In an aspect, this disclosure relates to methods and devices for calibration of capillary blood flow meters for measuring capillary blood flow in absolute flow units (such as mL/min×100 g of tissue). For example, the calibration method utilizes the combination of a wet model device and a dry model device to provide a convenience, easy-to-use, and accurate calibration and measurement in absolute flow units. In an aspect, the dry model device can use thermal conductivity parameters from the wet model device, which can be translated into thermal conductivity parameters in a dry model device, which can be used to calibrate the capillary blood flow meter in absolute units.

An apparatus for estimating blood glucose is provided. The apparatus for estimating blood glucose may include a spectrometer configured to measure a spectrum from an object, and a processor configured to monitor a change in a contact state between the object and the spectrometer, determine a calibration section based on the monitored change in the contact state, extract a background signal from a spectrum of the determined calibration section, and generate a personalized blood glucose estimation model based on the extracted background signal.

Systems and methods described provide dynamic and intelligent ways to change the required level of user interaction during use of a monitoring device. The systems and methods generally relate to real time switching between a first or initial mode of user interaction and a second or new mode of user interaction. In some cases, the switching will be automatic and transparent to the user, and in other cases user notification may occur. The mode switching generally affects the user’s interaction with the device, and not just internal processing. The mode switching may relate to calibration modes, data transmission modes, control modes, or the like.

A system for monitoring medical conditions including pressure ulcers, pressure-induced ischemia and related medical conditions comprises at least one sensor adapted to detect one or more patient characteristic including at least position, orientation, temperature, acceleration, moisture, resistance, stress, heart rate, respiration rate, and blood oxygenation, a host for processing the data received from the sensors together with historical patient data to develop an assessment of patient condition and suggested course of treatment, including either suspending or adjusting turn schedule based on various types of patient movement. Compliance with Head-of-Bed protocols can also be performed based on actual patient position instead of being inferred from bed elevation angle. The sensor can include bi-axial or tri-axial accelerometers, as well as resistive, inductive, capacitive, magnetic and other sensing devices, depending on whether the sensor is located on the patient or the support surface, and for what purpose.

An apparatus configured for application to a surface of a body, the apparatus comprising: an array of mechanomyography sensors spatially distributed across a substrate, each mechanomyography sensor configured to detect mechanomyography signals from the body to which the apparatus is applied; and a pressure bias system configured to provide a variation in contact pressure of the mechanomyography sensors to the body surface to receive mechanomyography signals at different levels of applied contact pressure.

A method for processing measurements, acquired by a measurement sensor at different measurement times, involves the measurement sensor being integrated into a connected device that is worn/borne by a user and configured to connect to a wireless communication network. The measurement sensor is configured to acquire, at each measurement time, a measurement representative of a movements of, or a physiological characteristic of, the user. The measurement sensor is parameterized by various parameters, the value of each parameter being encoded in a register. Measurements are acquired by the measurement sensor at various measurement times to form a sequence of measurements. Data, established from the sequence of measurements, is transmitted to an interpreting application programmed to estimate, from the transmitted data, a user state selected from a plurality of predetermined states. The method also includes, before or during the measurements acquisition, a verification of the parameters of the measurement sensor.

An optical transmitter includes a light source and an adjustment structure. The light source is configured to output an original light spot, to transmit a test optical signal to a skin of a user. The adjustment structure is located on an output optical path of the test optical signal. A test optical signal transmitted from an original light spot center of the original light spot is a central light spot optical signal, and the adjustment structure is configured to scatter the central light spot optical signal in a direction away from the original light spot center, to convert the original light spot

A method and apparatus for measuring a biopotential signal together with impedance changes uses electrodes on a subject’s skin and for compensating for such impedances to increase accuracy and usability of such devices for short-and long-term monitoring of biosignals. The apparatus can include a first terminal for connection to a first electrode, a second terminal for connection to a second electrode, a first circuitry configured for measuring the biopotential signal from the first and the second terminal, a third terminal for connection to the reference skin electrode, a first variable controlled resistance load connected to the first terminal, and a second variable controlled resistance load connected to the second terminal.

A psychological stress estimation method includes obtaining a physiological signal of a user corresponding to a current moment, determining a first stress indicator of the user based on the current moment and a cyclic stress model of the user, determining a second stress indicator of the user based on the physiological signal of the user corresponding to the current moment and an instantaneous stress model of the user, where the physiological signal is an input of the instantaneous stress model, and determining the current stress indicator of the user based on the first stress indicator and the second stress indicator.

The present invention relates to a detecting device for detecting a blood count parameter in a blood vessel. The detecting device comprises a signal generator, which is designed to generate a calibration measurement signal, wherein the calibration measurement signal comprises a superimposition of a first excitation signal and a second excitation signal, wherein the first excitation signal has a higher frequency than the second excitation signal and/or the second excitation signal is a direct signal and/or wherein the second excitation signal has a higher power than the first excitation signal; a transceiver arrangement which is designed to emit the calibration measurement signal towards the blood vessel and to receive a first system response signal in response to the emission of the calibration signal; wherein the transceiver arrangement is designed to emit a third excitation signal directed towards the blood vessel and to receive a second system response signal in response to the emission of the third excitation signal; and a processor which is designed to link the first system response signal and the second system response signal in order to obtain a measurement signal for determining the blood count parameter.