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1. 发明申请

US20160193010A1 MEDICAL ROBOTIC AND/OR CATHETER CONTROL SYSTEM 审中-公开
标题翻译：医疗机器人和/或导管器控制系统
公开(公告)号：US20160193010A1
公开(公告)日：2016-07-07
申请号：US14911315
申请日：2014-08-21
申请人： KONINKLIJKE PHILIPS N.V. , KONINKLIJKE PHILIPS N.V.
发明人： ERIC JOHANNES MARIA JANSSEN , ERIK MARTINUS HUBERTUS PETRUS VAN DIJK
IPC分类号： A61B90/50 , B25J9/00 , A61B6/00 , A61M25/01 , A61B34/30
摘要： The invention relates to a medical system for applying a medical procedure. The medical system (1) comprises a medical device (5) like a surgical robot with a surgical instrument (24) for performing the medical procedure, wherein the medical device is adapted to perform a movement, for instance, a movement of the surgical instrument, relative to a reference device like a patient table (9) for applying the medical procedure. The medical device is attached to a wall and/or a ceiling (3) of a room (2) by an attaching system (7) and rigidly attached to the reference device by a fixation element (8). Due to the attachment to the wall and/or the ceiling, the weight of the medical device does not need to be completely carried by, for instance, the patient table, wherein, due to the rigid attachment to the reference device, the medical procedure can still very accurately be performed.
摘要翻译：本发明涉及一种用于应用医疗程序的医疗系统。医疗系统（1）包括医疗装置（5），类似于具有用于执行医疗程序的外科器械（24）的手术机器人，其中医疗装置适于执行移动，例如外科器械相对于诸如用于施加医疗程序的患者台（9）的参考装置。医疗装置通过附接系统（7）附接到房间（2）的墙壁和/或天花板（3），并通过固定元件（8）刚性地附接到参考装置。由于附接到壁和/或天花板，医疗装置的重量不需要被例如患者台完全承载，其中，由于刚性地附接到参考装置，医疗程序仍然可以非常准确地执行。

2. 发明公开

US20240290502A1 VERIFYING A DIGITAL TWIN OF A SUBJECT 审中-公开
公开(公告)号：US20240290502A1
公开(公告)日：2024-08-29
申请号：US18572851
申请日：2022-06-23
申请人： KONINKLIJKE PHILIPS N.V.
发明人： MURTAZA BULUT , CORNELIS PETRUS HENDRIKS , LIEKE GERTRUDA ELISABETH COX , VALENTINA LAVEZZO , HARM CRONIE
IPC分类号： G16H50/70 , G16H10/20
CPC分类号： G16H50/70 , G16H10/20
摘要： Systems and methods are proposed for verifying whether a digital twin of abiological asset (or biological system) of a subject (110) indeed relates to the subject (110). Such proposals may be based on obtaining: a first signal comprising a value of a physiological parameter of the subject (e.g. determined by a physical and/or virtual sensor arrangement); and a second signal generated by the digital twin that simulates a value of a physiological parameter of the subject (110). By comparing the first and second signals, a verification result may then be determined.

3. 发明公开

US20240289951A1 DETERMINATION OF 3D POSITIONING IN AN MRI SYSTEM 审中-公开
公开(公告)号：US20240289951A1
公开(公告)日：2024-08-29
申请号：US18571233
申请日：2022-06-20
申请人： KONINKLIJKE PHILIPS N.V.
发明人： Karsten Sommer , Sascha Krueger , Jan Hendrik Wuelbern , Ingmar Graesslin , Lena Christina Frerking
IPC分类号： G06T7/00 , A61B6/00 , G06T17/10 , G06V10/25
CPC分类号： G06T7/0012 , A61B6/5264 , G06T17/10 , G06V10/25 , G06T2207/10088
摘要： The invention provides means for determining 3D position data in an MRI system. A method for motion correction of MR data, comprising: generating, by a calculation unit (51), a three-dimensional model, 3D model, of a region of interest (24) of a subject (23) comprising at least one landmark (27) inherent to the subject (23) (S10); obtaining, by a first measuring device (20, 25, 52), a two-dimensional image, 2D image, of at least a part of the subject (23) inside a MRI system (22), wherein the measuring device is arranged inside a bore of the MRI system (22) (S20); determining, by the calculation unit (53), at least one landmark (27) in the 2D image, wherein the at least one landmark (27) in the 2D image corresponds to the at least one landmark (27) of the 3D model (S30); determining, by the calculation unit (54), a 3D position of the region of interest (24) of the subject (23) in the MRI system (22) based on the determined at least one landmark (27) in the 2D image (S40); providing, by the calculation unit (55), the 3D position of the region of interest (24) of the subject (23) for motion correction of MR data (S50).

4. 发明公开

US20240285407A1 VALVE STENT FOR INTRAVASCULAR REPERFUSION THERAPY 审中-公开
公开(公告)号：US20240285407A1
公开(公告)日：2024-08-29
申请号：US18693487
申请日：2022-09-19
申请人： KONINKLIJKE PHILIPS N.V.
发明人： James David CEZO , Arjen VAN DER HORST
IPC分类号： A61F2/24 , A61B8/04 , A61B8/06 , A61B8/12 , A61F2/48 , A61F2/95
CPC分类号： A61F2/2476 , A61B8/04 , A61B8/06 , A61B8/12 , A61F2/2418 , A61F2/484 , A61F2002/9528 , A61F2250/001
摘要： A system includes a stent positionable within a coronary vein. The stent includes a valve and a stent body coupled to the valve and arranged to transition between a collapsed state and an expanded state. The system includes an intravascular reperfusion therapy device with a sensor and a catheter with a lumen shaped to receive the stent. The intravascular reperfusion therapy device delivers reperfusion therapy to a myocardium of a heart. The system includes a processor circuit that receives physiological data from the sensor, determines a progression of the reperfusion therapy, controls a configuration of the valve and/or the expansion state of the stent such that back pressure is controlled. With the stent in the expanded state, the stent body contacts a wall of the coronary vein and the valve obstructs blood flow in a first direction to generate the back pressure in an opposite, second direction.

5. 发明公开

US20240285259A1 METHODS AND SYSTEMS FOR VENTILATION MANAGEMENT USING LUNG ULTRASOUND 审中-公开
公开(公告)号：US20240285259A1
公开(公告)日：2024-08-29
申请号：US18571811
申请日：2022-06-21
申请人： KONINKLIJKE PHILIPS N.V.
发明人： Jochen Kruecker , Seyedali Sadeghi , Shyam Bharat , Claudia Errico , Samer Bou Jawde , Roberto Buizza , Balasundar Iyyavu Raju , Sven Peter Prevrhal
IPC分类号： A61B8/08 , A61B8/00 , G16H50/30
CPC分类号： A61B8/5223 , A61B8/08 , A61B8/463 , G16H50/30
摘要： A lung injury monitoring system (200) configured to monitor a patient's lungs during ventilation. comprising: an ultrasound device (280) configured to obtain an ultrasound image of the patient's lungs during ventilation of the patient: a processor (220) configured to: (i) receive the obtained ultrasound image: (ii) determine a ventilation phase of the ventilator: (iii) analyze the received ultrasound image: and (iv) determine a risk score for a potential ventilator-associated lung injury (VALI): and a user interface (240) configured to display the determined risk score for the potential VALI.

6. 发明公开

US20240285187A1 SNIFF DETECTION AND ARTIFACT DISTINCTION FROM ELECTROMYOGRAPHY AND ACCELEROMETER SIGNALS 审中-公开
公开(公告)号：US20240285187A1
公开(公告)日：2024-08-29
申请号：US18573480
申请日：2022-06-27
申请人： KONINKLIJKE PHILIPS N.V.
发明人： JAKOB VAN DE LAAR , JENS MUEHLSTEFF , MARIAN DEKKER
IPC分类号： A61B5/085 , A61B5/00 , A61B5/11 , A61B5/113 , A61B5/389
CPC分类号： A61B5/085 , A61B5/1126 , A61B5/113 , A61B5/389 , A61B5/7221 , A61B5/7225 , A61B2562/0219 , A61B2562/04 , A61B2562/06
摘要： Non-invasive systems and methods for quantifying respiratory muscle effort (RME) (or breathing effort, work-of-breathing) are provided. The systems and methods utilize simultaneously measured EMG and accelerometer signals. The measured EMG signal is preprocessed to produce both a signal accentuating regular breathing activity and a signal accentuating sniff activity (deep, sharp inhalations). Time intervals of candidate sniffs are determined from the preprocessed EMG signals. The measured accelerometer signal is preprocessed to produce multiple signals accentuating either upper or lower frequency band activity. Features of the preprocessed EMG and accelerometer signals corresponding to the time intervals of candidate sniffs are analyzed to determine if the candidate sniffs constitute actual sniffs or artifacts. Subsequently, after maximum sniff effort has been identified, RME is quantified by the ratio of the mean of the maxima of regular breathing activity to the value of the maximum sniff effort.

7. 发明授权

US12073940B2 Extracting sales and upgrade opportunities from utilization data 有权
公开(公告)号：US12073940B2
公开(公告)日：2024-08-27
申请号：US16758073
申请日：2018-10-22
申请人： KONINKLIJKE PHILIPS N.V.
发明人： Paul Richard Simons
IPC分类号： G16H40/40 , G06F21/62 , G06N20/00 , G06Q10/0637 , G06Q30/0601 , G16H40/20 , G16H50/20 , G06Q10/04
CPC分类号： G16H40/40 , G06F21/6254 , G06N20/00 , G06Q10/06375 , G06Q30/0631 , G16H40/20 , G16H50/20 , G06Q10/04
摘要： A non-transitory computer-readable medium stores instructions readable and executable by a workstation (20) including at least one electronic processor (22) to perform a method (100) for generating medical imaging device upgrade recommendations from utilization data. The method includes: retrieving, from at least one database (14), 5 utilization data (30) from logs of a plurality of installed medical imaging devices (16); applying a set of rules (29) to the utilization data to identify one or more upgrade recommendations wherein each upgrade recommendation comprises: an identification of one or more of the installed medical imaging devices or components of the installed medical imaging devices recommended to be upgraded or replaced; and at least one of a 10 replacement medical imaging device or component or a new medical imaging device or component for each of the installed medical imaging devices or components recommended to be upgraded or replaced; and displaying, on a display device (26), a list (38) of the at least one identified replacement or new medical imaging device or component.

8. 发明公开

US20240277294A1 MOTION REDUCTION IN DIAGNOSTIC IMAGING OR RADIATION THERAPY 审中-公开
公开(公告)号：US20240277294A1
公开(公告)日：2024-08-22
申请号：US18291368
申请日：2022-07-15
申请人： KONINKLIJKE PHILIPS N.V.
发明人： Christoph Günther Leussler , Steffen Weiss
IPC分类号： A61B5/00 , A61B5/055 , A61B5/372 , A61B6/00
CPC分类号： A61B5/721 , A61B5/055 , A61B5/372 , A61B6/527
摘要： The present invention relates to monitoring motion in diagnostic imaging or radiation therapy. In order to improve workflow, a device is proposed that comprises an input unit, a processing unit, and an output unit. The input unit is configured to receive an electroencephalogram (EEG) signal measured from a patient. The processing unit is configured to determine a readiness potential (RP) based on the received EEG signal, to determine whether patient motion is likely to happen based on the received EEG signal, and to provide a control signal via the output unit as output, if it is predicted that patient motion is likely to happen. The control signal is usable for controlling an apparatus to perform a function to reduce motion artefacts during the medical imaging or to assure that radiation dose is delivered according to a planned dose map during the radiation therapy.

9. 发明授权

US12068060B2 Record finding using multi-party computation 有权
公开(公告)号：US12068060B2
公开(公告)日：2024-08-20
申请号：US17051495
申请日：2019-04-22
申请人： KONINKLIJKE PHILIPS N.V.
发明人： Lu Zhang , Meilof Geert Veeningen , Peter Petrus van Liesdonk
IPC分类号： G06F16/00 , G06F16/14 , G06F16/24 , G06F16/245 , G06F16/2455 , G06F16/33 , G06F16/35 , G06F16/83 , G06F16/835 , G06F16/903 , G06F16/9032 , G06F16/906 , G16H10/60 , G16H50/70
CPC分类号： G16H10/60 , G06F16/14 , G06F16/148 , G06F16/24 , G06F16/245 , G06F16/2455 , G06F16/33 , G06F16/3331 , G06F16/334 , G06F16/35 , G06F16/83 , G06F16/835 , G06F16/903 , G06F16/9032 , G06F16/90335 , G06F16/906 , G16H50/70
摘要： Some embodiments are directed to a requesting device and a data device configured for multi-party computation to select a close record from a database. The data device performs a filtering of its candidate records by selecting candidate records from the database for which a received set of similarity values for a target record are close to a set of similarity values for a candidate record. For one or more selected candidate records, the requesting device and the data device performing a multiparty computation protocol to jointly compute a second closeness measure between the target record and the selected candidate record.

10. 发明授权

US12064300B2 Method and system for magnetorheological control of personal care device orifices 有权
公开(公告)号：US12064300B2
公开(公告)日：2024-08-20
申请号：US17637034
申请日：2020-08-19
申请人： KONINKLIJKE PHILIPS N.V.
发明人： Richard William Liptak , Anandh Balakrishnan
IPC分类号： A61C17/02 , A61C1/00 , B05B1/30
CPC分类号： A61C1/0015 , A61C17/02
摘要： A nozzle (14) for use with a personal care device (10), comprising: (i) a nozzle housing (50/52) defining a central channel (54) through which a stream of liquid and/or air is directed, and comprising a housing orifice (56) at the end of the central channel; (ii) a magnetorheological liquid housing (58) located over at least a portion of the nozzle housing at the housing orifice, and comprising a tip with an adjustable diameter orifice (59) through which the stream of liquid and/or air exits, wherein the adjustable orifice is adjustable between at least a first diameter and a second diameter; and (iii) one or more magnets (62) configured to control magnetorheological liquid (60) in the magnetorheological liquid housing to adjust between the at least first diameter and second diameter of the adjustable diameter orifice.

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