A myocardial infarction detection method and apparatus is described that includes a stiffness measurement step of measuring myocardial stiffness of a cardiac muscle of a subject, and a determination step of determining, based on the myocardial stiffness, whether or not infarction is present in the cardiac muscle.

An electronic device for identifying occurrence of hypotension and a method therefor are provided. The electronic device includes a housing, a user interface, a photoplethysmogram (PPG) sensor exposed through at least part of the housing, a motion sensor disposed in the housing, at least one processor operatively coupled with the user interface, the PPG sensor, and the motion sensor, and a memory operatively coupled with the at least one processor. The memory may store instructions which, when executed by the at least one processor, cause the at least one processor to, based on first data from the motion sensor indicating a change of a selected pattern, identify a blood pressure value based at least in part on second data from the PPG sensor, and based on the identified blood pressure value being lower than a first threshold, provide a notification through the user interface.

An electrode measuring the presence of an analyte is described as one embodiment. The electrode includes a working conductor with an electrode reactive surface and a first reactive chemistry that is responsive to the analyte. The electrode further includes a first transport material that enables flux of the first analyte to the first reactive chemistry and a second transport material that supplies a reactant to the first reactive chemistry. Wherein the first reactive chemistry does not contact the electrode reactive surface while at least partially shadowing a portion of the electrode reactive surface.

A non-invasive detection method and device, and a wearable apparatus for tissue element are provided. The method includes: acquiring, for a detected site of a detected object, a second light intensity measurement value for each predetermined wavelength of at least one predetermined wavelength at a measurement distance, and/or a second light intensity reference value for each predetermined wavelength of at least one predetermined wavelength at a reference distance, wherein the measurement distance is a source-detection distance corresponding to the first light intensity measurement value, and the reference distance is a source-detection distance corresponding to the first light intensity reference value; and determining a concentration of a tissue element to be detected according to the second light intensity measurement value of each predetermined wavelength and/or the second light intensity reference value for each predetermined wavelength.

A non-invasive detection method and device, and a wearable apparatus for tissue element are provided. The method includes: acquiring, for a detected site of a detected object, a second light intensity measurement value for each predetermined wavelength of at least one predetermined wavelength at a measurement distance, and/or a second light intensity reference value for each predetermined wavelength of at least one predetermined wavelength at a reference distance, wherein the measurement distance is a source-detection distance corresponding to the first light intensity measurement value, and the reference distance is a source-detection distance corresponding to the first light intensity reference value; and determining a concentration of a tissue element to be detected according to the second light intensity measurement value of each predetermined wavelength and/or the second light intensity reference value for each predetermined wavelength.

The present disclosure relates to optical methods and devices based on pulsate behavior of blood and optical absorption spectroscopy to measure the level of water and/or other substances or compounds, such as an alcohol or lipid, in the blood and the tissues surrounding blood vessels and arteries.

The present disclosure relates to optical methods and devices based on pulsate behavior of blood and optical absorption spectroscopy to measure the level of water and/or other substances or compounds, such as an alcohol or lipid, in the blood and the tissues surrounding blood vessels and arteries.

A method, system, apparatus, and/or device to determine a condition of a user using multiple sensors. The method, system, apparatus, and/or device may include: a band configured to extend at least partially around a body part of a user having a subdermal feature within body part; a light configured in the band to emit light into the body part; a miniaturized spectrometer positioned in the band to press against the body part to receive the light, where the miniaturized spectrometer comprises: an optical filter configured to isolate a relevant constituent wavelength of the light; a collimator configured to collimate the light; and an optical sensor configured to detect an intensity of the relevant constituent wavelength; and an impedance sensor integrated into the band and configured to be positioned against a same side of the body part as the miniaturized spectrometer.

A method, system, apparatus, and/or device to determine a condition of a user using multiple sensors. The method, system, apparatus, and/or device may include: a band configured to extend at least partially around a body part of a user having a subdermal feature within body part; a light configured in the band to emit light into the body part; a miniaturized spectrometer positioned in the band to press against the body part to receive the light, where the miniaturized spectrometer comprises: an optical filter configured to isolate a relevant constituent wavelength of the light; a collimator configured to collimate the light; and an optical sensor configured to detect an intensity of the relevant constituent wavelength; and an impedance sensor integrated into the band and configured to be positioned against a same side of the body part as the miniaturized spectrometer.

An adjustable measurement device is described that may include a housing, a power supply, a processor, a communication device, an elastic coupling member, a physiological sensor, and/or a clamp. The housing may be configured to attach to a wearable band that is wearable by a subject. The housing may include a chamber within the housing. The power supply, the processor, the communication device, the elastic coupling member, and or the physiological sensor may be disposed within the chamber. The elastic coupling member may couple the physiological sensor to the housing. A force exerted by the elastic coupling member on the physiological sensor may be in a direction through an opening towards a body part of a subject. As the subject wears the wearable band and the housing is coupled to the wearable band, the physiological sensor may be adjacent to or contact the subject.