Integrated Modular Health Platforms and Methods of Use

• US 20160042154A1
• Filed: 03/14/2014
• Published: 02/11/2016
• Est. Priority Date: 03/15/2013
• Status: Abandoned Application

• Current Assignee: Eli S. Goldberg, Scott A. Luchau
• Original Assignee: Eli S. Goldberg, Scott A. Luchau
• Inventors: Goldberg, Eli S., Luchau, Scott A.
• Application Number:
  US14/777,046
• Publication Number:
  US 20160042154A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: G06Q 10/10 Office automation; Time management
• CPC Class Codes: G06Q 40/08 Insurance
• CPC Class Codes: G16H 20/10 relating to drugs or medications, e.g. for ensuring correct administration to patients
• CPC Class Codes: G16H 40/20 for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
• CPC Class Codes: G16H 40/67 for remote operation
• CPC Class Codes: G16H 50/20 for computer-aided diagnosis, e.g. based on medical expert systems

Abstract

Integrated modular health platforms and methods of their use are provided. The integrated modular health platform may include one or more sensors (120) configured to monitor a patient usage of a medical device (110); a communication unit (130) communicatively coupled to the one or more sensors (120); and a processing unit (200) configured to receive a first communication from the communication unit (120), the communication being indicative of the patient usage of the medical device (110), to compare the patient usage of the medical device (110) with an expected usage of the medical device (110); and to generate a second communication indicative of a difference between the patient usage and the prescribed usage.

Claims

1. A method for monitoring a medical device comprising:

receiving a first communication indicative of one or more parameters associated with a patient usage of a medical device;

comparing the patient usage of the medical device with an expected usage of the medical device; and

generating a second communication indicative of a difference between the patient usage and the expected usage.

2. The method of claim 1 wherein the first communication is indicative of whether medical devices are being used by the patient;

whether monitored parameters conform to manufacturer operational constraints;

assessment of patient device usage against physician prescribed therapeutic regimens;

or a combination thereof.

3. The method of claim 1 wherein the one or more parameters are selected from the group consisting of amperage;

device generated sound volume;

device generated sound frequency;

temperature;

an on/off state;

time in the device on state at each use and accumulated total time in the device on state;

frequency of device use; and

combinations thereof.

4. The method of claim 1 wherein the expected usage comprises a range of acceptable device amperage readings;

a range of acceptable device generated sound volumes;

a range of acceptable device generated sound frequency;

a range of acceptable device temperature readings or combinations thereof.

5. The method of claim 1 wherein the expected usage is a physician prescribed therapy regimen comprising a device time in the on state for each use by the patient and accumulated total time in an on state;

temperature of medication storage;

temperature at which device sterilization is performed;

duration of equipment sterilization;

one or more frequencies generated by device operation or combinations thereof.

6. The method of claim 1 wherein the medical device may be selected from the group consisting of an air compressor;

a refrigeration unit;

a steam sterilizer;

a pulmonary percussion system;

a blood glucose monitor;

a blood pressure monitor;

a blood oxygen concentration monitor;

oxygen generation equipment;

IV fluid delivery;

spirometers, flowmeters, medicine delivery systems.

7. The method of claim 1 further comprising transmitting the first communication, the second communication, or both to a stakeholder for review.

8. The method of claim 1 further comprising monitoring with one or more sensors the one or more parameters associated with a patient usage of a medical device.

9. The method of claim 1 comprising reporting a patient adherence to the expected usage using a moving average of sensed device usage.

10. The method of claim 1 further comprising predicting future patient adherence to the expected usage using the moving average or a neural network NARX model.

11. A system for monitoring a medical device comprising:

one or more sensors configured to monitor a patient usage of a medical device;

a communication unit communicatively coupled to the one or more sensors; and

a processing unit configured to receive a first communication from the communication unit, the communication being indicative of the patient usage of the medical device, to compare the patient usage of the medical device with an expected usage of the medical device; and

to generate a second communication indicative of a difference between the patient usage and the prescribed usage.

12. The system of claim 11 wherein the first communication is indicative of whether medical devices are being used by the patient;

whether monitored parameters conform to manufacturer operational constraints;

assessment of patient device usage against physician prescribed therapeutic regimens;

or a combination thereof.

13. The system of claim 11 wherein the one or more sensors monitor amperage;

device generated sound volume;

device generated sound frequency;

temperature;

an on/off state;

time in the device on state at each use and accumulated total time in the device on state;

frequency of device use;

or combinations thereof.

14. The system of claim 11 wherein the expected usage comprises a range of acceptable device amperage readings;

a range of acceptable device generated sound volumes;

a range of acceptable device generated sound frequency;

a range of acceptable device temperature readings or combinations thereof.

15. The system of claim 11 wherein the expected usage is a physician prescribed therapy regimens comprising a device time in the on state for each use by the patient and accumulated total time in an on state;

temperature of medication storage;

temperature at which device sterilization is performed;

duration of equipment sterilization;

a frequency generated by device operation or combinations thereof.

16. The system of claim 11 wherein the medical device may be selected from the group consisting of an air compressor;

a refrigeration unit;

a steam sterilizer;

a pulmonary percussion system;

a blood glucose monitor;

a blood pressure monitor;

a blood oxygen concentration monitor;

oxygen generation equipment;

IV fluid delivery;

spirometers, flowmeters, medicine delivery systems.

17. The system of claim 11 wherein the processing unit is further configured to report a patient adherence to the expected usage using a moving average of sensed device usage and to predict future patient adherence to the expected usage using the moving average or a neural network narx model.

18. An integrated health platform comprising:

a chassis;

one or more medical devices supported by the chassis;

one or more sensors coupled to the one or more medical devices to monitor patient usage of the one or more medical devices; and

a communication unit communicatively coupled to the one or more sensors to receive the patient usage information from the one sensors and to transmit the patient usage information to a processing unit.

19. The integrated health platform of claim 18 wherein the medical devices comprise a refrigerator;

an air compressor, associated air-lines, and air barb;

a particulate and allergen filter;

a steam sterilizer;

a pulmonary percussion system;

a power hub; and

a spirometer.

20. The integrated health platform of claim 18 wherein the one or more sensors are configured to measure device amperage, device generated sound volume, device generated sound frequency, device temperature or combinations thereof for the one or more medical devices.