Abstract: Methods and devices for correcting electrocardiogram (EKG) indication saturation may include receiving an EKG indication from at least one sensor and determining that a saturation condition has been met in response to receiving the EKG indication. Additionally, the methods and devices may include incrementing an EKG saturation level based on a determination that the saturation condition has been met. Moreover, the methods and devices may include determining whether the EKG saturation level satisfies an EKG saturation threshold. The methods and device may include disregarding at least a second EKG indication in accordance with a determination that the saturation level satisfies the EKG saturation threshold. The methods and devices may further include transmitting the second EKG indication to an output device in accordance with a determination that the saturation level does not satisfy the EKG saturation threshold.

Abstract: This disclosure is directed to a catheter having an asymmetric basket-shaped electrode assembly at the distal end of the catheter body formed from a plurality of spines with electrodes. The plurality of spines are radially distributed across a first circumferential portion. One or more counter spines are radially distributed across a remaining second circumferential portion. Diagnostic electrodes are arrayed across the spines, while the counter spines may have one or more reference electrodes.

Abstract: A heart activity sensor structure includes a flexible substrate being substantially non-conductive, at least two electrodes printed on one side of the flexible substrate and configured to be placed against a skin of a user in order to measure biometric signals related to heart activity, and an electrostatic discharge shield printed on opposite side the flexible textile substrate, compared to the printing of the at least two electrodes, for protecting the at least two electrodes from static electricity.

Abstract: Medical catheterization is carried out by receiving a plurality of analog bioelectric signals in respective channels and multiplexing the bioelectric signals in respective selection events. The selection events comprise making a first connection with a reference voltage, thereafter breaking the first connection and making a second connection with one of the bioelectric signals. The method is further carried out by outputting the multiplexed bioelectric signals to an analog-to-digital converter.

Abstract: Method for processing a brain wave signal (4) obtained from a person using a brain wave detector (5). One or more stimuli are applied to the person in which each of the one or more stimuli comprises a pseudo random noise component modulating the stimulus intensity. A brain wave signal (4) is detected after applying the one or more stimuli. The detected brain wave signal is processed to calculate which of the one or more stimuli is present in the detected brain wave signal using correlation techniques. The pseudo random noise component comprises a pseudo random noise sequence of the class of maximum length sequences, which are further modulated with twice their associated bit frequency.

Abstract: The invention provides a sensor for measuring both impedance and ECG waveforms that is configured to be worn around a patient's neck. The sensor features 1) an ECG system that includes an analog ECG circuit, in electrical contact with at least two ECG electrodes, that generates an analog ECG waveform; and 2) an impedance system that includes an analog impedance circuit, in electrical contact with at least two (and typically four) impedance electrodes, that generates an analog impedance waveform. Also included in the neck-worn system are a digital processing system featuring a microprocessor, and an analog-to-digital converter. During a measurement, the digital processing system receives and processes the analog ECG and impedance waveforms to measure physiological information from the patient. Finally, a cable that drapes around the patient's neck connects the ECG system, impedance system, and digital processing system.

Abstract: Example methods, apparatus/systems and articles of manufacture for determining intensity of a biological response to a presentation are disclosed. An example method includes accessing galvanic skin response (GSR) data obtained from a subject while exposed to a presentation. The GSR data includes a plurality of trough-to-peak instances. The example method includes generating a GSR intensity profile by assigning trough-to-peak scores to corresponding ones of the trough-to-peak instances, defining a plurality of time windows, and assigning window scores to corresponding ones of the time windows based on the trough-to-peaks scores of the trough-to-peak instances occurring within the corresponding time windows. The example method also includes determining an effectiveness of the presentation based on the window scores of the GSR intensity profile.

Abstract: A method is provided for identifying a muscle abnormality. The method may include acquiring image data associated with a plurality of muscles in an area of interest of a living subject and generating a data model for the plurality of muscles based on the image data. The method further includes calculating the volume and/or length of one of the plurality of muscles based on the data model, and determining if the volume and/or length for the muscle, as calculated, deviates from volume and/or length associated with a healthy muscle. If it is determined that the volume and/or length for the muscle deviates from the volume and/or length associated with a healthy muscle, a muscle abnormality can be identified based on the deviation.

Abstract: In a magnetic resonance method and apparatus for determining an item of deformation information of an examination object that exhibits a cyclical movement within an examination subject, a spatial magnetization pattern is generated in an MR scanner, and MR signals are acquired from the subject during at least two cycles of the cyclical movement, with the spatial magnetization exhibiting differences in a subsequent cycle of the movement compared to an earlier cycle. Segmented subsequent MR images are acquired in a subsequent cycle and the examination object is localized therein. This localization of the examination object is then used to localize the examination object in segmented earlier MR images from the earlier cycle, and the item of deformation information is determined in a spatial direction from the segmented earlier MR images.

Abstract: An apparatus comprises an instrument including an elongated, flexible body and a shape sensor including an optical fiber extending at least partially along the elongated, flexible body. The apparatus also includes a radiopaque material incorporated with the optical fiber along an entire length of the optical fiber. The radiopaque material is incorporated such that the optical fiber is radiographically distinguishable from a remainder of the elongated, flexible body.

Abstract: A capsule device configured to navigate through a patient's GI track is disclosed. System and method to turn on the capsule device based on acceleration is described. First the capsule is monitored at a slow sampling mode. Then the capsule is monitored at a fast sampling mode. A user can input hand motion to change the acceleration to turn on the capsule device.

Abstract: There is provided a method for dynamically determining a breath related parameter, which includes averaging a breath related parameter over a first period of time, calculating a breath related value over a second period of time and adapting the duration of the first period of time according to the calculated breath related value.

Abstract: A method of diagnosing an air leak in a lung compartment of a patient may include: advancing a diagnostic catheter into an airway leading to the lung compartment; inflating an occluding member on the catheter to form a seal with a wall of the airway and thus isolate the lung compartment; measuring air pressure within the lung compartment during multiple breaths, using the diagnostic catheter; displaying the measured air pressure as an air pressure value on a console coupled with the diagnostic catheter; and determining whether an air leak is present in the lung compartment based on the displayed air pressure value during the multiple breaths.

Abstract: A wearable respiration monitoring system and associated method that is configured to (i) determine three dimensional displacement of the spine of a subject with respect to the axial displacement of the subject's chest wall, (ii) process the three dimensional anatomical data, (iii) determine at least one respiration parameter associated with the monitored subject as a function of the three dimensional anatomical data, and (iv) generate at least one respiration parameter signal representing the respiration parameter.

Abstract: A system and method for determining FRC, TGV, TLC and RV includes a hand-held unit with a shutter assembly designed to minimize measured air displacement due to shuttering. Measurements of flow and pressure are used to derive the lung parameters.

Abstract: Medical devices and methods for determining the size of blood vessels are disclosed. In one implementation, a blood vessel sizing device is configured for placement on an area of skin of a patient. The device includes a plurality of radiopaque concentric-circle elements. In one implementation, a blood vessel sizing method includes placing a marker having a plurality of concentric-circle elements on the skin of a patient, imaging a blood vessel of the patient and the device, and comparing the imaged blood vessel to the imaged circles to determine the blood vessel size, the concentric-circle elements allowing a determination of size without errors of parallax.

Abstract: A system and method for collecting a set of kinematic data streams from an activity tracking system with at least one activity monitoring system that is attached to a user; segmenting at least a subset of the kinematic data streams into a set of segments according to actions of the user; generating a set of biomechanical signals from the kinematic data streams wherein a biomechanical signal characterize a biomechanical property during a segment and includes generating a first integration data set through data integration and baseline error correction across the set of segments of the normalized kinematic data stream and determining at least a first biomechanical signal that is at least partially based on the first integration data set; and applying the set of biomechanical signals.

Abstract: Technology for use with a touchscreen user interface device that uses gesture swipe data to provide an early potential indication of onset of Parkinson's disease. Technology for use with a touchscreen user interface device that uses gesture swipe data to provide an information about motor skill development of a child. Technology for use with a touchscreen user interface device that uses gesture swipe data to provide an information about reading ability development of a child.

Abstract: Disclosed are a system, a method, and a program for initializing an attachment location of a measurement sensor. The method of initializing an attachment location of at least one measurement sensor includes requesting selection of the measurement sensor that is attached to a specific body unit (S100); recognizing identification information of the measurement sensor, which agrees with a selection manipulation of the measurement sensor (S200); matching the identification information with the body unit (S300); and determining sensing data received from the measurement sensor, which corresponds to the identification information, as motion data of the body unit. According to the inventive concept, because attachment locations of a plurality of measurement sensors are initialized, a terminal may accurately calculate a posture or motion of the user.

Abstract: A method, system and apparatus for image capture and registration are described. The method includes: obtaining a position of an imaging device in a tracking system frame of reference; obtaining a position of a patient in the tracking system frame of reference; determining, based on the position of the imaging device and the position of the patient, a transformation for registering an imaging device frame of reference with a patient frame of reference; receiving an instruction to capture an image, the instruction including coordinates identifying a target area in the patient frame of reference; applying the transformation to convert the coordinates to the imaging device frame of reference; and controlling the imaging device to capture an image based on the converted coordinates.

Abstract: The invention relates to a device for detecting analytes. In order to supply a need in alternative prenatal diagnostic methods which do not include the risks known in the state of art, the present invention provides a device for detecting analytes, including a polymer fiber and capturing molecules, wherein the capturing molecules bind to an analyte and/or a linker molecule.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: A biosensor including light emitting elements and a light receiving element disposed on a principal surface of a wiring board; a light shielding portion disposed between a light-emitting-element sealing portion and a light-receiving-element sealing portion; a base medium having light transmitting properties, disposed in parallel with the wiring board with the light shielding portion therebetween; an adhesion layer having light transmitting properties that bonds the base medium with the light-emitting-element sealing portion, the light-receiving-element sealing portion, and the light shielding portion; and a first electrocardiograph electrode attached to a principal surface of the base medium. Both end portions of the adhesion layer and both end portions of the base medium are disposed such that they overlap neither of the light-receiving-element sealing portion nor the light-emitting-element sealing portion when viewed from a direction normal to the principal surface of the wiring board.

Abstract: Disclosed herein is a sensor comprising a conduit; the conduit comprising an organic polymer; a working electrode; the working electrode being etched and decorated with a nanostructured material; a reference electrode; and a counter electrode; the working electrode, the reference electrode and the counter electrode being disposed in the conduit; the working electrode, the reference electrode and the counter electrode being separated from each other by an electrically insulating material; and wherein a cross-sectional area of the conduit that comprises a section of the working electrode, a section of the reference electrode and a section of the counter electrode is exposed to detect analytes.

Abstract: A support pad, including a first cushion layer, a second cushion layer, and a sensing device, is provided. The sensing device is positioned between the first and second cushion layers. The sensing device includes a plurality of sensing elements and a substrate. The substrate includes a plurality of tab portions and a plurality of expandable portions. The sensing elements are respectively mounted to the tab portions. The expandable portions are moveable between contracted and expanded positions in response to pressure applied thereto.

Abstract: A vocal dosimeter receives a first set of sensor data as sensor outputs through a sensor array including an acoustic sensor, a piezoelectric sensor, and an accelerometer. The dosimeter generates normalized sensor waveforms by filtering for an amplitude range from the quadratic mean of each individual raw sensor waveform through control of a first band-pass filter, and operates laryngeal activity detection to configure a vocalization filter with a vocalization threshold within a vocalization analysis window. A feedback control is generated in response to identifying a statistically similar vocalization amplitude in a vocal characteristic database.

Abstract: An eyelid position sensor system and/or an eye movement sensor system for an ophthalmic lens having an electronic system is described herein for recording data associated with sleep of the wearer. The eyelid position sensor system is part of an electronic system incorporated into the ophthalmic lens. The electronic system in at least one embodiment includes a system controller and a data manager. In at least one embodiment, the eyelid position sensor system is utilized to determine eyelid position and the eye movement sensor system is utilized to determine eye position for the system controller to determine if the wearer is awake, asleep, or in REM sleep.

Abstract: Monitoring patient compliance with a compression therapy regimen. Venous Refill Time (VRT) is monitored via a pressure sensor in a bladder of a compression system. A controller of the compression system correlates the monitored VRT to a predetermined threshold to determine whether the patient is using the compression system.

Abstract: Non-invasive monitoring of cardiovascular health is performed by monitoring changes in the volume of blood in the venous side of the vascular system. The blood volume changes are determined from measurements of bioimpedance of limbs or neck, in particular changes in bioimpedance in response to blood modulating events performed on the limbs or neck, where bioimpedance is measured and compared before and after such events.

Abstract: A method and an apparatus for recommending a route are provided. The route recommending method includes obtaining user's current body information; obtaining geographic information from a current position to a destination; and determining a recommended route to the destination on the basis of the body information and the geographic information.

Abstract: A electronic device, a system including the wearable electronic device, and an operating method of the wearable electronic device are disclosed. The electronic device includes a biosensor configured to sense bioinformation on a body of a user wearing the electronic device. The electronic device also includes a controller configured to determine a state of the user based on the bioinformation and surrounding environment information of a surrounding environment of the user, and control a change in a function of the electronic device based on the state of the user.

Abstract: Apparatus for improving health of a user is provided, including a first sensor, adapted to measure a first physiological variable, which is indicative of a voluntary action of the user. A second sensor is adapted to measure a second physiological variable, which is substantially governed by an autonomic nervous system of the user. Circuitry is adapted to receive respective first and second sensor signals from the first and second sensors, and, responsive thereto, to generate an output signal which directs the user to modify a parameter of the voluntary action.

Abstract: A method and system to deliver biomechanical feedback utilizes three major elements: (1) multiple hardware data capture devices, including optical motion capture, inertial measurement units, infrared scanning devices, and two-dimensional RGB consecutive image capture devices, (2) a cross-platform compatible physics engine compatible with optical motion capture, inertial measurement units, infrared scanning devices, and two-dimensional RGB consecutive image capture devices, and (3) interactive platforms and user-interfaces to deliver real-time feedback to motions of human subjects and any objects in their possession and proximity.

Abstract: An apparatus that monitors information associated with an oral cavity is provided, the apparatus comprising: a three-dimensional oral appliance; a data collection device having at least one sensor and/or hydrogel like material configured to sense the information associated with the oral cavity; an interface device cooperatively coupled to the data collection device, the interface device configured to transfer the information from the sensor device to a receiving device external to the oral cavity or the entire device is analyzed.

Abstract: A method for measuring body movement with a wearable device. The method includes receiving, from a magnetic sensor of the wearable device, first signal data indicative of a magnetic field of a wearable magnet, wherein the wearable device is placed on a first body segment and the wearable magnet is placed on a second body segment; determining, by a computing device based on the first signal data, a distance metric indicative of a relative distance between the wearable magnet and the wearable device, and an orientation metric indicative of an orientation relative to the wearable magnet; and determining a biomechanical model based on the type of body segment for the first body segment and the second body segment, wherein the biomechanical model includes a relationship constraint between the distance metric and the orientation metric.

Abstract: Provided are apparatuses for and methods of measuring a biological signal. The biological signal measuring apparatus includes reference point sensors configured to detect signals detected from at least two reference marks on a surface of a subject and a biological signal measuring position detector configured to generate information about a biological signal measuring position based on the signals detected from the at least two reference marks. The biological signal measuring apparatus measures the biological signal according to the information about the biological signal measuring position.

Abstract: A vaginal ring sensor device adapted to be placed within the vaginal vault of a user, the device including a ring body, at least one through hole that passes through the ring body, and at least one biosensor structured and arranged to sense and/or measure a parameter of vaginal fluid as such fluid passes through the at least one through hole.

Abstract: The present invention relates to a sensor guide wire (1) for intravascular measurements of at least one variable in a living body, which sensor guide wire (1) has a proximal region (2), a distal sensor region (3) and a tip region (4). The sensor guide wire (1) comprises, a sensor element arranged in said sensor region (3), a tip region core wire (5) having a longitudinal axis (6) and extending essentially along said tip region (4), and a coil (7) arranged in said tip region (4). The coil (7) at least partly encloses said tip region core wire (5), and a distal tip joint (8) is arranged at a distal end (9) of said sensor guide wire (1) for attaching said coil (7) to said tip region core wire (5). A major part of said tip region core wire (5) has a circular cross-section in a plane perpendicular to said longitudinal axis (6).

Abstract: A system and method of determining regions of interest for heart ablation using fractionation. The method can comprise detecting, via sensors, electro-cardiogram (ECG) signals, each ECG signal detected via one of the sensors and indicating electrical activity of a heart, determining, for each of the ECG signals, activation times (LATs) each indicating a time of activation of a corresponding ECG signal, generating, based on the determined LATs of each of the ECG signals, one or more driver maps and one or more perpetuator maps, each representing the electrical activity of the heart, deriving parameters from the driver and perpetuator maps, using at least fractionation, processing and combining the derived parameters into driver evidence and perpetuator evidence, and determining the regions of interest for heart ablation in accordance with the fractionation used to derive the driver evidence and the perpetuator evidence.

Abstract: A stand-on physiological sensor (e.g. floormat) measures vital signs and various hemodynamic parameters, including blood pressure and ECG waveforms. The sensor is similar in configuration to a common bathroom scale and includes electrodes that take electrical measurements from a patient's feet to generate bioimpedance waveforms, which are analyzed digitally to extract various other parameters, as well as a cuff-type blood pressure system that takes physical blood pressure measurements at one of the patient's feet. Blood pressure can also be calculated/derived from the bioimpedance waveforms. Measured parameters are transmitted wirelessly to facilitate remote monitoring of the patient for heart failure, chronic heart failure, end-stage renal disease, cardiac arrhythmias, and other degenerative diseases.

Abstract: According to one aspect there is provided a method comprising: loading, with an application, a webpage comprising an embedded activity recognition module; causing collection of activity sensor data from at least one sensor of a mobile device with a sensor polling module; causing transmission of the activity sensor data to the embedded activity recognition module; causing processing of the collected sensor data with the embedded activity recognition module to form processed activity sensor data; and receiving the processed activity sensor data from the activity recognition module.

Abstract: Provided is an apparatus and method of measuring a pulse wave. The method includes: causing receivers to respectively receive pulse wave signals that are detected at two points of an object, determining an effective pulse wave signal period by using the received pulse wave signals, and obtaining a pulse transit time (PTT) between the two points by using a result obtained after comparing a magnitude of an output signal of each of the receivers with a value that is less by a predetermined percentage than a peak value of an output signal of each of the receivers during the determined effective pulse wave signal period.

Abstract: Systems, methods, apparatuses, and software for measuring and determining physiological parameters of a patient are presented. In one example, a physiological measurement system includes an optical system configured to emit one or more optical signals into tissue of a patient, and detect the one or more optical signals after propagation through the tissue. The physiological measurement system includes a capacitance system configured to apply one or more electric field signals to a single side of the tissue to determine a capacitance signal based at least on changes in the one or more electric field signals, and a processing system configured to process at least the one or more detected optical signals and the capacitance signal to determine a physiological parameter of the patient.

Abstract: A technology for a wearable medical device for monitoring medical parameters. Medical measurement data can be received at the wearable medical device from a medical measurement sensor attached to the wearable medical device or a medical measurement sensor in communication with the wearable medical device. A calibration coefficient can be determined for calibrating the wearable medical device based on the medical measurement data. The wearable medical device can be calibrated based on the calibration coefficient.

Abstract: Methods and systems for performing T1 mapping. T1 samples are obtained from an acquisition including one or more inversion groupings. The acquisition may be designed to result in incomplete tissue magnetization recovery between inversion groupings. The acquisition may be designed for the use of non-uniform, non-180° preparatory pulses. The method may also include the combined use of data from different inversion groupings. A model is used in which fit parameters are variable dependent on the inversion grouping.

Abstract: Systems and methods for home monitoring and detection of febrile neutropenia in a patient are provided. The system includes a photoplethysmographic sensor for sensing photoplethysmographic signals of the patient, and one or more blood borne parameter sensors for sensing parameters in the patient's blood. A febrile neutropenia monitoring application receives information sensed by the photoplethysmography sensor and the one or more blood borne parameter sensors and determines, based on the received information, the presence or deterioration of febrile neutropenia.

Abstract: A method, system, and/or apparatus for automatically monitoring for possible mental or physical health concerns. The method or implementing software application uses or relies upon location information available on the mobile device from any source, such as cell phone usage and/or other device applications. The method and system automatically learns user activity patterns and detects significant deviations therefrom. The deviations are automatically analyzed for known correlations to mental or physical concerns, which can then be automatically communicated to a relevant friend, family member, and/or medical professional.

Abstract: Disclosed is a detector for a positron imaging unit, comprises a hollow body with an inner cylindrical wall and an outer wall spaced apart from the inner cylindrical wall. The hollow body includes a scintillating material, suitable to emit photons once hit by a 511 keV ?-ray, and one or more pairs of photo-detecting units (e.g. comprising PMTs or SiPM) for detecting photons emitted by the scintillating material; each photo-detecting unit of a pair being placed at opposite ends of the inner cylindrical wall along a radial direction. The scintillating material has scintillation decay time ? lower than 10 ns, an atomic number greater than 10, and a high scintillation yield greater than 8,000 photons/MeV, and comprises a mixture of xenon and argon. An imaging unit including the detector and a method to estimate the differential of the dose of radiation provided in a subject to cancer cells and to surrounding tissues in the course of hadrotherapy is also disclosed.

Abstract: A bed apparatus according to one embodiment, includes a top plate, a first slide actuator, an elevating actuator, and a second slide actuator. The first slide actuator supports the top plate to be slidable in the longitudinal direction. The elevating actuator supports the first slide actuator to be movable in the vertical direction, and is installed on the floor. The second slide actuator is provided between the first slide actuator and the elevating actuator and supports the first slide actuator such that the first slide actuator is slidable interlockingly with the vertical movement of the elevating actuator.

Abstract: A CT scanning system includes a rotatable gantry having an opening for receiving an object to be scanned, an x-ray tube, and a detector comprising an imaging area of pixels and a calibration area of pixels. The system further includes a pre-patient collimator positioned between the x-ray tube and the detector having first and second apertures that pass x-rays respectively to at least a portion of the imaging area of pixels, and to the calibration area of pixels, a motor configured to move the pre-patient collimator, and a computer programmed to determine a focal spot location using energy derived from x-rays that fall upon the calibration area of pixels, and issue commands to a motor to adjust a position of the pre-patient collimator based on the determination.