.

Diascan NOT ACTIVE No measurement possible. Confirm Mute time: Infinite Additional information: Appears when the Diascan is activated in Isolated UF mode. The Diascan function cannot perform measurement checks. This attention can also appear when an attempt to reactivate the Diascan is made after a Diascan failure attention has previously occurred. Confirm by pressing the flashing Kt/V button.

Diascan RESCHEDULED Press Kt/V to confirm Mute time: No buzzer Additional information: Appears when one of the following is done at the same time as a measurement check is in progress: - the blood flow rate is changed - the Blood pump button is pressed - the Start UF Stop button is pressed - the Fluid by button is pressed - a treatment alarm that produces dialysis fluid by or blood pump stop is generated The machine was not able to completely perform the measurement check as the measurement check has been interrupted. Confirm by pressing the flashing Kt/V button and the machine will automatically reschedule measuring as soon as possible.

14:20



EMPTY AND REMOVE CleanCart Close holder Mute time: 2 min Additional information: Open the upper latch of the holder and wait until the CleanCart has been emptied. Remove the CleanCart and close the holder. This attention can be removed by preset.

EXTRA PRIMING VOLUME ACHIEVED Check line in priming detector Mute time: 2 min Additional information: If this attention appears during initiation of the treatment, check that the venous blood line is properly inserted into the priming detector. If this attention appears during priming, the set extra priming volume has been achieved. Note that the buzzer can be muted for 2 min if the blood pump is running; if the blood pump is not running, the buzzer will be muted until the blood pump is started again1.

FLUID BY TIME EXPIRED Press BY key Mute time: 2 min Additional information: Appears after 5 min: will only appear when blood is detected.

FLUID MONITOR TEMPERATURE ALARM Insufficient internal cooling Mute time: 2 min Additional information: Check FAN filter at the rear.

12 HCEN9751 Revision.12.2005 Program version 8.xx

min mute time when the blood pump is not running can be preset AK 200 S Operator’s manual - Alarm

14:21

FLUID PATH OBSTRUCTION Check drain tube Mute time: 2 min Additional information: A "blockage" has been detected. Check drain tubing.

FLUID PATH OBSTRUCTION Check tubes and dialyzer paths Mute time: 2 min Additional information: A "blockage" has been detected. Check if particle filter after dialyzer is "clogged" by pressing Fluid by button - if attention disappears, the cause is probably the particle filter.

FLUID TUBES IN SAFETY BY Check position of fluid tubes Mute time: Infinite Additional information: Buzzer is delayed 2 min. Appears if the tubings are attached to the machine when blood is detected.

FLUID TUBES NOT IN SAFETY BY Mute time: 2 min Additional information: Buzzer is delayed 2 min. Disinfection mode cannot be started.

14:22



FUNCTIONAL CHECK STOPPED Remove line from primingdetector Mute time: 2 min Additional information: The priming detector detects blood during blood monitor function check. Remove blood filled line from priming detector. If priming detector is malfunctioning, call for technical service.

HDF KEY ERROR Press technical alarm key Mute time: 2 min Additional information: Technical error concerning HDF key. If confirmed with technical alarm key it is possible to continue in HD mode.

HEPARIN PUMP OVERLOAD Check syringe and tube Mute time: 2 min Additional information: Heparin pump stopped. Syringe empty?



14:23

HIGH INLET WATER COND x.xmS/cm Press LOW to confirm low K+ Mute time: 2 min Additional information: Appears during function check if the inlet water conductivity is between 0.5 and 2.5 mS/cm. When this attention alarm appears, the operator must consult the attending physician before the attention alarm is confirmed and a treatment is started. It will not be possible to start a treatment until the attention alarm is confirmed. Depending on the inlet water conductivity, minor electrolytes concentration (potassium, calcium, magnesium) will be reduced by 4 20% in the dialysis fluid. This attention alarm can only appear if it is possible to run the machine with inlet water conductivity above 0.5 mS/cm.

HIGH SYSTEM PRESSURE ALARM Mute time: 2 min Additional information: Blood pumps stop. Clotted dialyzer? Wrong insertion of the pump segments? May appear after treatment in double pump mode when the discontinuing is performed in single pump mode, without having removed the venous pump segment from the pump.

INCONSISTENT UF-RATE PARAMETERS Check parameter settings Mute time: 2 min Additional information: Buzzer is delayed 2 min. Calculated UF-rate is either below min UF-rate or above max UF-rate (4 l/h) a) Increase UF-rate by adjusting time or UF volume when set UF-rate is below min UF-rate b) Decrease min UF-rate c) Decrease UF-rate by adjusting time or UF volume when set UF-rate is above max limit (4 l/h)

14:24



INCORRECT ACETATE CONCENTRATE Check concentrate fluid Mute time: 2 min Additional information: Dialysis fluid flow byed

INCORRECT ACIDIC CONCENTRATE Check concentrate fluid Mute time: 2 min Additional information: Dialysis fluid flow byed

INCORRECT AUTO DISINFECTION TIME Check ready time parameters Mute time: 2 min Additional information: Real time and ready time are too close?

INCORRECT BICARBONATE CONC Check concentrate fluid Mute time: 2 min Additional information: Dialysis fluid flow byed



14:25

INCORRECT CLEANING AGENT Check cause, press HEAT key Mute time: 2 min Additional information: An insufficient citric acid amount or incorrect selection of cleaning agent has been detected, check cause and press HEAT key shortly to repeat fill phase. If the RINSE key is pressed for 3 seconds, a post chemical rinse will start.

INCORRECT CLEANING AGENT Check cause, press RINSE key Mute time: 2 min Additional information: An incorrect concentration or incorrect selection of cleaning agent has been detected, check cause. If the RINSE key is pressed for 3 seconds, a post chemical rinse will start.

INCORRECT CONDUCTIVITY MEASURED Check concentrate supply Mute time: 2 min Additional information: Function check stopped. Will only appear during function check

INCORRECT DISINFECTANT Check cause, press CHEM key Mute time: 2 min Additional information: A too low disinfectant concentration has been detected, check cause and press CHEM key shortly to repeat fill phase. If the RINSE key is pressed for 3 seconds, a post chemical rinse will start.

14:26



INCORRECT DISINFECTANT Check cause, press RINSE key Mute time: 2 min Additional information: A too high disinfectant concentration has been detected, check cause and press RINSE key shortly to repeat fill phase. If the RINSE key is pressed for 3 seconds, a post chemical rinse will start.

INCORRECT MAIN FLOW Mute time: 2 min Additional information: Appears when the BiCart Select system is being used. The protective and control systems for dialysis flow rate are not in agreement. To continue treatment if the attention remains, exchange the SelectCart and SelectBag for an acidic concentrate. Press the Bicarbonate button once to change concentrate alternative. Call for an authorized technician for trouble shooting to ensure further use with the Bicart Select system.

INCORRECT SelectBag FLOW Check SelectBag Mute time: 2 min Additional information: Check holder for leakage or air at the top of SelectBag. Remove and replace an empty SelectBag

INCORRECT SelectCart CONCENTRATE Check or replace SelectCart Mute time: 2 min Additional information: Dialysis fluid flow byed.



14:27

INCORRECT UF PARAMETER(S) Check parameter settings Mute time: Infinite Additional information: Buzzer is delayed 2 min. Max positive/negative pressure limit has been reached a) Increase UF-rate by adjusting time or UF volume (negative TMP) b) Decrease UF-rate by adjusting time or UF volume (positive TMP)

INFUSION PUMP FAILURE Deactivate HDF to continue Mute time: 2 min Additional information: Protective system is not in agreement with control system about the speed of the infusion pump. This means that the patient’s weight loss during treatment might be incorrect. The infusion pump and ultrafiltration are stopped. Press the HDF button for 3 seconds to confirm the alarm and simultaneously deactivate the HDF treatment. Do customary patient checks. To continue treatment: A calculation of the true infusion volume up to when the attention alarm occurred has to be made. Weigh the infusion bags in order to roughly estimate how much infusion fluid has been infused so far. Exclude the priming volume. Check, at the same time, the accumulated infusion volume measured by the control system by pressing the HDF button. Calculate the difference and adjust the set UF volume (patient weight loss) in order to achieve the correct weight loss for the patient. If possible, also weigh the patient in order to ensure that the calculation is correct. Continue the treatment in HD mode. CAUTION Incorrect weight loss may occur if confirmation of the alarm is done without adjusting the set UF volume for the rest of the treatment. CAUTION

14:28



INFUSION RATE LESS THAN XX.X L/H Adjust SET value Mute time: 2 min Additional information: 0.3 l/h is the min "total UF-rate". When infusion volume + UF volume = less than 0.3 l/h, this attention appears.

INFUSION RATE MORE THAN XX.X L/H Adjust SET value Mute time: 2 min Additional information: It is not possible to set the infusion rate above 2.1 l/h.



14:29

INFUSION VOLUME DEVIATION Check cause, press HDF key Mute time: 2 min Additional information: HDF procedure stops. Protective system has detected that the accumulated infusion volume during treatment measured up to this point is incorrect. This means that the patient weight loss during treatment is incorrect. The infusion pump and ultrafiltration are stopped. Check the infusion line and infusion bags for e.g. kinks. Press the HDF button for 3 seconds to confirm the alarm and simultaneously deactivate the HDF treatment. Do customary patient checks. To continue treatment: A calculation of the true infusion volume up to when the attention alarm occurred has to be made. Weigh the infusion bags in order to roughly estimate how much infusion fluid has been infused so far. Exclude the priming volume. Check, at the same time, the accumulated infusion volume measured by the control system by pressing the HDF button. Calculate the difference and adjust the set UF volume (patient weight loss) in order to achieve the correct weight loss for the patient. If possible, also weigh the patient in order to ensure that the calculation is correct. If the fault is rectified (e.g. a kinked line) it is possible to continue the HDF treatment. In this case, activate HDF again by pressing the HDF button for 3 seconds. If the attention reappears, deactivate HDF and redo the calculation as above. If it is not possible to rectify the fault, continue the treatment in HD mode. CAUTION Incorrect weight loss may occur if confirmation of the alarm is done without adjusting the set UF volume for the rest of the treatment. CAUTION

INSUFFICIENT DISINFECTANT Check disinfectant supply Mute time: 2 min Additional information: Check pick up tube and disinfectant container.

14:30



INSUFFICIENT WATER SUPPLY Check water supply Mute time: 2 min Additional information: Buzzer is delayed 2 min. The blood flow rate is decreased. It is however possible to increase the blood flow during the alarm state. Check water supply.

ISOLATED UF PHASE COMPLETED Press ISOL UF key to complete Mute time: Infinite Additional information: When the remaining time is 0.00 after isolated UF phase, this attention will occur and remain until the Isol UF button has been released.

Kt/V FORECAST TOO LOW Mute time: Infinite Additional information: Kt/V forecast value is below the Kt/V alarm limit set. Check cause, adjust treatment parameters or adjust the alarm limit for Kt/V. This is done by pressing the Kt/V button twice (to reach the second Diascan screen). Then press the lit Arrow button below LIMIT and adjust by using the Set knob.

Kt/V TARGET ACHIEVED Press Kt/V to confirm Mute time: Infinite Additional information: The set target value for Kt/V has been reached. Confirm by pressing the flashing Kt/V button. It is also possible to increase the Kt/V target value, and the machine will recalculate time to target. This is done by pressing the Kt/V button twice, (to reach the second Diascan screen). Then press the lit Arrow button below TARGET and adjust by using the Set knob.



14:31

LIMITED INPUT PUMP CAPACITY Adjust UF/TMP parameters Mute time: 2 min Additional information: AK 200 S cannot produce the min or max dialysis fluid pressure that is required a) Check for possible obstructed drain tube b) Check UF volume and UF rate c) If the attention remains, call for technical service. CAUTION Incorrect weight loss may occur if the machine is left for a longer period with this attention. CAUTION

LIMITED OUTPUT PUMP CAPACITY Adjust UF/TMP parameters Mute time: 2 min Additional information: AK 200 S cannot produce the min or max dialysis fluid pressure that is required a) Check UF volume and UF rate b) If the attention remains, call for technical service. CAUTION Incorrect weight loss may occur if the machine is left for a longer period with this attention. CAUTION

LOW BATTERY POWER Machine turns off in one minute Mute time: Infinite Additional information: -

14:32



LOW FLOW HEAT ABORTED Press lit arrow to confirm Mute time: Infinite Additional information: This attention alarm appears when performing integrated Heat disinfection program with WRO 300 H. The Low Flow Heat phase (where the machine receives hot water from the WRO 300 H) will not start. Press the lit Arrow button to confirm the attention alarm. The AK 200 S now enters drain phase as the circulation phase of the Heat disinfection program is complete. Call for an authorized technician. For information about the integrated Heat disinfection program with WRO 300 H, see the corresponding handling instructions for the program in chapter 12 of this manual.

LOW SYSTEM PRESSURE ALARM Check infusion bag Mute time: 2 min Additional information: HDF procedure stops. Check infusion line. Check if infusion bag is empty.

MAJOR AIR LEAKAGE Check fluid connectors and tubes Mute time: 2 min Additional information: Buzzer is delayed 2 min. Dialysis fluid flow byed, dialysis fluid pressure: -50 mmHg. CAUTION Incorrect weight loss may occur if the machine is left for a longer period with this attention. CAUTION



14:33

MEAN BLOOD FLOW TOO LOW Check settings Mute time: 2 min Additional information: Measured blood flow is less than 70% of set blood flow.

MINOR AIRLEAKAGE Check fluid connectors and tubes Mute time: Infinite Additional information: Buzzer is delayed 2 min.

NEGATIVE UF RATE Check and press UF volume Mute time: 2 min Additional information: Relative negative UF volume of 500 ml or negative UF rate >50 ml/min for 5 min. Check for "blockage" of the draining tube. After correction of the fault, press the UF volume button for 3 sec. for confirmation. Check the UF rate before leaving the machine, if this is not correct call for technical service. CAUTION Incorrect weight loss may occur if confirmation is done without having corrected the cause for the attention. CAUTION

NEW ULTRA FILTERS REQUIRED Replace ULTRA filters Mute time: Infinite Additional information: Will disappear as soon as priming is activated. See "Ultrafilters; how to change" in the “Hygiene and maintenance" chapter.

14:34



NO BACK-FILTRATION WARNING Press TMP to confirm Mute time: 2 min Additional information: The TMP low alarm limit is set below zero mmHg and no backfiltration warning will occur. This attention needs confirmation. This attention alarm can be activated by preset.

NO BPM VALUES Check BPM cuff Mute time: Infinite Additional information: Buzzer delayed 2 min. It was not possible to measure the patients blood pressure. Check that the cuff is correctly applied to the patient. It could also be that the patient is moving during the measurement check.

NO CHANGE IN BLOOD PRESSURE Check cause, press BLOODPUMP key Mute time: 2 min Additional information: Blood pump stopped, venous clamp closed. May appear just before "arterial revolution too high" attention. a) Kinks on system pressure transducer protector? b) Clotted discfilter? c) Clotted dialyzer? d) Check that the venous blood pump segment is inserted in the pump housing

NO CUFF ATTACHED Attach or check BPM cuff Mute time: Infinite Additional information: Buzzer delayed 2 min. Check for kinks or leakage from the cuff and the cuff hose. Check also that the cuff hose is properly connected to the machine.



14:35

NO CUVETTE IN BVS Insert cuvette or switch off BVS Mute time: 2 min Additional information: Buzzer delayed 2 min. The cuvette of the blood line is not inserted in the holder or a blood line without a cuvette is used. In the later case turn the BVS off.

NO HEPARIN VALUE SET Press HEPARIN key to confirm Mute time: 2 min Additional information: An attention also appears simultaneously.

POWER FAILURE, BATTERY OPERATION Battery operated for XX minutes Mute time: Infinite Additional information: Buzzer is delayed 2 min.

PRIMING VOLUME ACHIEVED Check line in priming detector Mute time: No buzzer Additional information: The blood pump stops. (If SN/double pump or HDF has been activated, the venous/infusion pump also stops.) If this attention appears during initiation of the treatment, check that the venous blood line is properly inserted into the priming detector.

14:36



PULSE RATE OUTSIDE ALARM LIMITS Check patient and press BPM key Mute time: Infinite Additional information: Pulse rate measurement value is outside the set alarm limits. Check patient. Confirm by pressing the flashing BPM button. The BPM screen will then be shown and the measured numerical value outside the set alarm limits will be flashing.

RECOVERED FROM POWER-FAILURE Press TIME key to confirm Mute time: 2 min Additional information: When Time is confirmed, both Blood leak as well as Air detect buttons have to be pressed in order to start again.

RECOVERED FROM TECHNICAL RESTART Press TIME key to confirm Mute time: 2 min Additional information: Appears after an automatic restart. When Time is confirmed, both Blood leak as well as Air detect buttons have to be pressed in order to start again

STROKE VOLUME NOT ACHIEVED Check blood line setup Mute time: 2 min Additional information: May appear if high system pressure limit was decreased too rapidly. a) Check for kinks on venous blood line b) Check system pressure change during whole phase. Adjust high system pressure limit. c) Decrease stroke volume



14:37

STROKE VOLUME NOT ACHIEVED Check cause, press SN DATA key Mute time: 2 min Additional information: a) Check/adjust level in expansion chambers b) Check/adjust system pressure window c) Decrease stroke volume d) Check/adjust blood pump segment setting

SelectBag FLOW NOT CALIBRATED Change concentrate alternative Mute time: 2 min Additional information: Protective and control system do not agree about the SelectBag flow. Press the Bicarbonate button once to change concentrate alternative.

SelectBag HOLDER IMPROPER POSITION Mute time: 2 min Additional information: Buzzer is delayed 2 min. Check holder position.

SelectCart HOLDER NOT CLOSED Close or check SelectCart holder Mute time: 2 min Additional information: Buzzer is delayed 2 min.

14:38



SelectCart NOT ATTACHED Attach or check SelectCart Mute time: Infinite Additional information: Buzzer is delayed 2 min.

TMP LIMITS ADJUST Press TMP key Mute time: 2 min Additional information: Alarm limits are too wide: will only appear when blood is detected

TOTAL UF-RATE TOO HIGH Adjust blood flow/infusion volume Mute time: Infinite Additional information: If a too low blood flow in combination with a too high "total UF rate" is of set blood set, this attention appears. Max "total UF rate" is 30% flow.

TREATMENT STOP TIME EXPIRED Press START UF key Mute time: 2 min Additional information: Appears after 5 min: will only appear when blood is detected



14:39

TREATMENT TIME EXPIRED Press TIME key to confirm Mute time: 2 min Additional information: When the flashing Time button is pressed, end of treatment will be confirmed and the TMP alarm limits will widen.

UF RATE HIGHER THAN EXPECTED Adjust UF parameters Mute time: 2 min Additional information: Buzzer is delayed 2 min. Min UF-rate is reached a) Increase UF-rate by adjusting time or UF volume b) Decrease min UF-rate

UF RATE LIMIT REACHED Re-adjust time or UF volume Mute time: 2 min Additional information: Buzzer is delayed 2 min. UF volume cannot be achieved within remaining time even though +20% limit on UF-rate is used a) Increase UF-rate limit (+20%) by pressing UF volume arrow for set (a new limit is calculated) b) Decrease UF-rate by adjusting time or UF volume

UF SELF TEST FAILED New test within 5 min Mute time: No buzzer Additional information: Will only appear during Fch, the function check will be prolonged.

14:40



UF VOLUME DEVIATION Check cause, press UF volume Mute time: 2 min Additional information: The protective system accumulated measured UF volume (SUPERV) is outside LOW or HIGH limit. The ultrafiltration is stopped and the blood flow is decreased. It is however possible to increase the blood flow during the alarm state. Check the machine for visual leakage. Check accumulated UF volume in both control and protective system. Check alarm limits for UF volume in protective system. Do customary patient checks as whenever the ultrafiltration volume is suspected to be incorrect. Evaluate if it is possible to continue the treatment. Confirm by pressing the UF volume button for 3 sec. After confirmation the estimated accumulated UF volume is recalculated in protective system. (See “Protective system for ultrafiltration" in chapter 3). If problem remains call for technical service. This attention can be removed by preset. CAUTION Incorrect weight loss may occur if confirmation is done without having corrected the technical cause for the attention alarm. CAUTION

UF VOLUME DEVIATION: NEGATIVE UF Check cause, press UF volume Mute time: 2 min Additional information: The protective system UF volume is more than 500 ml negative. Check for "blockage" of the draining tube. Confirm by pressing the UF volume button for 3 sec. If problem remains call for technical service. CAUTION Incorrect weight loss may occur if confirmation is done without having corrected the technical cause for the attention alarm. CAUTION



14:41

UF VOLUME HIGHER THAN EXPECTED Adjust time or UF volume Mute time: Infinite Additional information: Max positive dialysis fluid pressure is reached (negative TMP). a) Partly clotted dialyzer? b) Partly kinked venous blood line? c) Technical problem? Correct the cause. d) Check UF volume and UF rate CAUTION Incorrect weight loss may occur if confirmation is done without having corrected the technical cause for the attention alarm. If problems remains service technician. CAUTION

UF VOLUME LOWER THAN EXPECTED Adjust time or UF volume Mute time: Infinite Additional information: Max negative dialysis fluid pressure is reached (positive TMP). a) Partly clotted dialyzer or too small dialyzer? b) Technical problem? Correct the cause. c) Check UF volume and UF rate CAUTION Incorrect weight loss may occur if confirmation is done without having corrected the technical cause for the attention alarm. If problems remains service technician. CAUTION

UF VOLUME TOO HIGH Re-adjust time or UF volume Mute time: 2 min Additional information: The accumulated UF volume differs > 200 ml from the calculated volume. The blood flow will be decreased.

14:42



UNSTABLE CONDUCTIVITY Check SelectCart, press HIGH Mute time: 2 min Additional information: Appears in function check. It was not possible to complete conductivity test. The function check has been stopped. Check that the SelectCart cartridge is properly attached to SelectCart holder. Check for possible air leakage where the cartridge is attached into the holder. Confirm by pressing the lit HIGH Arrow button.

VENOUS PRESSURE LIMITS ADJUST Press VENOUS key Mute time: 2 min Additional information: Alarm limits are too wide: will only appear when blood is detected

VENOUS PUMP COVER NOT CLOSED Close cover Mute time: 2 min Additional information: Blood pump stopped, venous clamp closed

VENOUS PUMP OVERLOAD Press BLOODPUMP key Mute time: 2 min Additional information: Blood pump stopped, venous clamp closed



14:43

WRO COMMUNICATION FAILURE Check WRO Mute time: Infinite Additional information: The communication between the AK 200 S and the WRO has stopped. Call for an authorized technician.

WRO NOT READY Please wait Mute time: Infinite Additional information: Appears during function check, please wait. WRO inaccessible, check information on WRO.

14:44



Technical alarm list ERROR! CALL SERVICE Additional information: Call service to investigate cause of alarm and the possibility of continuing treatment. In case of a technical error in the fluid monitor during treatment the blood flow will be decreased. It is however possible to increase the blood flow during the alarm state. WARNING A restart attempt after technical error during treatment may create a potential hazard for the patient. WARNING

ERROR! RESTART OR CALL SERVICE Additional information: A restart attempt can be made before calling service.

TECHNICAL ERROR BUZZER Continued use confirmed Additional information: The technical symbol will remain lit during the treatment. When pressed, this information will be displayed.

TECHNICAL ERROR BUZZER Press LOW to confirm further use Additional information: One of the two buzzers is broken. The treatment can be completed and technical service should in this case be carried out after the treatment. In order to confirm further use, the left lit Arrow button should be pressed (LOW).



14:45

TECHNICAL ERROR HEPARIN PUMP Heparin pump not in use Additional information: The technical symbol will remain lit during the treatment. When pressed, this information will be displayed.

TECHNICAL ERROR HEPARIN PUMP Zero set value to continue Additional information: The heparin pump is broken. The treatment can be completed if the heparin set value is adjusted to 0.0. When suitable, call for technical service.

14:46



Chapter 15 Major changes in operator’s manual


AK 200 S Operator’s manual - Major changes

15:1

Major changes between program version 7.xx and 8.xx Chapter 1 A new section has been included; "How to use this manual". This is a brief explanation of how the chapters in the manual are structured and how they are intended to be used. A new manual symbol is also introduced in this section, in "Definitions of expressions used in this manual". The symbol; , indicates that it is possible to preset the value of a parameter, and appears throughout the manual.

Chapter 2 A small text has been added in the "Blood monitor" section, position 11. The level adjustment buttons are now only active for maximum 6 seconds at a time, when pressed and hold.

Chapter 3 A small information has been included in the "Concentrate stand-by mode" section, concerning the fact that the fluid flow is automatically decreased to 100 ml/min when Concentrate stand-by mode is active, to minimize the water consumption. As a consequence, it will now take one minute longer for the dialysis fluid preparation to be resumed. The section "Override possibilities" has been updated, especially note the new information about changed machine actions during air detector alarm override. A new section has been added; "ing treatment parameters" as it is now possible to certain treatment parameters from an external computer system. "BiCart/SelectCart change during treatment" has been rewritten. Information is included about the fact that the priming process of the cartridge is indicated by a cartridge symbol in the upper right corner of the information display.

Chapter 4 The section "Discontinuing" has been rewritten and updated with new instructions for the discontinuing procedure. If the BiCart Select system or the BiCart cartridge has been used during treatment, and if desired, the emptying procedure of the containers can now be started at any time during the discontinuing procedure after treatment end has been confirmed.

15:2



Chapter 5 The chapter has been rewritten based on, and with referrals to, chapter 4. A glossary of single needle parameters and key has been added, as well as instructions on how to perform single needle/single pump treatment with pressure-controlled arterial and venous phases.

Chapter 11 There is information included about the possibility for the machine to carry out a distribution volume calculation, displayed in litres, using the Watson formula. See "The second screen", "Distribution volume" and "Distribution volume calculation using the Watson formula".

Chapter 12 Changes have been made in the "Schedule for hygiene and maintenance". "Disinfection history" has been updated, as it is now possible for the machine to display the 50 most recently performed disinfection programs.

Chapter 14 The additional information to the attention alarm; EXTRA PRIMING VOLUME ACHIEVED, has been updated as the buzzer now can be muted when the blood pump is not running until the blood pump is started again.



15:3


15:4



Chapter 16 Index


AK 200 S Operator’s manual - Index

16:1

A Acetate button . . . . . . . . . . Air detector . . . . . . . . . . . . air detector head . . . . . . . Air gap . . . . . . . . . . . . . . . . Alarm . . . . . . . . . . . . . . . . . air detector . . . . . . . . . . . alarm indicators . . . . . . . alarm list . . . . . . . . . . . . . arterial pressure . . . . . . . . attention . . . . . . . . . . . . . attention alarm list . . . . . blood flow rate . . . . . . . . blood leak . . . . . . . . . . . . BPM attention . . . . . . . . BVS . . . . . . . . . . . . . . . . conductivitiy . . . . . . . . . . Diascan attention . . . . . . pH . . . . . . . . . . . . . . . . . technical . . . . . . . . . . . . . technical alarm list . . . . . . temperature . . . . . . . . . . time attention . . . . . . . . . transmembrane pressure . UF volume . . . . . . . . . . . venous pressure . . . . . . . Arrow buttons . . . . . . . . . . Arrows symbol . . . . . . . . . . Arterial blood line . . . . . . . . Arterial blood pump . . . . . . Arterial expansion chamber . Arterial line arterial line clamp . . . . . . arterial line guide . . . . . . . Arterial pressure transducer connector . . . . . . . . . . . . . Automatic heat button . . . . Automatic rinse button . . . .

. . . . . . 3:5 . . . . . 4:16 . . . . . . 2:2 . . . . . . 2:9 . . . . . 3:17 . . . . . 3:17 . . . . . 3:17 . . . . . 14:2 . . . . . 3:18 . . . . . 3:17 . . . . . 14:9 . . . . . 3:18 . . . . . 3:17 . . . . . 3:19 . . . . . 3:17 . . . . . 3:18 . . . . . 3:19 . . . . . 3:17 . . . . . 3:17 . . . . 14:45 . . . . . 3:18 . . . . . 3:19 . . . . . 3:18 . . . . . 3:18 . . . . . 3:18 . . . . . 3:23 . . . . 11:14 . . 4:12, 5:4 . . . . . . 2:2 . . . . . . 5:4 . . . . . 4:12 . . 2:3, 4:12 . . 2:2, 4:12 . . . . . . 3:4 . . . . . . 3:4

B Bargraph display . . . . . . . . . viewing angle adjustment . Battery back-up . . . . . . . . . . technical data . . . . . . . . . Bicarbonate button . . . . . . . BiCart automatic emptying . . . . . change during treatment . holder . . . . . . . . . . . . . . . how to connect . . . . . . . . Blood flow knob . . . . . . . . . Blood leak detector . . . . . . . how to maintain . . . . . . . Blood line arterial blood line . . . . . .

.. .. .. .. ..

. . . 3:10 . . . 3:10 . . . 3:38 . . 13:12 . . . . 3:5

.. .. .. .. .. .. ..

. . . 4:24 . . . 3:43 . . . . 2:5 . . . . 4:8 . . . 3:23 . . . . 2:5 . . 12:33

. . 4:12, 5:4

attaching . . . . . . . . . . . . . . . . . . 4:11 list of blood lines . . . . . . . . . . . . 1:14 venous blood line . . . . . . . . 4:16, 5:5 Blood monitor . . . . . . . . . . . . . . . . 2:2 Blood path . . . . . . . . . . . . . . . . . . 3:10 Blood pressure measurement accessories . . . . . . . . . . . . . . . . 1:15 cuff holder . . . . . . . . . . . . . . . . . 2:9 Blood pump . . . . . . . . . . . . . . . . . 4:12 arterial blood pump . . . . . . . . . . . 2:2 blood pump button . . . . . . . . . . 3:22 change of segment . . . . . . . . . . 3:42 emergency stop . . . . . . . . . . . . . 3:22 maintenance how to clean and disinfect the rotor . . . . . . . . . . . . . . . . . 12:33 how to remove and attach the rotor . . . . . . . . . . . . . . . . . 12:33 rotor . . . . . . . . . . . . . . . . . . . . 12:33 venous blood pump . . . . . . . 2:3, 5:5 Bolus infusion . . . . . . . . . . . . . . . . . 8:8 BPM BPM button . . . . . . . . . . . . . . . 10:5 BPM connection . . . . . . . . . . 2:6, 2:8 BPM cuff how to maintain . . . . . . . . . 12:34 technical data . . . . . . . . . . . . . . 13:3 BVS . . . . . . . . . . . . . . . . . . . . 2:2, 4:12 graph combinations . . . . . . . . . . . 9:5 technical data . . . . . . . . . . . . . . 13:3 By path . . . . . . . . . . . . . . . . . 3:10

C Caution . . . . . . . . . . . . . . . . . . . . . 1:4 CE-marking . . . . . . . . . . . . . . . . . 1:18 Central chemical disinfection . . . . 12:24 how to perform . . . . . . . . . . . . 12:24 Charging indicator . . . . . . . . . . . 2:7, 2:9 Chemical disinfection button . . . . . . 3:4 Chemical disinfection program how to perform . . . . . . . . . . . . 12:20 Clamps arterial line clamp . . . . . . . . 2:3, 4:12 infusion line clamps . . . . . . . . . . . 8:4 venous line clamp . . . . . . . . 2:3, 4:16 Clearance measurement . . . . . . . . . 11:2 Clinic automation button . . . . . . . . 3:13 Clock symbol . . . . . . . . . . . 10:6, 11:14 Concentrate stand-by mode . . . 3:5– 3:6 manual activation . . . . . . . . . . . . 3:7 Concentrates connect concentrates . . . . . . . . . . 4:6 list of concentrates . . . . . . . . . . 1:13 select concentrates . . . . . . . . . . . 4:4 Connect concentrates



acetate concentrate . . . . . . . . . . . 4:8 acidic and liquid bicarbonate concentrate . . . . . . . . . . . . . . . . 4:8 acidic concentrate and BiCart . . . 4:8 SelectCart, SelectBag and BiCart . 4:7 Connectors arterial pressure transducer . 2:2, 4:12 system pressure transducer . . 2:3, 5:5 venous pressure transducer . 2:2, 4:16 Control system . . . . . . . . . . . . . . . . 1:9 Copyright . . . . . . . . . . . . . . . . . . . 1:18

D Degressive graph . . . . . . . . . . . . . . 7:2 Dialysis dose measurement . . . . . . 11:2 Dialysis fluid preparation . . . . . . . . . . . . . . . . 1:12 preparation, technical data 13:4, 13:14 Dialysis fluid filter . . . . . . . . . . . . . . 2:9 Dialysis fluid tubes dialysis fluid inlet . . . . . . . . . . . . . 2:4 dialysis fluid outlet . . . . . . . . . . . . 2:4 Dialyzer . . . . . . . 1:14, 4:11– 4:12, 4:16 attaching . . . . . . . . . . . . . . . . . . 4:11 dialyzer holder arm . . . . . . . . . . . 2:4 dialyzer path . . . . . . . . . . . . . . . 3:10 Dialyzer path . . . . . . . . . . . . . . . . 3:10 Diascan key . . . . . . . . . . . . . . . . . 11:3 parameters . . . . . . . . . . . . . . . . 11:3 precautions . . . . . . . . . . . . . . . . 11:4 technical data . . . . . . . . . . . . . . 13:6 Disinfection ports . . . . . . . . . . . . . . 2:4 Drain air gap . . . . . . . . . . . . . . . . . . 2:9 Drain outlet from the machine . . . . . . . . . 2:7, 2:9 Dwell time . . . . . . . . . . . . . . . . . 12:18

E Electromagnetic environment Expansion chamber . . . . . . arterial expansion chamber holder . . . . . . . . . . . . . . . venous expansion chamber

. .. . .. .

. . 13:18 . . . . 8:4 . . . . 5:4 . . . . 2:3 . . . . 5:5

F Flow diagram . . . . Flow path cleaning . . . . . . decalcification . . maintenance . . . Fluid by button Fluid flow button . Fluid monitor . . . . Formaldehyde . . . .


. . . . . . . . . . . . 3:10 . . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

. . . . . . .

12:30 12:30 12:30 . 3:22 . . 3:9 . . 2:4 12:19

Function check . . . . . . . . . . . . . . . . 4:3 overview screen . . . . . . . . . . . . 3:26 Fuses . . . . . . . . . . . . . . . . . . . . 2:7, 2:9

G Goal flag symbol . . . . . . . .11:11– 11:12 GSS/PC connection . . . . . . . . . 2:6, 2:8

H Half-time . . . . . . . . . . . . . . . . . . . . 7:2 Halt button . . . . . . . . . . . . . . . . 2:7, 2:9 HDF button . . . . . . . . . . . . . . . . . . 3:9 Heat disinfection heat disinfection button . . . . . . . . 3:4 integrated . . . . . . . . . . . . . . . . 12:17 Heat disinfection program automatic start . . . . . . . . . . . . 12:16 automatic switch off . . . . . . . . 12:17 how to perform . . . . . . . . . . . . 12:11 with CleanCart . . . . . . . . . . . . 12:12 with liquid citric acid . . . . . . . . 12:13 with WRO 300 H Low Flow Heat . . . . . . . . . . 12:14 Heating vessel overflow . . . . . . . 2:7, 2:9 Heparin heparin button . . . . . . . . . . . . . . 3:9 heparinization . . . . . . . . . . . . 4:13 heparin pump . . . . . . . . . . . . . . . 2:3 attaching syringe . . . . . . . . . . 4:14 set values . . . . . . . . . . . . . . . . . 4:15 Hold button . . . . . . . . . . . . . . . . . 3:23 Hygiene and maintenance schedule 12:6

I Information display . . . . . . . Infusion infusion bags . . . . . . . . . . infusion fluid . . . . . . . . . . infusion line . . . . . . . . . . clamps . . . . . . . . . . . . infusion pole . . . . . . . . . . height adjustment . . . . infusion pump . . . . . . . . Inlet water quality . . . . . . . . . . . . . . . requirements . . . . . . . . . . Integrated Heat disinfection Intended use . . . . . . . . . . . . Isolated UF . . . . . . . . . . . . . isolated UF button . . . . .

. . . . . 3:23 . . . . . . 8:4 . . . . . 1:15 . . . . . . 8:4 . . . . . . 8:4 . 2:10, 2:12 . 2:10, 2:12 . . . 2:3, 8:4 .. .. .. .. .. ..

.. .. .. .. .. ..

. 13:9 . 1:12 12:17 . . 1:8 . . 6:1 . . 3:5

K Kt/V button . . . . . . . . . . . . . . . . . 11:5 Kt/V target supervision . . . . . . . . 11:2


L Latch for filter change . . . Level adjustment buttons Linear graph . . . . . . . . . . Lines . . . . . . . . . . . . . . . arterial blood line . . . . venous blood line . . . . Low Flow Heat . . . . . . . .

. . . . . . . . 2:9 . . . . . . . . 2:3 . . . . . . . . 7:2 . . . . . . . 1:14 . . . . 4:12, 5:4 . . . . 4:16, 5:5 . 12:14, 14:33

M Machine blood monitor . . . . . . . . . . . . . . . 2:2 BM 200 and BM 202 . . . . . . . . 2:2 fluid monitor . . . . . . . . . . . . . . . . 2:4 FM 202 . . . . . . . . . . . . . . . . . . 2:4 physical data . . . . . . . . . . . . . . 13:16 power supply . . . . . . . . . . . . . 13:10 rear of the machine options included . . . . . . . . . . . 2:8 without options . . . . . . . . . . . . 2:6 transportation and storage . . . . 13:18 Main switch . . . . . . . . . . . . . . . 2:7, 2:9 Mains supply inlet . . . . . . . . . . . 2:7, 2:9 Maintenance blood leak detector . . . . . . . . . 12:33 blood pump . . . . . . . . . . . . . . 12:33 BPM cuff . . . . . . . . . . . . . . . . 12:34 exterior . . . . . . . . . . . . . . . . . . 12:33 top tray . . . . . . . . . . . . . . . . . . 12:33 Manufacturer . . . . . . . . . . . . . . . . 1:18 Monitor stand bars, lifting positions . . . . . 2:10, 2:12 height control . . . . . . . . . . . . . . 2:13 power supply cord . . . . . . . . . . . 2:13 rear handle . . . . . . . . . . . . 2:10, 2:12 screws . . . . . . . . . . . . . . . 2:11– 2:12 Mute button . . . . . . . . . . . . . . . . . 3:22

N Note . . . . . . . . . . . . . . . . . . . . . . . . 1:4

O ON/OFF button . . . . . . . . Operator’s . . . . . . . . . Optional connection . . . . . . Override . . . . . . . . . . . . . . . air detector alarm . . . . . . arterial pressure alarm . . . blood leak alarm . . . . . . . low venous pressure alarm

.. .. .. .. .. .. .. ..

. . . . 3:4 . 2:3, 3:3 . 2:7, 2:9 . . . 3:20 . . . 3:20 . . . 3:20 . . . 3:21 . . . 3:20

P Parameter buttons . . . . . . . . . . . . . 3:12 Parameter settings

arterial pressure . . . . . . . . . . . . . 3:31 blood flow . . . . . . . . . . . . . . . . 3:30 blood pump segment . . . . . . . . . 3:30 BPM, BVS, Diascan . . . . . . . . . 3:31 conductivity . . . . . . . . . . 3:30– 3:31 dialysis fluid flow . . . . . . . . . . . . 3:31 heparin . . . . . . . . . . . . . . . . . . . 3:31 SN data . . . . . . . . . . . . . . . . . . 3:30 temperature . . . . . . . . . . . . . . . 3:30 time . . . . . . . . . . . . . . . . . . . . . 3:31 TMP . . . . . . . . . . . . . . . . . . . . . 3:31 UF rate . . . . . . . . . . . . . . . . . . . 3:31 UF volume . . . . . . . . . . . . . . . . 3:31 venous pressure . . . . . . . . . . . . 3:30 Per-Low . . . . . . . . . . . . . . . . . . . 12:20 Peracetic acid . . . . . . . . . . . . . . . 12:19 Physical data of the machine . . . . 13:16 Pick-up tube A pick-up tube . . . . . . . . . . . . . . 2:4 B pick-up tube . . . . . . . . . . . . . . 2:4 Potential equalization . . . . . . . . . . . 1:6 Potential equalization connection . . 2:6, 2:8 Power failure recovery . . . . . . . . . . . . . . . . . . 3:39 returning the blood . . . . . . . . . . 3:38 Power supply unit . . . . . . . . . . . 2:7, 2:9 Precautions . . . . . . . . . . . . . . . . . . . 1:5 Preparation of dialysis fluid . . . . . . 1:12 Preset can be preset . . . . . . . . . . . . . . . . 1:4 Priming in double needle mode, finishing in single needle/double pump mode . . . . . . . . . . . . . . . . . . . . 5:6 in HDF low volume . . . . . . . . . . 8:6 in single needle/double pump mode . . . . . . . . . . . . . . . . . . . . 5:9 priming button . . . . . . . . . . . . . . 3:9 priming detector . . . . . . . . . . . . . 2:3 Profiling activation . . . . . . . . . . . . . . . . . . 7:7 degressive graph . . . . . . . . . . . . . 7:2 half-time . . . . . . . . . . . . . . . . . . . 7:2 linear graph . . . . . . . . . . . . . . . . . 7:2 profiling button . . . . . . . . . . . . . . 3:9 progressive graph . . . . . . . . . . . . 7:2 technical data . . . . . . . . . . . . . . 13:5 UF rate . . . . . . . . . . . . . . . . . . . . 7:4 Progressive graph . . . . . . . . . . . . . . 7:2 Protective system . . . . . . . . . . . . . . 1:9 for low volume HDF . . . . . . . . . . 8:2 for ultrafiltration . . . . . . . . . . . . 3:35 Pulse rate symbol . . . . . . . . 10:6– 10:7



R Rear of the machine options included . . . . . . . . . . . . . 2:8 without options . . . . . . . . . . . . . . 2:6 Recirculation . . . . . . . . . . . . . . . . . 3:40 Relay interface connection . . . . . 2:6, 2:8 Reset . . . . . . . . . . . . . . . . . . . . . . 3:16 Residual test . . . . . . . . . . . . . . . . 12:23 Rinse/Drain button . . . . . . . . . . . . 3:4 Rinse/Drain program . . . . . . . . . 12:25 automatic start . . . . . . . . . . . . 12:28 automatic switch off . . . . . . . . 12:29 with CleanCart . . 12:17, 12:26, 12:29

S Safety coupling . . . . . . . . . . . . . . . . 2:4 Safety philosophy . . . . . . . . . . . . . . 1:9 SelectBag automatic emptying . . . . . . . . . . 4:24 holder . . . . . . . . . . . . . . . . . . . . . 2:5 how to connect . . . . . . . . . . . . . . 4:7 SelectCart automatic emptying . . . . . . . . . . 4:24 change during treatment . . . . . . 3:43 holder . . . . . . . . . . . . . . . . . . . . . 2:5 how to connect . . . . . . . . . . . . . . 4:7 Set knob . . . . . . . . . . . . . . . . . . . . 3:23 Single needle parameters and key . . . . . . 5:3 Single needle button . . . . . . . . . . . . 3:5 Smiley symbol . . . . . . . . . . . . . . . 11:14 Sodium hypochlorite . . . . . . . . . . 12:19 Standards . . . . . . . . . . . . . . . . . . 13:22 Start UF Stop button . . . . . . . . . . . 3:22 Substitution fluid . . . . . . . . 13:5, 13:15 Symbols arrows symbol . . . . . . . . . . . . . 11:14 clock symbol . . . . . . . . . . 10:6, 11:14 goal flag symbol . . . . . .11:11– 11:12 list of symbols . . . . . . . . . . . . . . 1:16 pulse rate symbol . . . . . . 10:6– 10:7 screen symbols, disinfection . . . . 12:4 smiley symbol . . . . . . . . . . . . . 11:14 time to target symbol . . . . . . . . 11:14


System pressure transducer connector . . . . . . . . . . . . . . . . 2:3, 5:5 System pressure transducer protector 8:4

T Time display . . . . . . . . . . . . . . Time to target symbol . . . . . . . Top tray . . . . . . . . . . . . . . . . . how to maintain . . . . . . . . . Tray for concentrate containers 2:13 Treatment overview screen . . . Treatment parameters . . . . . . . . . . . . . .

. . . 3:11 . . 11:14 . . . . 2:2 . . 12:33 . . .2:11, . . . 3:24 . . . 3:32

U UF calibration unit connection UF rate profiling . . . . . . . . . . . Ultrafiltered Dialysis Fluid . . . . Ultrafilters frequency of change . . . . . . ultrafilter . . . . . . . . . . . . . . . how to change . . . . . . . . . Ultrafiltration control . . . . . . . . . . . . . . . . control, technical data . . . . . technical data . . . . . . . . . . . ultrafiltration path . . . . . . . .

. 2:7, 2:9 . . . . 7:4 . . . 1:12 . . . 1:12 . . . 1:14 . . 12:31 .. .. .. ..

. 3:34 . 13:5 13:15 . 3:10

V Venous blood line . . . . . . . . Venous blood pump . . . . . . Venous expansion chamber . Venous line clamp . . . . . . . . Venous pressure transducer connector . . . . . . . . . . . . . Volume control button . . . .

. . 4:16, 5:5 . . . 2:3, 5:5 . . . . . . 5:5 . . 2:3, 4:16 . . 2:2, 4:16 . . . . . . 3:5

W Warning . . . . . Water inlet . . . Watson formula Wheels, lockable

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. . . . . . 1:4 . . . 2:7, 2:9 . . . . . 11:9 . 2:11, 2:13

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