Abstract: An earplug-type earphone is disclosed including: an earplug (10) for producing sound and an elastic support (30). The earplug (10) includes a front housing (200) and a rear housing (500) connected in that order. The elastic support (30) is positioned on an outer side of the rear housing (500). When the earplug (10) is inserted in the external auditory canal, the elastic support (30) is pressed and deformed and then applies resilience to the helix, by which the earplug can be stably positioned in the external auditory canal.

Abstract: A transdermal permeant delivery of at least one permeant composition into a tissue membrane of a subject including a disposable substrate having at least a portion of a bottom surface of a first release liner connected to an upper surface of the substrate and a patch having a backing layer and a reservoir that is selectively removable from the top surface of the first release liner. In a connected position, a first portion of the backing layer of the patch is releaseably mounted to a top surface of the first release liner in spaced registration with a poration area of the substrate.

Abstract: A system and method for signal processing to remove unwanted noise components including: (i) wavelength-independent motion artifacts such as tissue, bone and skin effects, and (ii) wavelength-dependent motion artifact/noise components such as venous blood pulsation and movement due to various sources including muscle pump, respiratory pump and physical perturbation. Disclosed are methods, analytics, and their uses for reliable perfusion monitoring, arterial oxygen saturation monitoring, heart rate monitoring during daily activities and in hospital settings and for extraction of physiological parameters such as respiration information, hemodynamic parameters, venous capacity, and fluid responsiveness. The system and methods disclosed are extendable to include monitoring platforms for perfusion, hypoxia, arrhythmia detection, airway obstruction detection and sleep disorders including apnea.

Abstract: The present invention provides techniques for measuring one or more parameters of a subject using a probe having an optical assembly configured and operable for applying optical measurements to a measurement location in a subject and generating optical measured data indicative thereof comprising at least one of pulsatile and occlusion measurements, a pressure system configured and operable for controllably applying pressure to the subject in the vicinity of the measurement location and measuring pressure inside the pressure system and generating pressure data indicative thereof, and a control system configured and operable for receiving and processing the pressure data to identify whether the optical measured data is valid, and for processing the valid optical measured data and determining at least one relation between the valid optical measured data and the corresponding pressure data indicative of at least one parameter of the subject.

Abstract: A method and apparatus for monitoring a blood oxygen saturation level within a subject's tissue is provided. The method includes the steps of: a) sensing the subject's tissue using a near infrared spectrophotometric oximeter, and producing a value representative of the oxygen saturation level within the sensed tissue; b) comparing the determined saturation value to a predetermined threshold oxygen saturation value; and c) determining at least one of a time under threshold (TUT) value or an area under threshold (AUT) value using the determined saturation value and the threshold value.

Abstract: Embodiments of the present disclosure disclose a method and system for determining health condition of a subject. First step of the method comprises receiving, by a computing unit, a first oxygen saturation level and a second oxygen saturation level from at least two sensors placed on the subject. Second step of the method comprises determining cerebral extraction of oxygen using the first and second oxygen saturation levels. Third step of the method comprises comparing the cerebral extraction of oxygen with a threshold level. Fourth step of the method comprises identifying a mental fatigue level of the subject based on outcome of the comparison, wherein the mental fatigue level indicates the health condition of the subject.

Abstract: In certain embodiments, a sampling assembly is for use with a main analyzer. The main analyzer is configured to sense an analyte in a body fluid obtained from a patient through a first fluid passageway extending from the main analyzer. The sampling assembly includes an instrument portion separate from the main analyzer and including at least one sensor. The instrument portion is removably engaged with the first fluid passageway. The at least one sensor is in sensing engagement with the first fluid passageway such that the at least one sensor can sense a property of a fluid within the first fluid passageway.

Abstract: A near infrared spectrometer and method for wavelength and path length correction are disclosed. The spectrometer includes a number of photodiodes that transmit broadband near infrared measurement light into the tissue and at least one broadband detector which measures the light signal transmitted through the tissue. A processor estimates chromophore concentrations through a comparison of measured light attenuation and modeled light attenuation. The light attenuation model utilizes a light path length distribution derived from a Monte Carlo model and accounts for the spectral shape of the light source as a function of temperature.

Abstract: Methods, devices, and systems are provided for correcting lag in measurements of analyte concentration level in interstitial fluid. The invention includes receiving a signal representative of sensor data from an analyte monitoring system related to an analyte level measured over time, computing rates of change of the sensor data for a time period of the sensor data, computing a rate distribution of the rates of change, transforming the rate distribution into a linear arrangement, determining a best-fit line for the transformed rate distribution, computing a slope of the best-fit line; and using the slope of the best-fit line as a representation of a variability of the analyte level to adjust an amount of lag correction applied to the sensor data. Numerous additional features are disclosed.

Abstract: The present invention relates to a biological probe structure, as well as apparatuses, systems, and methods employing this structure. In particular embodiments, the structure includes a hermetically sealed unit configured to receive and transmit one or more optical signals. Furthermore, the structure can be implanted subcutaneously and interrogated externally. In this manner, a minimally invasive method can be employed to detect, treat, and/or assess the biological target. Additional methods and systems are also provided.

Abstract: There are provided an endoscope system processor device, an endoscope system, an operation method for an endoscope system processor device, and an operation method for an endoscope system for calculating objective diagnostic information, which is easier to understand than the oxygen saturation, based on the oxygen saturation. The endoscope system processor device includes: a receiving unit that receives an image signal obtained by imaging an observation target with an endoscope; an oxygen saturation calculation unit that calculates an oxygen saturation based on the image signal; a pixel specification unit that specifies an out-of-range pixel in which the oxygen saturation deviates from a specific range set in advance; and a diagnostic information calculation unit that calculates diagnostic information as a numerical value using information of the out-of-range pixel.

Abstract: Sensors and methods for measurement of an analyte in a medium within a living animal are described. The sensor may include an inductive element that may receive power from an external device. The sensor may also include a charge storage device (CSD) and a memory. The sensor may perform analyte measurements initiated by the external device using power received from the external device and convey the analyte measurements to the external device using the inductive element. The sensor also may perform autonomous analyte measurements using the on board charge device's power and store the autonomous analyte measurements in the memory. The sensor may convey one or more stored analyte measurements to the external device using the inductive element using power received from the external device. The sensor may include a CSD-powered clock and a CSD-powered measurement scheduler that initiate the autonomous analyte measurements.

Abstract: A nanosensor for detecting an analyte can include a substrate, a photoluminescent nanostructure, and a polymer interacting with the photoluminescent nanostructure. The nanosensor can be used in in vivo for biomedical applications.

Abstract: A sensor cartridge according to embodiments of the disclosure is capable of being used with a non-invasive physiological sensor. Certain embodiments of the sensor cartridge protect the sensor from damage, such as damage due to repeated use, reduce the need for sensor sanitization, or both. Further, embodiments of the sensor cartridge are positionable on the user before insertion in the sensor and allow for improved alignment of the treatment site with the sensor. In addition, the sensor cartridge of certain embodiments of the disclosure can be configured to allow a single sensor to comfortably accommodate treatment sites of various sizes such as for both adult and pediatric applications.

Abstract: A system includes a mobile computing device, a sleeve, a contact surface, a sensor module, and a telemetry module. The mobile computing device has a first processor within a housing. The sleeve has an internal surface configured to fit the housing. The contact surface is disposed on an external surface of the sleeve. The sensor module is coupled to the contact surface and is configured to generate an electrical signal corresponding to a measured physiological parameter associated with tissue at the contact surface. The telemetry module is coupled to the sensor module and is configured to communicate data corresponding to the electrical signal to the mobile computing device.

Abstract: An endoscope system includes a light source unit, a band limiting unit, a light source control unit, an imaging sensor, an imaging control unit, and an oxygen saturation image generation unit. The light source unit includes a V-LED that emits violet light, a B-LED that emits blue light, a G-LED that emits green light, and an R-LED that emits red light. The band limiting unit generates measurement light having a specific wavelength band for measuring the oxygen saturation from the blue light. The light source control unit switches the control of the light source unit between a first light emission mode, in which the observation target is irradiated with the violet light, the measurement light, the green light, and the red light, and a second light emission mode, in which the observation target is irradiated with the measurement light.

Abstract: A physiological monitoring system may receive a sensor signal from a physiological sensor. The system may determine a first and second change metric based on the sensor signal, and may determine a venous signal based on the change metrics. In some embodiments, the sensor signal may be a photoplethysmograph signal that includes both arterial and venous information. By subtracting a second change metric from a first change metric, arterial contributions may be substantially removed, resulting in a signal primarily comprising venous information. The venous signal may be indicative of changes in the venous blood, and may be used to determine a physiological parameter, for example, blood pressure. The venous signal may also be used to trigger an event, for example, calibration of a blood pressure measurement.

Abstract: Provided is a biometric device including a light source unit arranged facing a first part on a surface of an organism and configured to irradiate the first part with excitation light, and a light-reception unit arranged facing a second part adjacent to the first part on the surface of the organism and configured to receive fluorescence light which is generated by the excitation light exciting a first body substance of the organism and emitted from the second part.

Abstract: A NIRS sensor assembly includes a light source, a light detector, a first insulating layer, an EMI shielding layer, and a second insulating layer. The first insulating layer covers an exposed portion of the light detector. An optically transparent portion of the first insulating layer is aligned with an active area of the light detector. The EMI shielding layer covers the first insulating layer. An optically transparent portion of the EMI shielding layer is aligned with the active area of the light detector. The second insulating layer covers the EMI shielding layer and the first insulating layer. An optically transparent portion of the second insulating layer is aligned with the active area of the at least one light detector.

Abstract: A sensor head for a compact oximeter sensor device includes light sources and light detectors. A compact oximeter sensor device implementation is entirely self-contained, without any need to connect, via wires or wirelessly, to a separate system unit. The sources and detectors are arranged in a circular arrangement having various source-detector pair distances that allow for robust calibration and self-correction in a compact probe. Other source-detector arrangements are also possible.