Abstract: The present disclosure relates to an automated grooming appliance (20) for hair processing procedures, the appliance (20) comprising a processing head (58) including a blade set (22) having a processing width (36), a length setting unit (26) that is operatively coupled to the blade set (22), and a control unit (40) that is arranged to operate the length setting unit (26) based on a hairstyle model (90) that correlates position data and hair processing data, wherein the control unit (40) is arranged to adjust a length setting dependent on an actual position and an actual orientation of the blade set (22). The present disclosure further relates to an automated hair processing system (10), to a method of operating an automated grooming appliance (20), and to a corresponding computer program.

Abstract: The present invention discloses a hair styling device (10, 20) comprising an inner cylindrical shell (121, 221) provided with through-holes; a rotatable cylindrical shell (122, 222) surrounding the inner cylindrical shell (121, 221); a drive assembly (123, 223) for driving the rotatable cylindrical shell (122, 222) to rotate around the inner cylindrical shell (121, 221) for winding hair around the inner cylindrical shell (121, 221); and a wind supply assembly (130, 230) for supplying hot air to any hair wound around the inner cylindrical shell (121, 221) through the through-holes. According to the present invention, hot air is supplied to the hair wound around the inner cylindrical shell (121, 221) so that the hair is heated evenly and shaped.

Abstract: An image-guided prosthetic valve deployment system employs a prosthetic valve (80), a catheter (70) and a delivery tracking system (90). The catheter (70) has an elongated body with a proximal tip (71a) and a distal tip (71b), and the elongated body includes a delivery section (72) adjacent the distal tip (71b) for deploying the prosthetic valve (80) relative to a heart valve (21) within an anatomical region (20). The delivery section (72) includes a delivery segment (73) for sensing a shape and an orientation of the delivery section (72) within the anatomical region (20) relative to a reference point (74). The delivery tracking system (90) tracks a position and an orientation of the prosthetic valve (80) relative to the heart valve (21) as a function of a sensed shape and a sensed orientation of the delivery section (72) within the anatomical region (20) relative to the reference point (74) by the delivery segment (73).

Abstract: A dual mode radiation detector includes an x-ray detector layer configured to convert incident x-ray radiation into x-ray electrical data, where the x-ray detector forms an incident face of the dual mode radiation detector. The dual mode radiation detector further includes a collimator disposed below the x-ray detector layer, and a gamma photon detector layer disposed below the collimator to convert incident gamma photons into gamma photon electrical data.

Abstract: A medical device for multiple treatment therapies includes a hollow tube (102) having a first end portion with an electrode (104) disposed at the first end portion and an insulator (108) configured over a length of the tube such that conductive materials of the tube, except for the electrode, are electrically isolated from an exterior surface the tube. A conductive connection (127) is configured to electrically couple to the electrode to provide a voltage thereto. A selectively closeable valve (106) is configured to dispense a medical fluid from the tube.

Abstract: An actuator (12) for a personal care appliance (10) having an eccentric core (21) to preload the actuator (12) to prevent rattling caused by detrimental reactionary forces. The eccentric core (21) includes a pole assembly (24) radially extending from a spindle (22) having at least a first set (25-1) and a second set (25-2) of pole members. The first set (25-1) has a greater length as measured from the center of the spindle (22) than the second set (24-2), reducing the magnet gap on one side of the spindle (22) to create an eccentric core and preload the actuator (12). Alternatively, the preload can be mechanically created by a set of bearings (28) disposed within housing (18) of the actuator (12), where the bearings (28) have a centerline (A3) offset from the principal axis (A1) of the housing (18).

Abstract: A system to generate medical monitor alarm settings (10) which includes a normative analyzer (36) and/or observational analyzer (48) configured to receive (130) data from logs (32, 34) of a plurality of medical monitors (12), and generate (134, 138) one or more suggested alarm settings (26) based on a constructed model of the received log data.

Abstract: Secretions that have accumulated at or near an airway of a subject (12) as the subject (12) is being mechanically ventilated are removed by suctioning. Before, during, and/or after the removal of the secretions, steps are taken to mitigated the impact of the suctioning used for secretion removal on the subject (12). As such, the timing of suction used to remove secretions may be influenced or controlled, ventilation of the subject (12) during suction may be adjusted, ventilation of the subject (12) prior to secretion removal may be adjusted to prepare the lungs of the subject (12) for secretion removal, ventilation of the subject (12) subsequent to suction for secretion removal may be adjusted, and/or other techniques for reducing the impact of suctioning for secretion removal on the subject (12) may be implemented.

Abstract: A defibrillator and method for using a defibrillator which adopts an ECG analysis algorithm that can detect a cardiac arrhythmia in the presence of noise artifact induced by cardio pulmonary resuscitation (CPR) compressions. The apparatus and method provides both of a continuous and scheduled mode of operation for interleaving periods of CPR with electrotherapy, in a manner that improves the effectiveness of the rescue, resulting in more CPR “hands-on” time, better treatment of refibriUation, and reduced transition times between CPR and electrotherapy.

Abstract: The present invention relates to medical imaging, and in particular a medical imaging detector. In order to improve and facilitate the collection of information, e.g. for medical diagnosis, a medical imaging detector is provided that comprises a first sensor arrangement (12) and a second sensor arrangement (14). The first sensor arrangement is configured to provide a first type of image data belonging to a first imaging modality. The second sensor arrangement is configured to provide a second type of image data belonging to a second imaging modality. The first imaging modality is an X-ray imaging modality, while the second imaging modality is a non-X-ray imaging modality. The first sensor arrangement comprises one or a plurality of first sensor segments (16) arranged within a first circumferential line (18) defining a first imaging area (20).

Abstract: The present disclosure pertains to a system configured to manage a sleep session of a subject. In some embodiments, the sleep session is a nap and the system is configured to increase the restorative value of the nap by enhancing and/or maintaining sleep slow waves (and/or slow wave activity estimated using an EEG) in the subject during the nap with sensory stimuli. The present system is configured to enhance restorative sleep during a nap by delivering sensory stimulation to the subject during lighter NREM sleep stages (e.g., during a portion of stage N2 sleep) while still avoiding arousals. In some embodiments, the system is configured to facilitate a “powernap” by delivering the sensory stimulation to the subject in such a way so as to prevent transition into deep sleep (e.g., stage N3 sleep).

Abstract: A method of transferring a flexible layer to a substrate makes use of a partial bulge in the flexible layer, which does not make contact with the substrate. The partial bulge advances to the location of an alignment marker on the substrate. When alignment adjustments are needed, they are made with the partial bulge in place so that more reproducible positioning is possible when fully advancing the flexible layer against the substrate.

Abstract: A device for positioning an energy-generating transducer probe a movement unit. The transducer probe may be configured for heat treatment of biological tissues and emits energy in one aiming direction which is located in an aiming plane. The movement unit is configured to alter the position of the transducer probe and, consequently, the aiming direction in the aiming plane around a target zone within the aiming plane.

Abstract: An automated external defibrillator (AED) is described which spends an increased proportion of a rescue in a CPR mode. This is accomplished by use of a single shock protocol which causes the AED to spend less time in shock analysis and delivery activities as compared with the typical multiple shock protocol. An AED of the present invention preferably is configured such that the rescue protocol can be modified or changed easily without the need to remove the battery or use specialized hardware or software. Preferably the shock waveform of the single shock is a biphasic waveform delivering at least 150 Joules of energy and more preferably at least 200 Joules of energy.

Abstract: A catalog (34) of molecular marker tests specifies molecular marker tests annotated with clinical applicability annotations. An electronic patient medical record (22) stores genetic sequencing data (20) of a patient. A clinical decision support (CDS) system (30) is configured to track the clinical context of the patient wherein the clinical context includes at least a disease diagnosis and a current patient care stage. A catalog search module (32) is configured to search the catalog of molecular marker tests to identify a molecular marker test having clinical applicability to the patient in the clinical context tracked by the CDS system. The search is automatically triggered by occurrence of a trigger event defined by a set of triggering rules. A testing module (44) is configured to perform a molecular marker test identified by the identification module in silico using the genetic sequencing data of the patient stored in the electronic patient medical record.

Abstract: A multi-channel transmit/receive radio frequency (RF) system for a magnetic resonance examination system with an RF antenna array includes multiple antenna elements and an RF power supply to supply electrical RF power to the antenna elements. Directional couplers are circuited between respective antenna elements and a power distributor. A monitoring module is configured to measure forward electrical wave amplitude(s) and reflected electrical wave amplitude(s) at individual directional couplers. An arithmetic module is configured to compute individual coil element currents on the basis of the measured forward and reflected electrical wave amplitudes.

Abstract: A radio-frequency (RF) coil apparatus for magnetic resonance (MR) systems (100, 200, 300, 400, 500, 600, 700, 900, 1000) includes a base (102, 502, 702, 902, 1002) having opposed sides (121), a surface (124) to support an object of interest (OOI) for scanning, and fasteners (127) situated at the opposed sides, A positioner (104, 304A, 304B, 504, 604, 704, 1004) is configured to be releasably attached to the base and has a body (130) extending between opposed ends and fasteners (134,) situated at the opposed ends of the body, The body is configured to form an arch between the opposed ends. An upper section (106, 606, 706, 906, 1006) has at least one RF coil array (142) for acquiring induced MR signals, and is configured to be positioned over the positioner.

Abstract: The invention relates to a system for zooming an image displayed in a viewport, wherein the image comprises a plurality of regions, each region of the plurality of regions having a zoom function associated with the region, the system comprising an input unit for receiving a region input for selecting a region of the plurality of regions and for receiving a zoom input for zooming the image, and a zoom unit for zooming the image based on the zoom input, using the zoom function associated with the selected region. The zoom function associated with each region of the plurality of regions may be defined in any way deemed useful. For example, it may be defined in such a way that the selected region or an interesting portion of it is displayed in the viewport or, vice versa, the selected region or an interesting portion thereof is removed from the displayed view of the image.