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公开(公告)号:US20230181037A1
公开(公告)日:2023-06-15
申请号:US18077264
申请日:2022-12-08
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: RAYMOND VAN EE , JOANNE HENRIËTTE DESIRÉE MONIQUE WESTERINK , MARIA ESTRELLA MENA BENITO , TIMMY ROBERTUS MARIA LEUFKENS , TIM ELISABETH JOSEPH WEIJSEN , STEFAN PFUNDTNER , TSVETOMIRA KIROVA TSONEVA
CPC classification number: A61B5/0022 , A61B5/11
Abstract: The present invention relates to an agenda generation system (10), comprising:
at least one first sensor unit (20); an input unit (30); a processing unit (40); and at least one output unit (50);
wherein the at least one first sensor unit is configured to acquire physiological data of a subject over an extended period of time prior to a current time point and provide the physiological data to the processing unit, wherein the physiological data is assigned to different times during the extended period of time, and wherein the physiological data comprises one or more of: heart rate, ventricular high rate, blood pressure, respiration rate, skin conductance, step count;
wherein the at least one first sensor unit is configured to acquire sleep data of the subject over the extended period of time and provide the sleep data to the processing unit, wherein the sleep data is assigned to different times during the extended period of time, and wherein the sleep data comprises one or more of: duration of sleep; total daily sleep duration, onset of sleep, quality of sleep,
wherein the input unit is configured to receive details of undertaken work data and undertaken leisure activity data of the subject over the extended period of time and provide the undertaken work data and undertaken leisure activity data to the processing unit, and wherein the undertaken work data and undertaken leisure activity data is assigned to different times during the extended period of time;
wherein the input unit is configured to receive details of planned work data and planned leisure activity data of the subject after the current time point and provide the planned work data and planned leisure activity data to the processing unit;
wherein the processing unit is configured to implement at least one trained machine learning algorithm to determine a sleep schedule comprising a planned onset and duration of sleep and/or determine a work schedule comprising scheduling of the planned work data and/or determine a leisure schedule comprising scheduling of the planned leisure activity data, and wherein the determination comprises analysis of: the physiological data, the sleep data, the undertaken work data, the undertaken leisure activity data, the planned work data, and the planned leisure activity data; and
wherein one or more of the at least one output unit is configured to output the sleep schedule and/or the work schedule and/or the leisure schedule.-
公开(公告)号:US20190159688A1
公开(公告)日:2019-05-30
申请号:US16309950
申请日:2017-06-14
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: KOEN THEO JOHAN DE GROOT , TON HERMANUS MARIA AKKERMANS , CORNELUS HENDRICUS BERTUS ARNOLDUS VAN DINTHER , STEFAN PFUNDTNER , DAVID ANTOINE CHRISTIAN MARIE ROOVERS , ALPHONSUS TARCISIUS JOZEF MARIA SCHIPPER , CORNELIS HARM TAAL
Abstract: The present invention relates to a device (10) for determining an arterial compliance of a subject (12). The device (10) comprises an inflatable cuff (14), a pressure sensor (18) which is configured to sense a pressure signal (52) that is indicative of a pressure within the cuff (14), a second sensor (20) which is at least partly integrated in the cuff (14) and configured to sense a second signal (56) that is responsive to expansions and contractions of the cuff (14) caused by a pulsating blood flow in an artery (50) of the subject (12), and a processing unit (22). The processing unit is configured to determine based on said part of the pressure signal (52) a pulse pressure of the subject (12), to determine based on said part of the second signal (56) an arterial volume change of the artery (50) of the subject (12) during at least one cardiac cycle, and to determine the arterial compliance of the subject (12) based on pulse pressure and the arterial volume change.
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公开(公告)号:US20190382025A1
公开(公告)日:2019-12-19
申请号:US16481614
申请日:2018-01-31
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: MARIA ESTRELLA MENA BENITO , YANNYK PARULIAN JULIAN BOURQUIN , CAIFENG SHAN , STEFAN PFUNDTNER
IPC: B60W40/08 , A61B5/00 , A61B5/0205 , A61B5/01 , A61B5/02 , A61B5/11 , A61B5/053 , A61B5/145 , A61B5/16 , A61B5/18 , B60W50/00
Abstract: In one embodiment, an apparatus (22) is presented that recognizes a user is driving and predicts a hypoglycemic event has reached a threshold probability of occurring based on one or more input parameters and alerts the user or activates a device based on the prediction.
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公开(公告)号:US20170340854A1
公开(公告)日:2017-11-30
申请号:US15525322
申请日:2015-11-11
Applicant: KONINKLIJKE PHILIPS N.V.
IPC: A61M21/02 , A61B5/0484 , A61B5/00 , A61M21/00
CPC classification number: A61M21/02 , A61B5/04845 , A61B5/4812 , A61B5/4836 , A61M2021/0027 , A61M2205/18 , A61M2205/3375 , A61M2205/505 , A61M2205/52 , A61M2205/581 , A61M2205/582 , A61M2205/583 , A61M2230/10 , A61M2230/005
Abstract: The present disclosure describes a system configured to adjust the duration of individual sensory stimuli provided to a subject. The system is configured to determine a current amount of slow wave activity in the subject, responsive to the subject being presently in slow wave sleep, control one or more sensory stimulators to provide the individual sensory stimuli to the subject, determine habituation of the subject to the individual sensory stimuli and, responsive to the slow wave activity in the subject for a period of time following the providing of the individual sensory stimuli showing habituation, adjust the duration of the individual sensory stimuli.
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公开(公告)号:US20240232746A1
公开(公告)日:2024-07-11
申请号:US18559122
申请日:2022-05-03
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: RAYMOND VAN EE , JOANNE HENRIETTE DESIREE MONIQUE WESTERINK , TIMMY ROBERTUS MARIA LEUFKENS , STEFAN PFUNDTNER , TIM ELISABETH JOSEPH WEYSEN , MARIA ESTRELLA MENA BENITO
IPC: G06Q10/0631
CPC classification number: G06Q10/063116
Abstract: According to an aspect, there is provided a computer-implemented method for determining a sleep schedule (20; 40; 60) for a subject. The method comprises obtaining (101) information indicating a shift working pattern for the subject, the shift working pattern comprising at least one night shift, information indicating a required duration of sleep for the subject, and information relating to any personal activities to be undertaken by the subject during the day before or day after the at least one night shift. The method also comprises analyzing (103) the obtained information to determine a sleep schedule (20; 40; 60) for the subject. The sleep schedule (20; 40; 60) comprises two or more sleep windows in the day before or day after the at least one night shift in which the subject is to sleep, with the two or more sleep windows being scheduled according to the required duration of sleep for the subject and according to any personal activities to be undertaken by the subject.
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公开(公告)号:US20230211117A1
公开(公告)日:2023-07-06
申请号:US18082991
申请日:2022-12-16
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: TSVETOMIRA KIROVA TSONEVA , DAAN ANTON VAN DEN ENDE , SANDER THEODOOR PASTOOR , STEFAN PFUNDTNER
IPC: A61M21/00
CPC classification number: A61M21/00 , A61M2021/0027 , A61M2205/13 , A61M2205/502 , A61M2205/702 , A61M2205/3303 , A61M2230/10
Abstract: Methods and systems are provided for assisting a user of a wearable biosignal monitoring device (2) in adjusting the device to achieve optimum fit and positioning. The biosignal monitoring devices considered use integrated bio sensors (5) to monitor the user’s physiological activity for various purposes such as tracking daily activity patterns, determining mood, and monitoring sleep stages, among others. It is determined either during device setup or during primary use of the device whether the current fit and positioning of the device (2) enable the bio sensors (5) to properly sense the physiological signals needed for the device to perform its primary function. The user is then informed either after initial device setup whether adjustments need to be made in order to optimize device function during primary use, or is informed after primary use whether adjustments need to be made in order to improve device function during future primary use.
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