IP Library Granted Patent US 8,628,510
Granted Patent B2
US 8,628,510 · App. 12/976,591 · Granted Jan 14, 2014

Monitoring the operating health of a force sensor in a fluid infusion device

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Quick Facts
Patent No.
US 8,628,510
App. No.
12/976,591
Granted
Jan 14, 2014
Kind
B2
Abstract

A device for delivering fluid to a user includes a housing, a drive motor assembly in the housing, a force sensor, and an electronics module. The drive motor assembly regulates delivery of fluid by actuating a piston of a fluid reservoir, and the force sensor generates output levels in response to force imparted thereto during, for example, fluid delivery operations. The electronics module processes the output levels of the force sensor to assess the operating health of the force sensor, to check for occlusions in the fluid delivery path, and to monitor the seating status of the fluid reservoir.

Claims (25)

1. A method of operating a fluid infusion device comprising a drive motor assembly and a force sensor associated with the drive motor assembly, the method comprising:

determining a measure of actuation force imparted to the force sensor during a fluid delivery action of the drive motor assembly, where the drive motor assembly regulates delivery of fluid by the fluid infusion device;

comparing the measure of actuation force against a range of valid values that represents normally expected measures of actuation forces; and

when the measure of actuation force is outside the range of valid values, detecting that an occlusion is present in a fluid flow path and initiating corrective action for the fluid infusion device,

wherein initiating the corrective action includes:

adjusting a threshold value of the range of valid values for the actuation force; and

allowing the fluid infusion device to continue fluid delivery for a set number of fluid delivery actions.

2. The method of claim 1 , wherein initiating corrective action comprises generating a user alert at the fluid infusion device.

3. The method of claim 1 , wherein initiating corrective action comprises:

recording an invalid force event for the measure of actuation force; and

analyzing a set of invalid force events to determine a course of action for the fluid infusion device.

4. The method of claim 3 , wherein analyzing the set of invalid force events is performed to reduce false alerts associated with operating health of the force sensor.

5. The method of claim 4 , further comprising generating a user alert that indicates a poor operating health of the force sensor.

6. The method of claim 3 , further comprising generating a user alert at the fluid infusion device in response to recording at least a threshold number of invalid force events corresponding to consecutive fluid delivery actions of the drive motor assembly.

7. The method of claim 3 , wherein recording the invalid force event comprises recording a delivery time of the fluid delivery action.

8. The method of claim 3 , wherein recording the invalid force event comprises recording the measure of actuation force.

9. The method of claim 3 , wherein recording the invalid force event comprises recording a current position of the drive motor assembly.

10. The method of claim 3 , further comprising generating a user alert at the fluid infusion device in response to recording at least a threshold number of invalid force events within a designated period of time.

11. A method of operating a fluid infusion device comprising a drive motor assembly and a force sensor associated with the drive motor assembly, the drive motor assembly regulating delivery of fluid by the fluid infusion device via an infusion set, the method comprising:

determining a measure of actuation force imparted to the force sensor during a fluid delivery action of the drive motor assembly;

comparing the measure of actuation force against a range of valid values that represents normally expected measures of actuation forces to detect an operating health of the force sensor;

when the measure of actuation force is outside the range of valid values, initiating a corrective action for the fluid infusion device;

using the force sensor to detect an occlusion of the infusion set; and

upon detecting an occlusion of the infusion set, adjusting a threshold value of the range of valid values for the actuation force and allowing the fluid infusion device to continue fluid delivery for a set number of fluid delivery actions,

wherein initiating the corrective action includes generating a user alert that indicates an operating health of the force sensor.

Assignments (1)
SECURITY INTEREST Recorded Jan 16, 2026
From: MEDTRONIC MINIMED, INC.; COMPANION MEDICAL, INC.
To: CITIBANK, N.A.
Reel/Frame 074394/0237 →