Abstract: A patient monitoring sensor having a communication interface, through which the patient monitoring sensor can communicate with a monitor is provided. The patient monitoring sensor includes a light-emitting diode (LED) communicatively coupled to the communication interface and a detector, communicatively coupled to the communication interface, capable of detecting light. The patient monitoring sensor includes a layer of material is provided over protruding components on the patient-side of the sensor to reduce the contact pressure of such protruding components.

Abstract: A real-time automated method to diagnose and/or detect stroke and engage the patient, care-takers, emergency medical system and stroke neurologists in the management of this condition includes the steps of continuously measuring natural limb activity, conveying the measurements to a cloud based real-time data processing system, identifying patient specific alert conditions, and determining solutions for acting upon needs of the patient. The system by which the method is implemented includes at least one body worn sensor continuously measuring natural limb activity and a patient worn data transmission device conveying the measurements to a cloud based real-time data processing system that identities patient specific alert conditions and determines solutions for acting upon needs of the patient.

Abstract: Devices, systems, methods and kits for releasably mounting a medical device on the body or skin of a user are provided. Embodiments include a holder or mounting unit or structure that retains a medical device in a fixed position on a body part of a user or host, such as on the surface of the skin, and/or provides physical and/or electrical coupling to one or more additional components which may be operatively positioned above and/or below the surface of the skin.

Abstract: A ring of detecting physiological information of a user includes a case and a detection assembly. The case has an inner space including an annular region and a sunken region. The sunken region has a first lateral side, a lower bottom and a second lateral side. The first lateral side and the second lateral side are located on two sides of the sunken region and respectively connected with two sides of the annular region. The annular region covers a back of the user's finger. The lower bottom of the sunken region contacts against a finger pulp of the user's finger. The first lateral side and the second lateral side respectively contact against lateral sides of the finger. The detection assembly is disposed inside the case and includes a first detection module and a second detection module respectively located on the first lateral side and the second lateral side.

Abstract: Provided is an information processing device including an acquisition unit configured to acquire load information based on a load applied to a load measurement device from a sole of a user and a feature amount extracting unit configured to extract a feature amount indicating a walking environment from time series data in at least one walking cycle included in the load information.

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 insertion device is an insertion device configured to insert a medical device into a living body, including a needle portion to which at least a portion of the medical device is adhered and being inserted into the living body together with the adhered medical device; and a movable portion configured to be movable relatively to the needle portion in a direction of insertion of the needle portion, wherein the movable portion moves relatively to the needle portion in the direction of insertion to cut an adhered region between the medical device and the needle portion and separate the medical device and the needle portion.

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: Various aspects of the present disclosure generally relate to a multispectral sensor device. In some aspects, a sensor device may obtain, from image data collected by a sensor of the sensor device, first image data regarding a first measurement location of a measurement target, and may obtain, from the image data, second image data regarding a second measurement location of the measurement target, wherein the first measurement location and the second measurement location are sub-surface measurement locations within the measurement target. The sensor device may determine, based on the first image data and the second image data, a pulse transit time measurement, and provide information identifying the pulse transit time measurement. Numerous other aspects are provided.

Abstract: The present disclosure relates to a continuous glucose monitoring device, in which a body attachment unit is manufactured so as to be assembled in an applicator, thereby minimizing additional work for a user in attaching the body attachment unit to a body, and allowing attachment of the body attachment unit to the body simply by operation of the applicator. In particular, a wireless communication chip is provided in the body attachment unit to enable communication with an external terminal, thereby enabling simple and convenient use without additional work of connecting a separate transmitter, and allowing easier maintenance. In addition, the continuous glucose monitoring device is activated by a user's operation after the body attachment unit is attached to the body, such that an activation start time can be adjusted to a time appropriate to the user's needs, and the continuous glucose monitoring device can be activated in a stabilized state, and thereby can monitor blood glucose more accurately.

Abstract: Aspects relate to a portable device that may be used to identify a critical intensity and an anaerobic work capacity of an individual. The device may utilize muscle oxygen sensor data, speed data, or power data. The device may utilize data from multiple exercise sessions, or may utilize data from a single exercise session. The device may additionally estimate a critical intensity from a previous race time input from a user.

Abstract: A measurement engine of a wearable electronic device may compensate for wavelength variations of light emitted as part of blood-oxygen saturation measurements. In some cases, determining an estimated blood-oxygen saturation value is based at least partially on temperature data that may be used to compensate for temperature-based wavelength variations of the emitted light, drive current data that may be used to compensate for drive-current-based wavelength variations of the emitted light, and/or calibration information that may be used to compensate for manufacturing variability across different light emitters. In various embodiments, the measurement engine may use temperature data, the drive current data, and/or calibration information in a variety of ways to determine estimated blood-oxygen saturation values, including using lookup tables or calibration curves, applying functions, and the like.

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 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: A physiological signal monitoring device includes a base including a base body that has a bottom plate and an opening, a biosensor mounted to the base, and a transmitter removably mounted to the base body. The base further includes a first coupling structure disposed on a top surface of the bottom plate, and the transmitter includes a second coupling structure coupled to the first coupling structure when the transmitter is mounted to the base body. When the first and second coupling structures are coupled to each other, they are disposed to be distal from a periphery cooperatively defined by the base and the transmitter. They are uncoupled from each other when an external force is applied through the opening of the base body to separate the transmitter from the base.

Abstract: Estimation of a characteristic of a user's physiological signals can be improved using one or more calibration relationships that may be dependent on a characteristic of the optical sensor. For example, different calibration relationships can be used that are dependent on a spatial characteristic and/or that are dependent on a wavelength characteristic of the light emitting component(s) of the respective emitter of a channel. In some examples, a unique calibration relationship can be used for each channel. In some examples, a common calibration relationship can be used for multiple channels with shared distance and/or wavelength characteristics. Utilizing distance-dependent and/or wavelength-dependent calibration relationships can improve robustness of pulse oximetry measurements.

Abstract: A wearable electronic device may include a display and a housing. The housing may include a chassis defining a first portion of a rear exterior surface of the wearable electronic device, a first portion of a side exterior surface of the wearable electronic device, and an internal wall. The housing may also include a glass shell defining a front wall positioned over the display and defining a front exterior surface of the wearable electronic device and a side wall extending from the front wall and overlapping the internal wall, the side wall defining a second portion of the side exterior surface of the wearable electronic device. The wearable electronic device may also include a touch sensing system within the housing and configured to detect a touch input applied to the front exterior surface of the wearable electronic device.

Abstract: The present invention relates to a body attachment unit for continuous glucose monitoring.

Abstract: An electronic valve with: a yoke including an end plate portion and a side plate portion; a pole piece; a solenoid coil; and a diaphragm made of a plate-shaped magnetic material. The pole piece has an opening at one end portion and a first fluid inlet/outlet communicating with the opening at the other end portion. A biasing unit biases the diaphragm in a direction away from one end portion of the pole piece in a manner of moving the diaphragm translationally in one direction. In a non-operating time, the electronic valve comes into an open state where the opening is open. In an operating time, the diaphragm approaches the one end portion of the pole piece against the biasing force of the biasing unit by a magnetic force generated by the solenoid coil, and the electronic valve can come into a closed state where the opening is closed.

Abstract: A sensing device for acquiring data via a finger. The device includes a wrap having a central portion with a tip wing, a first side wing, and a second side wing each extending therefrom. The wrap has an exterior side and an opposite finger side that faces towards the finger. An electronics system is coupled to the wrap and has a sensor configured to acquire the data from the finger. An adhesive is configured to adhere the sensing device to the finger. First and second attachment portions are positioned on finger side of the first side wing and on the exterior side of the second side wing, respectively, where the first and second attachment portions removably attach to each other to non-adhesively secure the wrap around the finger.