Mobile patient alarm display
US-2019320988-A1 · Oct 24, 2019 · US
US2024423485A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024423485-A1 |
| Application number | US-202418750980-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 21, 2024 |
| Priority date | Mar 20, 2020 |
| Publication date | Dec 26, 2024 |
| Grant date | — |
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Systems and methods are provided for remote patient management and monitoring. The patient is monitored with a wireless sensor system connected to an application executing on a patient user computing device. The system continuously monitors physiological parameters, such as, but not limited to, blood oxygen saturation (SpO 2 ), pulse rate, perfusion index, pleth variability index, and/or respiration rate from the photoplethysmograph. The system triggers alarms if the patient physiological data violates thresholds. Care providers review patient data and associated alarm(s) with graphical user interfaces.
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1 . (canceled) 2 .- 17 . (canceled) 18 . A system for patient care and monitoring, the system comprising: a wearable patient sensor device configured to measure physiological parameters from a patient; a patient device in communication with the wearable patient sensor device, the patient device comprising: a memory device configured to store instructions; and a hardware processor configured to execute instructions to: receive one or more physiological parameter values generated by the wearable patient sensor device; output a plurality of user interfaces configured to receive a plurality of patient inputs to configure a plurality of alarm threshold levels for one of the physiological parameters and a plurality of alerts, wherein different alerts are transmitted for the plurality of alarm threshold levels; and in response to one of the plurality of alarm threshold levels being exceeded by the one or more physiological parameter values, transmit a corresponding alert. 19 . The system of claim 18 , wherein the one of the physiological parameters comprises blood oxygen saturation or SpO2. 20 . The system of claim 18 , wherein a portion of the wearable patient sensor device is configured to be attached to a wrist of the patient. 21 . The system of claim 18 , wherein the wearable patient sensor device comprises a fingertip pulse oximeter. 22 . The system of claim 18 , wherein the wearable patient sensor device comprises a disposable device coupled to a reusable device. 23 . The system of claim 18 , wherein the patient device is in wireless communication with the wearable patient sensor device. 24 . The system of claim 18 , wherein the plurality of alarm threshold levels comprises an emergency level. 25 . The system of claim 24 , wherein the alert corresponding to the emergency level comprises notifying an emergency contact or emergency medical responders. 26 . The system of claim 25 , wherein the plurality of user interfaces are further configured to allow the patient to set an amount of time after the emergency level has been exceeded before notifying the emergency contact or emergency medical responders. 27 . The system of claim 26 , wherein the amount of time after the emergency level has been exceeded before notifying the emergency contact is different from the amount of time after the emergency level has been exceeded before notifying the emergency medical responders. 28 . The system of claim 25 , wherein the plurality of user interfaces are further configured to allow the patient to configure repeat notifications to the emergency contact. 29 . The system of claim 25 , wherein hardware processor is configured to execute further instructions to receive a patient input to set an address that the emergency medical responders respond to in response to being notified of the emergency level. 30 . The system of claim 18 , wherein the plurality of alarm threshold levels comprises a warning level. 31 . The system of claim 30 , wherein the alert corresponding to the warning level comprises outputting a warning message to the patient on a display of the patient device. 32 . The system of claim 31 , wherein the plurality of user interfaces are further configured to allow the patient to set an amount of time after the warning level has been exceeded before displaying the warning message. 33 . The system of claim 18 , wherein the plurality of user interfaces are further configured to allow the patient to set a different parameter value for each of the plurality of alarm threshold levels. 34 . The system of claim 18 , wherein the plurality of alarm threshold levels comprises a good range, a caution range, a serious range, and/or a critical range. 35 . The system of claim 34 , wherein the hardware processor is configured to execute further instructions to output for display a recent events element summarizing a number of events at one or more of the plurality of alarm threshold levels. 36 . The system of claim 18 , wherein the hardware processor is configured to execute further instructions to transmit an alert related to low sensor battery. 37 . The system of claim 18 , wherein the hardware processor is configured to execute further instructions to transmit a sensor-off alert.
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