Abstract: A piezoelectric film sensor (3) of a swallowing sensor (1) includes a plurality of sensing portions (3A) and (3B) in a longitudinal direction of the neck region. The piezoelectric film sensor (3) is located within a range of movement of thyroid cartilage (103), which occurs along with swallowing, and is attached to skin of an anterior neck region (102). The piezoelectric film sensor (3) individually outputs analog signals (S1a) and (S2a) along with deformation of the plurality of sensing portions (3A) and (3B). The swallowing sensor (1) includes pre-processing units (21) and (22) and a signal processing unit (23). Each of the pre-processing units (21) and (22) separates the analog signal (S1a) or (S2a) into a displacement signal that is a low frequency component and a sound signal that is a high frequency component. The signal processing unit (23) determines whether the swallowing occurs based on the displacement signal.

Abstract: Existing wearable device-based approaches to capture a_tremor signal have accuracy limitations due to usage of accelerometer sensor with inherent noisy nature. The method and system disclosed herein taps characteristics of the PPG sensor of being sensitive to the motion artifact, as an advantage, to capture tremor_signals present in the PPG sensor. The method disclosed herein describes an approach to extract tremor_signals of interest from the PPG signal by performing a Singular Spectrum Analysis (SSA) followed by spectrum density estimation. The SSA comprises performing embedding on the acquired PPG signal, performing Principal Component Analysis (PCA) on the embedded signal and reconstructing the rest tremor signal from the significant principal components identified post the PCA. Further, the spectrum density estimation detects a dominant frequency present in the principal components, which is the dominant frequency associated with the rest tremor.

Abstract: The disclosure provides wearable cardiac arrest detection and alerting device that incorporates a non-invasive sensor based on optical and/or electrical signals transmitted into and received from human tissue containing blood vessels, and that transcutaneously quantifies the wearer's heart rate. The heart-rate quantification enables the detection of the absence of any heart beat by the wearable detection and alerting device indicative of the occurrence of a cardiac arrest, wherein the heart is no longer achieving effective blood circulation in the individual wearing the device. The display on the wearable cardiac arrest detection and alerting device may include the elapsed time since the time of detection of a heart rate that is below a predetermine lower limit value, i.e., the detected occurrence of a cardiac arrest event.

Abstract: An orthopedic system configured for use in a pre-operative, intra-operative, and post-operative assessment. The orthopedic system comprises a first screw, a second screw, a first device, a second device, and a computer. The first device and the second device are respectively coupled to a first bone and a second bone of a musculoskeletal system. The first and second devices each include electronic circuitry, one or more sensors, and an IMU. A bracket, wrap, or sleeve can be used to hold the first and second devices to the musculoskeletal system. The first and second devices are configured to send measurement data to a computer. The first and second devices each have an antenna system. Electronic circuitry in the first or second devices are configured to harvest energy from a received radio frequency signal to recharge a battery to maintain operation.

Abstract: A personal impact monitoring system is described herein comprising a monitoring station that receives impact events sent from personal impact monitors using a monitoring station receiver. The impact events which specify impact parameters associated with the impact events are stored in a data storage location associated with the monitoring station. Software operating on the operating station is configured to receive the impact events from the data storage location and to perform calculations based on the impact events to identify notable impact events.

Abstract: A sensor including electrodes, a control module and a physical layer module. The electrodes are configured to (i) attach to a patient, and (ii) receive a first electromyographic signal from the patient. The control module is connected to the electrodes. The control module is configured to (i) detect the first electromyographic signal, and (ii) generate a first voltage signal. The physical layer module is configured to: receive a payload request from a console interface module or a nerve integrity monitoring device; and based on the payload request, (i) upconvert the first voltage signal to a first radio frequency signal, and (ii) wirelessly transmit the first radio frequency signal from the sensor to the console interface module or the nerve integrity monitoring device.

Abstract: Example systems, methods, and apparatus are provided for using data collected from the responses of an individual with the computerized tasks of a cognitive platform to derive performance metrics as an indicator of cognitive abilities, and applying predictive models to generate an indication of neurodegenerative condition. The example systems, methods, and apparatus also can be configured to adapt the computerized tasks to enhance the individual's cognitive abilities, and for using data collected from the responses of an individual with the adapted computerized tasks to derive performance metrics and applying predictive models to generate the indication of neurodegenerative condition.

Abstract: An electronic system for bioimpedance signal acquisition, comprises: a current signal injection module configured for generating a current signal to be applied to a subject; a bioimpedance signal measurement module configured for measuring a bioimpedance signal based on a voltage generated by the current signal; a data quality detection module configured for detecting an AC or a DC level of the measured bioimpedance signal and detecting whether the AC or DC level is within or outside an AC reference value range and a DC reference value range, respectively; and a signal adaptation module configured for modifying at least one parameter of the current signal injection module or the bioimpedance signal measurement module based on said detection of the AC or DC level in relation to the AC reference value range and the DC reference value range, respectively.

Abstract: A blood pressure measurement module includes a base, a valve plate, a top cover, a micro pump, a driving circuit board, and a pressure sensor. The valve plate is disposed between the base and the top cover. The micro pump is in the base. The pressure sensor is disposed on the driving circuit board. An inlet channel of the top cover and the pressure sensor are connected to a gas bag. The micro pump operates to inflate the gas bag to press the skin of a user. The pressure sensor detects a pressure change in the gas bag so as to detect the blood pressure of the user.

Abstract: A system and method of a sensor for monitoring a circulatory condition, the system including a layered structure having a graphite-composite bonded to a flexible substrate, wherein the sensor further includes a microstructure arranged to increase the sensitivity of the sensor.

Abstract: A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

Abstract: A method of measuring a bio signal using a bio signal measuring apparatus includes: positioning electrodes included as part of the bio signal measuring apparatus to contact a surface of an examinee; switching an impedance measurer included as part of the bio signal measuring apparatus and including a voltmeter and a current source; measuring a first impedance value of the examinee while operating the impedance measurer according to a first mode; switching the impedance measurer to a second mode; measuring a second impedance value of the examinee while operating the impedance measurer according to a second mode; and obtaining bio impedance of the examinee based on the first and second impedance values and an internal impedance of the current source.

Abstract: A blood pressure measuring device includes a device main body; a curler configured to bend along a circumferential direction of a wrist of a living body, including one end and another end separated from each other, also configured to come into contact with a portion of the wrist at least between a dorsal side and a palmar side; a strap provided to the device main body; a sensing cuff arranged in a region of the wrist where arteries exist; a back plate provided between the curler and the sensing cuff and extending in a circumferential direction of the wrist; a pressing cuff provided on a side of the curler nearer to the strap and configured to press the sensing cuff; and a cuff provided on a side of the curler nearer to the living body and arranged on the dorsal side of the wrist.

Abstract: A device for measuring contractions and/or relaxation of one or more muscles of a body cavity, the device having a hollow body which is for positioning in the body cavity and which is covered by a coating made of or having a biocompatible material, the body being formed of two half-shells which are each physically connected, permanently and continuously during the use of the device, with the aid of non-compressible or deformable connecting means, to at least one pressure sensor, or part of the pressure sensor, arranged in the body. Also, a method for measuring the contraction and/or relaxation of the muscles of a body cavity, a method for monitoring the contractions and/or relaxation of the muscles, and a method for exercising these muscles.

Abstract: A breathing sensing device that detects breathing of a subject, the breathing sensing device including a film-shaped sensor configured to adhere to a body surface of the subject from a region corresponding to a xiphoid process of a sternum of the subject to a region corresponding to an epigastrium of the subject. The sensor is configured to detect the breathing of the subject by detecting relative positional changes between the region corresponding to the xiphoid process and the region corresponding to the epigastrium.

Abstract: A blood pressure measuring device includes a holder configured to be mounted on a wrist of a living body and come into contact with a portion of the wrist at least between a dorsal side and a palmar side; a sensing cuff provided on a side of the holder nearer to the living body and arranged in a region of the wrist where arteries exist; and a cuff provided on a side of the holder nearer to the living body and arranged on the dorsal side of the wrist.

Abstract: An electronic device and method for measuring user body information are provided. The method for measuring user body information includes detecting a contact of a user's body portion on at least two spots of a touch screen of the electronic device, upon detecting the contact of the user's body portion on the at least two spots of the touch screen, applying power to a first coil in the electronic device, and measuring the user body information using at least one of a voltage and a second current measured after a first current is induced across the user's body by a first magnetic field generated from the first coil as the power is applied.

Abstract: A nerve integrity monitoring device includes a control module and a physical layer module. The control module is configured to generate a payload request. The payload request (i) requests a data payload from a sensor in a wireless nerve integrity monitoring network, and (ii) indicates whether a stimulation probe device is to generate a stimulation pulse. The physical layer module is configured to (i) wirelessly transmit the payload request to the sensor and the stimulation probe device, or (ii) transmit the payload request to a console interface module. The physical layer module is also configured to, in response to the payload request, (i) receive the data payload from the sensor, and (ii) receive stimulation pulse information from the stimulation probe device. The data payload includes data corresponding to an evoked response of a patient. The evoked response is generated based on the stimulation pulse.

Abstract: The wrist-type body component measuring apparatus includes: a band configured to be worn on a wrist of a user; a first input electrode and a first output electrode disposed on an inside surface of the band and configured to be in contact with the wrist of the user; a second input electrode and a second output electrode disposed on an outside surface of the band; a measuring unit configured to apply a current to the first and second input electrodes and detect a voltage from the first and second output electrodes to measure a body impedance of the user; and an electrode converter configured to convert a disposition of the first and second input electrodes and the first and second output electrodes based on a determination of whether the band is worn on a left wrist or a right wrist of the user.

Abstract: A device and method for treating a hone includes a bone plate including first and second portions joined to one another via a connecting portion, a rigidity of the connecting portion being less than rigidities of each of the first and second portions in combination with a first sensor mounted on the first portion measuring strain on the first portion and a second sensor mounted on the second portion measuring strain on the second portion.