User's Manual
Table Of Contents
- Table of contents
- List of figures
- CHAPTER 1 Description
- CHAPTER 2 Indications and contraindications
- CHAPTER 3 Personal Pump Communicator (PPC)
- CHAPTER 4 Pump implantation
- Preprogramming and pre-testing the Pump
- CHAPTER 5 Pump refill procedure
- CHAPTER 6 Explanting the Pump System
- CHAPTER 7 Warnings and precautions
- CHAPTER 8 Adverse reactions
- CHAPTER 9 System alarms and messages
- Pump alarms
- Alarm feedback
- Pump low battery
- Depleted pump battery
- System error
- Pump self test fail
- PPC low battery
- PPC alarms
- Low reservoir
- Empty reservoir
- Telemetry communication error
- Initialize alarm
- PPC not initialized
- Battery replacement
- Initialize to factory defaults
- Pump stopped
- Pump suspended
- Auto off
- Hourly maximum exceeded
- Pump alarm table
- Pump alarms
- CHAPTER 10 Troubleshooting Pump System under-delivery
- CHAPTER 11 Technical specifications
- APPENDIX A Label information symbol dictionary
- APPENDIX B Implant worksheet
- APPENDIX C Refill form
- APPENDIX D Precautions and general procedures
- APPENDIX E Pump rinse procedure
- APPENDIX F Side Port Catheter flush procedure
- Supplies and solutions
- Preparing for the procedure
- Flushing the Side Port Catheter
- Program minimal basal rate
- Remove insulin and fill with rinse buffer
- Equilibrate and pull rinse buffer through system
- Flush side port catheter
- Remove rinse buffer and fill with insulin
- Equilibrate and pull insulin through system
- Remove guide needles and record refill amount
- Program new basal rate
- Remove rinse buffer from catheter
- APPENDIX G Stroke volume measurement
97
CHAPTER 10 Troubleshooting Pump
System under-delivery
Potential under-delivery of insulin by the Medtronic MiniMed 2007D Implant-
able Insulin Pump System may result in an increase in daily programmed insulin
usage, difficulty maintaining euglycemia, occasional hyperglycemia, and prob-
lems calculating refill accuracy. This chapter describes how to diagnose potential
Pump System problems that may cause insulin under-delivery, and offers poten-
tial Pump and Catheter solutions to correct for under-delivery.
Diagnostic procedures
When refill procedures reveal the possibility of a Pump System under-delivery
problem, diagnostic procedures must be performed to verify if there is a problem
with either the Pump or Catheter. The Stroke Volume Measurement Procedure
tests Pump function, while the Pressure Measurement Procedure tests Catheter
patency. These diagnostic procedures should be performed according to the steps
outlined in Appendix G.
Under-delivery caused by backflow
Backflow results in the inverted flow of insulin through the Pump System. Back-
flow is caused by insulin deposits that compromise valve integrity, and allow the
negative reservoir pressure (vacuum) to pull insulin back into the reservoir. To
compensate for this under-delivery, the user can program appropriate increases in
their basal rates and bolus amounts.
Backflow conditions are characterized by increases in daily programmed insulin
usage, difficulty in maintaining euglycemia, increasingly negative refill accuracy
and sometimes hyperglycemia. Confirm a backflow condition by performing the
Stroke Volume Measurement Procedure. Then rinse the Pump System with
NaOH solution to dissolve insulin deposits, following the Pump Rinse Procedure
outlined in Appendix E.