AMBULATORY INFUSION DEVICE WITH REPLACEABLE ENERGY STORAGE AND METHOD OF MONITORING THE ENERGY STORAGE

• US 20130147490A1
• Filed: 02/07/2013
• Published: 06/13/2013
• Est. Priority Date: 08/18/2010
• Status: Active Grant

• Current Assignee: Roche Diabetes Care Inc. (Roche Holding AG)
• Original Assignee: Roche Diagnostics International AG (Roche Holding AG)
• Inventors: Lindegger, Stefan
• Granted Patent: US 9,377,513 B2
• Time in Patent Office: Days
• US Class Current: 324/435
• CPC Class Codes: A61M 5/14 Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
• CPC Class Codes: A61M 5/1413 Modular systems comprising interconnecting elements
• CPC Class Codes: A61M 5/14244 adapted to be carried by the patient, e.g. portable on the body
• CPC Class Codes: A61M 5/16831 Monitoring, detecting, signalling or eliminating infusion flow anomalies low-level float-valves causing cut-off A61M5/40; indicating or recording presence, absence or direction of flow in general G01P13/0066
• CPC Class Codes: A61M 5/172 electrical or electronic A61M5/16804, A61M5/16831 take precedence
• CPC Class Codes: G01R 31/3835 involving only voltage measurements

Abstract

An ambulatory infusion device comprising a replaceable energy storage for electrically powering its functional units is presented. Control units provide to a monitoring system data about energy consuming activities or consumed energy by the functional units. Based on this data, the monitoring system determines energy consumed by the functional units and triggers measurement of the voltage of the energy storage at a point in time which depends on the determined energy consumed in a time interval preceding the point in time. Adapting the time of measurement to the actual energy drawn from the energy storage makes it possible to detect reliably and early a low energy state of any conventional standard battery, regardless of its electrochemical design and electrical behavior.

Claims

1. An ambulatory infusion device, the ambulatory infusion device comprising:

a replaceable energy storage for electrically powering several functional units of the ambulatory infusion device;

a measuring module to measure a voltage of the replaceable energy storage; and

a monitoring system to determine on an ongoing basis energy consumed by the functional units by adding up amounts of energy based on data provided by control units associated with the functional units, to trigger the measuring module to measure the voltage of the energy storage at a point in time which depends on the energy consumed by the functional units in a time interval preceding the point in time, and to generate an alarm depending on the voltage of the energy storage.

2. The ambulatory infusion device according to claim 1, wherein the functional units comprise at least one functional hardware unit controlled by one of the control units which provide the monitoring system data about energy consuming activities or energy consumed by the hardware unit.

3. The ambulatory infusion device according to claim 2, wherein the monitoring system determines the energy consumed by the functional units based on the data provided by the control units controlling the hardware units.

4. The ambulatory infusion device according to claim 2, wherein the monitoring system compares a current value of energy consumed by the functional units to an energy threshold value, triggers the measuring module to measure the voltage of the energy storage for cases where the current value of consumed energy exceeds the energy threshold value, and resets the current value of energy consumed by the energy threshold value, upon having triggered the measuring module.

5. The ambulatory infusion device according to claim 4, wherein the monitoring system determines the energy threshold value depending on at least one of:

a type of energy storage used in the ambulatory infusion device, a current temperature value, a course of the temperature value, the voltage of the energy storage, and a course of the voltage of the energy storage.

6. The ambulatory infusion device according to claim 1, wherein the monitoring system generates a preliminary alarm indicative of a low energy level, sufficient for supporting further operation of the ambulatory infusion device for cases where the voltage of the energy storage meets alarm conditions associated with an upper voltage threshold value, and generates an end alarm indicative of a low energy level, insufficient for supporting further operation of the ambulatory infusion device for cases where the voltage of the energy storage meets alarm conditions associated with a lower voltage threshold value.

7. The ambulatory infusion device according to claim 1, wherein the monitoring system maintains counters for several voltage threshold values, increments a counter value when the voltage of the energy storage falls below the respective voltage threshold value and decrements the counter value when the energy storage subsequently exceeds the respective voltage threshold value again, up to a defined counter threshold value when the energy storage is considered to have fallen definitely below the respective voltage threshold value.

8. The ambulatory infusion device according to claim 7, wherein the monitoring system maintains an event log including for the voltage threshold values in each case a point in time when the energy storage is considered to have fallen definitely below the respective voltage threshold value.

9. A method of monitoring a replaceable energy storage of a medical device which includes several functional units electrically powered by the energy storage, the method comprising:

determining on an ongoing basis energy consumed by the functional units by adding up amounts of energy based on data provided by control units associated with the functional units;

measuring a voltage of the energy storage at a point in time determined based on the energy consumed by the functional units in a time interval preceding the point in time; and

generating an alarm depending on the voltage of the energy storage.

10. The method according claim 9, further comprises

receiving from the control units data about energy consuming activities or energy consumed by functional hardware units;

and

determining the energy consumed by the functional units based on the data about energy consuming activities or consumed energy or charge.

11. The method according claim 9, further comprises,

comparing a current value of energy consumed by the functional units to an energy threshold value;

measuring the voltage of the energy storage for the case where the current value of consumed energy exceeds the energy threshold value; and

resetting the current value of energy consumed by the energy threshold value upon having measured the voltage of the energy storage.

12. The method according to claim 11, further comprises,

determining the energy threshold value depending on at least one of:

a type of energy storage used in the medical device, a type of battery used as energy storage used in the medical device, a current temperature value, a change in the temperature value, the voltage of the energy storage, and a course of the voltage of the energy storage.

13. The method according to claim 9, further comprises,

generating a preliminary alarm indicative of a low energy level, sufficient for supporting further operation of the medical device for cases where the voltage of the energy storage meets alarm conditions associated with an upper voltage threshold value;

and

generating an end alarm indicative of a low energy level, insufficient for supporting further operation of the medical device for cases where the voltage of the energy storage meets alarm conditions associated with a lower voltage threshold value.

14. The method according to claim 9, further comprises,

maintaining counters for several voltage threshold values;

incrementing a counter value when the voltage of the energy storage falls below the respective voltage threshold value; and

decrementing the counter value when the energy storage subsequently exceeds the respective voltage threshold value again, up to a defined counter threshold value when the energy storage is considered to have fallen definitely below the respective voltage threshold value.

15. A computer program product comprising a computer readable medium having stored thereon computer program code configured to direct a processor of a medical device, which includes a replaceable energy storage for electrically powering several functional units of the medical device, such that the processor:

determines on an ongoing basis energy consumed by the functional units by adding up amounts of energy based on data provided by control units associated with the functional units;

triggers a measuring module of the medical device to measure the voltage of the energy storage at a point in time determined based on the energy consumed by the functional units in a time interval preceding the point in time; and

generates an alarm depending on the voltage of the energy storage.