Abstract: To accurately generate the three-dimensional ultrasound data and/or determine the position of the ultrasound scan relative to pre-operative data, a tracking sensor is releasably connected with the ultrasound probe. The connection positions the tracking sensor near a distal end of the probe for insertion into the patient. A needle guide may be similarly releasably connected with the probe and, at least in part, inserted into the patient.

Abstract: A magnetic field generator assembly (44) is configured to be associated with a table (20) supporting a body. The magnetic field generator comprises magnetic field transmitters (57A) that are thin (of minimal height) and transparent, or substantially transparent, to x-ray radiation. The magnetic field transmitters (57A) are configured to minimally obstruct components of an imaging system and to minimally interfere with image quality. A plurality of transmitters is arranged in a first layer of the assembly. Each transmitter (57A) comprises an elongate conductive element, such as a wire, arranged in a spiral form, such as a coil.

Abstract: System and method for ingestion event detection and monitoring are disclosed. The system comprises: an ingestible microsensor configured to generate a signal representing an ingestion event upon ingestion and contact with stomach fluid of a patient; and a reader device positioned external to the patient and configured to detect the signal representing the ingestion event with at least 95% accuracy.

Abstract: In a system, device and method for treating an aneurysm of a human or mammal patient an implantable member adapted to hold fluid is provided. The member is adapted to be placed in connection with a blood vessel having the aneurysm and to exercise a pressure on the aneurysm of said blood vessel.

Abstract: The invention is directed to a system and method for providing an ARDS indication of a patient comprising a sampling device for obtaining a gas sample of the exhaled breath of a patient, a measuring unit for measuring a content of n-octane in the exhaled breath of a patient, a controller which is able to distinguish if the patient has or may develop ARDS based on the content of n-octane in the exhaled breath of a patient resulting in a ARDS indication of the patient and provided with a protocol for providing output regarding the ARDS indication of the patient, and a user interface for indicating the ARDS indication to a user.

Abstract: Orthopedic systems and methods are provided for use in preparing joints for implants. Specifically, hip preparation systems and methods are disclosed which can include a surgical orientation device. The hip preparation systems and methods can be used, for example, to orient the hip during the procedure, determine the orientation of an anatomical plane or planes, and orient a prosthetic component or components.

Abstract: A method for evaluating positioning of an examination object on a patient-positioning apparatus in a magnetic resonance unit, a magnetic resonance unit, and a computer program product are provided. The method includes acquiring positioning data relating to the examination object using an acquisition unit. Using the acquired positioning data, positioning information relating to the examination object is determined using an analysis unit. Evaluation information is determined using the positioning information, using an evaluation unit. Using the evaluation information, an evaluation signal is transmitted using an output unit. Monitoring of a specific absorption rate may be adjusted using the evaluation signal.

Abstract: Systems and methods for monitoring the location of a patient using a double-release alarm belt. The belt may include a plurality of straps configured to be releasably attached to one another and an alarm system that is triggered when at least one of the straps is disengaged from the other strap or straps. One strap may be disengaged from another strap by pulling the first strap in a first direction and another strap may be disengaged from the yet another strap by pulling in a second direction. By requiring multiple straps to be released from one another, the amount of time it takes to remove the belt can be increased, which provides medical personnel additional time to reach a patient.

Abstract: Aspects of gait matching are described herein. In one embodiment, a method of gait matching includes identifying a gait cycle timing in a data sequence captured by an inertial sensor, splitting the data sequence into a gait cycle segment, resampling the gait cycle segment, and estimating a rotation matrix for the resampled gait cycle segment. The rotation matrix, in one embodiment, can be estimated by minimizing a root mean squared deviation between the resampled gait cycle segment and a reference gait cycle segment. The method further includes calculating an aligned gait cycle segment from the resampled gait cycle segment using the rotation matrix, and generating a similarity measure between the aligned gait cycle segment and the reference gait cycle segment.

Abstract: A method for monitoring a patient in a bed may involve capturing images of the patient with multiple cameras in a vicinity of the bed, wirelessly transmitting the images of the patient from the multiple cameras to a processor including a memory device, processing the images to provide processed image data pertaining to a position of the patient relative to the bed to a user, and analyzing the processed image data to determine whether the patient is exiting the bed. The method may also optionally involve providing an alarm indicating that the patient is exiting the bed.

Abstract: Low-cost, easy-to-use alignment target generators for aligning a user's own face or eye to a camera or scanner are based on field-of-view visual feedback from a filtered or apertured planar light source. These approaches may be made agnostic to the scanner's operating system or other software. Alternatively, software on the scanner or its host device may create a solid light-colored section of an existing display screen to use as a planar light source. In some embodiments, the planar light source may be the virtual image of an object viewed in a plane mirror.

Abstract: Provided are transdermal microneedle-based devices for sensing the presence and concentration of analytes such as electrolytes, biomarkers, drugs, and proteins in interstitial fluid. Also provided are methods and systems to transmit the data obtained by wired or wireless connection to a receiver and to relay the data to the user or a clinician.

Abstract: Systems, methods, and computer readable storage media manage low blood glucose levels. The system receives blood glucose readings, where each reading includes a blood glucose value and a respective timestamp. The system compares each blood glucose reading to a predefined hypoglycemic event threshold, and identifies hypoglycemic events when a respective blood glucose reading is below the predefined hypoglycemic event threshold. For at least a subset of the identified hypoglycemic events, the system prompts a user for information associated with each hypoglycemic event. The information requested includes one or more of: symptoms associated with the respective hypoglycemic event; perceived causes of the respective hypoglycemic event; and treatment for the respective hypoglycemic event. In response to the prompting, the system obtains feedback about the identified hypoglycemic events and provides a report that includes at least a subset of the obtained feedback.

Abstract: A glucose biosensor includes a plurality of optical fibers configured for placement within the ear canal. A first optical fiber emits light into the ear canal. A plurality of other optical fibers capture and transmit the reflected light back to the glucose biosensor. A plurality of photodetectors are configured in the glucose biosensor to detect the reflected light from the plurality of optical fibers. The glucose biosensor processes the detected light from each photodetector to determine a glucose level measurement. In an embodiment, the glucose biosensor also includes a wireless interface to transmit the glucose level measurements to a glucose meter and/or a gateway.

Abstract: The present invention relates to a pH sensor adapted to be inserted into all soft tissues, such as muscle, fat or other organs e.g. heart, lung, kidney, liver, pancreas, renal gland etc., comprising one or more of: a) means to provide sensor calibration performance information; b) a sensor dislodgement alert, providing an indication to the user if the pH reading falls outside a predetermined range; c) an alert to indicate that the sensor has exceeded its usage period; and d) an alert to indicate that the sensor had exceeded its shelf life. There is also provided a method of assessing the efficacy of a treatment regime comprising the steps of determining any change in the pH of the soft tissue during treatment, where any change in the pH towards the preferred range for the tissue type is indicative of an effective treatment regime and any change in the pH away from the preferred range for the tissue type is indicative of a worsening in the condition of the tissue, and thus an ineffective treatment regime.

Abstract: A near infrared spectrophotometric sensor assembly for non-invasive monitoring of blood oxygenation levels in a subject's body is provided. The assembly includes at least one light source, at least one light detector operable to detect light emitted by the light source, an electromagnetic interference shielding disposed around at least a portion of the light detector, wherein the electromagnetic interference shielding includes an electrically conductive substrate that is optically transparent, and one or both of a light blocking sheet disposed relative to at least one of the light detectors and an encapsulating material.

Abstract: Analyte sensor connectors that connect analyte sensors, e.g., conductive members of analyte sensors, to other devices such as sensor electronics units, e.g., sensor control units, are provided. Also provided are systems that include analyte sensors, analyte sensor connectors, and analyte sensor electronics units, as well as methods of establishing and maintaining connections between analyte sensors and analyte sensor electronics units, and methods of analyte monitoring/detection. Also provided are methods of making analyte sensor connectors and systems that include analyte sensor connectors.

Abstract: The present invention relates to the field of film materials for biosensors, in particular to a film for biosensors and a preparation method. Provided is an organosilicon polymer, the raw materials thereof comprising the following components: at least one active organosilane, at least one curing agent, at least one optional hydrophilic copolymer and at least one optional regulator and/or filling. The membrane prepared from the provided organosilicon polymer has outstanding oxygen permeability and is adjustable in water absorption rate, and can put regulation and restriction on the diffusion of analytes (e.g. glucose) and interferents (e.g. acetaminophen). Meanwhile, the provided organosilicon polymer film also has indispensable physical strength and superior biocompatibility, and can serve as a multifunctional polymer film material for biosensors, such as anti-interference layer, analyte regulating layer and biocompatible layer.

Abstract: A diagnostic Electrochemical Impedance Spectroscopy (EIS) procedure is applied to measure values of impedance-related parameters for one or more sensing electrodes. The parameters may include real impedance, imaginary impedance, impedance magnitude, and/or phase angle. The measured values of the impedance-related parameters are then used in performing sensor diagnostics, calculating a highly-reliable fused sensor glucose value based on signals from a plurality of redundant sensing electrodes, calibrating sensors, detecting interferents within close proximity of one or more sensing electrodes, and testing surface area characteristics of electroplated electrodes. Advantageously, impedance-related parameters can be defined that are substantially glucose-independent over specific ranges of frequencies. An Application Specific Integrated Circuit (ASIC) enables implementation of the EIS-based diagnostics, fusion algorithms, and other processes based on measurement of EIS-based parameters.

Abstract: Systems, methods and devices are disclosed for directing and focusing signals to the brain for neuromodulation and for directing and focusing signals or other energy from the brain for measurement, heat transfer and imaging. An aperture in the skull and/or a channel device implantable in the skull can be used to facilitate direction and focusing. Treatment and diagnosis of multiple neurological conditions may be facilitated with the disclosed systems, methods and devices.

Abstract: A method of detecting and measuring the condition of intraluminal esophageal mucosa. An esophagus is intubated with a catheter including an inflatable and deflatable balloon and one or more impedance sensing electrodes on an exterior surface of the catheter. The balloon is inflated to press the impedance sensing electrode(s) into a mucosa of the interior esophageal wall. An electric current is directed through the mucosa via the impedance sensing electrode(s) while the impedance sensing electrode(s) is/are pressed by the balloon against the mucosa and measure impedance of the mucosa.

Abstract: A cervical dilation reading apparatus and method of use to accurately and precisely determine cervical dilation measurements during labor and delivery. The apparatus includes a measuring device having a length with a first end and a second end, a fixed attachment configured to couple with a first finger and fixedly engage the first end of the measuring device, and a slidable attachment configured to couple with a second finger and slidably engage the measuring device along the length between the first and second ends.

Abstract: The invention is directed to methods and systems of hyperspectral and multispectral imaging of medical tissues. In particular, the invention is directed to new devices, tools and processes for the detection and evaluation of diseases and disorders such as, but not limited to diabetes and peripheral vascular disease and cancer, that incorporate hyperspectral or multispectral imaging.

Abstract: A method of analysis is disclosed. The method comprises: receiving from a mobile device of a subject sensor data and/or device state data, analyzing the data to provide at least one behavioral pattern associated with the subject, comparing the behavioral pattern with a reference behavioral pattern, and estimating the likelihood that the subject is experiencing or is expected to experience an abnormal condition based on the comparison.

Abstract: Methods, systems, and apparatus, including computer programs encoded on a computer storage medium, for determining sleep stages and sleep events using sensor data. In some implementations, sensor data is obtained over a time period while a person is sleeping. The time period is divided into a series of intervals. Heart rate and changes in the heart rate are analyzed over the intervals. Based on the analysis of the heart rate changes, sleep stage labels are assigned to different portions of the time period. An indication of the assigned sleep stage labels is provided.

Abstract: A multi-purpose wearable patch includes a stretchable and permeable substrate, a first sensing unit mounted in the stretchable and permeable substrate, the sensing unit that can conduct a first measurement of a user to produce a first measurement signal, a treatment unit that produces a first treatment field in the user's body; a circuit electrically connected with the treatment unit and the sensing unit; and a semiconductor chip in connection with the circuit and configured to receive the first measurement signal from the sensing unit. The semiconductor chip produces a first treatment control signal to control the treatment unit to produce a first treatment field in the user's body.

Abstract: This invention is smart clothing (such as a shirt or pair of pants) for ambulatory motion capture comprising: an article of clothing; an electromagnetic energy emitter; an electromagnetic energy receiver; a helical stretching and/or bending electromagnetic energy pathway that spans a body joint, wherein motion of the body joint stretches and/or bends the pathway, and wherein stretching and/or bending of the pathway changes the flow of electromagnetic energy from the emitter to the receiver; and a data processor, wherein the data processor analyzes changes in the flow in order to measure motion of the body joint.

Abstract: A mobile healthcare device and method of operating the same are provided. The method includes setting a mode of the mobile healthcare device to a measurement mode, displaying a screen for guiding a user to maintain a predetermined position during the measurement mode, and, in response to a predetermined amount of time passing from a time at which the screen begins to be displayed, obtaining state information of the user based on bio information of the user, the bio information being received from a sensor.

Abstract: Devices, methods, computer-readable media, and systems for determining an identity of a food are disclosed. For example, a method may receive at least one property of at least one component in a sample of a food from an intra-oral device including a spectrometer, the at least one property obtained via the spectrometer, compares the at least one property to a plurality of food signatures, and determines the identity of the food based upon the comparing. In another example, a system may include an intra-oral device and a wireless device. The intra-oral device may include a spectrometer for measuring at least one property of at least one component in a sample of a food. The wireless device may include a processor for receiving the at least one property, comparing the at least one property to a plurality of food signatures, and determining the identity of the food based upon the comparing.

Abstract: A cardiac electrophysiology system including a means for identifying the source of an arrhythmia in the heart is disclosed. The disclosed system may be an electrocardiograph device and may generate an enhanced electrocardiogram (EKG) of a cardiac structure. The disclosed system may include a disclosed catheter inserted into a chamber of the cardiac structure. The disclosed catheter may include electrodes configured to measure an analog electrical signal of the electrical activity of the cardiac structure over time, and a transformer configured to remove a direct current (DC) offset of the analog electrical signal to generate an analog electrical signal centered at 0 volts (V), which may be sampled by an analog-to-digital converter (ADC) and gain adjusted to a maximum resolution of the ADC to produce an enhanced digital electrocardiogram (EKG) signal.

Abstract: In at least one example, a medical device is provided. The medical device includes at least one therapy electrode, at least one electrocardiogram (ECG) electrode, at least one acoustic sensor, and at least one processor coupled with the at least one acoustic sensor, the at least one ECG electrode, and the at least one therapy electrode. The at least one processor can receive at least one acoustic signal from the at least one acoustic sensor, receive at least one electrode signal from the ECG electrode, detect at least one unverified cardiopulmonary anomaly using the at least one electrode signal, and verify the at least one unverified cardiopulmonary anomaly with reference to data descriptive of the at least one acoustic signal.

Abstract: A method for data display includes acquiring a three-dimensional (3D) map of a lumen inside a body of a subject, transforming the 3D map of the lumen into a two-dimensional (2D) image by projecting the 3D map onto an annulus, and presenting the 2D image on a display screen.

Abstract: A multiple sensor wireless wearable device measuring oxygen saturation and/or heart rate includes a single housing, two or more sensors, each having a pick up beam, an alarm generator, and a timer generator. The two or more sensors, the alarm generator, and the timer generator are all housed inside the single housing, and the two or more sensors are placed in specifically selected placements that avoid their respective pick up beams crossing each other. The housing is a garment specifically designed for containing the device.

Abstract: A medical imaging device is disclosed. In an embodiment, the medical imaging device includes an imaging area; a patient positioning device including a positioning table and a transfer plate for positioning a patient in a patient positioning area; a frame element for disposing at least one component relative to the imaging area and/or the patient positioning device, wherein the frame element has a first side arm, a second side arm and an apex area disposed between the first side arm and the second side arm; and a first mounting device and a second mounting device for retaining the frame element. The apex area is disposed above the transfer plate in respect of a vertical direction.

Abstract: A method is for generating CT image data with spectral information from an examination region of a patient. According to an embodiment, the examination region is exposed to polychromatic X-radiation. Data from the examination region, including a first projection measurement data record and at least one second projection measurement data record, is captured via a photon counting detector. At least one second projection measurement data record with reduced resolution is generated based upon the at least one second projection measurement data record. The first and at least one second projection measurement data records are then transmitted to an image generation unit. Finally, the resolution of the first projection measurement data record is transferred onto the at least one second projection measurement data record with reduced resolution and/or an image data record based on the at least one second projection measurement data record with reduced resolution. A system is also disclosed.

Abstract: A method for triggering image capture by a group of simultaneously X-ray exposed multiple wirelessly interlinked self-triggering direct radiography (DR) detector assemblies includes the steps of performing an initiation step to identify the group of participating DR detector assemblies prior to X-ray exposure, detecting the X-ray exposure by a first participating DR detector assembly, the first participating DR detector assembly performing a trigger step to signal all participating DR detector assemblies to start image capture.

Abstract: A mobile X-ray apparatus includes: an X-ray radiation device; a controller configured to control the X-ray radiation device; a power supply configured to supply operating power to the X-ray radiation device and the controller via a lithium ion battery and control overcurrent occurring during X-ray emission by the X-ray radiation device; and a charger configured to charge the power supply. Each of the controller, the power supply, and the charger is embodied in a physically separate module, and each of the power supply and the charger is encased in a metal case.

Abstract: A supporting device according to an embodiment includes a holder, a supporter, and a controller. The holder holds a user terminal that includes a detection surface that detects an input operation by an operator. The supporter is connected to the holder and is movably provided so as to locate a user terminal at a predetermined position, the user terminal being held by the holder. The controller fixes the supporter in a state where the supporter is located at a predetermined position when the detection surface detects the input operation.

Abstract: A myocardial blood flow analysis scan includes incorporating a pharmacological kinetic model with the standard factor analysis model where each time activity curve is assumed to be a linear combination of factor curves. Pharmacological kinetics based factor analysis of dynamic structures (K-FADS-II) model can be applied, whereby estimating factor curves in the myocardium can be physiologically meaningful is provided. Additional optional aspects include performing a discretization to transform continuous-time K-FADS-II model into a discrete-time K-FADS-II model and application of an iterative Improved Voxel-Resolution myocardial blood flow (IV-MBF) algorithm.

Abstract: Disclosed herein are workstation, medical imaging apparatus having the same and method for controlling thereof. The medical imaging apparatus includes an X-ray source configured to irradiate X-rays; an X-ray detector configured to obtain raw data by detecting X-rays irradiated from the X-ray source; and an image processor configured to determine a motion parameter to represent motion of at least one of an object, the X-ray source, and the X-ray detector from a medical image reconstructed based on the obtained raw data, and reconstruct a motion-compensated medical image of the object based on a virtual trajectory of the X-ray source generated based on the determined motion parameter.

Abstract: In an image analysis device, an image analysis method, and a non-transitory computer-readable recording medium, it is determined whether a radiographic image is captured by rocking a rocking imaging grid. The image analysis device includes: a radiographic image acquisition section; a dosage data acquisition section that acquires dosage data indicating, in a time-series manner, a dosage of radiation rays exposed to a specific position in an imaging area in a specific period; and a determining section that determines whether the dosage data has a first feature indicating a dosage variation as a plurality of radiation absorbing bodies and a radiation transmitting body disposed between adjacent radiation absorbing bodies pass through a space between the specific position and a radiation source, and determines that the radiographic image corresponding to the dosage data determined to have the first feature is a rocking grid use image captured by rocking a rocking imaging grid.

Abstract: A method and system provides improved auscultation training for medical students and other healthcare providers. The system includes an instructor stethoscope which generates an acoustic output corresponding to an ausculatory sound from the patient. The acoustic output is wirelessly transmitted to earpieces worn by one or more students such that the students can simultaneously listen with the instructor to the ausculatory sound. The acoustic output may be recorded for future listening and training. The instructor stethoscope includes a resonance chamber having a capacitive pickup to receive the ausculatory sound wave from the stethoscope chest piece. The acoustic wave is converted to an analog signal and then to a digital signal, which is broadcast and then re-converted to an analog signal for the listening students.

Abstract: Techniques, systems, and devices are disclosed for synthetic aperture ultrasound imaging using spread-spectrum, wide instantaneous band, coherent, coded waveforms.

Abstract: An endovascular navigation system and method are disclosed. The endovascular navigation system includes an elongate flexible member, a endovascular electrogram lead disposed at a distal end of the elongate flexible member and configured to sense an endovascular electrogram signal, a processor and an output device. The processor is configured to receive the endovascular electrogram signal, to determine a peak amplitude of a P-wave in the endovascular electrogram signal, and to determine that the position of the distal end of the elongate flexible member is within a predetermined structure within the venous vasculature of the patient. The output device is configured to display a visual indication that the distal end of the elongate flexible member is within the predetermined structure within the venous vasculature of the patient, where the visual indication is different from the endovascular electrogram signal of the venous vasculature of the patient.

Abstract: A hydraulic unit of an electronic control brake system including a modulator block; a pair of master cylinder connection portions; a first valve row having a plurality of first valve accommodation bores; a second valve row having a plurality of second valve accommodation bores; a pair of low-pressure accumulator bores arranged in a bottom side of the modulator block in the lateral direction; pump accommodation bores; a pair of shuttle valve ESV accommodation bores arranged between the first valve row and the second valve row; a pair of driving force control valve TC accommodation bores arranged between wheel cylinder connection portions formed in the modulator block and the first valve row; and a pair of high-pressure accumulator bores arranged in the modulator block in a longitudinal direction, wherein the pair of high-pressure accumulator bores are formed to have an arrangement parallel to the motor accommodation bores.

Abstract: Computerized characterization of cardiac wall motion is provided. Quantities for cardiac wall motion are determined from a four-dimensional (i.e., 3D+time) sequence of ultrasound data. A processor automatically processes the volume data to locate the cardiac wall through the sequence and calculate the quantity from the cardiac wall position or motion. Various machine learning is used for locating and tracking the cardiac wall, such as using a motion prior learned from training data for initially locating the cardiac wall and the motion prior, speckle tracking, boundary detection, and mass conservation cues for tracking with another machine learned classifier. Where the sequence extends over multiple cycles, the cycles are automatically divided for independent tracking of the cardiac wall. The cardiac wall from one cycle may be used to propagate to another cycle for initializing the tracking. Independent tracking in each cycle may reduce or avoid inaccuracies due to drift.

Abstract: Provided is a method of generating an ultrasound image corresponding to a cross-section of interest, which is performed by an ultrasound imaging apparatus. Exemplary embodiments include a method of generating an ultrasound image corresponding to a cross-section of interest of an object by storing ultrasound echo signals respectively corresponding to a plurality of frames that constitute a three-dimensional (3D) ultrasound image of the object, performing beamforming on a focal point on the cross-section of interest of the object, and generating beam focused data for the focal point.

Abstract: The present invention relates to formation of an image indicating viscoelastic characteristics in a specimen by a simple method. Stepwise pressurization in which, after pressure is instantaneously increased to a certain pressure value, the certain pressure value is kept for a certain time period is performed to measure the variation with time of strain distribution in the specimen and to calculate a stress from strain distribution at a saturation measurement time when the effect of the viscosity of a viscoelasticity measurement reference layer is saturated, thereby evaluating the modulus of elasticity and the coefficient of viscosity of a body tissue.

Abstract: In an ultrasound diagnostic apparatus of the present invention, the controller writes and reads element data of one frame into and out from two or more buffer memories 21a, 21b, . . . 21i sequentially frame by frame and assigns the element data of one frame sequentially read out from the buffer memories to a plurality of arithmetic blocks of a signal processor, wherein the element data assigned is subjected to processing by each of a plurality of arithmetic cores in the plurality of arithmetic blocks to produce an image signal.

Abstract: Systems and methods for relaying electrical signals representing acoustic response of a volume of tissue to light and ultrasound stimulation. In an embodiment, a plurality of ultrasound transducers receive acoustic energy from the volume and generate electrical energy, which is transmitted via an electrical path to a relay system. The ultrasound transducers are operated at a wide band frequency of at least 1 MHz to 5 MHz to receive acoustic energy from the volume of tissue responsive to light stimulation and at a narrower band frequency to receive acoustic energy from the volume of tissue responsive to acoustic stimulation. The relay system relays the electrical signals to an optoacoustic system or an ultrasound instrument for further processing depending on whether the electrical signals resulted from ultrasound or light stimulation. In an embodiment, optoacoustic, ultrasound, or other images are generated from the electrical signals and may be coregistered, overlayed, or displayed.