Fluid line occlusion detection system and methods

Patent metadata

Field	Value
Publication number	US-11826546-B2
Application number	US-202117371495-A
Country	US
Kind code	B2
Filing date	Jul 9, 2021
Priority date	Jun 26, 2013
Publication date	Nov 28, 2023
Grant date	Nov 28, 2023

Abstract

The systems, methods and articles described herein are directed to at least one pressure sensor along a downstream fluid line which senses fluid pressure and assists an occlusion detection feature in determining the presence of occlusions in the downstream fluid line. In addition, the system can dynamically adapt the occlusion detection feature based on a delivery of fluid, such as a bolus, in order to prevent the system from creating a false alarm regarding an occlusion of the downstream fluid line.

First claim

The invention claimed is:

1. A non-transitory computer readable medium comprising instructions executable by a processor to cause a programming module of a medical fluid delivery system to:
determine that a delivery of a bolus condition has commenced;
increase a maximum pressure limit that is compared to a sensed pressure of a fluid line between an infusion pump of the medical fluid delivery system and a patient; and
gradually lower the maximum pressure limit over a predetermined time period after commencement of the delivery of the bolus condition.

2. The non-transitory computer readable medium of claim 1 , wherein the programming module includes at least one processor and memory.

3. The non-transitory computer readable medium of claim 1 , wherein the programming module receives a sensed pressure of the fluid line.

4. The non-transitory computer readable medium of claim 1 , wherein the instructions executable by the processor further cause the programming module to automatically dynamically adapt upon commencing the delivery of the bolus.

5. The non-transitory computer readable medium of claim 1 , wherein the instructions executable by the processor further cause the programming module to determine at least one of a maximum pressure and a decay rate.

6. The non-transitory computer readable medium of claim 5 , wherein the decay rate includes an exponential decay rate.

7. The non-transitory computer readable medium of claim 5 , wherein the instructions executable by the processor further cause the programming module to use at least one of the maximum pressure and decay rate when monitoring the fluid line pressure at least during the delivery of the programmed bolus in order to prevent activation of a false occlusion alarm.

8. A medical fluid delivery system comprising:
a programming module;
a non-transitory computer readable medium comprising instructions executable by a processor to cause the programming module to:
an infusion pump; and
a non-transitory computer readable medium comprising instructions executable by a processor to cause a remote device separate from and in communication with the infusion pump to:
determine that a delivery of a bolus condition has commenced;
increase a maximum pressure limit that is compared to a sensed pressure of a fluid line between an infusion pump of the medical fluid delivery system and a patient; and
gradually lower the maximum pressure limit over a predetermined time period after commencement of the delivery of the bolus condition.

9. The medical fluid delivery system of claim 8 , wherein the programming module includes at least one processor and memory.

10. The medical fluid delivery system of claim 8 , wherein the instructions executable by the processor further cause the programming module receive a sensed pressure of the fluid line.

11. The medical fluid delivery system of claim 8 , wherein the instructions executable by the processor further cause the programming module to automatically dynamically adapt upon commencing the delivery of the bolus.

12. The medical fluid delivery system of claim 8 , wherein the instructions executable by the processor further cause the programming module to use at least one of the maximum pressure and decay rate when monitoring the fluid line pressure at least during the delivery of the programmed bolus in order to prevent activation of a false occlusion alarm.

13. The medical fluid delivery system of claim 8 , wherein the instructions executable by the processor further cause the programming module to determine at least one of a maximum pressure and a decay rate.

14. The medical fluid delivery system of claim 13 , wherein the decay rate includes an exponential decay rate.

Assignees

• Carefusion 303 Inc

Inventors

• Halbert Donald
• Guerra Jesse
• Bollish Stephen

Classifications

• A61M5/16854 Primary

  by monitoring line pressure · CPC title

• A61M5/14212 Primary

  Pumping with an aspiration and an expulsion action · CPC title

• A61M5/5086

  for indicating if defective, used, tampered with or unsterile · CPC title

• A61M5/14228

  with linear peristaltic action, i.e. comprising at least three pressurising members or a helical member · CPC title

• A61M5/16827

  controlling delivery of multiple fluids, e.g. sequencing, mixing or via separate flow-paths (infusion of multiple fluids without using a controller A61M5/1407) · CPC title