Abstract: A method for detecting cardiac arrhythmia based on a photoplethysmographic (PPG) signal is provided. The method includes: receiving a PPG signal and a motion signal corresponding to a motion made by a user; extracting PPG signal segments and motion signal segments corresponding to a time period from the PPG signal and the motion signal, respectively, at every time period; filtering out motion artifact noise in the PPG signal segments according to the PPG signal segments and the motion signal segments, and converting the PPG signal segments and the motion signal segments into PPG spectrum diagrams and motion spectrum diagrams, respectively; obtaining an estimated heart rate according to the PPG spectrum diagrams and the motion spectrum diagrams; and determining whether cardiac arrhythmia is present based on the filtered PPG signal segments and the estimated heart rate.

Abstract: A device for monitoring a health parameter in a person is disclosed. The device includes a semiconductor substrate, at least one transmit antenna configured to transmit millimeter range radio waves over a 3D space below the skin surface of a person, multiple receive antennas configured to receive radio waves, the received radio waves including a reflected portion of the transmitted radio waves, wherein the semiconductor substrate includes circuits for processing signals received on the multiple receive antennas, wherein processing signals includes mixing signals of two different frequencies, and wherein the semiconductor substrate includes at least one output configured to output a signal that corresponds to a health parameter of a person in response to received radio waves.

Abstract: Systems, devices, and methods are provided for changing the power state of a sensor control device in an in vivo analyte monitoring system in various manners, such as through the use of external stimuli (light, magnetics) and RF transmissions.

Abstract: According to one aspect of the invention, there is provided a method for assessing blood flow regulation performance based on hemodynamics, comprising the steps of: calculating second biometric information corresponding to a time differential of first biometric information on a hemoglobin concentration measured from a cerebral part of a subject; and assessing blood flow regulation performance of the subject with reference to a response that occurs in the second biometric information in correspondence to a change in a posture of the subject.

Abstract: A method for estimating an ear geometry of an ear of a user with a hearing device, the hearing device comprising an ear canal microphone, an external microphone, and a receiver, includes: obtaining an external input signal using the external microphone; providing an output signal by the receiver; obtaining an ear canal microphone input signal using the ear canal microphone; and estimating the ear geometry based on the external input signal and the ear canal microphone input signal.

Abstract: An electronic device for identifying occurrence of hypotension and a method therefor are provided. The electronic device includes a housing, a user interface, a photoplethysmogram (PPG) sensor exposed through at least part of the housing, a motion sensor disposed in the housing, at least one processor operatively coupled with the user interface, the PPG sensor, and the motion sensor, and a memory operatively coupled with the at least one processor. The memory may store instructions which, when executed by the at least one processor, cause the at least one processor to, based on first data from the motion sensor indicating a change of a selected pattern, identify a blood pressure value based at least in part on second data from the PPG sensor, and based on the identified blood pressure value being lower than a first threshold, provide a notification through the user interface.

Abstract: A wearable electronic device is disclosed, including: a housing having a front plate disposed facing in a first direction, a rear plate disposed facing in a second direction opposite to the first direction, at least a part of the rear plate substantially transparent, and a side member defining a space between the front plate and the rear plate, a substrate disposed within the space, a biometric sensor module disposed between the substrate and the rear plate including at least one light source configured to emit light to an exterior of the wearable electronic device and at least one light detector configured to receive reflected light corresponding to the emitted light reflected from the exterior, and at least one magnetic substance disposed between the light source and the light detector to limit an amount of light reaching the biometric sensor module other than the reflected emitted light.

Abstract: Systems, methods, and devices of a health device network may include: a non-invasive glucometer that non-invasively measures analyte levels; an invasive glucometer communicatively coupled directly to the non-invasive glucometer; a cloud-based server communicatively coupled to the non-invasive glucometer or the invasive glucometer; a user device communicatively coupled to the cloud-based server; and/or a user interface that displays the invasive glucose measurement, the non-invasive glucose measurement, a data batch, and/or processed data to the user. The non-invasive glucometer and/or the invasive glucometer may aggregate an invasive glucose measurement and a non-invasive glucose measurement into the data batch.

Abstract: Shaped liver biopsy sheaths and methods for transfemoral transcaval liver access are disclosed.

Abstract: A sensor system has a low-noise sensor controller providing communications between an active-temperature-regulated optical sensor and an external monitor. A low-noise sensor controller drives optical emitters, receives resulting detected signals after attenuation by a blood perfused tissue site and communicates the detector signals to the attached signal processor. An optically-isolated controller front-end receives and digitizes the detected signals. A controller serializer transmits the digitized detector signal to the processor via a single, shielded coaxial cable.

Abstract: An electronic device may include a housing and a PhotoPlethysmoGram (PPG) sensor disposed inside the housing. The PPG sensor may include a first Light Emitting Diode (LED) configured to generate light in a first wavelength band, a second LED configured to generate light in a second wavelength band, a third LED configured to generate light in a third wavelength band, a fourth LED configured to generate light in a fourth wavelength band, and a light receiving module including at least one photo diode. The electronic device may include a processor operatively coupled with the PPG sensor and a memory operatively coupled with the processor. The memory may include instructions that, when executed, cause the processor to measure optical densities of the light generated by the first LED to the fourth LED, and calculate a blood glucose value based at least in part on the measured optical densities.

Abstract: An interchangeable sensor device for a functional near-infrared spectroscopy system (fNIRS) is a non-invasive device intended to detect changes in the concentration of hemoglobin species on any body surface area. The device includes a plurality of measurement units having different elastic configurations, each intended to be adapted to a specific area of the body, and a control unit for controlling any of the measurement units. Each of the measurement units is equipped with a first connector and the control unit is equipped with a second connector, which connectors allow the control unit to be interchangeably connected to any of the measurement units.

Abstract: An embodiment of the present invention provides a sphygmomanometer that is worn on a measured part of the left wrist of a subject (user) for use. In the sphygmomanometer, on an inner peripheral surface of a band-like body that constitutes a base of a band, a portion for installing a pressure cuff and a protrusion for installing an antenna substrate are separately provided, and the pressure cuff and the antenna substrate are respectively installed on these portions.

Abstract: A retractor has an oximeter sensor at its tip, which allows measuring of oxygen saturation of a tissue being retracted by the retractor. The tip includes one or more openings for at least one source and detector. A specific implementation is a spinal nerve root retractor with an oximeter sensor.

Abstract: A pulse oximeter may include a photoelectric conversion device having wavelength selectivity so that a low output LED may be included in the pulse oximeter to prevent skin damage and to reduce power consumption. The pulse oximeter includes a light emitting device configured to emit white light and a sensor configured to detect transmitted light that is received from the light emitting device. The sensor includes a near infrared organic photoelectric conversion device configured to sense a particular near infrared wavelength spectrum of light and a red photoelectric conversion device configured to sense a particular red wavelength spectrum of light.

Abstract: A method differentiates a blood vessel from a nonvascular tissue during a minimally invasive surgery using a device. A device may be any penetration sensor device, such as a dilator sensor device, a hollow needle sensor device, or a trocar sensor device, which penetrates the skin and subcutaneous layers to reach a target location inside the body. The penetration sensor device includes a sensor probe which can make optical measurements to determine various parameters of the tissue at the tip of the sensor probe. These parameters may include an optical signal level returned from tissue contacting the tip of the sensor probe, an oxygen saturation level of the tissue, a total hemoglobin concentration, a blood flow, and a pulse. Based on these parameters, the presence or absence of a blood vessel at the tip of the penetration sensor device can be determined while the device travels towards the target location for surgery.

Abstract: An integrated window for a photosensor for use in an electronic device has first and second transparent regions separated by an opaque region. The first transparent region allows a transmitter to emit light out of the housing of the electronic device and the second transparent region allows a receiver to receive light through the housing. The opaque region is disposed between the first and second transparent regions to isolate them from one another such that the transmitted light is isolated from the received light.

Abstract: Systems and methods of optical transcutaneous oxygenation monitoring. The oxygenation monitor comprises a photoluminescent oxygen-sensitive probe, a photon source positioned to direct photons at the probe, a photodetector positioned to detect light emitted from the probe when the photon source directs photons at the probe, a controller in electrical communication with the photon source and the photodetector, the controller being configured to execute a program stored in the controller to calculate a level of oxygen adjacent the probe from an electrical signal received from the photodetector. The photon source, the photodetector, and the controller are disposed in or on a support structure.

Abstract: A device for collecting cardiovascular data relating to an individual user, comprising a control unit assembly with an electronic controller and a pneumatic unit, an arm band having an inflatable bladder and configured to surround the left arm of the individual, wherein the pneumatic unit has a pump and a pressure sensor, and is configured to inflate and deflate the inflatable bladder, so that the electronic controller can determine the arterial pressure of the user, the device further comprising an acoustic sensor being coupled to the external wall of the arm band and having a sensitive side such that in use configuration, the sensitive side is adjacent to the chest of the user, whereby at least a cardiovascular timing characteristic can be inferred from signals from the acoustic sensor and the pressure sensor. The device may also comprise a set of contact electrodes to provide additionally ECG functionality.

Abstract: A sensor module includes a ring-shaped member; and a semiconductor device that is provided on the ring-shaped member. The semiconductor device includes: a wiring substrate that has flexibility; and electronic components that are mounted on the wiring substrate. The wiring substrate has component mounting regions, wherein at least one electronic component is mounted in each of the component mounting regions, and component non-mounting regions, wherein no electronic component is mounted in each of the component non-mounting regions. The component mounting regions and the component non-mounting regions are provided alternately in a longitudinal direction of the wiring substrate. The component non-mounting regions are curved along an outer circumferential direction of the ring-shaped member.