Abstract: An electrode multiplexing physiological parameter monitoring ring, comprising a built-in power supply (2), a microprocessor module (1), an electrocardiogram monitoring analog front end (3), a skin conductance monitoring module (4), a first electrode (6), and a second electrode (7). The microprocessor module (1) is connected to the electrocardiogram monitoring analog front end (3) and the skin conductance monitoring module (4). The first electrode (6) and the second electrode (7) are connected to the electrocardiogram monitoring analog front end (3), and the electrocardiogram monitoring analog front end (3) processes electrocardiogram signals collected by the first electrode (6) and the second electrode (7). The first electrode (6) and the second electrode (7) are further connected to the skin conductance monitoring module (4), and the skin conductance monitoring module (4) processes skin impedance signals collected by the first electrode (6) and the second electrode (7).

Abstract: The process for classifying anesthetic depth includes: collecting of biological signals, conditioning of said signals, monitoring of activity of the central and autonomic systems, measurement of indexes and classification of patterns in anesthetic depth. The activity includes: i) Awake: Vigil—Ak. and recovery of verbal response—Rc. ii) Light Anesthesia: Light induction anesthesia—Li. Light recovery—Lr, Light dose, increase in drugs or patient movement (La), iii) General anesthesia: General anesthesia—Ga, one minute after the start of the surgery, and iv) Deep anesthesia: identification of the EEG burst-suppression pattern (BSP) associated with deep anesthesia.

Abstract: A light adjustable lens illumination system comprises an illumination source, for generating a light beam; a light delivery system, for projecting the light beam onto a Light Adjustable Lens (LAL), implanted into an eye, wherein a fraction of the light beam propagates past the LAL to a retina of the eye; and a protective beam-shaper, for shaping the light beam to have an intensity pattern with a relative central intensity reduction that varies along an axis; wherein the relative central intensity reduction at the retina is greater than the relative central intensity reduction at a LAL plane.

Abstract: A modular wearable health monitor having a substantially flexible attachment means connected to a housing comprising a power source and at least one processor through a relatively rigid and narrow spine disposed substantially centrally thereon having a variety of clinical and non-clinical uses that provides more comfortable and durable attachment of biometric sensors to a user by allowing the attachment means to contour to the user's body without the housing also being forced to do so along its entire width.

Abstract: A circadian rhythm entrainment platform can use medication circadian profiles that include mappings of medications to circadian rhythm disruptions and can make conversions of such circadian rhythm disruptions to administrations of light therapy to adjust for the disruptions. The circadian rhythm entrainment platform can specify how to entrain a patient's circadian rhythm using light therapy to compensate for or anticipate side effects of medications and for optimizing medication schedules for a patient's circadian rhythm so as to minimize side effects and increase medication effectiveness. The circadian rhythm entrainment platform can also gather information on the effects of medications on circadian rhythms and interact with patients, medical providers, and other providers in relation to light therapy.

Abstract: Concepts and technologies disclosed herein are directed to a smart automated external defibrillator (“AED”). According to one aspect of the concepts and technologies disclosed herein, the AED can present a menu that includes a plurality of modes. The plurality of modes can include a first responder mode, an Internet of Things (“IoT”) mode, and a general use mode. The AED can receive, via an input component, a selection, from the menu, of a mode from the plurality of modes. In response to the selection, the AED can configure a network connectivity component in accordance with a setting specified in the mode.

Abstract: Provided is a data processing apparatus including a signal data processor configured to collect signal data detected through polysomnography, to extract feature data by analyzing a feature of the collected signal data, and to transform the extracted feature data to time series data; and a sleep stage classification model processor configured to input the processed signal data to a pre-generated sleep stage classification model, and to classify a sleep stage corresponding to the signal data. The signal data processor is configured to extract feature data by analyzing a feature of each of an electroencephalographic (EEG) signal, an electro-oculographic (EOG) signal, and an electromyographic (EMG) signal with respect to the signal data, and to transform the extracted feature data to an epoch unit of time series data to input the extracted feature data to the pre-generated sleep stage classification model.

Abstract: Systems and methods for pacing cardiac conductive tissue are described. An embodiment of a medical system includes an electrostimulation circuit to generate His-bundle pacing (HBP) pulses to stimulate a His bundle, and a cardiac event detector to detect a His-bundle activity within a time window following an atrial activity. The cardiac event detector may use a cross-chamber blanking, or an adjustable His-bundle sensing threshold, to avoid or reduce over-sensing of far-field atrial activity and inappropriate inhibition of HBP therapy. The electrostimulation circuit may deliver HBP in the presence of the His-bundle activity. The system may further recognize the detected His-bundle activity as either a FFPW or a valid inhibitory event, and deliver or withhold HBP therapy based on the recognition of the His-bundle activity.

Abstract: One variation of a method for identifying homology of physiological signals comprises: receiving signal data of two different types of physiological signals; performing waveform matching on the signal data of the two different types of physiological signals to determine waveform matching information in the signal data of the two types of physiological signals; calculating an associative feature between the signal data of the two different types of physiological signals according to the waveform matching information; calculating a homology reference coefficient corresponding to the two different types of physiological signals according to the associative feature; and determining that the two different types of physiological signals are homologous when the homology reference coefficient is greater than a preset value.

Abstract: A hands-free LED device for the treatment of wrinkles and acne, or hair loss, includes a curved housing. Rigid areas contain the LED bulbs. The LED bulbs are interspaced therebetween the flexible areas; such that between each of the rigid LED bulb areas is a flexible area. The rigid LED bulb areas are between the flexible areas. A leg is provided on opposite sides of the housing, The legs being wider at the top of each leg and narrower at the bottom. The number of LED bulbs at each wavelength for treatment of wrinkles are: 126 LED bulbs of 605 nm; 210 LED bulbs of 630 nm, 126 LED bulbs of 660 nm, and 26 LED bulbs of 850 nm. The number of LED bulbs at each wavelength for treatment of acne are 280 LED bulbs at 415 nm and 210 LED bulbs of 630 nm. Hair loss uses 500-700 LED bulbs at 630 nm.

Abstract: Methods, systems, and apparatus for detecting configuration for a patient worn sensor assembly are described. In one aspect a method includes receiving, by a computer system, sensor assembly data for a particular sensor assembly, accessing, by the computer system, sensor assembly identifier information defining a plurality of sensor assembly identifiers, where each sensor assembly identifier is associated with a respective sensor assembly, identifying, by the computer system and based on the sensor assembly data, a particular sensor assembly identifier for the particular sensor assembly, and determining, by the computer system, configuration information for the particular sensor assembly based on the particular sensor assembly identifier.

Abstract: An ophthalmic device for treating an eye includes a laser source, a scanner system and an application head with a focusing optic and a patient interface for docking the application head onto the eye. Moreover, the ophthalmic device includes a measurement system for optically capturing eye structures when the application head is docked to the eye and a circuit which is configured to determine reference structures of the eye, which are arranged in ring-shaped fashion about the center axis of the anterior chamber of the eye, from the captured eye structures and to arrange a defined three-dimensional treatment model with respect to these reference structures in order to process a three-dimensional treatment pattern in accordance with the arranged three-dimensional treatment model in the eye.

Abstract: In some examples, a coil electrode assembly includes a coil electrode including a plurality of windings and extending from an electrode proximal end to an electrode distal end, the coil electrode defining an electrode lumen from the electrode proximal end to the electrode distal end. The coil electrode assembly further includes an insulative tube extending within the lumen of the coil electrode such that the coil electrode extends along an outer surface of the insulative tube. The coil electrode is partially embedded within the insulative tube when the insulative tube is in an expanded state to maintain a spacing between the windings.

Abstract: Various embodiments provide a wellness tracking device with a base plate that may be utilized as a combination electrode by a variety of sensors. The base plate may be a multi-material electrode that includes a conductor and a transparent or semi-transparent material to enable optical sensing. In certain embodiments, the base plate supports a plurality of different sensors, which may selectively utilize the base plate as an electrode.

Abstract: The invention relates mainly to an optical guide for diffusing a light radiation through a surface, which is essentially characterized in that it includes a base (3,31) comprising or able to hold at least one diffusion rod (2, 2a; 35a, 35b, 35c) whose lower diffusion end (7, 7a; 38a, 38b, 38c) protrudes from said base (3) and is intended to be applied on or near said surface, and whose upper collecting end (6,6a; 37a, 37b, 37c) is intended to be located near and opposite a power supplied light source (36a, 36b, 36c), and in that the diffusion rod (2, 2a; 35a, 35b, 35c) comprises a material able to transmit light from its collecting end (6,6a; 37a, 37b, 37c) up to its diffusion end (7, 7a; 38a, 38b, 38c). The invention also relates to an irradiation module and to an irradiation device adapted to the transcranial and/or transcutaneous irradiation by light radiation.

Abstract: A garment includes a fabric base layer and at least one side-emitting optical fiber retained to or integrated with the fabric base layer. The fabric base layer can stretch in the grain and cross grain direction of the fabric base layer. The at least one side-emitting optical fiber is located in at least one light-emitting zone to be located over a targeted body area of the person wearing the garment, and is configured to receive light from a light source and in the at least one light-emitting zone is configured to project light having a therapeutic wavelength toward the targeted body area.

Abstract: Modulated light therapy devices for treatment of dermatological disorders of the scalp are provided. An exemplary device includes a flexible printed circuit board (FPCB) supporting at least one light emitting device having an emitter height. The FPCB includes multiple interconnected panels and bending regions defined in and between at least some of the interconnected panels as to allow the FPCB to be configured in a concave shape to cover at least a portion of a cranial vertex of the patient. At least one light-transmissive layer proximate to the FPCB is configured to transmit (e.g., incoherent) light emissions generated by at least one light emitting device. At least one standoff is configured to be arranged between the FPCB and the scalp of the patient, wherein the at least one standoff includes a standoff height that exceeds the emitter height.

Abstract: A treatment tool includes an elongated shaft that has a bending mechanism at a distal end thereof; a bending operation part that is connected to a proximal-end side of the shaft in order to operate the bending mechanism; a connection sleeve that is provided at a connection section of the bending operation part where the bending operation part and the shaft are connected, and that rotatably holds the shaft; a rotation operation member that is provided at the proximal-end side of the shaft and that rotates the shaft; and a stopper member that can be made to slide outside the connection sleeve along a direction of a longitudinal axis of the shaft and that is engaged with both the rotation operation member and the connection sleeve at a specific position in a range of movement thereof, thereby locking rotation of the shaft with respect to the connection sleeve.

Abstract: A neurostimulation system includes an electromyographic (EMG) electrode; a neural electrode implantable in a deep cerebellar nuclei of a subject; a data acquisition unit in communication with the EMG electrode for receiving and transmitting a EMG signal; and a processor in communication with the data acquisition unit, the processor generates a EMG pattern based on the EMG signal and outputs a stimulation signal to the neural electrode when the EMG pattern is indicative of an abnormal motor movement. A method of modulating an abnormal motor movement of a subject by using the neurostimulation system.

Abstract: A medical handpiece having a laser irradiation unit connected to a body for generating a laser beam, so as to irradiate a subject with the laser beam; a laser tip which is brought into contact with a predetermined surgical site of the subject so as to guide the laser thereto; a sensor installed in the laser tip so as to measure pressure applied by the laser tip to the predetermined surgical site; and a processor for checking whether the measured pressure is within the pressure range set for the predetermined surgical site, determining, according to the result of the checking, whether the pressure applied to the predetermined surgical site needs to be adjusted, and performing control such that a guide signal for the laser tip is output.