A method of determining one or more vital sign parameters by a wireless vital-sign measurement device comprises: measuring motion information of a user wearing the wireless measurement device, the measurement device being in the idle mode in which at least one opto-electronic sensor in the measurement device is deactivated; switching the measurement device in an active mode if the motion information is below a predetermined threshold, wherein in the active mode the at least one opto-electronic sensor is activated; during a predetermined measuring period, exposing part of a skin tissue of the user to light and measuring one or more optical response signals associated with the exposed skin tissue and the motion sensor measuring motion information associated with movements of the user; and, selecting or rejecting one or more pulses in the one or more optical response signals on the basis of the motion information measured during the measuring period and determining one or more vital sign parameters on the basis of the one or more selected pulses.

Systems and methods are provided for measuring depth, position, and/or angle of a cannula in a medical drug delivery device. In particular, a drug delivery device having a cannula is positioned adjacent to tissue, a voltage pulse is provided to the cannula, a charge is measured at an electrode in the drug delivery device, and the depth of penetration of the cannula is determined based in part on the charge at the first electrode. Systems and methods described herein can be used to determine subcutaneous insertion depth in a wearable bolus injector. In some implementations, insertion depth determination is achieved through capacitive sensors which measure needle depth in a drug delivery device.

A biological information measuring device (100a) includes a light source configured to emit probe light; a total reflection member (16) configured to totally reflect the probe light with the total reflection member (16) brought into contact with a subject (S) to be measured; a light intensity detector configured to detect light intensity of the probe light reflected from the total reflection member (16); a biological information output unit (2a) configured to output biological information, the biological information being acquired based on the light intensity; and a display unit (506) configured to display the light intensity or an absorbance of the probe light, the absorbance being acquired based on the light intensity. Preferably a pressure detector is provided configured to detect a pressure of the subject (S) with respect to the total reflection member (16).

A probe with a blood circulation sensor and a force or pressure sensor is placed against a patient. One part of the probe applies a force to another part of the probe which is pressed against the patient at one or more locations. The variation of a measure of blood circulation is recorded as a function of the applied pressure, thereby giving the operator a specific knowledge of the Tissue Perfusion Pressure (TPP), a measure of circulatory health, at each location.

A pressure control system for providing an interventional pressure to be applied to a defined area of a patient during a pre-interventional imaging process with an imaging system is provided. Therein, the interventional pressure corresponds to an interventional pressure applied to the defined area of the patient during an intervention via a medical technology device. The pressure control system includes a pressure plate, a force module, and a positioning apparatus. Therein, the force module is configured to apply a force on the pressure plate. Therein, the force on the pressure plate generates the interventional pressure. Therein, the positioning apparatus is configured to position the pressure plate and the force module relative to the patient.

A device for determining muscle condition of a region of tissue. The device comprises an electrical impedance myography (EIM) portable probe bearing an electrode array. The electrode array comprises excitation electrodes used to apply multi-frequency electrical signals to the region of tissue and pickup electrodes that are used to collect electrical signals resulting from the application of the multi-frequency electrical signals to the region of tissue. To improve accuracy and reproducibility of EIM measurements, the electrode array is reconfigurable to select different subsets of excitation and pickup electrodes so that the electrodes are oriented differently with respect to muscle fibers. Additional devices may be associated with the EIM probe to measure such parameters as temperature, moisture content of the region, quality of contact of electrodes of the electrode array with a surface of the region and pressure with which the EIM probe is applied to the region. The EIM measurements may be adjusted based on these parameters. Also, ultrasound and electrical impedance tomography measurements may supplement the EIM measurements for more complete analysis of the muscle condition.

Provided are adaptive wearable devices that measure physiological conditions, methods of operating the device, and computer programs for use with the device. The adaptive wearable device provides improved reliability in data due to the adaptive structure and can be made waterproof with the incorporation of a polymer material. In the context of a wearable device, an apparatus is provided that includes a support structure configured to at least partially enclose the torso or an appendage of a user, a spring module disposed on the support structure, a first section of flexible circuitry disposed on the spring module and a first sensor disposed on the spring module and configured to monitor the user.

A system for monitoring vital signs, configured to be used in conjunction with a computerized mobile device, the system including: a cover sensor assembly adapted to be operably engaged with the computerized mobile device, the cover sensor assembly having integrated therein at least one physiological sensor; a physiological data acquisition module configured to generate a physiological parameter measurement descriptive of a physical stimulus received by the at least one physiological sensor; and a validation module configured to control a validity status of the physiological parameter measurement.

A device for detection of the tactile sensitivity of a user includes a base frame and a mechanical system joined to the base frame, the mechanical system being movable relative to the base frame and having a resting area for the fingertip of at least one finger of the user. The mechanical system includes a plurality of movable plate-shaped members arranged side by side to each other so that the resting area is defined by the thicknesses of at least part of the upper edges of the plate-shaped members. Each plate-shaped member is connected to an actuator, which can be operated to independently move each plate-shaped member from a minimum height position to a maximum height position, a control unit being further provided, which is adapted to operate the actuators.

An apparatus for estimating bio-information includes: a sensor part configured to obtain contact pressure of a contact surface contacted by an object, and configured to obtain a contact image of the object that contacts the contact surface; and a processor configured to obtain a pulse wave signal of a region of interest based on the contact image, and configured to estimate bio-information based on the obtained pulse wave signal and the contact pressure.