Abstract: There is provided herein a motion-based evaluation of reaction time that utilizes motion detection hardware of a mobile device to determine auditory and visual stimulated reaction time. In an embodiment, the subject holds a mobile computing device equipped with built-in triaxis accelerometer and gyroscope with both hands at arms length away from the face. A visual or auditory stimulus is then presented on screen via a software application that also records the response time for the individual to initiate a movement of the device. A simple reaction time test could include the movement of the device in any direction that exceeded a threshold of movement beyond what would be expected from static holding. An embodiment of a choice reaction time test would provide for specific directional movements as it related to an instructed stimulus.

Abstract: The blood pressure measuring device includes a device main body configured to form a flow path of a fluid and supply the fluid, and a cuff to be wound around a living body, the cuff provided with a bag-shaped connection portion with an opening and a connection plate with a hole communicating with the opening; the connection portion formed of a sheet member; the connection plate having a bending elastic modulus higher than that of the connection portion, bonded to the connection portion and adhered to the device main body; and the cuff configured to be inflated when the fluid is supplied to an internal space of the cuff.

Abstract: Disclosed are self-powering biofuel cell and sensor devices, systems and techniques. In some aspects, a self-powered biosensing system includes an electronic circuit; an anode including an enzymatic layer electrically coupled to a power supply voltage terminal of the electronic circuit and configured to interact with an analyte in a fluid, such as glucose or lactate; and a cathode electrically coupled to a ground voltage terminal of the electronic circuit, where the electronic circuit is operable to control and use the electrical energy generated at the anode and cathode for powering the biosensing system and detecting a concentration of the analyte in the fluid.

Abstract: A physical area network for detecting head injuries described herein enables significantly improved cranial health monitoring and treatment by utilizing internal (in-body) mechanisms and information and external mechanisms and information.

Abstract: A push-type blood collection needle includes a housing having an accommodating cavity therein, a rear cover and a needle body disposed in the accommodating cavity. The rear cover is movably disposed on the housing, and the rear cover has a supporting leg extending into the accommodating cavity. The needle body is provided with a rib. The accommodating cavity is internally provided with a projecting part that cooperates with and blocks the bottom of the rib. The supporting leg is provided with a stopper that cooperates with and blocks the side wall of the rib. And an elastic member is disposed between the needle body and the rear cover.

Abstract: A measurement chamber that is essentially dome shaped and has a base area with a membrane and has at least two connection points fora fluid flow. The measurement chamber has two outer webs opposite each other, one of the webs engaging a clamping edge of a coupling element.

Abstract: A flexible planar patch suitable for application to a patient's skin is provided. The planar patch comprises a capture layer (100) and a cover layer (200). The capture layer (100) comprises an analyte capture zone (105) and a fastener zone (104). The analyte capture zone (105) consists of a first water permeable material comprising a ligand capable of binding specifically to an analyte. The fastener zone (104) is impermeable to water and/or delimited from said analyte capture zone by a water impermeable barrier zone (108) and comprises an adhesive (133) capable of fastening the capture layer (100) removably to a surface. The cover layer comprises an adhesive (233) capable of fastening the cover layer (200) removably to the capture layer (100). In addition, a kit for assembly of the patch and a diagnostic method using the patch are provided.

Abstract: An apparatus includes a disposable assembly and a reusable assembly. The disposable assembly includes a fluid input port, a fluid output port, and a tube configured to provide fluid communication between the fluid input port and the fluid output port. The reusable assembly includes a housing, a fluid management assembly that is configured to transition between an open position and a closed position, and a sensing assembly. The fluid management assembly is configured to prevent fluid from traveling past the tube to the fluid output port in the closed position. The sensing assembly is configured to sense fluid accumulating within the tube while the fluid management assembly is in the closed position. The sensing assembly is also configured to drive the fluid management assembly from the closed position to the open position when the sensing assembly detects fluid within the tube at a predetermined range.

Abstract: A method of determining an indication of the hydration status relating to a subject. The method includes determining a measured impedance value for at least one body segment, and then; for each body segment, using the measured impedance values to determine at least one indicator at least partially indicative of a level of extracellular fluid. Indicators can then be used to determine an indication of the hydration status.

Abstract: Provided is an apparatus for measuring implant osseointegration, and the apparatus for measuring implant osseointegration includes: a vibration generation unit configured to apply multiple vibrations with frequencies in different bands, respectively, to an implant fixture; a vibration sensor configured to measure three-axis vibration information of the implant fixture caused by the vibrations from the vibration generation unit; and a control unit configured to determine the degree of osseointegration based on the measured vibration information.

Abstract: An exemplary system includes a photodetector configured to generate a plurality of photodetector output pulses over time as a plurality of light pulses are applied to and scattered by a target, a TPSF generation circuit configured to generate, based on the photodetector output pulses, a TPSF representative of a light pulse response of the target, and a control circuit configured to direct the TPSF generation circuit to selectively operate in different resolution modes.

Abstract: A non-invasive method and system is provided for determining an internal component of respiratory effort of a subject in a respiratory study. Both a thoracic signal (T) and an abdomen signal (A) are obtained, which are indicators of a thoracic component and an abdominal component of the respiratory effort, respectively. A first parameter of a respiratory model is determined from the obtained thoracic signal (T) and the abdomen signal (A). The first parameter is an estimated parameter of the respiratory model that is not directly measured during the study. The internal component of the respiratory effort is determined based at least on the determined first parameter of the respiratory model. The first model parameter is determined based on the thorax signal (T) and the obtained abdomen signal (A) without an invasive measurement.

Abstract: A method for manufacturing a blood pressure measurement cuff includes preparing an outer cloth, preparing an inner cloth, and forming a bag-shaped portion. The bag-shaped portion has an opening on a peripheral edge of the bag-shaped portion. A curler is inserted into the bag-shaped portion through the opening, the curler being flexible and configured to curve and conform to the measurement site. An air bladder is formed by welding the opening of the bag-shaped portion such that the air bladder surrounds an inner side and an outer side of the curler thereby containing the curler. The outer cloth is attached to an outer surface on a first side of the air bladder configured to be opposite to the measurement site, and the inner cloth is attached to an outer surface on a second side of the air bladder configured to be towards the measurement site.

Abstract: Disclosed is an apparatus for diagnosing vertigo and balance related ailment using Craniocorpography (CCG) technique. The apparatus includes a helmet adapted to be worn over a head of a patient. The helmet includes a plurality of light emitting diodes (LEDs). Further, the apparatus includes a camera placed directionally above at a vertical distance from the helmet while the helmet is being worn over the head of the patient. The camera is adapted to track movement of the patient when the CCG is performed on the patient. Furthermore, the apparatus includes an interface card adapted to connect the camera. The interface card is adapted to relay images captured by the camera. A computing system in communication with the interface card is also provided. The computing system is adapted to analyze and present at least a plurality of patient alignment parameters based on the images captured by the camera.

Abstract: One aspect relates to a catheter system, a use of such catheter system and a manufacturing method for such catheter system. The catheter system includes an at least partially flexible catheter body, at least a ring electrode, and at least a strain gauge. The ring electrode surrounds at least a portion of the flexible catheter body. The strain gauge is allocated to the ring electrode and the strain gauge is configured to measure a deformation of the flexible catheter body at a position allocated to the ring electrode to detect a contact between the ring electrode and tissue.

Abstract: The disclosure describes a wearable, low-cost and low-power Electrical Impedance Tomography system for gesture recognition. The system measures cross-sectional bio-impedance using electrodes on wearers' skin. Using all-pairs measurements, the interior impedance distribution is recovered, which is then fed to a hand gesture classifier. This system also solves the problem of poor accuracy of gesture recognition often observed with other gesture recognition approaches.

Abstract: Embodiments of the presently-disclosed subject matter include methods and systems for measuring a level of a neurotransmitter in a subject. Embodiments of the present methods comprise displaying a fixation point, a reward target, and a non-reward target, and measuring one or more saccade movement parameters for reward saccades and non-reward saccades. The saccade movement parameters can include velocity, amplitude, reaction time, or a combination thereof. The present methods can further include determining a reward modulation of the subject, the reward modulation being equal to a difference between the reward and the non-reward values for a respective saccade movement parameter. Some embodiments further include identifying the subject as including a deficiency of the neurotransmitter if there is a statistically measurable difference between the reward modulation of the subject and a reference reward modulation and/or if the non-reward and the reward saccade movement parameters are statistically equivalent.

Abstract: An electronic device according to one embodiment of the present disclosure may include: a housing; an optical element unit which may be configured to emit light toward a user's body, receive light reflected from the user's body, and convert the received light into a first signal; an IC element which may be configured to convert the first signal provided from the optical element unit into a second signal, and provide the second signal to a main circuit board disposed in the housing; a first circuit board that may be disposed between the optical element unit and the IC element and may be electrically connected to the optical element unit and the IC element; and a second circuit board that may include at least one first opening in which the IC element is mounted. The housing may include at least one transparent region such that the light generated by the optical element unit is transmitted through the transparent region to an exterior of the housing.

Abstract: A wearable device for monitoring medical properties of a patient, the device having a rigid frame, multiple members coupled to the rigid frame, and a housing having an electrical circuit, where the housing is secured to the rigid frame, where the rigid frame surrounds a void, and where the void is configured to accommodate a bottom surface of the housing.

Abstract: The systems and methods described herein determine metrics of cardiac or vascular performance, such as cardiac output, and can use the metrics to determine appropriate levels of mechanical circulatory support to be provided to the patient. The systems and methods described determine cardiac performance by determining aortic pressure measurements (or other physiologic measurements) within a single heartbeat or across multiple heartbeats and using such measurements in conjunction with flow estimations or flow measurements made during the single heartbeat or multiple heartbeats to determine the cardiac performance, including determining the cardiac output. By utilizing a mechanical circulatory support system placed within the vasculature, the need to place a separate measurement device within a patient is reduced or eliminated. The system and methods described herein may characterize cardiac performance without altering the operation of the heart pump (e.g., without increasing or decreasing pump speed).