Abstract: Embodiments of apparatuses and methods for determining an emplacement of sensors in a wound dressing are disclosed. In some embodiments, a wound dressing includes a plurality of sensors configured to measure wound or patient characteristics. One or more processors are configured to receive wound or patient characteristics data as well as emplacement data. The received data can be used to determine an emplacement of the plurality of sensors, the wound dressing, or a wound. The sensors can include a set of nanosensors. The wound dressing can include pH sensitive ink which can be utilized for determining a placement of the wound dressing and determining a pH associated with the wound. The wound dressing can be used in a negative pressure wound therapy system.

Abstract: Disclosed is a device for non-invasively sampling interstitial fluid including one or more analytes from dermis to the skin surface by employing the magneto-hydrodynamic effect and/or reverse iontophoresis. According to a preferable embodiment the device includes a first frame including a first electrode and a second frame including a second electrode, power source and preferably also a first magnet. The first frame is connected to the second frame by a formable connector adapted to provide mechanical connection between the first frame and the second frame and electrical connection between the power source and the first electrode. The direction of the magnetic field and the direction of the electric current produced by the magnet and the power source is such that the Lorenz force drives the fluid from the dermis towards the skin surface.

Abstract: A system, devices, and methods are described for imaging and measuring the mechanical properties of both surface and subcutaneous tissues found in living organisms, animals, and in natural and synthetic materials, and may include a first device configured to determine a modulus of a portion of bulk material or subcutaneous tissue (via measurement of vibrations), and/or determine resonant frequency of the vibrations, and a second device operably connected to the first device and configured to generate vibrations. The first device may be an optical coherence tomography device. The system may include a processor and data storage device with instructions which when executed by the processor, cause the processor to process of the frequency data and the displacement data to determine a resonant frequency of the material under investigation and calculate the mechanical modulus of elasticity of the material from a resonance frequency spectrum of the analyzed spectral image.

Abstract: There is provided an apparatus (12) for use in measuring blood pressure. The apparatus (12) comprises a processor (102) configured to acquire a signal indicative of pressure oscillations detected inside a cuff inflated to pressurize a measurement site of a subject undergoing cardiopulmonary resuscitation. The pressure oscillations detected inside the cuff are indicative of a pulse of the subject. The processor (102) is also configured to trigger a blood pressure measurement for the subject based on the pressure oscillations detected inside the cuff.

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: An optical based patient monitoring system employing an optical sensor and providing an indication of an optical change which does not correlate to a change in a physiological blood parameter and based on that indication, providing a care provider an indication of a condition of a patient. The optical based patient monitoring system providing the indication of the patient condition in relation to a patient using an IV setup.

Abstract: An image-based hemoglobin estimation tool for measuring hemoglobin can be embedded in hand held devices such as smartphones, and similar known and to be developed technology. The hand-held device acquires video data of a finger illuminated from the dorsal surface by a first near infrared light responsive to hemoglobin and a second near infrared light near responsive to plasma. The acquired video is segmented into frames and processed to produce a Photoplethysmography (PPG) waveform. The features of the PPG waveform can then be identified, and the waveform and corresponding features evaluated by a predictive hemoglobin model. The predictive hemoglobin model can be provided at a remote computer, enabling non-invasive hemoglobin analysis from point of care locations. Near infrared lights of 850 nm and 1070 nm are particularly effective in the process.

Abstract: The present disclosure relates to gastrointestinal (GI) tract detection methods, devices and systems.

Abstract: An apparatus is described for measuring hemodynamic or metabolic function of an organ or tissue region of a subject comprising a super-continuum laser operating in the near or short-wave infrared wavelength range and comprising a multi-stage amplifier. A source fiber delivers the super-continuum emission to the organ or tissue region, and a collection fiber receives reflected emission from the region. A detector followed by a processor is used to determine a metabolic state and an oxygenation state of the organ or tissue region. A signal-to-noise ratio of the signal is improved using a dual-arm differential measurement technique.

Abstract: A non-invasive monitoring device for monitoring physiological condition of a subject may include at least one light source for emitting light at at least one predetermined narrow spectral wavelength band onto a living tissue of the subject and two or more light sensors. Each of the two or more light sensors may correspond to a specific substance in a living tissue of the subject and may be configured to measure a change in a concentration of the specific substances to which the sensor corresponds. The distance of each of the two or more sensors from the light source, may be determined so that intensity of light scattered by each specific substance, may have a maximal signal to noise ratio at the determined distance of the corresponding sensor.

Abstract: A wearable electronic device (e.g., an electronic watch) may detect and analyze one or more sensing signals corresponding to light detected by the device to determine whether the device is in a sensing state (e.g., the device is within a maximum sensing distance of a user). If the wearable electronic device is in the sensing state, the device may determine one or more physiological parameters from the same signals used to determine whether the device is in the sensing state.

Abstract: A device for obtaining a biological sample, such as a capillary blood collection device, that has the ability to lance and squeeze the finger, collect the sample, stabilize the sample, and subsequently dispense the sample in a controlled manner is disclosed. The device also simplifies and streamlines the capillary blood collection by eliminating workflow variabilities which are typically associated with low sample quality including hemolysis and micro-clots.

Abstract: Methods and systems are provided for lowering power consumption in an optical sensor, such as a pulse oximeter. In one example, a method for an optical sensor includes illuminating a light emitter of the optical sensor according to set sensor parameters, the sensor parameters set based on hardware noise or external interference characterization and light transmission or reflection of a tissue contributing to a signal output by the optical sensor, the sensor parameters including current drive parameters of the light emitter, and adjusting the current drive parameters of the light emitter to maintain a target signal to noise ratio of the signal output by the optical sensor.

Abstract: The present disclosure provides systems and methods for calibrating a medical device utilizing LED emission by characterizing the spectrum distribution of the LED emission and mapping such characterized spectrum distribution to calibration coefficients, e.g., gamma coefficients.

Abstract: The present disclosure relates to a device, method and system for calculating, estimating, or monitoring the blood pressure of a subject. At least one processor, when executing instructions, may perform one or more of the following operations. A first signal representing heart activity of the subject may be received. A second signal representing time-varying information on at least one pulse wave of the subject may be received. A first feature in the first signal may be identified. A second feature in the second signal may be identified. A pulse transit time based on a difference between the first feature and the second feature may be computed. The blood pressure of the subject may be calculated according to a first model based on the computed pulse transit time and a first set of calibration values, the first set of calibration values relating to the subject.

Abstract: An oximetry probe and an operating method thereof, and an oximetry sensor. The oximetry probe includes an oximetry sensor which includes a detection end and an output end, and an adapter. The detection end includes a photodetector and multiple light-emitting elements connected in series. The output end has multiple output ports. Adjacent output ports are electrically connected to two sides of the corresponding light-emitting element. The adapter has a first adapter end and a second adapter end between which multiple wires are provided. The first adapter end is electrically connected with an input end of the monitor. When the second adapter end is connected to the output end, the wires are electrically connected with the output ports to form closed circuit to enable the light-emitting element to emit light which is received by the photodetector to generate a signal involving blood oxygen saturation to be displayed on the monitor.

Abstract: The present invention relates to an apparatus and a method for determining an indication of blood flow in a limb. According to an embodiment, the apparatus comprises an orientation sensor, a blood volume (BV) measuring device and a control unit. The orientation sensor is configured to determine an orientation of the limb and output an orientation signal indicative thereof. The blood volume measurement device is configured to measure an indication of blood volume (BV) in the limb and output a BV signal indicative thereof. The control unit is arranged to receive the orientation signal and the BV signal, determine a change in orientation of the limb in dependence on the orientation signal, and correlate the change in orientation with a change in blood volume of the limb determined in dependence on the BV signal.

Abstract: A wearable device is described. The wearable device includes a housing having a back cover, and an optical mask on first portions of the back cover. The back cover includes a set of windows, with a first subset of windows in the set of windows being defined by an absence of the optical mask on second portions of the back cover, and a second subset of windows in the set of windows being inset in a set of openings in the back cover. An optical barrier surrounds each window in the second subset of windows. A set of light emitters is configured to emit light through at least some of the windows in the set of windows. A set of light detectors is configured to receive light through at least some of the windows in the set of windows.

Abstract: A method for calculating blood oxygen saturation includes defining the extreme value point of a non-red light signal as the extreme value point of a red light signal, and calculating the blood oxygen saturation according to the extreme value point of the red light signal. The method for calculating blood oxygen saturation of the present disclosure proposes to use other light source signals to assist in finding the period of the red light signal, so that the calculation result of the red light signal is more accurate.

Abstract: A device for the continuous and real-time monitoring of bilirubin, comprises a housing that encloses a waterproof/splash proof body. The body comprises a bilirubin and temperature measuring module; a wearable biocompatible strap; a buckle; a display unit; a safety module; a learning module; a battery and charging unit; a switch; and a wireless connectivity facilitator. The bilirubin and temperature measuring module comprises: one or more light emitting sources; a microprocessor; one or more photodetectors; a filter; and an analogue to digital converter. The device can be configured to be mounted on a patient's wrist or any other body part like palm, earlobe, cheek, finger, forehead, and feet.