A method for predicting simulated patient admissions, comprising: receiving healthcare records for a plurality of patients; adapting the received healthcare records to a common data format; parameterizing the adapted healthcare records to generate a plurality of patient parameters comprising for each patient a day of the week admission parameter, a time of day admission parameter, and a patient type parameter; generating a length of stay parameter for each of the plurality of different patient types; generating a transition probability for each of the plurality of different patient types; predicting, for a time period in the healthcare environment, patient admissions; predicting a care pathway for some or all of the predicted patient admissions during the time period; and reporting, via a user interface, the predicted patient admissions and predicted care pathways.
G16H 40/20 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
A cradle style cushion includes a central sealing body portion including a front wall, a rear wall, a top wall and a bottom wall. The top wall includes a central sealing surface, a first stabilizing surface and a second stabilizing surface, the first and second stabilizing surfaces each extending upwardly and outwardly with respect to the central sealing surface and a top edge of the front wall and being structured to wrap around and engage an outside of the nostrils when the patient interface device is donned by the patient, wherein the first stabilizing surface includes a first front side edge portion and the second stabilizing surface includes a second front side edge portion, and wherein the top edge of the front wall, the first front side edge portion and the second front side edge portion together define a front opening of the central sealing body portion.
A diaphragm for a breast pump comprises a cavity having an open end for receiving a nipple of a user and a closed end. A valve closure element is provided for forming part of a valve, the valve closure element extending from a bottom edge of the open end controlling a flow path to a milk container through a first part of a container opening. The diaphragm also defines a lid for sealing a second part of the container opening. In this way, the container can have a large lid opening, and the diaphragm seals one part of the opening as well as defining a fluid path through a valve to another part of the opening.
A catheter (200) includes a jacket (110), a chamber (120) and an adjustable material (230). The jacket (110) has a first stiffness and includes an outer surface (112) and an inner surface (114). The chamber (120) is enclosed within the inner surface (114). The adjustable material (230), when adjusted, provides the catheter (200) with a second stiffness which is stiffer than the first stiffness.
A computer-implemented method of providing guidance for a treatment procedure on an occluded vessel, is provided. The method includes: analyzing CT data to determine one or more properties of an occlusion in the vessel; determining, based on the one or more properties, a recommended intravascular treatment device for treating the occluded vessel; and outputting an indication of the recommended intravascular treatment device.
A system and method are provided for reducing radiation exposure in a procedure room using a radiation shield. The method determines first position data indicating a position of a clinician in the procedure room and determines second position data indicating a position of an imaging source of an imaging system in the procedure room. The method further applies a radiation model to estimate a radiation pattern of radiation emitted by the imaging source based on the first position data and the second position data. The method further applies a shield positioning model to predict an optimal position of the radiation shield that minimizes exposure of the at least one clinician to the emitted radiation based on the estimated radiation pattern, the first position data, and the second position data.
The present invention relates to a method, apparatus, and system for secure communication wherein an end device is adapted to: receive a first system information message from or through a first primary station, decode the first system information message and obtaining a "protection field", use the "protection field" to determine the location of "security information", and use "security information" to verify the received message and/or first primary station and/or send a subsequent secure message to the first primary station or a third primary station.
H04L 9/32 - Arrangements for secret or secure communications; Network security protocols including means for verifying the identity or authority of a user of the system
9.
METHODS AND SYSTEMS FOR PREDICTING BASELINE CREATININE VALUES
A method (100) for determining a baseline creatinine value for a subject, comprising: obtaining (130) a set of features about the subject; analyzing (140), using a trained baseline creatinine determination model, the obtained set of features to generate a baseline creatinine value for the subject; reporting (150), via a user interface, the generated baseline creatinine value for the subject.
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
An X-ray detector (100) includes a pixelated array (110) of X-ray detector elements (130i,j) configured to determine detection times of received X-ray quanta from detection events representing the received X-ray quanta; and a processor (120) estimates an amount of scattered X-ray quanta received by the X-ray detector elements (130i,j) based on a count of pairs of detection events detected within a predetermined time interval of each other by adjacent X-ray detector elements (130i,j, 130i,j(a . . . h)) in the pixelated array (110).
The present invention relates to a method (1), resp. a device, system and computer-program product, for material decomposition of spectral imaging projection data. The method comprises receiving (2) projection data acquired by a spectral imaging system and reducing (3) noise in the projection data by combining corresponding spectral values for different projection rays to obtain noise-reduced projection data. The method comprises applying (6) a first projection-domain material decomposition algorithm to the noise-reduced projection data to obtain a first set of material path length estimates, and applying (7) a second projection-domain material decomposition algorithm to the projection data to obtain a second set of material path length estimates. The second projection-domain material decomposition algorithm comprises an optimization that penalizes a deviation between the second set of material path length estimates being optimized and the first set of material path length estimates.
Systems, methods, and apparatuses for confidence mapping of shear wave measurements are disclosed. Confidence maps of shear wave image measurements may be generated from one or more confidence factors. Masking of graphical overlays of tissue stiffness values, based at least in part on the confidence map is disclosed. The confidence map and/or masked graphical overlays of tissue stiffness values may be superimposed on ultrasound images and provided on a display.
Devices (110,120) and methods are described to establish secure communication between a first and a second device over a physical channel according to a security protocol. The protocol establishes first integrity data in the first device and second integrity data in the second device. The protocol has at least two security levels. The applied security level is selectable based on grading information transferred via the physical channel. Advantageously, a grading indicator indicative of a minimum security level as minimally required in at least one of the first device (110) and second device (120) is transferred via the physical channel, while integrity protection of the grading indicator is provided based on the integrity data. Thereby, a man-in-the-middle attack by a further device (130) to downgrade the security level may be prevented.
Systems and apparatuses for lead extraction using a lead locking device are provided. The apparatus includes a lead extraction assistance device for use with a lead locking device (LLD) in a lead extraction procedure, the apparatus includes a lead locking device (LLD); a lead locking assist device coupled to the LLD wherein the lead locking assist device includes an assembly configured with a center shaft that has an inlet that for entry of the lead (10) and configured with an outlet for exiting the LLD wherein the assembly clamps both an entered lead and an exited LLD; and a module disposed in the assembly and coupled to both the entered lead and the exited LLD, the module configured to apply, a first action by a rotational motor (60) to twist the entering lead and a second action by a hammering device (87) for hammering the entered lead to assist in pulling out the lead.
A system and method for achieving more accurate results when applying an image processing task to a series of medical images of a patient, without significantly increasing processing resource. The proposed system and method is based on receiving a plurality of image sequences of a particular anatomical region, each capturing cyclical movement of an anatomical object. Each image sequence is supplied to a classifier module which employs use of one or more machine learning algorithms to derive at least one score for each image sequence indicative of predicted success or quality of a result of the image processing task if applied to the given image series. This permits an assessment to be made in advance of which of the plurality of image series is most likely to result in the best (e.g. highest quality, or greatest amount of information) results from the image processing task. This allows maximization of the quality of image processing results, without the need to actually process each of the image series with the image processing task, which would consume a large amount of processing resource and consume time.
G06V 10/764 - Arrangements for image or video recognition or understanding using pattern recognition or machine learning using classification, e.g. of video objects
The invention relates to a method for operating a communication system including a primary station linked to a Core Network, said primary station serving a cell, a relay station served by the primary station and a secondary station served by the primary station, the method comprising the steps of the relay station establishing a connection with the primary station, including receiving in at least one first secure message from the primary station a first set of configuration parameters, the secondary station establishing a connection with the primary station, including receiving from the primary station in at least one second secure message a second set of configuration parameters linked to an upcoming data session, the relay station transmitting at least one transmitted service code from the first set, the secondary station establishing a direct communication with the relay station upon determination that the transmitted configuration parameters is included in the second set.
A system (10) for positioning a sensor patch on a user is provided, the system comprising a band (20) for creating a pressing force to the sensor patch when the band is stretched, the band comprising a stretchable part (22), and a first marker (25) located on the stretchable part, and a non- stretchable element (30), having a second marker (35), wherein the non-stretchable element (30) is a ribbon, mounted on the band (20) with a connector (55) or an elastic joint (51b) at one end and an elastic joint (51, 51a) at the other end, the ribbon even when taut, permitting the stretching of the band, and wherein a relative position of the first and second marker indicates an amount of stretch of the stretchable part. The user guided by the relative position of the first (25) and second (35) markers may take actions for the stretchable part (22) of the band to reach a desired stretch, which corresponds to a desired pressing force to the sensor patch. A corresponding method (100) for positioning a sensor patch on a user is also provided.
A61B 5/256 - Wearable electrodes, e.g. having straps or bands
G01L 5/04 - Apparatus for, or methods of, measuring force, work, mechanical power, or torque, specially adapted for specific purposes for measuring tension in flexible members, e.g. ropes, cables, wires, threads, belts or bands
G01L 5/06 - Apparatus for, or methods of, measuring force, work, mechanical power, or torque, specially adapted for specific purposes for measuring tension in flexible members, e.g. ropes, cables, wires, threads, belts or bands using mechanical means
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
18.
MEDICAL IMAGE ACQUISITION UNIT ASSISTANCE APPARATUS
The present invention relates to a medical image acquisition unit assistance apparatus (10), the apparatus comprising: - at least one sensor (20); and - a processing unit (30); wherein one or more sensors of the at least one sensor is configured to acquire sensor data of a person observing a patient undergoing a medical scan by a medical image acquisition unit; wherein the one or more sensors is configured to provide the acquired sensor data of the person observing the patient undergoing the medical scan to the processing unit; wherein the processing unit is configured to determine a state of the person observing the patient undergoing the medical scan comprising utilization of the acquired sensor data of the person observing the patient undergoing the medical scan; wherein the processing unit is configured to determine an overall state of the patient comprising utilization of the determined state of the person.
A method for retrieving relevant images from an image database based on converting linguistic search criteria into image-based search criteria. User inputs are used to construct a base image from a combination of pre-formed graphical or visual image elements, and an image database is then queried with the base image using image-based searching. The resulting retrieved images may be exported to a user training system for use in training a user using the images.
A system (200) for providing guidance information for an implantable device extraction procedure, is provided. The system includes one or more processors (210) configured to: receive (S 110) attenuation data (110) representing an implantable device (120) in an anatomical region, the attenuation data defining X-ray attenuation within the anatomical region; analyze (S120) the attenuation data (110) to determine an amount of adhesion (130) between the implantable device (120) and a tissue (140) contacting the implantable device; and output (S130) guidance information for the implantable device extraction procedure based on the amount of adhesion (130).
A61B 6/12 - Devices for detecting or locating foreign bodies
A61B 6/00 - Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
A61N 1/05 - Electrodes for implantation or insertion into the body, e.g. heart electrode
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
21.
MAGNETO-MECHANICAL RESONATORS WITH REDUCED MUTUAL ATTRACTION
A system for monitoring and/or diagnosing the transit through the gastro-intestinal tract of a mammal, such as a human is described. The system comprises a micromechanical resonator (MMR) device and a tracking system. The sensing device comprises a casing and a first magnetic object with a permanent magnetic moment, wherein the first magnetic object is coupled to the casing in such a way, that it is configured for oscillating around an equilibrium position when excited by a magnetic or an electromagnetic excitation field and wherein the tracking system comprises at least one coil for generating the magnetic or electromagnetic excitation field configured for detecting the magnetic response field generated by the sensing device.
A computer-implemented method of providing biomechanical plaque data (110) for an interventional device simulation system (100) includes: extracting plaque data from spectral CT data, the plaque data representing a spatial distribution of plaque (140) within a vascular region (130); converting the plaque data into biomechanical plaque data (110), the biomechanical plaque data representing a spatial distribution of a mechanical constraint to apply to an interventional device (150) of the interventional device simulation system (100) in response to a contact between the interventional device (150) and the plaque (140); and outputting the biomechanical plaque data (110).
An input data preprocessor (IDP) and related methods for facilitating image segmentation. The preprocessor may comprise an input port (IN) for receiving an input image to be segmented by an interactive machine learning based segmentor (SEG). A subset specifier (SS) determines, based on the input image, a size specification (b) for an in-image subset. An output interface (OUT) passes the size specification to a user interface (UI) for interaction with the segmentor (SEG). The proposed input data preprocessor (IDP) may preferably be used in interactive segmentation, to reduce the number of iteration cycles.
Proposed concepts aim to provide schemes, solutions, concepts, designs, methods and systems pertaining to the transmitting, receiving and/or communicating medical imaging data for remote real-time examination. In particular, a medical image is encoded (120) with an identifier based on at least part of metadata associated with the medical image. As the medical image and the metadata may have different transmission requirements (i.e. bandwidth, latency, loss, etc.), they are communicated through different communication channels (130, 140). In this way, the medical image and the metadata may be communicated appropriately, while the identifier enables the medical image and the metadata to be matched at a receiver.
An apparatus estimates vital signs of a person from video images with color channels representing a digitization of optical sensor signals. A first detector (203) detects a first image area being a skin area of the person and a second detector (205) detect a second image area corresponding to a different area of the person than the first image area. A determiner (207) determines color channel distributions for pixels of the first image area. A processor (209) provides a skin tone indication and a reference processor (211) provides a reference color channel distribution property for the skin tone. A gain processor (213) determines gains for the optical sensor signals in dependence on a luminance property of the second image area and on a comparison of the reference distribution property and a property of the color channel distributions. A gain controller (215) accordingly controls gain values applied to the optical sensor signals and a vital sign determiner (217) estimates a vital sign property for the person from the images.
09 - Scientific and electric apparatus and instruments
10 - Medical apparatus and instruments
35 - Advertising and business services
41 - Education, entertainment, sporting and cultural services
42 - Scientific, technological and industrial services, research and design
44 - Medical, veterinary, hygienic and cosmetic services; agriculture, horticulture and forestry services
Goods & Services
Apparatus and instruments for accumulating and storing electricity; batteries; battery packs; batteries for use in defibrillators; battery packs for external defibrillators; defibrillator batteries and chargers therefor; electronic devices in the nature of adaptors, connector cables, electric cables and USB cables used with defibrillators; electrodes; software; software application for medical apparatus; downloadable mobile software applications in relation with defibrillators; mobile phone software applications, downloadable; measuring, signaling, checking, safety, instructional and life saving equipment and apparatus. Medical apparatus and instruments; apparatus and instruments for resuscitation; defibrillators; wearable defibrillators; automated external defibrillators; electrodes for use with defibrillators; defibrillator electrode cartridges; defibrillator electrode pads; defibrillator monitors; medical cardiac defibrillator; cardiac electrodes; cardiac defibrillation electrodes. Retail services, wholesale services and marketing services, including the importing, wholesaling, retailing, selling and marketing of defibrillators and components, parts and accessories for defibrillators; the wholesaling, retailing and marketing of services related to CPR and life support and to training related to CPR and life support. Training services including teaching and instructional services, all being related to or connected with life support, life saving (including without limitation defibrillation and resuscitation), safety and therapy. Scientific research and advice, industrial research and advice, health research and advice; health equipment and service information services, therapy information services, medical and paramedical information services, quality assurance information services. Provision of information all being related to or connected with life support, life saving (including without limitation defibrillation and resuscitation), safety and therapy; guidance and advice all being related to or connected with life support, life saving (including without limitation defibrillation and resuscitation), safety and therapy.
09 - Scientific and electric apparatus and instruments
10 - Medical apparatus and instruments
35 - Advertising and business services
41 - Education, entertainment, sporting and cultural services
42 - Scientific, technological and industrial services, research and design
44 - Medical, veterinary, hygienic and cosmetic services; agriculture, horticulture and forestry services
Goods & Services
Apparatus and instruments for accumulating and storing electricity; batteries; battery packs; batteries for use in defibrillators; battery packs for external defibrillators; defibrillator batteries and chargers therefor; electronic devices in the nature of adaptors, connector cables, electric cables and USB cables used with defibrillators; electrodes; software; software application for medical apparatus; downloadable mobile software applications in relation with defibrillators; mobile phone software applications, downloadable; measuring, signalling, checking, safety, instructional and life saving equipment and apparatus. Medical apparatus and instruments; apparatus and instruments for resuscitation; defibrillators; wearable defibrillators; automated external defibrillators; electrodes for use with defibrillators; defibrillator electrode cartridges; defibrillator electrode pads; defibrillator monitors; medical cardiac defibrillator; cardiac electrodes; cardiac defibrillation electrodes. Retail services, wholesale services and marketing services, including wholesaling, retailing and marketing of defibrillators and components, parts and accessories for defibrillators and Import services of defibrillators and components, parts and accessories for defibrillators; business intermediary services in the field of rendering services related to CPR and life support and to training related to CPR and life support. Training services including teaching and instructional services, all being related to or connected with life support, life saving (including without limitation defibrillation and resuscitation), safety and therapy. Scientific research and advice, industrial research and advice; health equipment and service information services, therapy information services, medical and paramedical information services, quality assurance information services. medical services; medical assistance; health care services; providing medical information; therapy services; medical equipment rental; medical information regarding health equipment.
28.
INSTANTLY GELLING COMPOSITIONS FOR ARTIFICIAL SALIVA AND ULTRASOUND GELS
A method (100) for generating an instantly-formed artificial saliva gel or an ultrasound gel, comprising: (i) providing (110) a first composition comprising a pH-sensitive polymer, wherein the first composition is maintained at an acidic pH; (ii) providing (110) a second composition comprising a pH agent configured to maintain the second composition at an alkaline pH; and (iii) combining (120) the first composition and the second composition to generate a single instantly-formed gel, wherein the pH of the single instantly-formed gel is at a level required to increase viscosity of the pH-sensitive polymer to a level suitable for an artificial saliva gel or an ultrasound gel; wherein either the first composition or second composition comprises a solvent, and wherein the acidic pH of the first composition and the alkaline pH of the second composition are configured such that the pH of the single instantly-formed gel is between approximately 6.5 and 7.5.
A mechanism for synthesizing additional points for generating an anatomical model of an anatomical cavity. The additional points are positioned to lie partway between points directly derived from respective electrical responses of an interventional device positioned within the anatomical cavity.
G16H 50/50 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for simulation or modelling of medical disorders
A61B 34/10 - Computer-aided planning, simulation or modelling of surgical operations
30.
METHOD, APPARATUS AND COMPUTER PROGRAM PRODUCT FOR ANALYSING A PULSE WAVE SIGNAL TO DETERMINE AND INDICATION OF BLOOD PRESSURE AND/OR BLOOD PRESSURE CHANGE
According to an aspect, there is provided a computer-implemented method for analysing a pulse wave signal, PWS, obtained from a subject to determine an indication of the blood pressure or a change in blood pressure of the subject. The PWS comprises pulse wave measurements for a plurality of cardiac cycles of the subject during a first time period. The method comprises (i) analysing (111) the PWS to determine a first average cardiac cycle waveform for a first time point in the first time period and a second average cardiac cycle waveform for a second time point in the first time period; (ii) determining (113) a difference signal representing a change in morphology from the first average cardiac cycle waveform to the second average cardiac cycle waveform; (iii) determining (115) an absolute value of the change in morphology from the difference signal; (iv) determining (117) a direction of the change in morphology; and (v) determining (119) a relative blood pressure change by combining the absolute value and the direction of the change in morphology.
A system is provided for determining the position of an interventional device inside a lumen. The interventional device comprises a distal portion inside the lumen and a proximal portion outside the lumen and the system comprises a processor. The processor is configured to receive a first estimated position of the distal portion of the interventional device inside the lumen from a first system and receive an estimated displacement of the distal portion of the interventional device inside a lumen from a second system, wherein the estimated displacement is representative of the movement of the distal portion of the interventional device inside the lumen. The processor is further configured to determine a second estimated position of the distal portion of the interventional device inside the lumen based on the first estimated position and the estimated displacement.
An expression assembly for breast pump comprises a diaphragm, a cover over the diaphragm to define a sealed space between them, and a breast shield to which the cover and diaphragm are coupled. The diaphragm defines a cavity having an open end for receiving a nipple of a user and a closed end. The open end is angled back at the top to cover more of the top of the breast. This enables the diaphragm to provide better stimulation of the breast as well reducing leakage.
A first responder network is a network that is used by first responders for communicating between devices typically used by first responding officers. An MCI describes an incident in which emergency medical services are overwhelmed by the number and severity of casualties. A wireless communication system for first responder networks is proposed that can securely register (onboard) a variety of wireless devices to ensure a quicker response time in the MCI area. Existing wireless devices belonging to both triage officers and casualties in the MCI area can automatically be registered to a first responder network to enhance coverage in the MCI area. Expansion of a wireless infrastructure of the first responder network can be enabled by securely registering alien central nodes (e.g., base stations) on an on-demand basis.
A system for processing voice audio includes a local device and a remote personal health data ecosystem. The local device includes (1) a local speech-to-text transcriber configured to generate voice text based on voice audio spoken by a user; (2) a local NLP configured to extract spoken phrases from the voice text; and (3) an ML classifier configured to classify the voice audio as either personal health or non-personal health voice audio. The remote personal health data ecosystem includes (1) a remote speech-to-text transcriber configured to generate personal health voice text based on the personal health voice audio; (2) a remote NLP configured to extract personal health spoken phrases from the personal health voice text; (3) a text response generator configured to generate a text response based on the personal health spoken phrases; (4) a text-to-speech translator configured to generate a voice response based on the text response.
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G10L 13/02 - Methods for producing synthetic speech; Speech synthesisers
G10L 15/18 - Speech classification or search using natural language modelling
G10L 15/22 - Procedures used during a speech recognition process, e.g. man-machine dialog
G10L 15/30 - Distributed recognition, e.g. in client-server systems, for mobile phones or network applications
Disclosed in some embodiments are microdevices, medical devices and a registration apparatuses that allow for tracking of medical device(s) in an ultrasound image while maintaining the quality of the ultrasound image. The microdevice comprises a casing and a magneto mechanical resonator. The magneto mechanical resonator comprises at least two magnetic objects providing a permanent magnetic moment. The magneto mechanical resonator is adapted to transduce an external excitation field into a mechanical movement of the at least two magnetic objects relative to each other such that a changing magnetic response field is generated. A pressure sensor is arranged such that an external ultrasound signal induces an additional movement of the magnetic objects such that the changing magnetic response field is changed in dependency of the external ultrasound signal.
An ultrasound imaging system may acquire an image of a liver. The liver may be segmented from the image. Parameters, such as image homogeneity map, intensity probability chart, and/or speckle size diagram, may be extracted from the liver portion of the image. The parameters may be used to determine whether fatty liver deposits are diffuse or inhomogeneous. In some examples, inhomogeneous regions may be excluded from the calculation of liver fat quantification measurements. In some examples, the inhomogeneous regions may be displayed so that a user may select a region of interest that excludes the inhomogeneous regions to calculate the liver fat quantification measurements.
G06V 10/764 - Arrangements for image or video recognition or understanding using pattern recognition or machine learning using classification, e.g. of video objects
A61B 8/08 - Detecting organic movements or changes, e.g. tumours, cysts, swellings
G06V 10/22 - Image preprocessing by selection of a specific region containing or referencing a pattern; Locating or processing of specific regions to guide the detection or recognition
G06V 10/26 - Segmentation of patterns in the image field; Cutting or merging of image elements to establish the pattern region, e.g. clustering-based techniques; Detection of occlusion
G06V 10/50 - Extraction of image or video features by summing image-intensity values; Projection analysis
G06V 10/82 - Arrangements for image or video recognition or understanding using pattern recognition or machine learning using neural networks
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
37.
COUPLING ELECTRICAL SIGNALS ACROSS AN ELECTRICALLY INSULATING BARRIER
A system for coupling electrical signals between an interventional device (110) and a control unit (120) through an electrically insulating barrier (130), is disclosed. The system includes a connector (140). A device connector portion (140′) of the connector (140) includes at least one transmitter (160) that transmits electrical signals representing i) transducer signals and 5 ii) synchronisation signals for the transducer signals. The transducer signals are generated at a distal portion (110″) of the interventional device (110), and the synchronisation signals are generated at a distal portion (110″) of the interventional device or in the device connector portion (140′). A control unit connector portion (140″) of the connector (140), or the control unit (120), receives the electrical signals, extracts the transducer signals and the 10 synchronisation signals from the electrical signals, and performs a timing correction on the transducer signals using the synchronisation signals.
An apparatus includes an intraluminal dilator with a flexible elongate member and a balloon. The flexible elongate member can be positioned within a body lumen. The flexible elongate member includes a first diameter. The balloon includes an unexpanded state and an expanded state. In the expanded state, the balloon includes a second diameter larger than the first diameter and a leading edge including a length between a first portion coupled to the flexible elongate member and a second portion with the second diameter. The leading edge extends at an angle between the first diameter and the second diameter. The balloon can engage an anatomical wall along the leading edge as the intraluminal dilator moves through an opening in the anatomical wall to enlarge the opening such that the second portion of the balloon engages the anatomical wall only after the first portion of the balloon has engaged the anatomical wall.
System and related method for medical image processing, comprising an input interface (IN) through which is receivable input data. The input data included spectral input imagery of a part of a vascular system (VS) of a patient (PAT). The spectral input imagery is based on data reconstructable from projection data acquired by a spectral imaging apparatus of the tomographic type, with presence of contrast agent in the part of the vascular system. A predictor module (PM) of the system is configured to predict, based on the input imagery, an increase or decrease in flow caused by presence of contrast agent. An output interface (u-OUT) provides output data indicative of the predicted flow increase or decrease.
An intraluminal device includes a flexible elongate member configured to extend within a body lumen of a patient, and a sensor disposed at a distal region of the flexible elongate member, and is configured obtain intraluminal data associated with the body lumen. A housing at least partially surrounds the sensor. A spacer is located between a portion of the sensor housing and a proximal face of the sensor, and includes: a base; a through-hole extending through the base; a recess disposed distal of the base and surrounded at least partially by a side wall; a plurality of support ledges projecting from the side wall and configured to contact the proximal surface of the sensor; and at least one retention feature extending distally from at least one support ledge of the plurality of support ledges and configured to contact a side surface of the sensor.
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
A61B 1/05 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances characterised by the image sensor, e.g. camera, being in the distal end portion
41.
PATIENT MONITOR COMPRISING ONE OR MORE UNIVERSAL PORTS
The present invention relates to a patient monitor (10) comprising one or more universal ports (12) each configured to connect a cable having a universal connector (36) fitting into a universal port (12) for providing a measurement signal from a subject (30) to the patient monitor (10), wherein the patient monitor (10) comprises a selection unit (14), a distribution network (16), an analog front end unit (18) and one or more processing units (20).
An intravascular lesion crossing device (10) includes a guidewire support catheter (12) having a guidewire lumen (14) configured to receive an associated guidewire (16) for delivery of a distal end (18) of the guidewire support catheter to an occlusion in a blood vessel; and a helical profile (20) provided at an outer surface of the distal portion of the guidewire support catheter.
Proposed concepts thus aim to provide schemes, solutions, concept, designs, methods and systems pertaining to updating a magnetic field (B0) map of a subject during a magnetic resonance imaging (MRI) examination or during image reconstruction. In particular, when a subject moves, the magnetic field inside the magnetic bore changes. As a result, any B0 map obtained prior to the movement of the subject may be inaccurate. Accordingly, an initial B0 map is updated to reflect changes in the B0 map caused by the movement of the subject. This can be achieved by determining a B0 map of the subject based on a B0 prediction model, instead of spending additional scanning time to acquire another B0 map.
The present disclosure provides a medical system (100) comprising at least one data processing unit (111, 121, 130), a mechanical ventilator (110), configured to be operated to cause a ventilation status at a to-be-ventilated subject, and a medical imaging device (120), configured as a mobile device. The at least one data processing unit (111, 121, 130) is configured to obtain, from the mechanical ventilator (110), ventilation status information associated with the ventilation status of the to-be-ventilated subject. Further, the at least one data processing unit (111, 121, 130) is further configured to trigger acquisition of a first image if the ventilation status meets a first image acquisition criterion. Furthermore, the at least data processing unit (111, 121, 130) is further configured to trigger acquisition of at least one subsequent, further image if the ventilation status meets a second image acquisition criterion.
G16H 20/40 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
G16H 30/20 - ICT specially adapted for the handling or processing of medical images for handling medical images, e.g. DICOM, HL7 or PACS
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
A method for localizing structural connectivity biomarkers in neurological diseases, includes dividing a diffusion magnetic resonance imaging brain volume into a set of connected brain regions; extracting three-dimensional voxels along fiber connections which structurally connect the connected brain regions, wherein the brain regions comprise bundles of neurons; applying a deep neural network to diffusion magnetic resonance imaging features extracted from the three-dimensional voxels for each set of fiber connections which structurally connect brain regions; outputting a disease classification based on applying the deep neural network; and applying multi-instance learning to predict whether each fiber connection is indicative of a healthy brain or a diseased brain.
G06T 7/73 - Determining position or orientation of objects or cameras using feature-based methods
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
46.
PARAMETRIC STEREO UPMIX APPARATUS, A PARAMETRIC STEREO DECODER, A PARAMETRIC STEREO DOWNMIX APPARATUS, A PARAMETRIC STEREO ENCODER
A parametric stereo upmix method for generating a left signal and a right signal from a mono downmix signal based on spatial parameters includes predicting a difference signal comprising a difference between the left signal and the right signal based on the mono downmix signal scaled with a prediction coefficient. The prediction coefficient is derived from the spatial parameters. The method further includes deriving the left signal and the right signal based on a sum and a difference of the mono downmix signal and said difference signal.
H04S 5/00 - Pseudo-stereo systems, e.g. in which additional channel signals are derived from monophonic signals by means of phase shifting, time delay or reverberation
G10L 19/008 - Multichannel audio signal coding or decoding using interchannel correlation to reduce redundancy, e.g. joint-stereo, intensity-coding or matrixing
H04S 3/02 - Systems employing more than two channels, e.g. quadraphonic of the matrix type, i.e. in which input signals are combined algebraically, e.g. after having been phase shifted with respect to each other
47.
SYSTEMS AND METHODS FOR PLANNING CORONARY INTERVENTIONS
A method and system are provided for planning a medical intervention, such as a coronary intervention. At least one image is retrieved, where the image includes at least a portion of a coronary artery. Based on the at least one image, a position and composition of plaque in the coronary artery are determined. A mechanical model of the portion of the coronary artery and the plaque in the coronary artery is generated, and a plurality of potential interventions is simulated in the context of the mechanical model. Following such simulations, an intervention for implementation is selected from the plurality of potential interventions.
Image processing system (SYS) and related method for image-based sliding interface detection. The system comprises an input port (IN) for receiving two medical input images (I1, I2), previously acquired at different times of a patient (PAT) during sliding motion of one anatomical features (AF1, AF2) of the patient against one other of the two anatomical features (AF1, AF2). The sliding motion defines a sliding interface (SI). A sliding motion evaluator (SME) applies a registration algorithm to compute a series of metric maps that are configured to respond to the sliding motion by varying the values of a parameter of the algorithm. A sensitivity analyzer (SA) computes a sensitivity map that represents the variation in the series of metric maps as a function of the values of the said parameter. A sliding interface detector (SD) detects, based on the sensitivity map, an image-based location of a representation of the sliding interface.
G06V 10/46 - Descriptors for shape, contour or point-related descriptors, e.g. scale invariant feature transform [SIFT] or bags of words [BoW]; Salient regional features
G06T 3/00 - Geometric image transformation in the plane of the image
49.
A MEDICAL MICRODEVICE AND REGISTRATION APPARATUS FOR REGISTERING AN ULTRASOUND SYSTEM AND A LOCALIZATION SYSTEM OF THE MICRODEVICE
Disclosed are a medical microdevice, a medical device and a registration apparatus that allow for tracking a medical device in an ultrasound image while maintaining the quality of the ultrasound image. The microdevice comprises a casing and a magneto mechanical resonator. The magneto mechanical resonator comprises at least two magnetic objects providing a permanent magnetic moment. The magneto mechanical resonator is adapted to transduce an external excitation field into a mechanical movement of the at least two magnetic objects relative to each other such that a periodically changing magnetic response field is generated. A pressure sensitive element is arranged such that an external ultrasound signal induces an additional movement of the magnetic objects such that the periodically changing magnetic response field is changed in dependency of the external ultrasound signal.
A61B 34/20 - Surgical navigation systems; Devices for tracking or guiding surgical instruments, e.g. for frameless stereotaxis
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
A61B 17/00 - Surgical instruments, devices or methods, e.g. tourniquets
50.
ACCELERATED SESSION RESUMPTION ON LOAD-BALANCED NETWORK SERVICES
The invention relates to a method and apparatus for increasing likelihood of a device being able to resume a previously established session (e.g., a transport layer security session) with a load-balanced network service (e.g., a cloud service) which may only support load balancing at node level. This can be achieved by maintaining one or more network addresses and valid session tickets (or identifiers) of individual nodes (e.g., servers) of the network service, that were used for previous communication sessions and by selecting a particular node for a subsequent communication session from a list of potential nodes returned by an address lookup (e.g., a domain name system (DNS) lookup), based on its match with one of the one or more network addresses and session tickets or identifiers.
H04L 67/145 - Termination or inactivation of sessions, e.g. event-controlled end of session avoiding end of session, e.g. keep-alive, heartbeats, resumption message or wake-up for inactive or interrupted session
H04L 67/146 - Markers for unambiguous identification of a particular session, e.g. session cookie or URL-encoding
H04L 67/1027 - Persistence of sessions during load balancing
A mechanism for generating a position space anatomical model of an anatomical cavity. Electrical responses, of an electrode positioned within the anatomical cavity, are obtained. A response space anatomical model is constructed based on the electrical responses. The response space anatomical model is then converted into a position space anatomical model using a mapping function.
G16H 50/50 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for simulation or modelling of medical disorders
A61B 5/367 - Electrophysiological study [EPS], e.g. electrical activation mapping or electro-anatomical mapping
G06T 17/20 - Wire-frame description, e.g. polygonalisation or tessellation
G06T 19/20 - Editing of 3D images, e.g. changing shapes or colours, aligning objects or positioning parts
53.
SYSTEMS AND METHODS TO SELECT AND SHARE LEARNING CONTENT BASED ON SIMILAR ACTIVITIES
At least one database stores reference content. In an annotation method, an annotation to an item of the reference content is received via a user interface, an annotation context of the annotation is determined at least based on analysis of content of the annotation, and the item of the reference content is updated in the database with the annotation tagged with the annotation context. In a reference content presentation method, an item of the reference content is presented via the user interface, a presentation context of the presenting is determined, and it is determined whether a comparison of the annotation context and the presentation context satisfies a sharing filter. In response to the sharing filter being satisfied, the annotation is presented via the user interface. The annotation is not presented if the sharing filter is not satisfied.
G16H 40/40 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
G06F 21/62 - Protecting access to data via a platform, e.g. using keys or access control rules
G06F 40/117 - Tagging; Marking up ; Designating a block; Setting of attributes
G06F 40/169 - Annotation, e.g. comment data or footnotes
G06Q 10/20 - Administration of product repair or maintenance
54.
ASSESSING A SUBJECT'S ADHERENE TO A TREATMENT FOR A CONDITION
According to an aspect, there is provided a computer-implemented method (100) for assessing a subject's adherence to a treatment for a condition, the method comprising receiving (102) adherence data indicative of the subject's past adherence to the treatment; receiving (104) medical data indicative of physiological details and a medical history of the subject; determining (106), based on the received adherence data, a non-adherence risk score indicative of a likelihood that the subject will not adhere to the treatment within a defined time period in the future; determining (108), based on the medical data, an adverse event risk score indicative of a likelihood that the subject will experience an adverse medical event; determining (110), based on the non-adherence risk score and the adverse event risk score, a priority classification to be assigned to the subject; and generating (122), based on the priority classification, an instruction signal to be delivered to a recipient
G16H 50/30 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for individual health risk assessment
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
G16H 20/30 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
A mobile device being a member of a communication group and configured to communicate with one or more other members of the communication group and to exchange control information with the one or more other members, wherein the mobile device is configured to create an identification information and to transmit the identification information on a physical layer of the control information, wherein the identification information assigns the communication group.
A capacitive micro-machined ultrasonic transducer, CMUT, device in which integrated probe circuitry includes both the ultrasound transmission and reception circuitry and a DC-DC converter for generating a bias voltage for the CMUT cell. The high voltage pulses of a pulser circuit and a high voltage DC bias voltage are both generated by a single probe circuit, which is local to the CMUT cell.
The power transmitter (101) providing power to a power receiver (105) comprises a communicator (309) communicating with the power receiver (105) and a negotiator (305) negotiating a guaranteed power level with the power receiver (105) prior to a power transfer phase. The guaranteed power level is a minimum power level guaranteed by the power transmitter (101) throughout the power transfer phase. During the power transfer phase, a determiner (307) dynamically determines an available power level based on the prevailing operating parameters. The available power level is one that can currently be provided but is not guaranteed. The power controller (309) is arranged to, during the power transfer phase, increase the power level above the guaranteed minimum level in response to power control messages, and to reduce the power level regardless of the power control messages in response to a detection that the power level exceeds the available power level.
H02J 50/80 - Circuit arrangements or systems for wireless supply or distribution of electric power involving the exchange of data, concerning supply or distribution of electric power, between transmitting devices and receiving devices
H02J 50/10 - Circuit arrangements or systems for wireless supply or distribution of electric power using inductive coupling
The present invention relates to a medical device movement control apparatus (10), comprising: - an input unit (20); - at least one distance sensor (30); and - a controller (40); wherein the input unit is configured to receive a required location of the medical device; wherein the input unit is configured to provide the required location of the medical device to the controller; wherein the at least one distance sensor is configured to be mounted to a medical device (50) or is configured to be integrated with the medical device; wherein the at least one distance sensor is configured to acquire distance data from the medical device for a plurality of angular directions about the medical device; wherein the at least one distance sensor is configured to provide the distance data for the plurality of angular directions about the medical device to the controller; and wherein the controller is configured to control a movement system (60) of the medical device to move the medical device from an initial location of the medical device to the required location along a route between the initial location and the required location that maintains a distance of at least a guard range distance between the medical device and one or more of objects comprising utilization of distance data for a subset of the plurality of angular directions acquired at a plurality of locations along the route.
The present invention relates to an imaging X-ray source assembly (200) with multiple filaments (FL, FS). The X-ray source assembly comprises a plurality of filaments (FL, FS, FX) configured to emit electrons when a respective current passes through the filament (FL, FS, FX); a filament transformer (T1) configured to transfer electrical energy to the plurality of filaments (FL, FS, FX); a filament driver (FD1) configured to supply electrical energy to the plurality of filaments (FL, FS, FX) via the filament transformer (T1); a plurality of switches (S1, S2, SX) each connected to a respective one of the filaments (FL, FS, FX) and configured to regulate the respective current through the respective filament (FL, FS, FX); and a control unit (CTRL) connected to the plurality of switches (S1, S2, SX) and the filament driver (FD1). The connection between the filament driver (FD1) and the control unit (CTRL) is galvanically isolated. The filament driver (FD1) is configured to provide a filament driver output signal to the control unit (CTRL), and the control unit (CTRL) is configured to control the plurality of switches (S1, S2, SX) by respective switch control signals based on the filament driver output signal.
A method (10) for improving receive sensitivity of a cMUT transducer element (32) by dynamically adjusting the bias volage (20, 26) between the transmit (12) and receive (16) phases of the drive cycle while keeping the cMUT in collapsed operation mode at all times.
A laser catheter assembly (10) includes a laser catheter (12) including a bundle of optical fibers (14); and a coupler (16) attached to a proximal end of the laser catheter. The coupler includes a connector (18) configured to mate with an associated light source; and a holding member (22) secured within the connector and having a through hole (24) positioned at an end of the channel, an end of the proximal portion of the bundle of optical fibers being disposed in the through hole, the through hole having a light input end (26) arranged to receive light from the associated light source when the connector is mated with the associated light source and a flared end (28) opposite the light input end.
A61B 18/24 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibre; Hand-pieces therefor with a catheter
A61B 17/00 - Surgical instruments, devices or methods, e.g. tourniquets
A61B 18/22 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibre; Hand-pieces therefor
A personal care system comprises a personal care device and a cleaning device. The personal care device has a motion sensor, and the cleaning device has a supporting structure for supporting the personal care device in a cleaning position for cleaning the personal care unit, and it used a cleaning device motor. The cleaning device implements a cleaning device cleaning program in response to a user action, and the personal care device implements a corresponding personal care device cleaning program in response to detection of the cleaning device cleaning program from the motion sensor signals.
B26B 19/38 - Clippers or shavers operating with a plurality of cutting edges, e.g. hair clippers, dry shavers - Details of, or accessories for, hair clippers or dry shavers, e.g. housings, casings, grips or guards
63.
IDENTIFIABLE ANTI-SCATTER GRID FOR A RADIOGRAPHIC IMAGING DEVICE
The present invention provides methods and devices for making an anti-scatter grid for a radiographic imaging device identifiable. A method for providing an anti-scatter grid (100) for a radiographic imaging device comprises forming, by an additive manufacturing process, a grid pattern (110) in accordance with a product specification of the anti-scatter grid (100) to be provided; and forming, by an additive manufacturing process, a number of structural modifications (121) in or at the grid pattern in a manner making the number of structural modifications (121) image-based recognizable when the anti-scatter grid (100) is viewed according to its intended use in a viewing direction from a radiation source of the radiographic imaging device, and in a unique identification pattern (120) creating a unique identifier to make the anti-scatter grid to be provided identifiable among one or more others.
A method (100) for managing an organization's compliance, comprising: (i) receiving (120) information about the organization's assets; (ii) receiving (130) a compliance requirement for a business facet of the organization; (iii) generating (140), from the compliance requirement, one or more of a rule and a workflow; (iv) parsing (150) each of the assets into a parsed asset; (v) analyzing (160) the business facet; (vi) identifying (170) one or more lack of compliance issues based on the analysis, wherein a lack of compliance issue comprises a determination that the business asset fails to utilize the asset according to the rule and/or workflow; (vii) prioritizing (180), when multiple lack of compliance issues are identified, the multiple lack of compliance issues into a prioritized list based on one or more prioritization rules; and (viii) reporting (190) the one or more lack of compliance issues for the business facet to a user via a user interface.
A method of administering sleep consolidation therapy to a patient to treat a sleep disorder of the patient. The method includes monitoring, via a first number of sensors, a number of characteristics and/or activities of the patient during a number of wake periods of the patient. The method further includes determining, at least in-part from the monitoring of the number of wake periods, a recommended bedtime for the patient for starting a particular sleep period and providing the recommended bedtime for starting the particular sleep period to the patient.
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
A61B 5/11 - Measuring movement of the entire body or parts thereof, e.g. head or hand tremor or mobility of a limb
G16H 20/70 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mental therapies, e.g. psychological therapy or autogenous training
66.
ASSESSING OPERATOR BEHAVIOR DURING A MEDICAL PROCEDURE
A computer-implemented method of assessing operator behavior during a medical procedure involving medical equipment, is provided. The method includes: receiving operator interaction data representing operator interactions with the medical equipment during the medical procedure; inputting the operator interaction data into a machine-learning model; and outputting a characteristic of the operator behavior based on a position of a latent space encoding of the operator interaction data generated by the machine-learning model, with respect to a distribution of latent space encodings of training data representing operator interactions with the medical equipment having known characteristics of the operator behavior.
G16H 40/20 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
An image registration system 111 for registering a live stream of ultrasound images 112 of a beamforming ultrasound probe 113 with an X-ray image 114 is described. The image registration 111 system identifies, from the X-ray image 114, the position of a medical device 116 represented in the X-ray image 114; and determines, based on ultrasound signals transmitted between the beamforming ultrasound probe 113 and an ultrasound transducer 115 disposed on the medical device 116, a location of the ultrasound transducer 115 respective the beamforming ultrasound probe 113. Each ultrasound image from the live stream 112 is registered with the X-ray 114 image based on the identified position of the medical device 116. The registration includes determining an offset from said identified position that is based on i) a predetermined spatial relationship of the ultrasound transducer 115 respective the medical device 116 and ii) the determined location of the ultrasound transducer 115 respective the beamforming ultrasound probe 113.
Ultrasound image devices, systems, and methods are provided. An ultrasound imaging system, comprising an array of acoustic elements configured to transmit ultrasound energy into an anatomy in accordance with a first preset acquisition setting, and to receive ultrasound echoes associated with the anatomy; and a processor circuit in communication with the array of acoustic elements and configured to receive, from the array, ultrasound channel data corresponding to the received ultrasound echoes; generate a first set of beamformed data by applying a predictive network to the ultrasound channel data, wherein the first set of beamformed data is associated with a second preset acquisition setting different than the first preset acquisition setting; generate an image of the anatomy from the first set of beamformed data; and output, to a display in communication with the processor circuit, the image of the anatomy.
G01S 15/89 - Sonar systems specially adapted for specific applications for mapping or imaging
G01S 7/52 - RADIO DIRECTION-FINDING; RADIO NAVIGATION; DETERMINING DISTANCE OR VELOCITY BY USE OF RADIO WAVES; LOCATING OR PRESENCE-DETECTING BY USE OF THE REFLECTION OR RERADIATION OF RADIO WAVES; ANALOGOUS ARRANGEMENTS USING OTHER WAVES - Details of systems according to groups , , of systems according to group
A method for tracking patient recovery status following a treatment or consultation. The method is based on capturing sensor data during personal care sessions of a user, and using this to infer user pain information. For example, pain can be inferred from a biological sensor or from patterns in force/motion sensors integrated in the personal care device. The pain data can be converted into a value of a metric for each personal care session, and by trending this metric over time, patient recovery progress can be inferred. A report can be generated based on the trended metric and exported for example to a clinical practitioner.
The present disclosure is related generally to fluid flow systems, and more specifically to systems for accelerating pressure and flow capability in fluid pump systems. The fluid flow systems of the present disclosure are configured to deliver a fluid output that achieves a target pressure within an associated inflatable device within a target duration. In various embodiments, these fluid flow systems comprise a flow pathway including one or more fluid inputs and a fluid output that is connectable to the inflatable device, a first pump, and a second pump connected in series with the first pump. Also provided herein are methods of accelerating pressure and flow capability in fluid pump systems. The systems and methods described herein may find particular application in environments subjected to high magnetic field environments.
A system and method are provided for performing stiffness measurements of an anatomical structure in a patient using ultrasound shear wave elastography. The method includes acquiring multiple elastography frames from ultrasound images of the anatomical structure, where the multiple elastography frames are provided by a cine loop performed by an ultrasound imaging system; automatically identifying a preferred elastography frame of the multiple elastography frames for making stiffness measurements of the anatomical structure; automatically identifying a preferred area of the preferred elastography frame based on confidence; automatically selecting at least one region of interest (ROI) based on stiffness measurements within the preferred area of the preferred elastography frame; and measuring stiffness of the anatomical structure in the at least one ROI.
A61B 8/08 - Detecting organic movements or changes, e.g. tumours, cysts, swellings
A61B 8/00 - Diagnosis using ultrasonic, sonic or infrasonic waves
G01S 7/52 - RADIO DIRECTION-FINDING; RADIO NAVIGATION; DETERMINING DISTANCE OR VELOCITY BY USE OF RADIO WAVES; LOCATING OR PRESENCE-DETECTING BY USE OF THE REFLECTION OR RERADIATION OF RADIO WAVES; ANALOGOUS ARRANGEMENTS USING OTHER WAVES - Details of systems according to groups , , of systems according to group
72.
EVALUATION OF ARTIFACT REMOVAL FROM MAGNETIC RESONANCE IMAGES USING NEURAL NETWORKS
Disclosed herein is a medical system (100, 300). The execution of the machine executable instructions (120) causes a computational system (104) to: receive (200) a measured magnetic resonance image (124); calculate (202) a gradient-based saliency map (126) for a first output of an image-to-image neural network (122) with the measured magnetic resonance image as input to the image-to-image neural network, wherein the gradient-based saliency map is calculated using a patch based algorithm with a predetermined patch size; determine (204) an evaluation mapping (130) using at least the gradient-based saliency map; produce (206) a warning signal (134) if the evaluation mapping meets a predetermined criterion; and receive (208) an output image (128) as a second output of the measured image-to-image neural network in response to inputting the measured magnetic resonance image into the image-to-image neural network.
A computed tomography, CT, imaging system (100) includes a rotatable gantry (110), and a component (120). The component (120) is mechanically coupled to the gantry (110), and the gantry is configured to rotate the component around an axis of rotation (130). The component includes a reservoir (140) for containing a fluid, and a chamber (150). The chamber (150) is fluidically coupled to the reservoir (140), and the chamber is configured to receive bubbles (160) or particles (170) in the fluid which are forced radially (180) with respect to the axis of rotation (130) of the gantry (110) as a result of centrifugal forces acting on the fluid during the rotation of the component around the axis of rotation.
A mechanism for detecting the presence/absence of an occlusion of an anatomical cavity by an interventional device, and therefore the presence/absence of a leak around the interventional device within the anatomical cavity. A plurality of electrical measurements between different electrode pairs are obtained, each electrode pair containing a device electrode carried by the interventional device and an external electrode positioned on the subject. The electrical measurements are processed to derive an occlusion indicator.
Provided is an infant feeding equipment-sterilizing apparatus (100). The apparatus comprises a chamber (102, 104) for receiving infant feeding equipment to be steam sterilized. A vent (108) is provided for venting air and/or steam from the chamber, e.g. to atmosphere. A valve assembly (110) restricts venting via the vent during steam sterilizing and allows venting from the chamber via the vent following the steam sterilizing. The venting being allowed following the steam sterilizing may assist to dry the infant feeding equipment following the steam sterilizing. However, by the valve assembly restricting, e.g. blocking, venting from the chamber via the vent during steam sterilizing, more of the steam supplied into the chamber can be retained therein during the steam sterilizing, thereby assisting to make the steam sterilization more energy efficient. Further provided is a chamber wall portion, e.g. lid, for an infant feeding equipment-sterilizing apparatus, and a method for sterilizing infant feeding equipment using such an apparatus.
The invention relates to an electrically conducting wire, the wire (4) being formed as a flexible helix with constant or changing slope, with constant or changing diameter and with straight or curved extension, wherein the wire comprises a superconductor. In this way, a wire is provided that comprises a superconductor and that allows small bending radii, especially lower than 15 cm.
H01F 6/06 - Coils, e.g. winding, insulating, terminating or casing arrangements therefor
H01F 27/30 - Fastening or clamping coils, windings, or parts thereof together; Fastening or mounting coils or windings on core, casing, or other support
The present invention relates to providing cable guidance in an at least partly moving medical appliance. In order to provide a cable connection with less impact on the usability of the medical facility, a cable guidance (10) with a feedthrough movable along a guide rail is provided. The cable guidance comprises a cable duct (12) and a cover arrangement (14). The cable duct is extending along a longitudinal direction (DL) and comprises a cable receiving and guiding space (16). The cable duct is configured to accommodate a cable connection comprising a number of cables. The cover arrangement comprises a floor section (18) for permanently delimiting the cable duct and for forming a floor part (20). A support mechanism (22) is provided comprising a longitudinal support element (24) that is configured to support a cantilevering edge of the floor section in the region of the cable duct. The support element is configured to be partly temporarily displaced to provide a movable passageway (26) from the cable duct to a connection opening.
System (SYS) and related method for image processing, comprising an input interface (IN) to receive input data comprising i) spectral projection imagery of a region of interest including a conduit (CN) for passage of a liquid (CA), the spectral projection imagery obtainable in an imaging procedure by a spectral X-ray imagining apparatus (IA1) with contrast agent (CA) present in the liquid, and ii) additional image data acquirable by a further imaging apparatus (IA2) of the non-ionizing type, the said additional image data representative of 3D information of the conduit. A predictor component (PC) predicts based on the spectral projection imagery and the additional image data, a concentration of contrast agent in the said conduit.
Some embodiments relate to machine learnable image segmentation. An image segmentation model may be applied to a set of input images thus obtaining a corresponding set of segmentation images. Corrected segmentation images obtained from expert judgement may be used to train a further image segmentation model predicting an expected error image.
Proposed is a head component for an oral hygiene product for cleaning teeth by emitting a cleaning fluid. The head component comprises a nozzle configured, in use, to emit a burst of cleaning fluid to the teeth of user via a fluid outlet located at the end of the first nozzle. The nozzle is configured to be moveable by emitting the burst of cleaning fluid to rotate the fluid outlet from a resting position to a different, cleaning position.
A61C 17/02 - Rinsing or air-blowing devices, e.g. using fluid jets
A61C 17/028 - Rinsing or air-blowing devices, e.g. using fluid jets with intermittent liquid flow
A61C 17/36 - Power-driven cleaning or polishing devices with brushes, cushions, cups or the like reciprocating or oscillating driven by electric motor with rinsing means
: A toothbrush has a toothbrush head and a motion sensor integrated into the toothbrush for tracking a location of the toothbrush head. Brushing instructions are provided to a user while they perform tooth brushing, and the instructions are to follow a template brushing routine, which may be a real brushing routine being followed by another person or a virtual brushing routine. Brushing instructions are provided in real time for improving the correspondence between a current location in the template brushing routine and a current tracked location.
A method for obtaining an overall score indicative of the presence of a target pathology of a subject during a medical scan procedure. The method comprises acquiring images during the medical scan procedure and iteratively identifying whether a newly acquired image corresponds to one of a set of pre-determined views. For the newly acquired images which correspond to one of the pre-determined views, a predictive model is selected from a set of predictive models each trained on one or more of the pre-determined views for the target pathology. The selected predictive model is trained on the pre- determined view or multiple predetermined views that have been acquired. The newly acquired image is input into the selected predictive model and an overall score is updated, or generated using the output of the selected predictive model. The overall score is indicative of the presence of the target pathology in the subject.
G16H 30/40 - ICT specially adapted for the handling or processing of medical images for processing medical images, e.g. editing
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
83.
ASSESSING A SUBJECT'S ADHERENE TO A TREATMENT FOR A CONDITION
According to an aspect, there is provided a computer-implemented method (100) for assessing a subject's adherence to a treatment for a condition, the method comprising receiving (102) adherence data indicative of the subject's past adherence to the treatment; receiving (104) medical data indicative of physiological details and a medical history of the subject; determining (106), based on the received adherence data, a non-adherence risk score indicative of a likelihood that the subject will not adhere to the treatment within a defined time period in the future; determining (108), based on the medical data, an adverse event risk score indicative of a likelihood that the subject will experience an adverse medical event; determining (110), based on the non-adherence risk score and the adverse event risk score, a priority classification to be assigned to the subject; and generating (122), based on the priority classification, an instruction signal to be delivered to a recipient.
G16H 20/00 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
G16H 50/30 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for individual health risk assessment
G16H 50/70 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
A61B 5/0205 - Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
The invention provides a method for obtaining a measure of user pain at home. The proposed concept is to measure the pain by utilizing sensor data obtained from force and/or motion sensors integrated in a personal care device, e.g. an oral care device, over the course of each of one or more personal care sessions of the user. Patterns in the sensor data, or changes in said patterns, can be used to infer pain information, such as an overall pain level, pain reaction events at certain points during the personal care session and/or at certain locations, or increased sensitivity at certain body areas. This provides a more objective and reliable estimation and monitoring of user oral pain that relying on patient (subjective) reporting of pain.
A face mask comprises a filter portion and a fan module for driving air which passes through the filter portion. A magnetic coupling is used to couple the fan module to the filter portion, The filter portion comprises a recessed area having a base wall, a non-recessed area which extends around the recessed area and a side wall extending between the recessed area and the non-recessed area. The magnetic coupling comprises first and second magnetic parts disposed on opposite faces of the side wall.
Proposed concepts provide schemes, solutions, concepts, designs, methods and systems pertaining to improving the utilization of privacy-sensitive datasets (i.e. increasing security and/or concealment) for training a machine-learning algorithm. In particular, embodiments may address the technical problem of protecting privacy-sensitive datasets while utilizing them as training data in machine-learning applications. Proposed embodiments may therefore help to enable stand-along and federated deep-learning platforms to be executed on private datasets.
Disclosed herein is a medical system comprising: —a memory storing machine executable instructions; —a computational system, wherein execution of the machine executable instructions causes the computational system to perform a mismatch check comprising: —receive posture recognition system data, wherein the posture recognition system data comprises a set of subject coordinates and a set of coil coordinates described using a current coordinate system, wherein the set of subject coordinates are descriptive of anatomical features of a subject, wherein the set of coil coordinates are descriptive of a coil location of a magnetic resonance imaging coil, wherein coil data comprising a predefined range of coil positioning coordinates referenced to the anatomical features is associated with the magnetic resonance imaging coil; —determine an allowed range of coil coordinates by mapping the predefined range of coil positioning coordinates to the current coordinate system using the set of subject coordinates and the anatomical features; and —provide a warning signal in case of a mismatch between the set of coil coordinates and the allowed range of coil coordinates.
There is proposed a mechanism for determining whether or not an imaging probe, such as an ultrasound imaging probe, is at a desired orientation and/or position with respect to an anatomical structure. Image data of the imaging probe is processed to generate a 3D landmark model that contains anatomical landmarks of the anatomical structure. The 3D landmark model is then processed to determine whether or not the imaging probe is at the desired orientation and/or position.
A breast pump comprises abreast shield for fitting over at least the nipple of a breast thereby to create a cavity over the breast. A pump is used to deliver an under pressure to the cavity. In addition, a compressible chamber is used to manually create a reduced pressure in the cavity, in particular to function as a baseline pressure for holding the breast shield against the breast.
A coffee machine has a test function, by which a user can instruct suitable operating settings to be determined, e.g. for a new coffee bean type to be used. A series of one or more test brewing cycles is then carried out to measure operating characteristics of the coffee machine, and thereby derive a set of suitable operating settings, for example for those new coffee beans.
A method predicts an interpretation time for a medical image examination of a subject comprising one or more medical images. A plurality of data inputs is obtained, where the data inputs are associated with the medical image examination or the subject of the medical image examination, and the data points represent parameters affecting the interpretation time. The plurality of data inputs are input to a trained artificial intelligence algorithm, wherein the algorithm automatically provides a predicted interpretation time based on said plurality of data inputs. The predicted interpretation time is output to a clinical management system. A clinical management system incorporating the aforementioned method and a computer program product encoded with the aforementioned method are also provided.
G16H 30/40 - ICT specially adapted for the handling or processing of medical images for processing medical images, e.g. editing
G16H 40/20 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
93.
ADAPTIVE WATER-FAT SHIFT IN NON-CARTESIAN MAGNETIC RESONANCE IMAGING
Disclosed herein is a medical system (100, 300) comprising a memory (110) storing machine executable instructions (120). The medical system further comprises a computational system (104). Execution of the machine executable instructions causes the computational system to: receive (200) initial pulse sequence commands (122), wherein the initial pulse sequence commands are configured for controlling a magnetic resonance imaging system (302) to acquire k-space data (332) following a non-Cartesian k-space sampling pattern (604, 604′), wherein the initial pulse sequence commands are configured for controlling the magnetic resonance imaging system to sample the non-Cartesian k-space sampling pattern by repeatedly sampling a Cartesian k-space sampling pattern (126) that is rotated for each acquisition, wherein the non-Cartesian k-space sampling pattern has an effective water-fat shift direction (606, 606′); receive (202) a chosen water-fat shift direction (124); and construct (204) modified pulse sequence commands by rotating the non-Cartesian k-space sampling pattern such that the effective water-fat shift direction is aligned with the water-fat shift direction.
According to an aspect, there is provided a method for minimising error in ambient light corrected image due to motion, the method comprising: capturing a plurality of primary images with controlled intensity of illumination varying over time, estimating an error value due to motion for each of a plurality of sub-sets of the plurality of primary images, and performing ambient light correction on an error minimised sub-set of primary images having the lowest estimated error value to generate an ambient light corrected (ALC) image with a minimised error. Estimating the error value for each sub-set of the plurality of primary images comprises identifying a pair of primary images in the sub-set including a first primary image and a second primary image, wherein the first primary image is captured temporally before the second primary image, determining a displacement vector matrix between the pair of primary images, and estimating the error value for the sub-set of primary images based on the displacement vector matrix between the pair of primary images. Determining the displacement vector matrix includes dividing the first primary image into a plurality of first grid elements and dividing the second primary image into a plurality of second grid elements, matching first grid elements to second grid elements which correspond to the same position on the object, and determining a displacement vector between each matched first grid element and second grid element to determine a displacement vector matrix describing the displacement vector of each grid element.
An apparatus for stabilizing a tongue of a user during sleep. The apparatus includes a mouthpiece member structured and configured to rest on the user's teeth, and a stabilization mechanism fixed to the mouthpiece member. The stabilization mechanism includes a first stabilization assembly having a first roller member structured to rotate about a first axle and a second stabilization assembly having a second roller member structured to rotate about a second axle, the first roller member being spaced from the second roller member to form a gap between the first roller member and the second roller member. The gap is configured to receive a frontal portion of the tongue to enable the tongue to be engaged and be held by the first roller remember and the second roller member when the tongue is received in the gap.
A coupling arrangement for use in an air delivery circuit includes a first connector tube defining a first passage therethrough and a second connector tube defining a second passage therethrough. The second connector tube telescopically receives a portion of the first connector tube within the second passage. A release mechanism includes wedges coupled to the first or second connector tube. The first and second connector tubes have a number of corresponding features that latch the first connector tube within the second passage of the second connector tube when the first connector tube is axially inserted along the longitudinal axis a predetermined distance. Actuation of the wedges radially toward the longitudinal axis causes axial movement among the first connector tube and the second connector tube a second predetermined distance that is sufficient to unlatch the corresponding features.
A respiratory interface system for use in delivering a flow of a positive pressure breathing gas to an airway of a patient that includes a patient interface device with a tubing assembly structured to be disposed on the head of the patient, a mask having a sealing element structured to sealingly engage about the airway of the patient, and an adaptor. The adapter includes a flange portion that extends generally radially outward from a central aperture and a hollow male connector extending from the flange portion and coupled with a correspondingly-shaped female connector of the tubing assembly or the mask. The mask is coupled to the tubing assembly via the adaptor, and the tubing assembly, the mask, and the adapter define a pathway structured to conduct the flow of the positive pressure breathing gas to the airway of the patient.
A method 100 of displaying a three dimensional volume of an image on a two dimensional display. For each pixel in the two dimensional display, the method comprises sequentially stepping 102 through a plurality of points along a line of sight from the pixel into the three dimensional volume and determining 104 a first point along the line of sight at which the three dimensional volume has a value that satisfies a first criteria indicating that the first point comprises a surface of interest in the three dimensional image. From the first point, the method then comprises determining 106 a second point that lies normal to the surface of interest at the first point, and determining 108 a value for the pixel based on a first value associated with the second point.
Provided is a system (300) for determining a sweat rate per gland and measuring biomarker concentration. The system comprises an apparatus and a sensor (166). The apparatus receives sweat from the skin and transports the sweat as discrete sweat droplets to the sensor. The sensor senses each of the counted sweat droplets. The system further comprises a processor which counts the number of sensed sweat droplets during a time period. The processor also determines time intervals between consecutive sensed sweat droplets, and receives a measure of the volume of each of the counted sweat droplets. The time intervals and the measure of the volume are then used by the processor to identify sweat burst and rest periods of the sweat gland or glands producing the sweat. This identification process necessarily involves assigning the sweat burst and rest periods to the sweat gland or glands, such that the processor is permitted to determine the number of sweat glands involved in producing the sweat. The sweat rate per gland may then be determined from the number of sweat droplets, the measure of the volume of each of the counted sweat droplets, and the determined number of sweat glands. Further provided is a method for determining a sweat rate per gland.
A computer-implemented method of providing plaque data (110) for a plaque deposit (120) in a vessel (130), is provided. The method includes: receiving (S110) computed tomography, CT, data (140) representing the vessel (130); generating (S120), from the CT data (140), a cross-sectional representation (150) of the vessel (130) at each of a plurality of positions (A - A', B - B') along the vessel; extracting (S130), from the cross-sectional representations, plaque data (110) comprising at least one measurement of the plaque deposit (120) at the plurality of positions along the vessel; and outputting (S140) a graphical representation of the plaque data (110).
