Control of a peripheral device with a bandage-type analyte sensor
US-10046114-B1 · Aug 14, 2018 · US
US10492986B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10492986-B2 |
| Application number | US-201615281395-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 30, 2016 |
| Priority date | Sep 30, 2016 |
| Publication date | Dec 3, 2019 |
| Grant date | Dec 3, 2019 |
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A system for monitoring performance of a resuscitation activity on a patient by an acute care provider is provided. The system includes: a first wearable sensor configured to sense movement of a first portion of an acute care provider's hand; a second wearable sensor configured to sense movement of a second portion of the acute care provider's hand; and a controller. The controller is configured to: receive and process signals representative of performance of a resuscitation activity from the first sensor and the second sensor; identify from the processed signals information indicative of at least one of a relative distance, a relative orientation, a change in relative distance and a change in relative orientation between the first sensor and the second sensor during performance of the resuscitation activity; and determine at least one resuscitation activity parameter based, at least in part, on the identified information.
Opening claim text (preview).
What is claimed is: 1. A system for monitoring performance of a resuscitation activity on a patient by an acute care provider, the system comprising: a first wearable sensor configured to sense movement of a first portion of an acute care provider's hand; a second wearable sensor configured to sense movement of a second portion of the acute care provider's hand; and a controller configured to: receive and process signals representative of performance of a resuscitation activity from the first wearable sensor and the second wearable sensor; identify from the processed signals information indicative of movement of the first wearable sensor in a first direction and information indicative of movement of the second wearable sensor in a second direction, the first direction being different from the second direction; and determine at least one resuscitation activity parameter based, at least in part, on the identified information for the first wearable sensor and the identified information for the second wearable sensor. 2. The system of claim 1 , wherein the at least one resuscitation activity parameter comprises one or more of compression depth, compression rate, ventilation volume, and ventilation rate. 3. The system of claim 1 , further comprising a feedback device, wherein the controller is configured to cause the feedback device to provide feedback to the acute care provider about performance of the resuscitation activity based, at least in part, on the determined at least one resuscitation activity parameter. 4. The system of claim 3 , wherein the feedback device comprises one or more of a haptic output component, a visual indication component, and an audio output component. 5. The system of claim 3 , wherein the feedback is based on a comparison between the determined at least one resuscitation activity parameter and target performance values for the resuscitation activity being performed. 6. The system of claim 5 , wherein the controller is configured to cause the feedback device to provide feedback according to varying haptic patterns to the acute care provider regarding performance of the resuscitation activity, the varying haptic patterns being based on a comparison of the determined at least one resuscitation activity parameter and the target performance values. 7. The system of claim 3 , wherein the feedback device comprises a haptic output component, and wherein the controller is configured to cause the haptic output component to provide vibration according to a first haptic pattern to encourage the acute care provider in performance of the resuscitation activity and according to a second haptic pattern to instruct the acute care provider to modify performance of the resuscitation activity. 8. The system of claim 7 , wherein the first haptic pattern and/or the second haptic pattern comprise one or more of a low intensity vibration, a high intensity vibration, a vibration having an intensity that varies in a saw tooth pattern, a pulse vibration at predetermined intervals, and/or a vibration including groups of haptic pulses of predetermined intensity and duration followed by intervals without haptic pulses. 9. The system of claim 3 , wherein the feedback device comprises a haptic output component and an audio feedback component, and wherein the controller is configured to cause the audio feedback component to provide audio feedback to encourage the acute care provider to perform a first aspect of the resuscitation activity and cause the haptic output component to provide feedback to encourage the acute care provider to perform a second aspect of the resuscitation activity. 10. The system of claim 4 , wherein the haptic output component comprises one or more linear vibrating motors. 11. The system of claim 4 , wherein the haptic output component comprises an annular or partially annular vibrating motor. 12. The system of claim 1 , further comprising at least one wireless transmitter associated with the first wearable sensor and/or the second wearable sensor, the at least one wireless transmitter being configured to wirelessly transmit the signals received from the sensors to the controller. 13. The system of claim 1 , further comprising a wireless transceiver associated with the controller, the transceiver being configured to receive wireless signals from the first wearable sensor and/or the second wearable sensor and to transmit information based on the received signals to a remote computing device. 14. The system of claim 13 , wherein the remote computing device comprises one or more of a portable computer, smartphone, laptop computer, and computer network. 15. The system of claim 13 , wherein the wireless transceiver comprises a device using one or more of Bluetooth, Zigbee, cellular, 3G, 4G, and Wi-Fi data transmission protocols. 16. The system of claim 13 , wherein the controller is configured to determine location and/or proximity information for the first wearable sensor and/or the second wearable sensor based, at least in part, on a quality of the signals wirelessly received by the wireless transceiver. 17. The system of claim 16 , wherein the controller is configured to determine the resuscitation activity being performed based, at least in part, on the determined location and/or proximity information for the first wearable sensor and/or the second wearable sensor. 18. The system of claim 1 , wherein the first wearable sensor is configured to sense movement of the acute care provider's thumb and the second wearable sensor is configured to sense movement of one of the acute care provider's fingers. 19. The system of claim 1 , further comprising a glove, wherein the first motion sensor and the second motion sensor are integrated with and/or attached to the glove. 20. The system of claim 1 , wherein the first wearable sensor and/or the second wearable sensor are disposed in ring-shaped housings, the housing being configured to be worn about the acute care provider's thumb or a finger. 21. The system of claim 1 , wherein the resuscitation activity comprises performance of chest compressions for an infant, and wherein the at least one resuscitation activity parameter comprises changes in anterior/posterior distance for the compressions. 22. The system of claim 1 , wherein the resuscitation activity comprises manually compressing a ventilation bag, and wherein the at least one resuscitation activity parameter comprises at least one of air volume expelled from the bag by the compression and flow rate of air expelled from the bag. 23. The system of claim 1 , wherein the resuscitation activity comprises administering a therapeutic agent to the patient using a syringe, and wherein the at least one resuscitation activity parameter comprises one or more of injection volume, unused fluid volume in the syringe, and injection flow rate. 24. The system of claim 1 , further comprising a proximity sensor configured to be worn by the acute care provider for identifying a position of the acute care provider relative to the patient, other medical devices at the emergency scene, and/or other acute care providers at the emergency scene. 25. The system of claim 24 , wherein the proximity sensor comprises a near-field communication sensor configured to identify one or more radio-frequency signals in proximity to the first wearable sensor and/or the second wearable sensor. 26. The system of claim 25 , wherein the con
Interfaces to the user · CPC title
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wireless · CPC title
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