Disclosed is a system for evaluating brain trauma via regional changes in tissue impedance. The present disclosure describes a system for non-invasive intracranial monitoring, comprising two or more affecting electrodes arranged between a conductive location of a cranium of a patient and a location on a scalp of the patient, two or more effected electrodes arranged between the conductive location of the cranium of the patient and the location on the scalp of the patient, and processing circuitry configured to apply an electrical stimulus between the two or more affecting electrodes, measure an electrical stimulus differential between the two or more effected electrodes, calculate, for the two or more effected electrodes, a value of an impedance metric, and identify, based on the calculated value of the impedance metric, a health condition of the patient.

An electromyography (EMG) device according to an aspect of the present disclosure includes a main circuit board having opposing first and second faces. A plurality of first connectors of a first type are provided on the first face, and a plurality of input contacts are provided on the second face. An EMG circuit is provided on the main circuit board. The EMG circuit is configured to utilize the input contacts as inputs to obtain an EMG input signal, and process the EMG input signal to provide an EMG output signal that is based on, but different from, the EMG input signal. For each of the input contacts, there is no conductive path directly between the input contact and any of the first connectors.

A system includes signal acquisition circuitry and a processing unit. The signal acquisition circuitry is configured to receive multiple intra-cardiac signals acquired by multiple electrodes of an intra-cardiac probe in a heart of a patient. The processing unit is configured to select a group of the intra-cardiac signals, extract a respective most-likely annotation value from each of the intra-cardiac signals in the group, in accordance with a likelihood criterion, identify in the group an intra-cardiac signal whose most-likely annotation value is statistically deviant in the group by more than a predefined measure of deviation, extract, from the intra-cardiac signal having the statistically deviant annotation value, at least a second-most-likely annotation value in accordance with the likelihood criterion, and, responsive to a statistical deviation of the second-most-likely annotation value, select a valid annotation value for the corresponding intra-cardiac signal.

Systems, devices, and methods for electroporation ablation therapy are disclosed, with a protection device for isolating electronic circuitry, devices, and/or other components from a set of electrodes during a cardiac ablation procedure. A system can include a first set of electrodes disposable near cardiac tissue of a heart and a second set of electrodes disposable in contact with patient anatomy. The system can further include a signal generator configured to generate a pulse waveform, where the signal generator coupled to the first set of electrodes and configured to repeatedly deliver the pulse waveform to the first set of electrodes. The system can further include a protection device configured to selectively couple and decouple an electronic device to the second set of electrodes.

A bed has a mattress. One or more temperature sensors are used, each sensor configured to: sense a temperature for the sleeper; and transmit, to a controller, temperature readings; one or more pressure sensors, each pressure sensor configured to: sense a pressure applied to the mattress by the sleeper; and transmit, to a controller, pressure readings. A controller may include a processor and memory, the controller configured to: receive, from the temperature sensors, the temperature readings; determine a skin temperature for the sleeper based on the temperature readings; receive, from the pressure sensors, the pressure readings; determine at least one cardiac parameter for the sleeper; and determine, from the skin temperature and the cardiac parameter, a core temperature for the sleeper that is different than the skin temperature and represents thermal state of a core of a body of the sleeper.

The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Described herein are systems, devices, and methods to assess and correct for instability of baseline pressure of pressure sensors applied for measuring pressures inside a human body or body cavity, such as intracranial pressure (ICP) and arterial blood pressure (ABP). The present disclosure includes systems for assessing instability of baseline pressure by computing differences in single pressure wave parameters between single pressure waves, calculating pressure stability levels, determining differences between pressure stability levels and creating baseline pressure indicator plots. The baseline pressure indicator plots define instability of baseline pressure as a function of defined thresholds applied to parameters of the pressure stability levels. The disclosure also provides means for correcting mean pressure caused by baseline pressure instability.

The bioelectrical impedance measurement device mainly includes a portable casing, a control member inside the portable casing, and an electrode assembly joined to the portable casing and electrically connected to the control member. The control member includes current generation element, a current collection and processing element, and a current protection element. The electrode assembly includes a left-hand contact and a right-hand contact, both configured on the portable casing. The electrode assembly further includes a left-foot contact, and a right-foot contact, both extended from the portable casing. The left-hand contact, right-hand contact, left-foot contact, and right-foot contact are respectively connected to a user's left hand, right hand, left foot, and right foot. The current generation element generates an electrical current, which enters the user's body through the limbs and then collected to calculate various bioelectrical impedances and to determine a required biological information.

A computer system for simultaneously sampling multiple light channels is configured to emit a first pulse-oximetry light signal from a first light source and to emit a second pulse-oximetry light signal from a second light source. The computer system then captures a combined pulse-oximetry signal from both the first pulse-oximetry light signal and the second pulse-oximetry light signal simultaneously at a photoreceptor sensor. The computer system identifies information within the combined pulse-oximetry signal, wherein the first light source and the second light source capture different attributes of the information.

A method for localizing gingival inflammation using an oral care device, comprising: (i) simultaneously emitting (520) light by a plurality of light sources (48) of the oral care device, wherein at least some of the plurality of light sources emit light of different wavelengths to result in a plurality of emitted light wavelengths, wherein each of the different wavelengths is modulated with a distinct code; (ii) obtaining (530), by a light detector (40) of the oral care device, reflectance measurements from a location within the user's mouth to generate reflectance data for the location; (iii) demodulating (540), by a controller (30) of the oral care device, the obtained reflectance data; and (iv) determining (560), by the controller using the demodulated reflectance data, whether gingiva at the location is inflamed.