Abstract: The present disclosure generally relates to user interfaces and more specifically to techniques for displaying user interfaces associated with physical activities. Exemplary user interfaces related to activity competitions are described. Exemplary user interfaces related to a friends list for activity sharing are described. Exemplary user interfaces associated with alerts presented to a user in response to automatically determining a boundary of a workout are described. Exemplary user interfaces associated with configuring a pace alert for a workout application are described.

Abstract: Devices for determining the likelihood that a user of a primary monitoring device (“PMD”) has developed a medical condition, generally comprising sensors coupled to the PMD, wherein the PMD detects changes to sensor readings over time, and wherein the changes indicate a change in the likelihood that a user of the PMD has developed a medical condition. In some embodiments, motion sensors are operably coupled to the PMD, and the PMD monitors and saves data relating to characteristics of motion detected, which are used to determine whether there has been a change in a likelihood that a user is undergoing a medical event. In further embodiments, the PMD comprises cameras, and the PMD monitors and saves data relating to movement of a user's eyes, which is utilized to determine whether there has been a change to a likelihood that the user is currently undergoing a medical event.

Abstract: The present disclosure describes systems and methods to evaluate auditory efferent function by exposing a patient to short-duration acoustic click stimuli to generate a click-evoked otoacoustic emission (CEOAE) occurring in each ear of the patient, and in response to exposing the patient to click stimuli, concurrently sampling outer hair cell activity (OHC) and medial olivocochlear reflex (MOCR; efferents) in each ear of the patient, monitoring the middle ear muscle reflex (MEMR) in each ear of the patient, and measuring a change in cochlear activity in the patient based on the CEOAE, MOCR, and MEMR of each ear of the patient.

Abstract: An analyte sensor system may include a first communication circuit configured to transmit a wireless signal in a first communication mode and a second communication mode, and a processor, wherein the processor determines whether a first condition is satisfied, the first condition relating to the sensor signal or to communication by the first communication circuit, and shifts the system to a second communication mode responsive to the first condition being satisfied.

Abstract: An analyte sensor system is provided. The system includes a base configured to attach to a skin of a host. The base includes an analyte sensor configured to generate a sensor signal indicative of an analyte concentration level of the host, a battery, and a first plurality of contacts. The system includes a sensor electronics module configured to releasably couple to the base. The sensor electronics module includes a second plurality of contacts, each configured to make electrical contact with a respective one of the first plurality of contacts, and a wireless transceiver configured to transmit a wireless signal based at least in part on the sensor signal. The system includes a first sealing member configured to provide a seal around the first and second plurality of contacts within a first cavity. Related analyte sensor systems, analyte sensor base assemblies and methods are also provided.

Abstract: Disclosed is a fully implantable sensor for detecting at least one analyte in a sample of body fluid. The sensor has a measurement chamber plate that receives the sample of bodily fluid and a quantum cascade laser illumination source that generates an illumination light beam in the spectral range and transmits it to the measurement chamber plate. The illumination light beam at least partially illuminates the measurement chamber plate and the measurement chamber plate generates a reflection light beam in response to the illumination by the illumination light beam. The reflection light beam at least partially illuminates the sample of body fluid within the measurement chamber plate. An optical detector detects at least one property of the reflection light beam and generates a sensor signal dependent on the presence of the analyte. A controlled evaluates the sensor signal. A method using an inventive fully implantable sensor is also disclosed.

Abstract: Systems and methods for processing sensor data and self-calibration are provided. In some embodiments, systems and methods are provided which are capable of calibrating a continuous analyte sensor based on an initial sensitivity, and then continuously performing self-calibration without using, or with reduced use of, reference measurements. In certain embodiments, a sensitivity of the analyte sensor is determined by applying an estimative algorithm that is a function of certain parameters. Also described herein are systems and methods for determining a property of an analyte sensor using a stimulus signal. The sensor property can be used to compensate sensor data for sensitivity drift, or determine another property associated with the sensor, such as temperature, sensor membrane damage, moisture ingress in sensor electronics, and scaling factors.

Abstract: Disclosed herein are devices and methods for detecting blood glucose levels in a subject that involve passively quantifying mid-infrared emissions from the eye of the subject.

Abstract: Various analyte sensor systems for controlling activation of analyte sensor electronics circuitry are provided. Related methods for controlling analyte sensor electronics circuitry are also provided. Various analyte sensor systems for monitoring an analyte in a host are also provided. Various circuits for controlling activation of an analyte sensor system are also provided. Analyte sensor systems utilizing a state machine having a plurality of states for collecting a plurality of digital counts and waking a controller responsive to a wake up signal are also provided. Related methods for such analyte sensor systems are also provided. Systems for controlling activation of analyte sensor electronics circuitry utilizing a magnetic sensor are further provided. One or more display device configured to display one or more analyte concentration values are also provided.

Abstract: An analyte sensor system is provided. The system includes a base configured to attach to a skin of a host. The base includes an analyte sensor configured to generate a sensor signal indicative of an analyte concentration level of the host, a battery, and a first plurality of contacts. The system includes a sensor electronics module configured to releasably couple to the base. The sensor electronics module includes a second plurality of contacts, each configured to make electrical contact with a respective one of the first plurality of contacts, and a wireless transceiver configured to transmit a wireless signal based at least in part on the sensor signal. The system includes a first sealing member configured to provide a seal around the first and second plurality of contacts within a first cavity. Related analyte sensor systems, analyte sensor base assemblies and methods are also provided.

Abstract: An analyte sensor system is provided. The system includes a base configured to attach to a skin of a host. The base includes an analyte sensor configured to generate a sensor signal indicative of an analyte concentration level of the host, a battery, and a first plurality of contacts. The system includes a sensor electronics module configured to releasably couple to the base. The sensor electronics module includes a second plurality of contacts, each configured to make electrical contact with a respective one of the first plurality of contacts, and a wireless transceiver configured to transmit a wireless signal based at least in part on the sensor signal. The system includes a first sealing member configured to provide a seal around the first and second plurality of contacts within a first cavity. Related analyte sensor systems, analyte sensor base assemblies and methods are also provided.

Abstract: A flexible sensor pad includes a cavity to hold a sensor unit with an attached cable. According to one aspect of the present invention, a light-shielding layer is coupled to a bottom surface of the sensor pad, surrounds the sensor unit, and extends past two sides of the sensor pad. A transparent adhesive layer is coupled to the light-shielding layer and extends past two sides of the light-shielding layer. Another light shielding layer is coupled to a top surface of the sensor pad and covers the sensor unit. The cable divides the sensor pad into a first side and a second side which are mirror images of each other.

Abstract: In a non-invasive optical detection system and method, sample light is delivered into a scattering medium. A first portion of the sample light passing through a volume of interest exits the scattering medium as signal light, and a second portion of the sample light passing through a volume of non-interest exits the scattering medium as background light that is combined with the signal light to create a sample light pattern. Reference light is combined with the sample light pattern to create an interference light pattern having a holographic beat component. Ultrasound is emitted into the volume of non-interest in a manner that decorrelates the background light of the sample light pattern from the holographic beat component. The holographic beat component is detected during the measurement period. An optical parameter of the volume of interest is determined based on the detected holographic beat component.

Abstract: In some embodiments, the present invention generally relates to the separation of blood within a device to form plasma or serum. In some embodiments, the present invention generally relates to the removal of fluids, such as blood, contained within a device. In one aspect, the present invention is generally directed to systems and methods for receiving blood from a subject and processing the blood to form plasma or serum. For example, a device may be applied to the skin of a subject to receive blood from the subject and pass the blood through a separation membrane, which separates the blood into plasma and a portion concentrated in blood cells. As another example, blood or plasma may be allowed to clot within the device and serum (the unclotted portion of the blood) may be withdrawn from the device. The device may contain, in some cases, a vacuum source such as a pre-packaged vacuum to facilitate receiving of blood and/or passage of the blood through the separation membrane to produce plasma or serum.

Abstract: A data processing device that performs data processing of monitoring a person, the data processing device includes: a calculator configured to calculate pupil movement and head movement of the person; an evaluator configured to evaluate a suitability degree of a situation in calculating the VOR; a provision unit configured to provide the suitability degree evaluated by the evaluator to data calculated by the calculator; a selector configured to select a first technique of calculating the sleepiness based on the VOR of the person or a second technique different from the first technique based on the suitability degree provided to the data; a first sleepiness calculator configured to calculate the sleepiness based on the first technique when the selector selects the first technique; and a second sleepiness calculator configured to calculate the sleepiness based on the second technique when the selector selects the second technique.

Abstract: An optical measurement system comprises an optical source configured for generating source light having an optical wavelength spectrum. The optical measurement system compises an interferometer configured for splitting the source light into sample light and reference light. The interferometer is further configured for delivering the sample light into an anatomical structure, such that the sample light is scattered by the anatomical structure, resulting in physiological-encoded signal light that exits the anatomical structure. The interferometer is further configured for combining the signal light and the reference light into interference light having the optical wavelength spectrum encoded with depths of the anatomical structure. The optical measurement system further comprises a dispersive spectrometer configured for generating an optical wavelength spectrum-intensity profile from the interference light.

Abstract: One or both of epilepsy seizure detection and prediction at least by performing the following: running multiple input signals from sensors for epilepsy seizure detection through multiple classification models, and applying weights to outputs of each of the classification models to create a final classification output. The weights are adjusted to tune relative output contribution from each classifier model in order that accuracy of the final classification output is improved, while power consumption of all the classification models is reduced. One or both of epilepsy seizure detection and prediction are performed with the adjusted weights. Another method uses streams from sensors for epilepsy seizure detection to train and create the classification models, with fixed weights once trained. Information defining the classification models with fixed weights is communicated to wearable computer platforms for epilepsy seizure detection and prediction.

Abstract: The present invention relates to a portable device and a method for measuring skin hydration using the same.

Abstract: The present invention provides for a system and method for the diagnosis of skin cancer, wherein visual data is acquired from a skin lesion by a passive or active optical, electronical, thermal or mechanical method, processing the acquired visual field image into a classifier, applying a dermoscopic classification analysis to the image and converting, by sonification techniques, the data to raw audio signals, wherein the raw audio signals are analyzed with a second machine learning algorithm to increase interpretability and the precision of diagnosis.

Abstract: A controller controls a temperature sensation provider that provides temperature sensations to an object contacting a contact surface of the temperature sensation provider. The controller includes a database including control information that associates values of a temperature of the contact surface with values of a controlled variable of the temperature sensation provider for each of the temperature sensations, and a temperature controller that controls the temperature sensation provider based on a measured temperature of the contact surface, a temperature sensation to be provided, and the control information.

Abstract: A method for managing urinary incontinence is provided. The method includes receiving historical information through an application; receiving input through an application; and making a recommendation to the user regarding an absorbent article.

Abstract: A method, system, and computer program for non-invasively monitoring a physiological parameter and providing biofeedback. The method, system, and computer program provide for the non-invasive detection of a physiological parameter by detecting changes in color channel values of a user in a live video feed and presenting biofeedback to the user indicating the relative position of the physiological parameter to an optimal range.

Abstract: Disclosed is an information processing method executed by a computer. The information processing method includes identifying a sleep onset time and an awakening time based on time series data relating to an activity status of a user; calculating a first midpoint at which an interval between the sleep onset time and the awakening time is evenly divided into two; and outputting information indicating a time at the calculated first midpoint.

Abstract: Systems and methods for monitoring sleep are disclosed. According to an aspect, a method includes emitting light into tissue. The method also includes detecting light backscattered from the tissue. Further, the method includes determining a sleep pattern based on the backscattered light.

Abstract: A pain measurement and diagnostic system (PMD) for bioanalytical analysis of pain matrix activity and the autonomic nervous system to diagnose and validate patient treatments, health status and outcomes to diagnose and validate patient treatments and outcomes. The PMD is implemented using medical devices for measuring and reporting objective measurements of pain through patient monitoring and analyzing related biological, psychological, social, environmental, and demographic factors that may contribute to and effect physiological outcomes for patients and through the analysis, improve diagnosis of pain, the evaluation of related disease states, and treatment options.

Abstract: The circuit may include bio-stimulating signal generating circuit which generates a bio-stimulating signal in a bio-stimulating mode, a bio-signal electrode which delivers the bio-stimulating signal generated in the bio-stimulating mode and receives a bio-signal in a bio-signal measuring mode, a switch block which is turned on when a voltage of the bio-stimulating signal is greater than a first reference voltage which is greater than a second reference voltage or lower than the second reference voltage, first and second resistors, and a bio-signal measuring circuit which measures voltage signals divided by the first and second resistors or measures a signal of the bio-signal electrode according to whether the switch block is turned on. The first and second resistors may be serially connected between the bio-signal electrode and the switch block, and divide a voltage of a signal of the bio-signal electrode when the switch block is turned on.

Abstract: Disclosed embodiments concern a system for monitoring one or more mechanical properties of an assembly of rigid bodies, comprising: at least one first transducer that is operative to excite mechanical waves that propagate from a first rigid body of the assembly via a contact interface to a second rigid body of the assembly; at least one distant sensor that is operative to sense one or more physical stimuli relating to the mechanical waves propagating in the second rigid body; a memory; and a processor that is operative to execute instructions stored in the memory to perform the following steps: receiving electronic signals that relate to the mechanical waves propagating in the first and second rigid body; and determining, based on the received electronic signals, a state and/or a change in a state of a structural feature of the assembly.

Abstract: A method for calculating a representation of energy expenditure, according to one embodiment, includes receiving input from multiple source, the sources including at least one sensor. An energy expenditure value is calculated based on the input. A method for utilizing real-time sensor data to guide breathing, according to one embodiment, includes receiving biometric sensor data about a user wearing a wearable device. An output is selected based on the sensor data for guiding a breathing rate and/or a breathing depth of the user. The selected output is sent to an output subsystem selected from the group consisting of an output subsystem of the wearable device and an output subsystem of a host. A different output is selected in response to detecting a change in the biometric sensor data.

Abstract: An intraoperative neurophysiological monitoring (IONM) system for identifying and assessing neural structures comprises at least one probe, at least one reference electrode, at least one strip or grid electrode, at least one sensing electrode, and a stimulation module. Threshold responses determined by stimulation during a surgical procedure are used to identify and assess functionality of neural structures. The identified neural structures are avoided and preserved while diseased or damaged tissue is resected during said surgical procedure.

Abstract: A wearable breath analysis device is disclosed that may be worn, for example, around the neck or wrist of a user. The wearable device may be a stand-along device (in which case it may include a display that provides a user interface), or may operate in conjunction with a smartphone or other command device. The wearable device may include auditory and/or vibratory notice and communications features or capabilities, for example, such as a reminder or notice to conduct a breath analyte measurement, instructions to the user in the course of conducting the measurement, and notice of the breath analyte measurement results. The auditory or vibratory notice may be provided at the wearable, and/or at the command device where a command device is used. Related methods also are provided.

Abstract: A device for measuring biological information includes at least one light emitting element configured to emit light having predetermined wavelength, a light receiving element configured to receive returned light from a subject with respect to the emitted light, an attachment determination unit configured to determine whether the device is attached to the subject with respect to the light receiving element based on an amount of returned light received, and a measurement-point determination unit configured to determine whether or not a point where the device is attached to the subject is suitable for measuring the biological information based on the amount of returned light received, when the attachment determination unit determines that the device is attached to the subject.

Abstract: In some examples, determining a heart failure status includes using an implantable medical device configured for subcutaneous implantation and comprising a plurality of electrodes and an optical sensor. Processing circuitry of a system comprising the device may determine, for a patient, a current tissue oxygen saturation value based on a signal received from the at least one optical sensor, a current tissue impedance value based on a subcutaneous tissue impedance signal received from the electrodes, and a current pulse transit time value based on a cardiac electrogram signal received from the electrodes and at least one of the signal received from the optical sensor and the subcutaneous tissue impedance signal. The processing circuitry may further compare the current tissue oxygen saturation value, current tissue impedance value, and current pulse transit time value to corresponding baseline values, and determine the heart failure status of the patient based on the comparison.

Abstract: In some examples, determining a health status includes using an implantable medical device configured for subcutaneous implantation and comprising at least one optical sensor. Processing circuitry of a system comprising the device may determine, for a patient, a current tissue oxygen saturation value based on a first signal received from the at least one optical sensor and a current pulsatile oxygen saturation value based on a second signal received from the at least one optical sensor. The processing circuitry may further compare the current tissue oxygen saturation and current pulsatile oxygen saturation values to corresponding baseline values, determine corresponding heart failure and pulmonary statuses of the patient based on the comparisons, and determine the health status of the patient based on the statuses.

Abstract: An adhesive patch for a medical device having a hub, such as an infusion device, is provided. The adhesive patch includes a first backing layer to be coupled to the medical device. The first backing layer is composed of a first material. The adhesive patch includes a first adhesive layer coupled to the first backing layer and a second backing layer coupled to the first adhesive layer. The second backing layer is composed of a second material, and the second material is different than the first material. The adhesive patch includes a biocompatible second adhesive layer coupled to the second backing layer, and the second adhesive layer is to be coupled to an anatomy.

Abstract: In nuclear medical imaging, respiratory motion is corrected. Rather than pairwise estimation of motion from projection views, a sequence-based technique is used to jointly estimate parameters for a motion model across many projection views. In one approach, this sequence-based method is iteratively solved with a maximum likelihood objective function incorporating the motion model. A surrogate respiration signal is used to gate for the joint estimation and used to convert gated motion parameters to temporal motion parameters.

Abstract: The methods and apparatuses presented herein determine and/or improve the quality of one or more physiological assessment parameters, e.g., response-recovery rate, based on biometric signal(s) and/or motion signal(s) respectively output by one or more biometric and/or motion sensors. The disclosed methods and apparatuses also estimate a user's stride length based on a motion signal and a determined type of user motion, e.g., walking or running. The speed of the user may then be estimated based on the estimated stride length.

Abstract: A monitoring device configured to be attached to a subject includes a photoplethysmography (PPG) sensor configured to detect/measure physiological information from the subject, and a processor configured to process the physiological information to detect subject stress, and to determine an origin of the subject stress. The processor can determine the origin of the subject stress by increasing a sampling rate of the PPG sensor to collect higher acuity physiological information. The processor also can determine the origin of the subject stress by processing data from the PPG sensor to determine whether the subject is likely to have atrial fibrillation. In response to determining that the subject is likely to have atrial fibrillation, the processor can increase a frequency of pulsing of an optical emitter of the PPG sensor and/or increase a sampling rate of the PPG sensor to collect higher acuity data for diagnosing that atrial fibrillation is truly occurring.

Abstract: A method is provided for determining a movement-corrected B1 field map on contrast medium injection, wherein before the injection, a B1 field map is determined. Following the contrast medium administration, a position change is determined at the position at which the B1 field map was determined. With the position change and the B1 field map, the movement-corrected B1 field map is determined.

Abstract: Computer implemented methods and systems for detecting noise in cardiac activity are provided. The method and system obtain a far field cardiac activity (CA) data set that includes far field CA signals for a series of beats, overlay a segment of the CA signals with a noise search window, and identify turns in the segment of the CA signals. The method and system determine whether the turns exhibit a turn characteristic that exceed a turn characteristic threshold, declare the segment of the CA signals as a noise segment based on the determining operation, shift the noise search window to a next segment of the CA signal and repeat the identifying, determining and declaring operations; and modify the CA signals based on the declaring the noise segments.

Abstract: Systems and methods are disclosed for estimating patient-specific blood flow characteristics. One method includes acquiring, for each of a plurality of individuals, a geometric model and estimated blood flow characteristics of at least part of the individual's vascular system; executing a machine learning algorithm on the geometric model and estimated blood flow characteristics for each of the plurality of individuals; identifying, using the machine learning algorithm, features predictive of blood flow characteristics corresponding to a plurality of points in the geometric models; acquiring, for a patient, a geometric model of at least part of the patient's vascular system; and using the identified features to produce estimates of the patient's blood flow characteristic for each of a plurality of points in the patient's geometric model.

Abstract: Apparatus for assessing medical risks of a patient includes an analytics engine and equipment that provides data to the analytics engine. The analytics engine analyzes the data from the equipment to determine a sepsis risk score, a falls risk score, and a pressure injury score. The apparatus further include displays that are communicatively coupled to the analytics engine and that display the sepsis, falls, and pressure injury risk scores. The displays include a status board display located at a master nurse station, an in-room display provided by a room station of a nurse call system, an electronic medical records (EMR) display of an EMR computer, and a mobile device display of a mobile device of a caregiver assigned to the patient.

Abstract: An interferometer grating support (118) of an imaging system (100) configured for grating-based x-ray imaging includes at least two elongate supports (302) separated from each other by a non-zero distance, wherein the at least two elongate supports have a first end (312) and a second end (316). The grating support further includes a first arc shaped grating (202) affixed to the first end and a second arc shaped grating (204) affixed to a second end (316). A non-transitory computer readable medium is configured with computer executable instructions which when executed by a processor of a computer cause the processor to: move a grating support, which supports G0 and G1 gratings of an interferometer and a bowtie filter, into a region between a low energy photon filter and a beam collimator, which are between a radiation source and an examination region, for a grating-based x-ray imaging scan.

Abstract: The invention relates to a problem of setting mutual position of an anatomy being imaged and imaging means of a computed tomography imaging apparatus so that specifically the very volume of the anatomy desired to be imaged actually is imaged. To further the positioning, a positioning tool in a form of a three-dimensional virtual positioning model (40), generated from the anatomy to be imaged, is shown on a display from which the volume (41) of the anatomy desired to be imaged can be pointed, selected or defined.

Abstract: In general, radiation shielding systems that shield radiation from multiple directions are described. In one embodiment, a method of shielding radiation is provided, including supporting a shielding device on an object proximate a radiation source, positioning a first shielding portion in a vertical position relative to the object, positioning a second shielding portion to extend away from the first portion, the second shielding portion attached to the first portion, and shielding radiation from the radiation source by the first shielding portion and the second shielding portion such that the first and second shielding portions provide a radiation shielding zone for a healthcare practitioner.

Abstract: According to one embodiment, an X-ray computed tomography apparatus includes an X-ray tube, a detector, and processing circuitry. The X-ray tube emits X-rays. The detector detects X-rays that have been emitted from the X-ray tube and have passed through the subject. The processing circuitry sets an imaging condition. The processing circuitry evaluates the imaging condition based on information on a lower limit range of a count value of the detected X-rays that may cause image degradation.

Abstract: A support apparatus for positioning a C-arm of a mobile x-ray apparatus in a horizontal position, enables a standard mobile x-ray device to perform CBCT acquisitions on an upright standing object or patient.

Abstract: The present approaches relates to the use of silicon-based energy-discriminating, photon-counting detectors, such as for use in X-ray based imaging including computed tomography. The described approaches address the resolution and classification of X-ray photons affected by Compton scatter, which may be detected as having energy levels below their proper level due to collision or deflection events.

Abstract: A mobile medical imaging robot is disclosed. The robot comprises a medical imaging device, and a vehicle configured to carry the medical imaging device. The vehicle is motorized so as to move on a surface, such the floor of an examination room. The robot further comprises a cable designed to link said vehicle to a wall of a room, such as a medical examination room. In at least one non-limiting embodiment, motorized robot movements along the surface are controlled manually by a user.

Abstract: A system for performing robotic surgery on a patient disposed on a bed includes a gantry comprising a computed tomography (CT) diagnostic device, a platform supporting the gantry, and a robotic arm assembly attached to the platform. The gantry slides along the platform via a first carriage to allow entry of at least part of the patient into the bore of the CT device. The robotic arm assembly is attached to the platform via a pivot arm and a second carriage to allow the assembly to slide along the platform to enable surgery to be performed on the patient. The pivot arm is substantially parallel to the upper surface of the platform.

Abstract: An X-ray device includes a camera to image an object and output the image of the object, a display member using a touch screen to display the image of the object output from the camera, and an X-ray irradiation region of the object, an X-ray irradiation region controller to control a region of the object to which an X-ray is irradiated, and a control member to enable the irradiation region controller to control the region of the object to which an X-ray is irradiated according to the X-ray irradiation region, when the X-ray irradiation region is determined, based on the image of the object displayed in the display member.