Abstract: A positional pattern of an irradiation unit for irradiating a patient with treatment radiation is determined based on optimal order data describing an order of the irradiation unit positions for which the statistical value is optimal. The optimal order data is determined based on irradiation unit position data describing irradiation unit positions of the irradiation unit for which the imaging device has a free viewing direction onto the position of the patient, position orders data describing all possible orders of the irradiation unit positions for which the imaging device has a free viewing direction onto the position of the patient, and intersection angle data describing a statistical quantity of the intersection angles between free viewing directions of the imaging unit for irradiation unit positions which are immediately subsequent in the order described by the position orders data.

Abstract: A method is proposed for recording diagnostic measurement data of a head of an examination object in head imaging via a magnetic resonance device. The method comprises performing an overview scan of the head of the examination object, wherein overview measurement data is acquired in the overview scan and performing various diagnostic scans of the head of the examination object based on the acquired overview measurement data, wherein diagnostic measurement data is acquired in the various diagnostic scans.

Abstract: Ultrasound imaging systems for automatically adjusting settings according to an position and/or orientation of one or more interfaces. The ultrasound imaging systems can include a probe configured to send and receive ultrasound signals for performing a medical exam, a medical procedure, or both; and a processor configured to: select a diagnostics mode or a procedural mode based on an operating orientation of the ultrasound imaging system or a portion thereof, and adjust one or more settings of the imaging system according to the selected diagnostics mode or the selected procedural mode.

Abstract: The present invention relates to an MRS 1D or 2D method and system for obtaining spectral data of the brain of a subject and using neurochemical markers to enable whether a subject is experiencing acute pain, and providing the capacity to monitor response to therapy on an individual basis. The markers can be an increase of Fuc II, III, IV, VII and lactate.

Abstract: Disclosed is a system and a method to analyze spectrophotometry and ultrasound images and data in a complex way to diagnose malignant skin tumors in early stages. The system consists of a high-frequency portable ultrasonic imaging device for in vivo skin examinations, an optical spectrophotometer with light sources of different wavelengths for skin chromophore registration, and a complex data processing algorithm providing an advisory diagnostic evaluation. This enables automatically aggregating data and quantitative estimates obtained by different imaging techniques for melanocyte-derived skin tumors, facilitating the decision support for acceptance of the final clinical diagnosis and treatment planning.

Abstract: An ultrasound probe 11 includes a housing 12 having a transducer array accommodation portion 14 and a battery storage portion 13B, a transducer array accommodated in the transducer array accommodation portion 14, and a battery 21 stored in the battery storage portion 13B. The housing 12 has an attachable and detachable battery cover 17 that covers the battery storage portion 13B, a nameplate 22 is disposed on an inside or an outside of the battery storage portion 13B with respect to the battery cover 17 in a visible manner, and a waterproof structure for restraining water from entering the nameplate 22 is provided.

Abstract: A method of generating a 4D model includes capturing imagery of a catheter and a vessel as the catheter is directed through the vessel to a location of interest, wherein the catheter is disposed on a guidewire, constructing a 3D time varying reference curve describing a trajectory of the guidewire, and constructing a time varying 3D model of the artery using the reference curve.

Abstract: An apparatus is provided that is visible by both a three dimensional (3D) scanner system of a medical navigation system and a camera of the medical navigation system. The apparatus involves a rigid member and a plurality of markers attached to the rigid member. Each of the plurality of markers includes a reflective surface portion visible by the camera and a distinct identifiable portion visible by the 3D scanner system. The apparatus further involves a connector mechanism to connect the apparatus to a reference location. The apparatus is in a field of view of the 3D scanner system and the camera within a timeframe of the 3D scan.

Abstract: An ultrasound probe includes a housing; a transducer array housed in the housing; a transmission/reception unit which is housed in the housing, transmits ultrasonic wave from the transducer array, and generates a sound ray signal on the basis of a reception signal acquired by the transducer array; an image information data generation unit which is housed in the housing, and generates image information data on the basis of the sound ray signal generated by the transmission/reception unit; a wireless communication unit which is housed in the housing, and wirelessly transmits the image information data generated by the image information data generation unit; a light emission unit which is housed in the housing, and emits light to an outside of the housing; and a light emission control unit which is housed in the housing, and causes the light emission unit to emit light in synchronization with a transmission timing of the ultrasonic wave by the transmission/reception unit in a case of a manufacturing inspection.

Abstract: An intravascular sensor device can be used to guide treatment of a diseased blood vessel in the body of a patient. In some examples, the intravascular sensor device includes a pressure sensor and an ultrasound transducer. The intravascular sensor device is used to measure a pressure within the diseased blood vessel and acquire an ultrasound image of the diseased blood vessel. The pressure may be measured during hyperemic blood flow that is caused by a pharmacologic vasodilator drug. The measured pressure can be used to calculate a fractional flow reserve value. The ultrasound image can be used to determine a physical dimension of the blood vessel, such as cross-sectional area. The fractional flow reserve value and physical dimensions of the blood vessel can be used to optimize patient treatment.

Abstract: Devices, systems, tools and methods are disclosed during diagnosis and treatment of spinal conditions. A cervical plumb line device is disclosed which can be used to produce a measurement of the sagittal vertical axis associated with a target part of a patient's cervical spinal anatomy from two or more radiographic images. Also disclosed is an apparatus for measuring the angulation of a patient's spinal anatomy relative to a cervical plumb line which uses a plurality of bolsters. A device that can be used to assist in implantation of an interbody device during spinal fusion device is also disclosed. Systems which produce geometric data describing optimized spinal fusion geometric at a spine level selected to receive spinal fusion.

Abstract: A device and system for and methods of using an ultrasound probe housing containing ultrasound probes configured to produce images inside the body of a patient for procedures requiring needle or probe insertion. The ultrasound probe housing can be configured with a guide channel cut-out or aperture between the ambient side and body side of a patient. A needle guide assembly may be pivotally connect internal to the guide channel cut-out or aperture of the ultrasound probe housing at a pivot point such that during use the needle enters the patient through the needle guide assembly within the ultrasonic probe housing so that the needle can be visualized by the ultrasonic probes in real time. The ultrasound probe housing may also provide an adhesion or suction quality to the body side of the device to facilitate aspects of the invention.

Abstract: A device and system for and methods of using an ultrasound probe housing containing ultrasound probes configured to produce images inside the body of a patient for procedures requiring needle or probe insertion. The ultrasound probe housing can be configured with a guide channel cut-out or aperture between the ambient side and body side of a patient. A needle guide assembly may be pivotally connect internal to the guide channel cut-out or aperture of the ultrasound probe housing at a pivot point such that during use the needle enters the patient through the needle guide assembly within the ultrasonic probe housing so that the needle can be visualized by the ultrasonic probes in real time. The ultrasound probe housing may also provide an adhesion or suction quality to the body side of the device to facilitate aspects of the invention.

Abstract: A device and system for and methods of using an ultrasound probe housing containing ultrasound probes configured to produce images inside the body of a patient for procedures requiring needle or probe insertion. The ultrasound probe housing can be configured with a guide channel cut-out or aperture between the ambient side and body side of a patient. A needle guide assembly may be pivotally connect internal to the guide channel cut-out or aperture of the ultrasound probe housing at a pivot point such that during use the needle enters the patient through the needle guide assembly within the ultrasonic probe housing so that the needle can be visualized by the ultrasonic probes in real time. The ultrasound probe housing may also provide an adhesion or suction quality to the body side of the device to facilitate aspects of the invention.

Abstract: A device comprises an ultrasound probe housing containing ultrasound probes configured to produce images inside the body of a patient for procedures requiring needle or probe insertion. Each of a first subset of the ultrasound probes is positioned such that a direction of ultrasound waves generated thereby is through a body side of the ultrasound probe housing and perpendicular thereto. Each of a second subset of the ultrasound probes is positioned non-perpendicular to the body side of the ultrasound probe housing such that a direction of ultrasound waves generated thereby is toward a site of needle penetration directly beneath a guide channel cut-out or aperture of the ultrasound probe housing. A first ultrasound probe in the first subset of ultrasound probes may be located further from the body side of the ultrasound probe housing that a second ultrasound probe in the first subset of ultrasound probes.

Abstract: A device and system for and methods of using an ultrasound probe housing containing ultrasound probes configured to produce images inside the body of a patient for procedures requiring needle or probe insertion. The ultrasound probe housing can be configured with a guide channel cut-out or aperture between the ambient side and body side of a patient. A needle guide assembly may be pivotally connect internal to the guide channel cut-out or aperture of the ultrasound probe housing at a pivot point such that during use the needle enters the patient through the needle guide assembly within the ultrasonic probe housing so that the needle can be visualized by the ultrasonic probes in real time. The ultrasound probe housing may also provide an adhesion or suction quality to the body side of the device to facilitate aspects of the invention.

Abstract: A device and system for and methods of using an ultrasound probe housing containing ultrasound probes configured to produce images inside the body of a patient for procedures requiring needle or probe insertion. The ultrasound probe housing can be configured with a guide channel cut-out or aperture between the ambient side and body side of a patient. A needle guide assembly may be pivotally connect internal to the guide channel cut-out or aperture of the ultrasound probe housing at a pivot point such that during use the needle enters the patient through the needle guide assembly within the ultrasonic probe housing so that the needle can be visualized by the ultrasonic probes in real time. The ultrasound probe housing may also provide an adhesion or suction quality to the body side of the device to facilitate aspects of the invention.

Abstract: The present disclosure relates to technology for estimating bio-information by using a foldable electronic device. The foldable electronic device includes a main body part, having a first main body and a second main body, configured to fold along a folding line; a first sensor provided on the first main body, and configured to obtain a contact image of an object of a user; a second sensor provided on the first main body, and configured to measure a degree of folding of the main body part; and a processor configured to estimate bio-information of the user, based on the contact image of the object and the degree of folding.

Abstract: A system for rod bending for use in robotic spinal surgery, enabling the correct bending of a fusion rod to match the shape required to accurately pass through the heads of the pedicle screws. The system uses data generated by information provided to the robot by the surgeon's preoperative plan, optionally augmented by feedback from the robot control system of deviations encountered intraoperatively. Such deviations could occur, for example, when the surgeon decides intraoperatively on a different trajectory or even to skip screws on one vertebra, in which case, the robot will be commanded to perform the alternative procedure, with commensurate instructions relayed to the control system of the rod-bending machine. The system is also able to thin down the rod at predetermined locations along its length, adapted to be at selected intervertebral locations, for maintaining limited flexibility between vertebrae, instead of fixating them.

Abstract: A method for quantitative flow analysis of a fluid flowing in a conduit from a sequence of consecutive image frames of such a conduit, where such image frames are timely separated by a certain time interval, the method comprising: a) selecting a start image frame and an end image frame from the sequence either automatically or upon user input; b) determining a centerline of the conduit in the start image frame; c) determining a centerline of the conduit in the end image frame; d) selecting a common start point on the centerline of the start image frame and on the centerline of the end image frame either automatically or upon user input; e) selecting an end point on the centerline of the start image frame; f) selecting an end point on the centerline of the end image frame; g) calculating centerline distance between the start point and the end point of the start image frame; h) calculating centerline distance between the start point and the end point of the end image frame; and i) calculating a local flow ve