Systems, Devices and Methods for the Prevention and Treatment of Pressure Ulcers, Bed Exits, Falls, and Other Conditions
US-2016256080-A1 · Sep 8, 2016 · US
US10278638B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10278638-B2 |
| Application number | US-201414336910-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 21, 2014 |
| Priority date | Jul 21, 2014 |
| Publication date | May 7, 2019 |
| Grant date | May 7, 2019 |
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A sleep assist system to monitor and assist the user's sleep, comprising: a bedside device adapted to be positioned near the user's bed, the bedside device optionally comprising a loudspeaker, a light source, a microphone, a light sensor, a temperature sensor, a control unit, an air quality sensor, a display unit, a user interface. The system further comprises a first sensing unit positioned in the user's bed comprising one or more sensors adapted to sense at least pressure and changes in pressure exerted by the user lying in the bed; an additional sensor device to be in contact with the user's body, and to be coupled to the bedside device; the system is configured to correlate the data obtained from both the first sensing unit and the additional sensor device.
Opening claim text (preview).
The invention claimed is: 1. A system to monitor a user's sleep and to assess various physiological parameters of the user, the system comprising: a bedside device comprising at least a processing unit and a memory unit having non-transitory computer executable instructions, the bedside device further comprising at least one of the following: a loudspeaker, a light source, a microphone, a light sensor, a temperature sensor, a humidity sensor, a control unit, an air quality sensor, a display unit, and a user interface; a first sensing unit adapted to be positioned in the user's bed, the first sensing unit comprising one or more sensors adapted to sense at least pressure and/or changes in pressure exerted by the user lying in the bed, the first sensing unit comprising an air bladder the first sensing unit being adapted to measure ballistocardiography signals, an additional sensor device, configured to be in contact with the user's body, such that the additional sensor device is worn by the user on the user's wrist, having a photopléthysmography sensor and configured to measure at least heart pulses of the user, wherein the first sensing unit is coupled to the bedside device, wherein the additional sensor device is coupled to the bedside device, the processing unit is configured to correlate the data obtained from both the first sensing unit and the additional sensor device, and to deduce therefrom cardiovascular parameters including at least user's heart rate, user's heart rate variability and user's breathing frequency, wherein the processing unit is further configured to determine a first instant sensed by ballistocardiography of the first sensing unit, said first instant being representative of the user's heart ventricular contraction, to determine a second instant of an arrival of a corresponding pulse at the user's wrist, sensed by photopléthysmography of the additional sensor device, and to measure a pulse transit time defined as the time difference between first and second instants, and wherein the processing unit is further configured to assess the stiffness of the user's arteries based on the measurements of pulse transit time. 2. The system as in claim 1 , wherein the bedside device further comprises a wherein the processing unit is further configured to: monitor the user's sleep, assess the user's sleep cycles and the phase of sleep cycle, by using data collected from the first sensing unit and the additional sensor device, and provide the user with at least one light and sound program via the bedside device, the light and sound program being based on the assessment of the user's sleep cycles and the phase of sleep cycle. 3. The system as in claim 1 , wherein the processing unit is configured further configured to assess heart volume stroke and/or its evolutions based on the amplitude of the signal measured by the first sensing unit, and from the pulse transit time. 4. The system as in claim 3 , wherein the processing unit is further configured to assess blood pressure or at least its evolutions based on the combination of arterial stiffness, heart volume stroke and heart rate. 5. The system as in claim 1 , the bedside device further comprising a microphone, wherein the processing unit is further configured to determine when a user suffers from sleep apnea based on a pause in breathing cycle sensed via the first sensing unit and a blood oxygenation drop sensed via the additional sensor. 6. The system as in claim 1 , wherein the system further comprising a mobile terminal, the mobile terminal being configured to receive and to display the information obtained by the bedside unit, the sensing unit and/or the additional sensor device, wherein the mobile terminal is further configured to receive feedback from the user. 7. A system to monitor a user's sleep, and to assess various physiological parameters of the user, the system comprising: a mobile terminal comprising at least a control unit and a display, a first sensing unit adapted to be positioned in the user's bed, the first sensing unit comprising one or more sensors adapted to sense at least pressure and/or changes in pressure exerted by the user lying in the bed, the first sensing unit comprising an air bladder, the first sensing unit being adapted to measure ballistocardiography signals, an additional sensor device, configured to be in contact with the user's body, such that the additional sensor device is worn by the user on the user's wrist, having a photopléthysmography sensor and configured to measure at least heart pulses of the user, wherein the first sensing unit is coupled to the mobile terminal, wherein the additional sensor device coupled to the mobile terminal, the mobile unit is configured to correlate the data obtained from both the first sensing unit and the additional sensor device, and to deduce therefrom cardiovascular parameters including at least user's heart rate, user's heart rate variability and user's breathing frequency wherein the mobile unit is further configured to determine a first instant sensed by ballistocardiography of the first sensing unit, said first instant being representative of the user's heart ventricular contraction, to determine a second instant of an arrival of a corresponding pulse at the user's wrist, sensed by photopléthysmography of the additional sensor device, and to measure a pulse transit time defined as the time difference between first and second instants, and wherein the mobile is further configured to assess the stiffness of the user's arteries based on the measurements of pulse transit time. 8. The system as in claim 7 , wherein the mobile unit is further configured to assess heart volume stroke and/or its evolutions based on the amplitude of the signal measured by the first sensing unit, and from the pulse transit time. 9. The system as in claim 7 , wherein the mobile unit is further configured to assess blood pressure or at least its evolutions based on the combination arterial stiffness, heart volume stroke and heart rate. 10. The system as in claim 7 , wherein the bedside device further comprising a microphone, and wherein the mobile unit is further configured to determine when a user suffers from sleep apnea based on a pause in breathing cycle sensed via the first sensing unit and a blood oxygenation drop sensed via the additional sensor.
of pulse wave propagation time · CPC title
Displaying user selection data, e.g. icons in a graphical user interface · CPC title
Details of sensor (A61B5/02427 takes precedence) · CPC title
Wristwatch-type devices · CPC title
occurring during breathing · CPC title
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