Abstract: An apparatus for estimating blood pressure may include: a photoplethysmogram (PPG) sensor configured to measure a PPG signal from a user; and a processor configured to: extract a cardiovascular feature from the PPG signal; calculate a first variation in the extracted cardiovascular feature compared to a reference cardiovascular feature measured at a reference time; determine a measurement posture of the PPG signal based on a time interval between two waveform components of the PPG signal; in response to the measurement posture corresponding to the reference posture, estimate the blood pressure based on the first variation; and in response to the measurement posture not corresponding to the reference posture, obtain a second variation by correcting the first variation; and estimate blood pressure based on the second variation.

Abstract: Provided is a measuring device that can ensure a level of a measurement signal while noise derived from the body movement of a subject is curbed. A measuring device according to the embodiments includes a first fixing body, a sensor fixing body configured to fix a sensor for detecting a biological signal, and the sensor, in which the first fixing body and the sensor fixing body have separate structures.

Abstract: Systems and methods include a device management platform for managing a plurality of devices (e.g., for a clinic system). A system can include a patient system such as a patient device (e.g., an implanted cardiac device, a mobile device, etc.) which transmits data to the device management platform and/or a clinic system. The device management platform tracks measured physiological parameters of the patient. Transmission data received from the patient system includes data corresponding to the measured physiological parameters. The device management platform generates a workflow interface at the clinic system based on a care pathway, a billing pathway, and the measured physiological parameters. Additionally, the device management platform can determine an outcome goal value and one or more benchmark values to reach the outcome goal value, and can send action instructions (e.g., to the patient system) based on comparing the measured physiological parameters to the one or more benchmark values.

Abstract: An example of a digital artery blood pressure monitor may include a tactile sensor array disposed on an inner surface of a cuff, the tactile sensor array including a plurality of capacitive sensors to detect pressure changes within a digital artery of a finger due to blood flow, where the pressure changes cause changes to capacitance values of one or more capacitive sensors of the tactile sensor array, and control circuitry coupled to the tactile sensor array to receive the capacitance values from the tactile sensor array, and determine a blood pressure based on the capacitance values.

Abstract: The present application discloses a PPG circuit, a biological characteristics detection device and a biological characteristics detection method. The PPG circuit is configured to control a light source and N photoelectric converters to sense biological characteristics of an object under test; the PPG circuit includes: a transmitting channel, K receiving channels, wherein the N photoelectric converters are divided into K sets of photoelectric converter sets, and the K receiving channels respectively correspond to K sets of photoelectric converter sets; and a controller, configured to control the PPG circuit to operate in a partial sampling phase or an full sampling phase, so as to generates J or K biological characteristics sampling results during each of the pulse repetition cycles.

Abstract: This application discloses a method for controlling an electronic device to perform photoplethysmography detection. The method includes obtaining historical detection data of a photoplethysmography sensor, calculating a confidence of the historical detection data, determining, based on the calculated confidence of the historical detection data, whether a light source to be turned on by the photoplethysmography sensor in a next detection time segment includes a light source different from a light source turned on when the historical detection data is obtained, and determining that a photoelectric sensing element to be turned on in the next detection time segment is a photoelectric sensing element corresponding to the determined light source to be turned on.

Abstract: A probe apparatus includes a sensor including at least one element, a plurality of electrically conductive wires each of which has a connection portion at which electrical connection is made between the electrically conductive wire and the sensor so that a signal used in the sensor can flow through the electrically conductive wire, and an insulative member configured to cover at least one of the electrically conductive wires at a place nearer to a tip than the connection portion in the at least one electrically conductive wire. The insulative member having an electrical insulating property.

Abstract: A method of non-invasively monitoring hematocrit levels includes monitoring a first emission response to the light provided at the first excitation wavelength, wherein the first emission response is monitored at a first wavelength and monitoring a second emission response to the light provided at the first excitation wavelength, wherein the second emission response is monitored at a second wavelength. A ratiometric value is calculated based on a ratio of the first emission response to the second emission response, wherein the ratiometric value corresponds with hematocrit level of the patient.

Abstract: An electronic device and a method for controlling the electronic device are provided. The electronic device includes a motion sensor and optical sensors. Each of the optical sensors includes a light emitter and a light receiver. The optical sensors are separately driven to determine a respective signal characteristic of each of the optical sensors. A current state of an object to be measured is determined, based on at least one signal received through the motion sensor or the optical sensors. A light emitter of at least one of the optical sensors is driven, based on the respective signal characteristics of the optical sensors according to the current state of the object to be measured. Based on the respective signal characteristics of the optical sensors, a light signal sensed through a light receiver of at least one of the optical sensors is selected and received.

Abstract: This instant disclosure provides a heart rate detecting device which includes an image sensor. The image sensor generates a first mixed signal within a first interval and generates a second mixed signal within a second interval, wherein the first mixed signal contains light information of first multiple light wavelengths having a first intensity ratio from one another, and the second mixed signal contains light information of second multiple light wavelengths having a second intensity ratio, different from the first intensity ratio, from one another.

Abstract: A core body temperature measurement device includes a body and an operation unit. The body is fixed to an ear canal of user. The operation unit is combined with a front side of the body, and is configured to be exposed to the ear canal or to be concealed inside, and has a sensor part. the sensor part measures a core body temperature of user when the operation unit is exposed to the ear canal.

Abstract: The present invention discloses a flexible sensor detection system for medical care and health, including: an information collection module, which uses a wearable device as a carrier, where flexible sensors are respectively arranged on the wearable device; an information transmission module, configured to wirelessly transmit collected information to an information processing and feedback module; and the information processing and feedback module, configured to perform grading treatment on received data information and feed back a health condition corresponding to the data information to the information transmission module, where the information transmission module compares feedback health condition data with a preset health threshold to determine whether to give an alarm. A heart rate ECG band, a breathing band, a shell temperature band, a blood flow rate band, a blood glucose band, a blood oxygen band, and a deep temperature band of the present invention are provided with the built-in flexible sensors.

Abstract: Systems, methods, apparatuses, and computer program products for contact-free heart rate monitoring and/or measurement are provided. One method may include receiving video(s) that include visual frame(s) of individual(s) performing exercises, detecting some exposed skin from the video(s), and performing motion compensation to generate color signals for the exposed skin to precisely align frames of the exposed skin. The method may also include generating the color signals by estimating a skin color for each frame by taking a spatial average over pixels of a cheek of the face(s) for R, G, and B channels, respectively, applying an operation to remove remaining motion traces from the frames such that the heart rate traces dominate, and extracting and/or outputting the heart rate of the individuals using a frequency estimator of the skin color signals.

Abstract: The invention provides a body-worn system that continuously measures pulse oximetry and blood pressure, along with motion, posture, and activity level, from an ambulatory patient. The system features an oximetry probe that comfortably clips to the base of the patient's thumb, thereby freeing up their fingers for conventional activities in a hospital, such as reading and eating. The probe secures to the thumb and measures time-dependent signals corresponding to LEDs operating near 660 and 905 nm. Analog versions of these signals pass through a low-profile cable to a wrist-worn transceiver that encloses a processing unit. Also within the wrist-worn transceiver is an accelerometer, a wireless system that sends information through a network to a remote receiver, e.g. a computer located in a central nursing station.

Abstract: A pulse photometer includes: an interface receiving a first signal and a second signal; and a processor configured to calculate a concentration of at least one blood light absorber in the subject, based on the first and second signals. The processor is configured to: acquire a first variation of the first light due to blood pulsation in the subject, acquire a second variation of the second light due to the pulsation, and calculate the concentration of the at least one blood light absorber, based on a first correction amount and a second correction amount. The first correction amount is based on at least one of a first constant, the first variation and the second variation, which are statistically determined. The second correction amount is based on at least one of a second constant, the first variation and the second variation, which are statistically determined.

Abstract: A probe device includes an optical device including at least one of a photodetector or a first light source. A cover structure is included and is arranged in front of the optical device. The cover structure includes an electrode which contacts, in use, a body tissue.

Abstract: A patient monitor can diagnose whether its speaker is blocked, malfunctioning, or at a volume that is too low. For example, the monitor can include a processor that can diagnose the speaker by recording a microphone input signal. The processor can compare the microphone input signal to an expected alarm signal that should be output by the speaker. If the two do not match or reasonably correspond to one another, then the processor may increase the volume of the alarm to determine whether doing so can overcome an obstruction, noise, or potential malfunction. The microphone can again detect the speaker output, and the processor can again make another comparison or analysis of the input with the speaker output. If the speaker output as detected via the microphone is still insufficiently loud, then the patient monitor may output an indication that the speaker has a problem.

Abstract: A non-contact temperature measurement system for calculating estimated core body temperature is disclosed. The temperature measurement system can include a sensor that can detect the temperature of a patient and the temperature of ambient surrounding. The temperature of the patient and the ambient temperature can then be used to determine a core body temperature. The temperature measurement system includes an optical module having a light emitter and a light detector. The light emitter emits a beam of light towards the patient and the light detector detects a beam of light reflected by the patient. The reflected beam is analyzed to determine a distance between the temperature measurement system and the patient.

Abstract: A surgical robotic system comprises a surgeon console, remote surgical robot, and a control unit. The surgeon console comprises a base connected to a hand controller by a linkage, the linkage comprising a plurality of joints whereby the configuration of the linkage can be altered. The surgeon console comprises a driver to drive each joint to move. The surgeon console further comprises a presence sensor to sense the presence of a surgeon's hand on the hand controller.

Abstract: In some embodiments, a blood flow sensor device such as a non-invasive cardiac arrest monitor (NICAM) that uses ultrasound to detect blood flow is used to monitor blood flow during cardiopulmonary resuscitation. One or more gating signal generation devices transmit gating signals to a blood flow monitoring computing device. The blood flow monitoring computing device uses the gating signals to determine time periods during which blood flow information generated by the blood flow sensor device is most likely to be accurate. The blood flow monitoring computing device measures blood flow during the time periods. In some embodiments, the blood flow monitoring computing device presents the measured blood flow to a user. In some embodiments, the blood flow monitoring computing device transmits a command to a chest compression device based on the measured blood flow.

Abstract: A device includes source and detector sensors. In a specific implementation, the device has two near detectors, two far detectors, and two sources. The two near detectors are arranged closer to the two sources than the two far detectors. A light-diffusing layer covers the two near detectors. The device may be part of a medical device that is used to monitor or measure oxygen saturation levels in a tissue. In a specific implementation, light is transmitted into the tissue and received by the detectors. An attenuation coefficient is first calculated for a shallow layer of tissue. The attenuation coefficient is then used to calculate an attenuation coefficient for a deep layer of tissue.

Abstract: A monitoring device configured to be attached to a subject includes a photoplethysmography (PPG) sensor configured to measure physiological information from the subject, a blood flow stimulator, and a processor configured to process signals from the PPG sensor to determine a confidence score of the signals. In response to a signal-to-noise level determination, the processor is configured to instruct the blood flow stimulator to increase blood perfusion at a location where the PPG sensor is attached to the subject. The confidence score is an indication of how strongly the signals can be trusted.

Abstract: A device, a substrate including a connection port. The substrate includes traces to enable a circuit of the substrate. The circuit is connected to the connection port. A light sensor mechanically and electrically attached respectfully to a first planar surface of the substrate and the circuit. A light source is mechanically and electrically attached respectively to the first planar surface and the circuit. The light source is located lateral to the light sensor at a first distance. A light signal of the light source emanates from the light source at an angle perpendicular to the first planar surface and a reflector mechanically attached to the first planar surface and located between the light sensor and the light source. The light signal is substantially reflected by the reflector away from the light sensor.

Abstract: The present disclosure provides methods and apparatus for evaluating the flow of blood in damaged or healing tissue. The present disclosure also provides methods of identifying a patient at the onset of risk of pressure ulcer or at risk of the onset of pressure ulcer, and treating the patient with anatomy-specific clinical intervention selected based on perfusion or blood oxygenation values, or a combination thereof. The present disclosure also provides methods of stratifying groups of patients based on risk of wound development and methods of reducing incidence of tissue damage in a care facility. The present disclosure also provides methods to analyze trends of perfusion or oxygenation measurements to detect tissue damage before it is visible, and methods to compare bisymmetric perfusion values to identify damaged tissue.

Abstract: A microscope is provided to measure HbA1c fraction. The microscope measures the HbA1c fraction of a single red blood cell (RBC) in a trace blood sample. The HbA1c fraction can be measured through a non-invasive way while the RBC flows in a human epidermal microvessel, too. The microscope comprises a laser device, an upright microscope, a light splitter, a light detector, and a mainframe. Unlike traditional methods, the HbA1c fraction can be measured in vitro or in vivo at the level of a single RBC. Accurate measurement is achieved. Misdiagnosis rate is reduced. The microscope provides HbA1c fractions from hundreds of RBCs, instead of averaging HbA1c fractions obtained from a large number of blood samples. Hence, the present invention is a method of detecting a HbA1c fraction of a single RBC, and is a microscope supporting blood-drawing measurement and non-invasive measurement simultaneously.

Abstract: The present invention provides a personal hand-held monitor comprising a signal acquisition device for acquiring signals which can be used to derive a measurement of a parameter related to the health of the user, the signal acquisition device being integrated with a personal hand-held computing device. The present invention also provides a signal acquisition device adapted to be integrated with a personal hand-held computing device to produce a personal hand-held monitor as defined above.

Abstract: Disclosed is an electronic device comprising: a biometric sensor, including at least one light emitting diode (LED) and at least one light receiving unit, for acquiring biometric information by means of the at least one light emitting device and the at least one light receiving unit; a power receiving circuit configured to receive a wireless power signal from an external electronic device; and a processor operatively coupled to the biometric sensor and the power receiving circuit. The processor may be configured to receive a designated wireless power signal from the external electronic device by using the power receiving circuit and to perform optical communication with the external electronic device by using the biosensor when the designated wireless power signal is received. Other various embodiments identified from the specification are also possible.

Abstract: A wearable sensor decal may include a flexible wrapper layer, an intermediate layer, and a porous film layer. A first plurality of electrodes may be deposited on the wrapper layer. A heating element may be conductivity coupled to the first plurality of electrodes. A second plurality of electrodes may be deposited on the intermediate layer. A biosensor may be conductively coupled to the second plurality of electrodes. The flexible film may be hydrophilic to allow biofluids pass to the biosensor and the wrapper layer may be hydrophobic to provide waterproofing to the biosensor and heating element. The heating element may be powered to reduce thermal variance in biosensor measurements.

Abstract: An infant monitoring device is disclosed having a band or sock configured to wrap around the foot or other portion of an infant. The sock houses a removable sensing module configured to couple to the sock and measure health parameters of the infant. The sensing module is removably couplable with a base station that charges the sensing module. The sensing module transmits and receives information from the base station. Both the base station and the sensing module can transmit and receive information from a remote location.

Abstract: Various embodiments of systems, devices, components, and methods for providing external therapeutic vibration stimulation to a patient are disclosed and described. Therapeutic vibration stimulation is provided to at least one location on or adjacent to a patient's skin (such as through clothing or a layer disposed next to the patient's skin), and is configured to trigger or induce resonance or high amplitude oscillations in a cardiovascular system of the patient. Inducing such resonance can aid in training autonomic reflexes and improve their functioning.

Abstract: A method for verifying a periodic useful signal component of a sensor signal of a flowmeter. To distinguish a useful signal from a noise signal, a periodic measured variable is detected over a period, and a periodic sensor signal is output, the sensor signal is subjected to a time/frequency analysis, and a time-dependent frequency spectrum of the sensor signal is determined, the time-dependent frequency spectrum is examined for a characteristic feature of the useful signal, and if the expected characteristic feature is found in the time-dependent frequency spectrum, the portion of the sensor signal having the characteristic feature is verified as the useful signal component and a flow measured value is determined on the basis of the verified useful signal component, or if the expected characteristic feature is not found, the portion of the sensor signal which does not have the characteristic feature is rejected as the noise signal component.

Abstract: A controller and a distal sensor module are used to emit optical emissions to a liquid sample being tested in a human body and detect desired optical data which the controller uses to electronically calculate a concentration measurement of a targeted analyte (e.g., glucose). The distal sensor module is held in place by a retention mechanism while a clamping system applies clamping pressure to the liquid sample during a test period to maintain a specified sample height of the liquid sample. An optical cable is intermediate the controller and the distal sensor module and is pluggably connected to the controller. Continuous monitoring of the analyte is possible without disconnecting the controller from the optical cable or the distal sensor module from the patient while clamping pressure on the test sample is reduced outside of the test period.

Abstract: A device for monitoring the respiratory status of a user is disclosed. The device may comprise a nasal cannula comprising a nasal chamber including first and second prongs, a connector configured to couple the nasal cannula to a remote device, and a tube configured to couple the nasal chamber to the connector. The nasal cannula may also comprise optical fibers passing through at least a portion of the tube. A first optical fiber may be configured to transmit light to a first nasal passage of the user, a second optical fiber may be configured to receive light passing through a nose septum and into a second nasal passage of the user.

Abstract: Systems and methods for monitoring sleep are disclosed. According to an aspect, a method includes emitting light into tissue. The method also includes detecting light backscattered from the tissue. Further, the method includes determining a sleep pattern based on the backscattered light.

Abstract: A biological monitoring device includes a sensor included in a sensor device, performing a detection process of detecting a medical condition in a body of a patient, and performing a process of generating first detection data indicating a result of the detection process, a generation unit indicating contents related to the detection process, and performing a process of generating second detection data having a smaller data volume than the first detection data, on the basis of the first detection data, a communication unit realized by the sensor device, and performing a process of transmitting the second detection data to a terminal associated with the patient, and a control unit that is configured to cause the communication unit to perform the process of transmitting the second detection data to the terminal, when it is determined that the sensor device exists in the body of the patient.

Abstract: A sensor electric wire that is not readily affected by external noise, and a sensor circuit that uses the same, including a first internal conductor covered by a piezoelectric material, a second internal conductor provided on the outside of the piezoelectric material, and an external shield conductor surrounding the first internal conductor and the second internal conductor, an insulating body being disposed between the first internal conductor and second internal conductor, and the external shield conductor.

Abstract: This document provides devices and methods for monitoring health patient parameters using a wearable monitoring device. For example, this document provides monitoring devices with multiple sensors, multiple types of sensors, algorithms for managing the multiple sensors to enhance monitor performance, and for detection of health events using health parameter data that is acquired by the monitoring system.

Abstract: The device uses pulsed electric fields to prevent the growth of biofilm and the attachment of bacteria to targeted surfaces. The device sets up an electric field around or surrounding the surface itself. These pulsed electric fields disrupt biofilm formation and bacterial attachment to surfaces. The device is meant to prevent the formation of biofilm or attachment of bacteria to a surface as opposed to disinfecting the surface.

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: 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: In accordance with some embodiments, systems, methods, and media for estimating compensatory reserve and predicting hemodynamic decompensation using physiological data are provided. In some embodiments, a system for estimating compensatory reserve is provided, the system comprising: a processor programmed to: receive a blood pressure waveform of a subject; generate a first sample of the blood pressure waveform with a first duration; provide the sample as input to a trained CNN that was trained using samples of the first duration from blood pressure waveforms recorded from subjects while decreasing the subject's central blood volume, each sample being associated with a compensatory reserve metric; receive, from the trained CNN, a first compensatory reserve metric based on the first sample; and cause information indicative of remaining compensatory reserve to be presented.

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: A bone oximeter probe includes an elongated member and a sensor head at an end of the elongated member to make measurements for a bone. The measurements can indicate the viability or nonviability of the bone. In an implementation, the probe is advanced through an incision in soft tissue, towards the underlying bone, and positioned so that the sensor head faces the bone to be measured. Optical signals are sent from the sensor head and into the bone. The bone reflects some of the optical signals which are then detected so that measurements for the bone can be made. Some of these measurements include an oxygen saturation level value, and a total hemoglobin concentration value of the bone.

Abstract: Systems and methods for detection and/or intervention of stress episodes such as nightmares during sleep activity or flashbacks or anxiety attacks during waking or sleep activity. In some embodiments, sensors, such as gyroscopes, accelerometers, heart rate sensors, and/or other sensors, may be used for monitoring stress indicators indicative of a user's stress level. The sensed stress indicators may be used to calculate a stress level. If the stress level meets or exceeds a stress level threshold, haptic, audio, visual, and/or other feedback or alerts may be used to draw a user's attention and thus interrupt the stress episode.

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: The present disclosure encompasses embodiments of nucleic acids comprising genetic elements which are useful for the detection of diseased cells.

Abstract: An aspect of the disclosure pertains to a wrist-worn device that may be characterized by the following features: an external surface that is not in contact with the user when the wrist-worn device is worn; a force sensor; a PPG sensor disposed on the wrist-worn device; and control logic configured to: (i) generate one or more sensor data samples, each sensor data sample including data that links force data generated by the force sensor when a user presses a against the external surface at a given time with heart rate data obtained from the PPG sensor at the given time; and (ii) calculate an estimate of blood pressure from the one or more sensor data samples. As examples, the force sensor may be a force sensitive touch screen or film, a strain gauge integrating into the device, or a calibrated spring element configured to be pressed by the user.

Abstract: A customized in-ear hearing device includes a light source, photodetector, light emission window, and light transmission window. The light source and the photodetector together function as a physiological sensor by emitting light from the light source through the light emission to the skin of a user's ear canal, and detecting at the photodetector light reflected by the skin that passes through the light detection window. The light emission window and light detection window are located at a customized portion of the sidewall of the device that contacts the skin in the ear canal.

Abstract: A method and a device for non-contact determination of temporal color and/or intensity variations in objects in a scene. Monoscopic overview images of the scene are detected with first and second overview cameras from two different viewing directions, and calculated to form a stereoscopic overview map. A two-dimensional detail image is detected by a detail camera from a third viewing direction and is projected on the overview map. Measurement surfaces in the scene are selected based on criteria which are predetermined depending on parameters on which conclusions are to be drawn from the color variations and/or intensity variations. Light emitted by the measurement surfaces is detected in a spatially-resolved and wavelength-resolved manner in a continuously-captured series of measurement images in a predetermined spectral range. The measurement surfaces are analyzed in the measurement images with respect to temporal variation of the intensity and/or color of the light, and the results displayed.

Abstract: Medical monitoring systems and methods are disclosed. A medical monitoring system can receive physiological parameter data and first physiological parameter alarm data from a plurality of patients. The first physiological parameter alarm data can be indicative of alarm conditions experienced by the plurality of patients. The alarm conditions can have been detected based upon first alarm criteria. The system can also generate second physiological parameter alarm data using a processor. The second physiological parameter alarm data can be indicative of simulated alarm conditions, which can be detected based upon a second alarm criteria. The system can compare the first and second physiological parameter alarm data using a processor.