Sequential compression therapy compliance monitoring systems and methods
A system includes a sequential compression device (SCD) used by a patient as part of a sequential compression therapy (SCT) protocol. The system also includes a computer device that determines whether the SCD is in use in substantially real time in compliance with the protocol. The computer device initiates a notification to a caregiver if noncompliance with the SCT protocol is detected.
1. A person support apparatus for use with a compression sleeve, the person support apparatus comprising
a frame,
a fluid supply carried by the frame and operable to inflate the compression sleeve,
a controller coupled to the frame and configured to control operation of the fluid supply, and
at least one sensor coupled to the controller, the controller being configured to determine whether a patient is present on the patient support apparatus based on one or more signals from the at least one sensor, the controller being configured to determine whether the compression sleeve should be in use based on a protocol, wherein the controller is configured to initiate a notification to a caregiver if noncompliance with the protocol is detected, and wherein the controller determines compliance with the protocol only after the controller determines that the patient is present on the patient support apparatus based on the one or more signals from the at least one sensor.
2. The person support apparatus of claim 1 , wherein the controller is configured to communicate data with a communication network.
3. The person support apparatus of claim 1 , wherein the controller is configured to communicate with an electronic medical record system.
4. The person support apparatus of claim 1 , wherein the controller is configured to communicate with a nurse call system.
5. The person support apparatus of claim 1 , further comprising a pressure sensor configured to communicate pressure to the controller.
6. The person support apparatus of claim 5 , wherein the pressure sensor is configured to measure pressure inside the compression sleeve.
7. The person support apparatus of claim 5 , wherein the pressure sensor is configured to measure pressure that the compression sleeve applies to a person wearing the compression sleeve.
8. The person support apparatus of claim 1 , wherein the controller is configured to compare data relating to usage of the compression sleeve with a predetermined threshold to determine compliance with the protocol.
9. The person support apparatus of claim 8 , wherein the data relating to usage comprises one or more of frequency data, amplitude data, and duration of usage data.
10. The person support apparatus of claim 1 , further comprising at least one physiological sensor configured to communicate at least one physiological signal to the controller.
11. The person support apparatus of claim 10 , wherein the controller is configured to trigger an alarm if A) said at least one physiological signal is outside a predetermined range, or B) the duration of inflation of the compression sleeve is below a predetermined threshold, or C) the at least one physiological signal is outside the predetermined range, and the duration of inflation of the compression sleeve is below the predetermined threshold.
12. The person support apparatus of claim 1 , wherein the controller is configured to record a frequency of compressive therapy provided by the compression sleeve.
13. The person support apparatus of claim 1 , wherein the controller is configured to record an amplitude of compression applied by the compression sleeve.
14. The person support apparatus of claim 1 , wherein the controller is configured to record a duration of application of compressive therapy by the compression sleeve.
15. The person support apparatus of claim 1 , further comprising a display unit coupled to the frame, wherein the display unit is configured to display data relating to usage of the compression sleeve.
16. The person support apparatus of claim 1 , wherein the controller is configured to determine whether the compression sleeve is in use according to the protocol in substantially real time if the patient is present on the patient support apparatus.
17. The person support apparatus of claim 1 , wherein the controller is configured to determine whether an excused non-use condition exists such that the notification for noncompliance with the protocol is not initiated by the controller.
18. The person support apparatus of claim 17 , wherein the excused non-use condition corresponds to a caregiver being present in a room with a patient.
19. The person support apparatus of claim 17 , wherein the excused non-use condition corresponds to a patient being off of the person support apparatus.
20. The person support apparatus of claim 1 , further comprising an electrical stimulation device coupled to the controller and configured to stimulate nerves or muscles of a patient.