Control unit for monitoring patient compliance with a compression therapy regimen
Monitoring patient compliance with a compression therapy regimen. Venous Refill Time (VRT) is monitored via a pressure sensor in a bladder of a compression system. A controller of the compression system correlates the monitored VRT to a predetermined threshold to determine whether the patient is using the compression system.
1. A compression garment control unit for monitoring compliance of a user with respect to wearing a compression garment in accordance with a compression treatment regimen, the control unit comprising:
a display configured to display patient compliance with a compression treatment regimen;
an alarm;
a pressure sensor;
at least one computer readable storage medium configured for storing one or more monitored parameters;
one or more processors coupled with the at least one computer readable storage medium; and
computer-executable instructions embodied on the at least one computer readable storage medium, the computer-executable instructions including instructions for causing the one or more processors to:
direct a flow of fluid from a pressurized fluid flow source to cyclically inflate and deflate at least one inflatable bladder of a compression garment configured to be wrapped around a limb of a wearer of the garment;
receive pressure signals indicative of fluid pressure in the at least one inflatable bladder from the pressure sensor communicatively coupled thereto during at least one of inflation and deflation of the at least one inflatable bladder in a plurality of successive compression cycle, with each compression cycle comprising pressurizing the inflatable bladder to a compression pressure and subsequently pressurizing the inflatable bladder to a refill pressure, with the compression pressure being greater than the refill pressure;
process the received pressure signals to determine a venous refill time (VRT); and
initiate the alarm in response to the received pressure signals indicating an interruption of operation or non-compliance with compression therapy when the VRT is lower than a predetermined threshold.
2. The compression garment control unit of claim 1 , wherein the alarm comprises one or more of an audio alarm and a visual alarm.
3. The compression garment control unit of claim 1 , wherein the pressure sensor is external to the at least one inflatable bladder.
4. The compression garment control unit of claim 1 , wherein the pressure sensor is coupled with the at least one inflatable bladder via a connection tubing.
5. The compression garment control unit of claim 1 , wherein the one or more processors are further configured to increment an active therapy time in response to the received pressure signals indicating compliance with the compression therapy.
6. The compression garment control unit of claim 5 , wherein the one or more processors are further configured to display the active therapy time and compliance on the display in response to the received pressure signals indicating compliance with the compression therapy.
7. The compression garment control unit of claim 1 , wherein the one or more processors are further configured to increment an active therapy time in response to receiving an override command in response to the alarm.
8. The compression garment control unit of claim 7 , wherein the one or more processors are further configured to display the active therapy time and compliance on the display in response to the received override command.
9. The compression garment control unit of claim 1 , wherein the one or more processors are further configured to store an active therapy time in response to receiving a stop command in response to the alarm.
10. A compression garment system comprising:
a compression garment; and
a compression garment control unit comprising:
a display configured to display patient compliance with a compression treatment regimen;
an alarm;
a pressure sensor;
at least one computer readable storage medium configured for storing one or more monitored parameters;
one or more processors coupled with the at least one computer readable storage medium; and
computer-executable instructions embodied on the at least one computer readable storage medium, the computer-executable instructions including instructions for causing the one or more processors to:
direct a flow of fluid from a pressurized fluid flow source to cyclically inflate and deflate at least one inflatable bladder of a compression garment configured to be wrapped around a limb of a wearer of the garment;
receive pressure signals indicative of fluid pressure in the at least one inflatable bladder from the pressure sensor communicatively coupled thereto during at least one of inflation and deflation of the at least one inflatable bladder in a plurality of successive compression cycle, with each compression cycle comprising pressurizing the inflatable bladder to a compression pressure and subsequently pressurizing the inflatable bladder to a refill pressure, with the compression pressure being greater than the refill pressure;
process the received pressure signals to determine a venous refill time (VRT); and
initiate the alarm in response to the received pressure signals indicating an interruption of operation or non-compliance with compression therapy when the VRT is lower than a predetermined threshold.
11. The compression garment system of claim 10 , wherein the alarm comprises one or more of an audio alarm and a visual alarm.
12. The compression garment system of claim 10 , wherein the pressure sensor is external to the at least one inflatable bladder.
13. The compression garment system of claim 10 , wherein the pressure sensor is coupled with the at least one inflatable bladder via a connection tubing.
14. The compression garment system of claim 10 , wherein the one or more processors are further configured to increment an active therapy time in response to the received pressure signals indicating compliance with the compression therapy.
15. The compression garment system of claim 14 , wherein the one or more processors are further configured to display the active therapy time and compliance on the display in response to the received pressure signals indicating compliance with the compression therapy.
16. The compression garment system of claim 10 , wherein the one or more processors are further configured to increment an active therapy time in response to receiving an override command in response to the alarm.
17. The compression garment system of claim 16 , wherein the one or more processors are further configured to display the active therapy time and compliance on the display in response to the received override command.
18. The compression garment system of claim 10 , wherein the one or more processors are further configured to store an active therapy time in response to receiving a stop command in response to the alarm.
19. A method for a compression garment control unit for monitoring and expressing compliance with a compression device comprising steps of:
directing, by the compression garment control unit, a flow of fluid from a pressurized fluid flow source to cyclically inflate and deflate an inflatable bladder of a compression garment configured to be wrapped around a limb of a wearer of the compression garment;
receiving, by the compression garment control unit, pressure signals indicative of fluid pressure in the inflatable bladder from a pressure sensor of the compression garment control unit, with the pressure sensor communicatively coupled thereto during an inflation and deflation of the inflatable bladder in a plurality of successive compression cycle, with each compression cycle comprising pressurizing the inflatable bladder to a compression pressure and subsequently pressurizing the inflatable bladder to a refill pressure, with the compression pressure being greater than the refill pressure;
processing, by the compression garment control unit, the received pressure signals to determine a venous refill time (VRT); and
initiating, by the compression garment control unit, an alarm in response to the received pressure signals indicating an interruption of operation or non-compliance with compression therapy when the VRT is lower than a predetermined threshold.