Abstract: An example method includes, determining, based on data received from a plurality of sensors that are each attached to a respective finger of a plurality of fingers of a hand of a patient, data that represents movements of one or more fingers of the plurality of fingers; and determining, based on the data that represents the movements of the one or more fingers, one or more objective indications of motor control of the patient.

Abstract: A health care system acquires data determines whether a patient is at risk of hypervolemia or hypovolemia. The method comprises (a) acquiring from a device memory a patient's absolute intrathoracic impedance data over a pre-specified time period, (b) determining a running average of the intrathoracic impedance data over the pre-specified time period, and (c) determining by the system whether the running average of the intrathoracic impedance data over the pre-specified time period exceeds one of a first and second range, the first range being a higher value boundary of intrathoracic electrical impedance and the second range being a lower value boundary of intrathoracic electrical impedance.

Abstract: The present invention comprises methods and devices comprising a scraping element used to contact circumferentially and longitudinally the surface walls of the uterine cavity to provide for broad contact of the intended surface with the device, resulting in attainment of a sufficient volume and comprehensive tissue sample for analysis as an endometrial biopsy or screening uterine cancer. The device may provide for a reservoir for the obtained sample to be contained when removing from the uterine cavity, cervical canal, and vagina. The device may be comprised of a detachable means or be of a material that allows the user to cut the sampling head of the device for placement in collection means to maximize the amount of tissue or cells being sent to the laboratory for analysis.

Abstract: A non-invasive system and method for measuring blood pressure variability includes a cuff (20) pneumatically connected to a pump (14) to inflate the cuff to be wrapped around a limb (21) of a subject. A pressure sensor (18) is associated with the cuff for measuring cuff pressure (52). A photoplethysmogram sensor (26) attached to a fingertip in the same limb (21) of the subject and placed distal to the cuff for monitoring blood flow and recording a pulse plethysmograph signal. A control unit (12) connected to the pressure sensor (18) and the photoplethysmogram sensor (26) for simultaneously recording the cuff pressure and the plethysmograph signal such that an empirical relationship is derived between the cuff pressure and an amplitude measure of the plethysmograph signal (54) to measure short-term variation in systolic and diastolic blood pressures at a frequency corresponding to respiratory cycle.

Abstract: An ergonomic suction syringe and method for performing medical procedures in which suction is generated and can be delivered to a medical device by a single-handed compression motion, with suction actuated by forward motion of a piston into a cylinder, and in which suction can be maintained essentially permanently once activated without any further effort by the operator, even hands-free.

Abstract: A surgical instrument includes a proximal control mechanism. The proximal control mechanism has an opening through which a resilient latch arm can be inserted to engage a locking surface of a fixed latch structure contained within the proximal control mechanism. The resilient latch arm is contained entirely within the proximal control mechanism when engaged. A release channel extends from an outer periphery of the proximal control mechanism to the resilient latch arm entrance opening. The release channel provides a passage through which a release tool can be inserted to engage the resilient latch arm and provides a fulcrum for the release tool where the release channel is joined to the outer periphery of the proximal control mechanism. The surgical instrument can be released by prying the resilient latch arm away from the locking surface of the fixed latch structure with the release tool used as a lever on the fulcrum.

Abstract: Adaptive respiratory condition assessment can include capturing signals generated by sensors of a portable device positioned to sense a user's body. The sensors can generate the signals in response to sensor-detected movements of the user's body measured along multiple axes and corresponding to lung activity in the user's body during respiratory cycles. A preferred axis of measurement can be selected using signal processing performed by a signal processor embedded in the portable device. Waveforms generated from signals corresponding to signals generated in response to movements of the user's body measured along the preferred axis can be filtered for extracting biomarkers from the waveforms using the signal processor. The one or more biomarkers extracted correspond to the lung activity. Based on the biomarkers, a respiratory condition of the user can be determined. A notification based on the respiratory condition as determined can be generated and conveyed with the portable device.

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: 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: 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: 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: 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.