Abstract: A blood pressure measurement device includes an outer case; a base; a pump provided on the base such that the pump is shifted from a center of the outer case and located on one side as viewed in a circumferential direction of a living body; a drive unit provided on the base and located on one side of the pump as viewed in a direction orthogonal to the circumferential direction; an on-off valve provided on another side of the pump as viewed in the direction orthogonal to the circumferential direction; a pressure sensor provided on said another side of the pump as viewed in the direction orthogonal to the circumferential direction; and packing provided between the on-off valve and the pressure sensor and the base.

Abstract: A blood pressure measurement device includes an outer case; a base; a pump provided on a surface of the base such that the pump is shifted from a center of the outer case and located on one side as viewed in a circumferential direction of a living body; a first pressure sensor and a second pressure sensor that are provided such that the first pressure sensor and the second pressure sensor are arranged side by side in the circumferential direction and located on one side as viewed in a direction orthogonal to the circumferential direction; and a first on-off valve and a second on-off valve that are provided such that the first on-off valve and the second on-off valve are arranged side by side in the circumferential direction with reference to the first pressure sensor and the second pressure sensor.

Abstract: Devices, systems and methods that track various aspects of a person's sleep and environment to optimize one or more aspects of the user's environment and sleep conditions, quality and duration, together or alone, and help make the one or more users maintain and prolong his or her deep sleep status and improve the their sleep duration and quality.

Abstract: Systems, apparatuses and methods are provided for identifying the position of a catheter relative to internal tissue and controlling injection of a therapeutic substance(s) into the internal tissue. In one embodiment, a catheter includes one or more position sensing electrodes disposed at or near a distal end of the catheter that allow identifying the position of the catheter relative to the internal tissue. The catheter also includes one or more contact sensors that provide an indication of contact and/or contact forces between the catheter and internal tissue before and after a therapy delivery needle is extended from the catheter into the internal tissue. Outputs of the contact sensor(s) allows for confirming insertion of the therapy delivery needle into the internal tissue to a desired depth. Once inserted to the desired depth, a therapeutic substance may be injected into the internal tissue at the desired depth.

Abstract: A blood pressure measurement device includes a bag-like pressing cuff wound around a measurement target site of a living body; a back plate arranged on the living body side of the pressing cuff; a bag-like sensing cuff arranged on the living body side of the back plate; a supply device configured to supply a fluid into the cuffs; first guides arranged on the living body side of the pressing cuff and configured to form wrinkles in a direction intersecting the winding direction; and second guides arranged on the living body side of the sensing cuff and configured to form wrinkles in the direction intersecting the winding direction.

Abstract: An example of a system for monitoring and treating respiratory distress in a patient may include one or more non-invasive monitoring devices to acquire patient condition signals and a respiratory distress monitoring circuit to monitor a state of the respiratory distress using the patient condition signals. The respiratory distress monitoring circuit may include a signal processing circuit to generate patient condition parameters using the patient condition signals and a respiratory distress analyzer, which may include a parameter analysis circuit and a notification circuit. The parameter analysis circuit may be configured to produce a patient condition metric being a function of the patient condition parameters and to perform prediction and/or detection of an exacerbation of the respiratory distress based on the patient condition metric. The notification circuit may be configured to produce an alert notifying a result of the performance of the prediction and/or detection.

Abstract: High blood pressure measurement accuracy can be achieved with a blood pressure monitor employing a double cuff structure. A blood pressure monitor of the present invention includes a pressing member that includes a pressure cuff having a bag shape capable of containing fluid and generates a pressing force toward a measurement site of a subject when the pressing member is wound around the measurement site and the pressure cuff is inflated, and a controller that controls an operation of the adjuster such that the fluid is contained in the sensing cuff in an amount corresponding to biometric information about the subject and the pressure cuff is inflated or inflated and deflated in this state when performing a blood pressure measurement, and calculates a blood pressure value of the subject based on an output from the pressure sensor.

Abstract: A sphygmomanometer includes: a bag-shaped sensing cuff to be worn to wrap a measurement site; a back plate disposed on the sensing cuff along a surface opposite to the measurement site; a pressing member for pressing the back plate toward the measurement site; and a blood-pressure calculating part calculating a blood pressure based on a pressure of a fluid stored in the sensing cuff. Regarding a longitudinal direction perpendicular to a circumferential direction of the measurement site to be wrapped by the sensing cuff, a surface facing the measurement site in edge potions on both sides in a width direction along the longitudinal direction of the back plate is curved in a direction away from the measurement site toward tips.

Abstract: A fluid pressure detection device capable of accurately detecting a pressure change of a fluid flowing inside a tube includes a substrate, a piezoelectric element formed on the top surface of the substrate, a support body which is annular and surrounds the piezoelectric element and supports the top surface of the substrate, and a lid body which is provided to close the top opening of the support body, and deforms the tube with the bottom surface of the substrate by pressing the substrate through the support body.

Abstract: A physiological signal sensing system and a physiological signal sensing method are provided. The physiological signal sensing system includes a signal processing device and a physiological signal sensing device having a plurality of sensing electrodes. The sensing electrodes are used to contact the skin of an organism to sense a plurality of physiological signals. The signal processing device is coupled to the physiological signal sensing device to receive the physiological signals, compares these physiological signals with the reference physiological signal pattern to obtain a comparison result, selects a selected electrode pair from the sensing electrodes based on the comparison result, and uses the selected electrode pair to perform physiological signal measurement on the organism during a normal operation period.

Abstract: A method, system, apparatus, and/or device for measuring a physiological condition of a user. The method, system, apparatus, and/or device may include: a band configured to attach to a body part of a user; a housing coupled to the band; a processing device integrated into the band or disposed within the housing; an interface integrated into the band or disposed within the housing; and a miniaturized impedance sensor.

Abstract: Monitoring vital parameters of a wearer of a compression garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Analyzing the pressure signal waveform for an oscillating amplitude as a function of time and/or a representation of a pulse of the wearer provides an indication of blood pressure of the wearer.

Abstract: A pulse wave measurement device including: a belt to be worn around a measurement target site; first and second pulse wave sensors that are mounted on the belt spaced from each other with respect to a width direction of the belt, and that detect pulse waves of opposing portions of an artery passing through the measurement target site; a pressing unit that is mounted on the belt is capable of changing pressing forces of the pulse wave sensors against the measurement target site; a waveform comparing unit that acquires pulse wave signals which are time-sequentially output by the pulse wave sensors respectively, and compares waveforms of the pulse wave signals; and a pulse wave sensor pressing force setting unit that variably sets the pressing forces by the pressing unit such that the waveforms of the pulse wave signals compared by the waveform comparing unit become identical to each other.

Abstract: In one aspect, a computer-implemented method includes receiving signals corresponding to wavelengths of light detected by an optical sensor placed in proximity to a patient's body, and for each received signal: separating the signal into an AC signal and a DC signal; separating the AC signal into component signals; analyzing the component signals through a fractional phase transformation to identify a desired component signal and harmonic signals associated with the desired component signal; smoothing the desired component signal, the harmonic signals, and the DC signal; and combining the smoothed desired component signal, the smoothed harmonic signals, and the smoothed DC signal to generate a modulation signal. A modulation ratio signal is generated based on the modulation signals derived from the signals, and a peripheral oxygen saturation (SpO2) of the patient's body is determined based on the modulation ratio signal.

Abstract: This disclosure relates generally to health monitoring and assessment systems, and more particularly to perform postural stability assessment of a user and quantify the assessed postural stability. In an embodiment, the system, by monitoring specific actions (which are part of certain tests done for the postural stability assessment) being performed by a user, collects inputs which are then processed to determine SLS duration, the body joint vibration, and the body sway area of the user, while performing the tests. By processing the SLS duration, the body joint vibration, and the body sway area together, a postural stability index score for the user is determined, and based on this score, postural stability assessment for the user is performed.

Abstract: Embodiments herein relate to reflective optical medical sensor devices. In an embodiment, a reflective optical medical sensor device including a central optical detector and a plurality of light emitter units disposed around the central optical detector is provided. A plurality of peripheral optical detectors can be disposed to the outside of the plurality of light emitter units. Each of the plurality of peripheral optical detectors can form a channel pair with one of the plurality of light emitter units. The reflective optical medical sensor device can also include a controller in electrical communication with the central optical detector, the light emitter units, and the peripheral optical detectors. The controller can be configured to measure performance of channel pairs; select a particular channel pair; and measure a physiological parameter using the selected channel pair. Other embodiments are also included herein.

Abstract: Disclosed is a method for initializing an analyte measurement system (1, 2, 3), the analyte measurement system (1, 2, 3) being designed for continuous in-vivo measurement of a body fluid analyte concentration.

Abstract: A technique for determining skin sodium content using bioimpedance spectroscopy includes applying a current at a predetermined frequency to skin of a subject, measuring a voltage across the skin of the subject produced by the current, determining a resistance across the skin of the subject at the predetermined frequency using the measured voltage, and determining skin sodium content using the measured voltage.

Abstract: An apparatus for measuring bio-information may include a pulse wave sensor that may measure a pulse wave signal from an object in contact with a measurement surface. The apparatus may include a force sensor that may measure a contact force between the pulse wave sensor and the object. The apparatus may include a fastener configured to fasten the pulse wave sensor to an electronic device such that the pulse wave sensor is rotatable around a center axis in a length direction of the pulse wave sensor. The apparatus may include a processor that may determine a direction in which a measurement region of the pulse wave signal or the measurement surface of the pulse wave sensor is oriented, select a measurement mode from among a plurality of measurement modes, and estimate bio-information of the object.

Abstract: A biopsy incision device (100) comprising a proximal side (101), to be arranged on a skin surface, and a distal side (102), said distal side (102) comprising a blade actuator (103) associated with at least one cutting blade (104), is provided. The blade actuator (103) and said at least one cutting blade (104) being suspended at a pivoting point (105) on said distal side (102), such that said blade actuator (103) and said at least one cutting blade (104) may pivot around a pivoting axis (A), such that said at least one cutting blade (104) may cut said skin surface.