Network-enabled systems for mitigating pressure applied to a living body by an underlying surface
Introduced here are pressure-mitigation systems able to mitigate the pressure applied to a human body by the surface of an object. A system can include a pressure-mitigation device with chambers whose pressure can be varied by a controller that regulates the flow of fluid produced by a pump. The controller may be deployed as part of a closed loop system that autonomously infers information related to the health of a patient based on data related to the pressure of these chambers. For example, the data may be examined to determine whether the values indicate the patient is properly situated. A notification may be presented responsive to determining that the patient is not situated on the pressure-mitigation device, the patient has been improperly situated on the pressure-mitigation device for a certain amount of time, etc. Thus, real-time feedback may be provided to those responsible for monitoring the patient.
1. A method for establishing whether a pressure-mitigation device that is deployed beneath a human body is being used in compliance with a treatment regimen, the method comprising:
determining, by a controller, that the pressure-mitigation device is fluidly connected to the controller;
identifying, by the controller, a programmable pattern from among a series of programmable patterns based on an arrangement of magnets contained in the pressure-mitigation device and detected by the controller;
causing, by the controller, chambers of the pressure-mitigation device to be inflated or deflated to varying degrees in accordance with the programmable pattern,
wherein the chambers are arranged in a geometric pattern that is designed to alleviate force applied to an anatomical region of the human body;
obtaining, by the controller, data that indicates pressure of each chamber of the pressure-mitigation device;
examining, by the controller, the data so as to establish a location of the human body with respect to the geometric pattern; and
producing, by the controller based on the location, an output that indicates whether the human body is properly positioned on the pressure-mitigation device as required by the treatment regimen.
2. The method of claim 1 ,
wherein the data is based on electrical signals generated by transducers mounted in the controller, and
wherein each electrical signal is generated by a corresponding one of the transducers based on the pressure of a corresponding one of the chambers of the pressure-mitigation device.
3. The method of claim 1 ,
wherein the data is based on measurements generated by pressure sensors embedded within the pressure-mitigation device, and
wherein each measurement is generated by a corresponding one of the pressure sensors based on the pressure of a corresponding one of the chambers of the pressure-mitigation device.
4. The method of claim 1 , further comprising:
transmitting, by the controller, information related to the output to a destination across a network.
5. The method of claim 4 , further comprising:
determining, by the controller, that the output indicates the human body is not properly positioned on the pressure-mitigation device as required by the treatment regimen; and
transmitting, by the controller, a notification to a computing device associated with a caregiver responsible for managing the human body.
6. The method of claim 5 , wherein the caregiver is a healthcare professional.
7. The method of claim 1 , wherein said obtaining, said examining, and said producing are performed continually over an interval of time in order to produce a coverage metric that is indicative of a portion of the interval of time that the human body was properly positioned on the pressure-mitigation device.
8. The method of claim 1 , wherein each programmable pattern in the series of programmable patterns is associated with a different type of pressure-mitigation device having a different number of chambers and/or a different arrangement of chambers.
9. A method for establishing whether a pressure-mitigation device that is deployed beneath a human body is being used in compliance with a treatment regimen, the method comprising:
determining, by a controller, that the pressure-mitigation device is fluidly connected to the controller;
identifying, by the controller, a programmable pattern from among a series of programmable patterns based on an electronic signature emitted by a beacon in the pressure-mitigation device and detected by the controller;
causing, by the controller, chambers of the pressure-mitigation device to be inflated or deflated to varying degrees in accordance with the programmable pattern,
wherein the chambers are arranged in a geometric pattern that is designed to alleviate force applied to an anatomical region of the human body:
obtaining, by the controller, data that indicates pressure of each chamber of the pressure-mitigation device;
examining, by the controller, the data so as to establish a location of the human body with respect to the geometric pattern; and
producing, by the controller based on the location, an output that indicates whether the human body is properly positioned on the pressure-mitigation device as required by the treatment regimen.
10. The method of claim 9 ,
wherein the data is based on electrical signals generated by transducers mounted in the controller, and
wherein each electrical signal is generated by a corresponding one of the transducers based on the pressure of a corresponding one of the chambers of the pressure-mitigation device.
11. The method of claim 9 ,
wherein the data is based on measurements generated by pressure sensors embedded within the pressure-mitigation device, and
wherein each measurement is generated by a corresponding one of the pressure sensors based on the pressure of a corresponding one of the chambers of the pressure-mitigation device.
12. The method of claim 9 , further comprising:
transmitting, by the controller, information related to the output to a destination across a network.
13. The method of claim 12 , further comprising:
determining, by the controller, that the output indicates the human body is not properly positioned on the pressure-mitigation device as required by the treatment regimen; and
transmitting, by the controller, a notification to a computing device associated with a caregiver responsible for managing the human body.
14. The method of claim 13 , wherein the caregiver is a healthcare professional.
15. The method of claim 9 , wherein said obtaining, said examining, and said producing are performed continually over an interval of time in order to produce a coverage metric that is indicative of a portion of the interval of time that the human body was properly positioned on the pressure-mitigation device.
16. The method of claim 9 , wherein each programmable pattern in the series of programmable patterns is associated with a different type of pressure-mitigation device having a different number of chambers and/or a different arrangement of chambers.