Occlusion detection system and method

• US 10,314,969 B2
• Filed: 12/22/2017
• Issued: 06/11/2019
• Est. Priority Date: 10/10/2008
• Status: Active Grant

• Current Assignee: Deka Products Limited Partnership
• Original Assignee: Deka Products Limited Partnership
• Inventors: Mandro, Marc A., Bryant, Robert J.
• Primary Examiner(s): Yacob, Sisay
• Application Number:
  US15/851,906
• Publication Number:
  US 20180117242A1
• Time in Patent Office: 536 Days
• CPC Class Codes: A61M 2005/14573 with a replaceable reservoir for quick connection/disconnection with a driving system
• CPC Class Codes: A61M 2005/16863 Occlusion detection
• CPC Class Codes: A61M 2205/332 Force measuring means
• CPC Class Codes: A61M 2205/52 with memories providing a history of measured variating parameters of apparatus or patient
• CPC Class Codes: A61M 2205/8206 battery-operated
• CPC Class Codes: A61M 5/1452 pressurised by means of pistons
• CPC Class Codes: A61M 5/14566 with a replaceable reservoir for receiving a piston rod of the pump
• CPC Class Codes: A61M 5/5086 for indicating if defective, used, tampered with or unsterile

Abstract

A method, computer program product, and infusion pump assembly for determining a first rate-of-change force reading that corresponds to the delivery of a first dose of an infusible fluid via an infusion pump assembly. At least a second rate-of-change force reading is determined that corresponds to the delivery of at least a second dose of the infusible fluid via the infusion pump assembly. An average rate-of-change force reading is determined based, at least in part upon the first rate-of-change force reading and the at least a second rate-of-change force reading.

Claims

1. An infusion pump assembly comprising:

a control system configured to;

monitor a displacement of one or more displaceable mechanical components included within the infusion pump assembly;

determine if the one or more displaceable mechanical components were displaced an expected displacement in response to delivery of one or more of a first dose of an infusible fluid and a second dose of the infusible fluid by comparing the monitored displacement to the expected displacement;

determine an initial force reading from a force sensor prior to dispensing the one or more of the first dose and the second dose of the infusible fluid;

determine a final force reading from the force sensor after dispensing the one or more of the first dose and the second dose of the infusible fluid;

compare, to a threshold, one or more of the initial force reading or the final force reading to determine if one or more of the initial force reading or the final force reading exceeds the threshold; and

if the one or more displaceable mechanical components were not displaced the expected displacement in response to delivery of one or more of the first dose of the infusible fluid and the second dose of the infusible fluid or if one or more of the initial force reading or final force reading exceeds the threshold, initiate an alarm sequence on the infusion pump assembly.

2. The infusion pump assembly of claim 1 wherein the control system further configured to:

determine a first initial force reading prior to dispensing the first dose of the infusible fluid;

dispense the first dose of the infusible fluid;

monitor a volume of the infusible fluid dispensed in the first dose;

determine a second initial force reading prior to dispensing the second dose of the infusible fluid;

set a first final force reading value as being equal to the second initial force reading;

dispense the second dose of the infusible fluid;

monitor a volume of the infusible fluid dispensed in the second dose;

determine a second final force reading subsequent to dispensing the second dose of the infusible fluid;

determine a first rate-of-change reading that corresponds to the delivery of the first dose of the infusible fluid via an infusion pump assembly by subtracting the first initial force reading from the first final force reading value;

determine at least a second rate-of-change reading that corresponds to the delivery of the second dose of the infusible fluid via the infusion pump assembly by subtracting the second initial force reading from the second final force reading;

normalize the first rate-of-change reading and the second rate-of-change reading to be indicative of the rates-of-change sensed for an equivalent quantity of infusible fluid; and

determine an average rate-of-change reading based, at least in part upon the normalized first rate-of-change reading and the normalized at least a second rate-of-change reading.

3. The infusion pump assembly of claim 2 further configured to:

compare the average rate-of-change reading to a threshold rate-of-change reading to determine if the average rate-of-change reading exceeds the threshold rate-of-change reading; and

if the average rate-of-change reading exceeds the threshold rate-of-change reading, initiate an alarm sequence on the infusion pump assembly.

4. The infusion pump assembly of claim 1 wherein the infusion pump assembly includes a battery assembly configured to power the infusion pump assembly, the control system further configured to:

compare an actual voltage level of the battery assembly to a minimum voltage requirement to determine if the actual voltage level meets the minimum voltage requirement; and

if the actual voltage level does not meet the minimum voltage requirement, initiate an alarm sequence on the infusion pump assembly.

5. An infusion pump assembly comprising:

a computer program product residing on a non-transitory computer readable medium in the infusion pump assembly having a plurality of instructions stored thereon which, when executed by a processor, cause the processor to perform operations comprising;

monitoring a displacement of one or more displaceable mechanical components included within the infusion pump assembly;

determining if the one or more displaceable mechanical components were displaced an expected displacement in response to delivery of one or more of a first dose of an infusible fluid and a second dose of the infusible fluid by comparing the monitored displacement to the expected displacement;

determining an initial force reading from a force sensor prior to dispensing the one or more of the first dose and the second dose of the infusible fluid;

determining a final force reading from the force sensor after dispensing the one or more of the first dose and the second dose of the infusible fluid;

comparing, to a threshold, one or more of the initial force reading or the final force reading to determine if one or more of the initial force reading or the final force reading exceeds the threshold; and

if the one or more displaceable mechanical components were not displaced the expected displacement in response to delivery of one or more of the first dose of the infusible fluid and the second dose of the infusible fluid or if one or more of the initial force reading or final force reading exceeds the threshold, initiating an alarm sequence on the infusion pump assembly.

6. The infusion pump assembly of claim 5 further comprising:

wherein the computer program product causes the processor to perform further operations comprising;

determining a first initial force reading prior to dispensing the first dose of the infusible fluid;

dispensing the first dose of the infusible fluid;

monitoring a volume of the infusible fluid dispensed in the first dose;

determining a second initial force reading prior to dispensing the second dose of the infusible fluid;

setting a first final force reading value as being equal to the second initial force reading;

dispensing the second dose of the infusible fluid;

monitoring a volume of the infusible fluid dispensed in the second dose;

determining a second final force reading subsequent to dispensing the second dose of the infusible fluid;

determining a first rate-of-change reading that corresponds to the delivery of the first dose of the infusible fluid via an infusion pump assembly by subtracting the first initial force reading from the first final force reading value;

determining at least a second rate-of-change reading that corresponds to the delivery of the second dose of the infusible fluid via the infusion pump assembly by subtracting the second initial force reading from the second final force reading;

normalizing the first rate-of-change reading and the second rate-of-change reading to be indicative of the rates-of-change sensed for an equivalent quantity of infusible fluid; and

determining an average rate-of-change reading based, at least in part upon the normalized first rate-of-change reading and the normalized at least a second rate-of-change reading.

7. The infusion pump assembly of claim 5 further comprising:

wherein the computer program product causes the processor to perform further operations comprising;

comparing the average rate-of-change reading to a threshold rate-of-change reading to determine if the average rate-of-change reading exceeds the threshold rate-of-change reading; and

if the average rate-of-change reading exceeds the threshold rate-of-change reading, initiating an alarm sequence on the infusion pump assembly.

8. The infusion pump assembly of claim 5 further comprising:

wherein the computer program product causes the processor to perform further operations comprising;

comparing an actual voltage level of the battery assembly to a minimum voltage requirement to determine if the actual voltage level meets the minimum voltage requirement; and

if the actual voltage level does not meet the minimum voltage requirement, initiating an alarm sequence on the infusion pump assembly.