Method And System For Monitoring Physiological And Athletic Performance Characteristics Of A Subject
US-2016249826-A1 · Sep 1, 2016 · US
US9826932B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9826932-B2 |
| Application number | US-201615133076-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 19, 2016 |
| Priority date | Apr 19, 2016 |
| Publication date | Nov 28, 2017 |
| Grant date | Nov 28, 2017 |
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This document describes automated abdominojugular reflux (AJR) testing. To automate AJR tests, a pressure cuff wrapped around a person's abdomen applies pressure while video of their neck is captured. By way of example, a medical professional wraps a pressure cuff around the person's abdomen and records video of the person's neck using a smartphone, which communicates with the pressure cuff to synchronize the application of pressure with video capture. The video is processed to detect and track the response of jugular venous pulse (JVP), which is compared to AJR test thresholds to determine test results. While determining JVP, and thereby results of AJR tests, from reconstructed videos may not result in data that is as accurate as invasive intra-heart tests, it requires little if any risk to patients and is easy for medical professionals to perform. Further, these techniques enable AJR tests to be performed automatically and without relying on estimates made by skilled medical professionals.
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What is claimed is: 1. A computer-implemented method for automating an abdominojugular reflux (AJR) test, the method comprising: communicating an indication to a pressure cuff wrapped around a person's abdomen to apply pressure to the person's abdomen; capturing video of the person's neck before, during, and after the pressure is applied to the person's abdomen; processing the captured video to measure a dynamic response of a jugular venous pulse (JVP) of the person while application of the pressure is initiated, maintained, and released; comparing measurements indicative of the dynamic response to one or more thresholds associated with AJR tests to determine a result of the AJR test that is indicative of cardiac functional performance of the person. 2. The computer-implemented method as described in claim 1 , wherein the one or more thresholds include an initial JVP rise threshold, the measurements include a measurement indicative of an initial rise of the person's JVP, and the comparing includes comparing the measurement indicative of the initial rise to the initial JVP rise threshold. 3. The computer-implemented method as described in claim 2 , wherein a negative AJR test result is determined if the initial rise of the person's JVP does not exceed the initial JVP threshold within a set time interval after the application of pressure is initiated. 4. The computer-implemented method as described in claim 2 , wherein the initial rise threshold is 3 centimeters from an initial location of the person's JVP detected before the application of pressure. 5. The computer-implemented method as described in claim 1 , wherein the one or more thresholds include a sustained JVP rise threshold, the measurements include metrics indicative of sustained rises of the person's JVP, and the comparing includes comparing metrics indicative of the sustained rises to the sustained rise threshold. 6. The computer-implemented method as described in claim 5 , wherein a negative AJR test result is determined if the metrics indicate that a sustained rise of the person's JVP falls below the sustained JVP rise threshold within a set time interval while the pressure is applied. 7. The computer-implemented method as described in claim 5 , wherein a positive AJR test result is determined based, at least in part, on the metrics indicating that a sustained rise of the person's JVP remains above the sustained JVP rise threshold for a set time interval while the pressure is applied. 8. The computer-implemented method as described in claim 1 , wherein the one or more thresholds include a JVP descent threshold, the measurements include a measurement indicative of a fall in the person's JVP after the application of pressure is released, and the comparing includes comparing the measurement indicative of the fall to the JVP descent threshold. 9. The computer-implemented method as described in claim 8 , wherein a positive AJR test result is determined based, at least in part, on a comparison that indicates the person's JVP falls by at least the JVP threshold within a set time interval after the application of pressure is released. 10. The computer-implemented method as described in claim 1 , wherein the application of pressure is maintained for a predetermined period of time in a range of 10-15 seconds. 11. The computer-implemented method as described in claim 1 , further comprising: receiving one or more readiness indications from the pressure cuff that indicate a readiness to apply the pressure to the person's abdomen; and responsive to the one or more readiness indications indicating that the pressure cuff is ready to apply the pressure, communicating to the pressure cuff the indication to apply the pressure to the person's abdomen. 12. The computer-implemented method as described in claim 11 , further comprising communicating a request to the pressure cuff that requests the one or more readiness indications responsive to receiving a user input to initiate the AJR test. 13. A device comprising: a transceiver to communicate with a pressure cuff wrapped around a person's abdomen to control pressure applied to the person's abdomen; a video camera to capture video of the person's neck while the pressure is applied to the person's abdomen; and a processing system to implement an abdominojugular reflux (AJR) testing manager configured to: process the captured video to measure characteristics of pulsatile motions that occur in the person's neck and are indicative of a jugular venous pulse (JVP) of the person; compare measurements of the characteristics to one or more thresholds associated with AJR tests; and determine a result of an AJR test for the person based on the comparison. 14. The device as described in claim 13 , wherein the one or more thresholds include at least one of an initial JVP rise threshold, a sustained JVP rise threshold, and a JVP descent threshold. 15. The device as described in claim 13 , further comprising a display device to display at least one of: instructions regarding how to position the pressure cuff around the person's abdomen; feedback regarding a positioning of the pressure cuff around the person's abdomen; instructions regarding how to position the device to enable the video camera to capture the video of the person's neck; a reconstructed video of the person's neck in which visually amplified pulsatile motions are perceptible to the human eye, the reconstructed video generated by processing the captured video to visually amplify the pulsatile motions that occur in the person's neck using one or more video motion amplification or other video enhancement techniques; the result of the AJR test for the person; and one or more messages based on the result of the AJR test. 16. A pressure cuff for abdominojugular reflux (AJR) testing, the pressure cuff comprising: a band configured to wrap around a person's abdomen; a pressure application assembly integral with the band to apply pressure to a particular region of the person's abdomen; and a processing system to implement a pressure application manager configured to: employ the pressure application assembly to apply the pressure to the particular region of the person's abdomen in conjunction with an AJR test of the person; and cause the pressure application assembly to cease application of the pressure after an amount of time associated with performing AJR tests lapses. 17. The pressure cuff as described in claim 16 , further comprising a transceiver to wirelessly communicate with a computing device configured to detect jugular distensions in the person's neck indicative of a jugular venous pulse (JVP) while the pressure application assembly applies the pressure to the particular region, a result of the AJR test being determinable based on the JVP. 18. The pressure cuff as described in claim 16 , further comprising a transceiver to communicate over a wired communication connection with a computing device configured to detect jugular distensions in the person's neck indicative of a jugular venous pulse (JVP) while the pressure application assembly applies the pressure to the particular region, a result of the AJR test being determinable based on the JVP. 19. The pressure cuff as described in claim 16 , further comprising a transceiver to communicate with another computing device to control the pressure cuff to initiate the application of pressure, release the pressure, and control a level of the pressure applied by the pressure cuff. 20. The pressure cuff as descri
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