Abstract: Disclosed is an extensible electrode array (102) for accurately locating a pelvic floor muscle, and its design method and an extensible pelvic floor electrode.

Abstract: A physiological information acquisition device configured to acquire physiological information of a subject includes: an input interface configured to receive waveform data corresponding to a measurement waveform of the physiological information from a sensor; a prediction unit configured to extract a feature from the waveform data using a convolutional neural network and predict a probability of the waveform data being classified into each of a plurality of classes; an importance specification unit configured to specify an importance of the feature with respect to a prediction result of the probability for at least one of the plurality of classes; and an output unit configured to output an indicator indicating the importance together with the measurement waveform.

Abstract: Status messages are wirelessly broadcast from medical devices (e.g., defibrillators) as advertisements that don't require the establishment of a wireless connection with listeners. The listeners are configured to act on, or forward received status messages as appropriate. The listeners may optionally include supplemental information supplied by the listener device when forwarding a status message to a management server. The listener may optionally analyze received status messages to determine whether an action should be taken based at least in part on status information in the message. Actions performed by the listener may include initiating a connection with the transmitting device to facilitate uploading new information from the defibrillator, updating the defibrillator's firmware, etc. Optionally, some of the advertisements are configured as beacons. The advertisements/beacons may be transmitted using a Bluetooth Low Energy or other suitable protocols.

Abstract: A system for controlling delivery of electrical stimulation to a subject. The system comprises a control device configured to send stimulation instructions to an electrical stimulation generator to cause the electrical stimulation generator to deliver transcranial electrical stimulation to one or more electrodes arranged to be positioned in proximity to a targeted region of the brain of the subject. The stimulation instructions comprise stimulation parameter value(s). The control device is configured to receive sensor data from optical sensor(s) arranged to be positioned in proximity to the targeted region and transmit updated stimulation instructions comprising updated simulation parameter value(s) to the electrical stimulation generator to cause the electrical stimulation generator to modify characteristic(s) of the stimulation. The system is configured to analyse the sensor data to determine an activity measure and determine updated stimulation parameter value(s) based on the determined activity measure.

Abstract: A medical display controlling apparatus and a display controlling method capable of enhancing convenience of medical providers includes generating a three-dimensional model of an observed object based on a right-eye medical captured image and a left-eye medical captured image taken by an imaging device configured to image the observed object; and causing a display screen to display a combination of the three-dimensional model with a right-eye special light observation image and a left-eye special light observation image, or a combination of the three-dimensional model with biological information acquired from an external biological information acquiring apparatus.

Abstract: A device, system and method for performing or conducting laser therapy, and more specifically, for performing Class IV laser therapy in an unattended and hands-free manner is provided herein. The system and method includes a support assembly with a laser treatment device supported thereon. The laser treatment device is configured to provide hands-free Class IV laser therapy treatment and includes a plurality of preprogrammed treatment protocols, each of the plurality of preprogrammed treatment protocols being associated with at least one of a plurality of body locations. A positionable arm extends from the support assembly and terminates at a laser emitter directed toward the selected body location. Upon selection of one of the plurality of body locations on the laser treatment device, the laser emitter will perform laser therapy treatment according to a corresponding one of the preprogrammed treatment protocols.

Abstract: Nocturia has been defined as the need for an individual to wake up one or more times during the night to void. Further, Nocturia detection also requires analysis of sleeping pattern of the person. In such cases a lot of assumptions are made when the person is not in bedroom during nights. A method and system for detection and validation of Nocturia in the person has been provided. The system is utilizing a statistical based analysis, a rule based analysis, a machine learning based analysis and analysis of sleeping pattern of the person to detect and validate Nocturia. The system ensures that the person is not disturbed in his/her daily activities. Further, the processes deployed in the system are completely un-supervisory in nature meaning it does not have the dependency of needing to have trained machine learning dataset.

Abstract: Disclosed is an ECG sensor having a packaging label form factor. The ECG sensor may comprise a set of electrodes configured to sense heart-related electrical activity when in contact with skin of a user and produce electrocardiogram (ECG) waveforms representing the sensed heart-related electrical activity. The ECG sensor may further comprise a processor configured to: identify, using a machine learning model, the user based on the ECG waveforms, convert the ECG waveforms to a modulated signal that carries the ECG waveforms representing the sensed heart-related electrical activity, and transmit the modulated signal wirelessly to a computing device using a transmitter. The ECG sensor may also comprise a housing having a first layer and a second layer, wherein the set of electrodes, the processor, and the transmitter are all disposed between the first layer and the second layer of the housing, and wherein the housing has a packaging-label form factor.

Abstract: Classification of heartbeats based on intracardiac and body surface electrocardiogram (ECG) signals are provided. Intracardiac ECG (IC-ECG) signals and body surface ECG (BS-ECG) signals are processed to perform heartbeat classifications. A BS annotation of BS-ECG signals reflective of a sensed heartbeat is defined, the BS annotation including a BS annotation time value. IC annotations of IC-ECG signals which reflect atrial-activity or ventricular activity of the sensed heartbeat are also defined, each IC annotation including an IC annotation time value. The IC-ECG signals are discriminated as A-activity or V-activity and IC annotations are designated as IC-A annotations or IC-V annotations, respectively. A respective A/V time sequence comparison of IC annotations reflective of the sensed heartbeat is made with one or more time sequence templates for heartbeat classification.

Abstract: The approach presented here relates to an analysis device (100) for analyzing a viscosity of a fluid (217). The analysis device (100) comprises a detection device (110) and a provisioning device (115). The detection device (110) is formed to determine the viscosity of the fluid (217) using at least one Doppler parameter of a Doppler spectrum of the fluid (217). The provisioning device (115) is formed to provide or transmit a viscosity signal that represents the viscosity determined by the detection device (110).

Abstract: A system includes a collar that is worn around a neck of the user. A stimulator is coupled to the collar such that the stimulator is positioned adjacent to an airway of the user. The sensor is coupled to the collar and configured to generate data associated with the airway of the user. The memory is coupled to the collar and storing machine-readable instructions. The control system is coupled to the collar and includes one or more processors configured to execute the machine-readable instructions to determine, based at least on an analysis of the generated data, that the user is currently experiencing an apnea event. In response to the determination, the control system causes the stimulator to provide electrical stimulation, at a first intensity level, to one or more muscles of the user that are adjacent to the airway to aid in stopping the apnea event.

Abstract: A sphenopalatine ganglion (SPG) stimulating device for stimulating an SPG of a patient is provided. The SPG stimulating device includes a sheath having a proximal end portion and a distal end portion, the distal end portion shaped to define at least one electrode opening. A nasal stabilizer is disposed around the sheath and configured to stabilize the sheath with respect to a nostril of a nose of the patient when the sheath is disposed within the nose. An electrode mount is slidably disposed within the sheath, and at least one electrode is coupled to the electrode mount and deployable out of the sheath through the at least one electrode opening to position the at least one electrode to stimulate the SPG. Other applications are also described.

Abstract: An illumination system (1) for photodynamic therapy is provided, the illumination system comprising an illumination source (2), which is configured to emit an electromagnetic radiation (3) to illuminate a target surface (4) during operation, and an electronic control unit (5), wherein the illumination source is configured such that the intensity of the electromagnetic radiation emitted by the illumination source can be varied, wherein the electronic control unit is operatively connected to the illumination source and configured to control operation of the illumination source according to an illumination protocol during an illumination session performed with the illumination system, and wherein the illumination protocol comprises instructions to operate the illumination source during the illumination session in a plurality of different modes, the modes comprising: a) a first mode, wherein, in the first mode, the electronic control unit controls operation of the illumination source such that the intensity of th

Abstract: Systems and methods are disclosed for a surgical laser system with illumination. In some embodiments, a laser system comprises a surgical laser and an illumination source having their outputs combined into a fiber-optic cable and directed by the fiber-optic cable to a target surface. The illuminating visible light may be continuous and/or in pulses. Surgical laser pulses and illumination pulses may be synchronized for a stroboscopic effect. The laser system may also monitor laser electromagnetic radiation that is returned back through the fiber-optic cable.

Abstract: A shared resource medical system for monitoring a patient during emergency situations includes a primary medical device including a processor configured to wirelessly receive and transmit data, at least one secondary medical device communicatively coupled to the primary medical device and configured to collect physiological information from a patient, and transmit the physiological information to the primary medical device, and a remote computing device disposed at a location remote from the primary medical device and the at least one secondary medical device, wherein the primary medical device is configured to receive the physiological information from the at least one secondary medical device, and transmit the physiological information to the remote computing device, and wherein the remote computing device is configured to monitor the physiological information collected by the at least one secondary medical device.

Abstract: A variety of electrode pad cartridges are described that are suitable for use with a defibrillator. In one aspect the cartridge includes a housing, a tray that carries one or more defibrillation electrode pads and a presence sensor. The presence sensor configured to detect the presence of the tray at a home position. In some embodiments, the AED is configured to be activated when the tray is pulled from the home position.

Abstract: Embodiments of the present invention provide systems and methods for the treatment of pain through activation of select neural fibers. The neural fibers may comprise one or more afferent neural fibers and/or one or more efferent neural fibers. If afferent fibers are stimulated, alone or in combination with efferent fibers, a therapeutically effective amount of electrical stimulation is applied to activate afferent pathways in a manner approximating natural afferent activity. The afferent fibers may be associated with primary receptors of muscle spindles, golgi tendon organs, secondary, receptors of muscle spindles, joint receptors, touch receptors, and other types of mechanoreceptors and/or proprioceptors. If efferent fibers are stimulated, alone or in combination with afferent fibers, a therapeutically effective amount of electrical stimulation is applied to activate intrafusal and/or extrafusal muscle fibers, which results in an indirect activation of afferent fibers associated therewith.

Abstract: A wearable device is provided. The wearable device includes an electronic component and an encapsulant. The encapsulant includes a low-penetrability region encapsulating the electronic component and a high-penetrability region physically separated from the electronic component.

Abstract: Methods and apparatuses for treating a patient having a brain lesion (e.g., a stroke patient) by applying a charge-balanced, low-frequency alternating current stimulation (ACS) to a region of the patient's brain immediately before and/or during a directed movement. The charge-balanced, low-frequency ACS may have a depolarizing phase that is slower than the hyperpolarizing phase (e.g., the depolarizing phase may have a frequency of 15 Hz or less and the hyperpolarizing phase with a frequency greater than 15 Hz). The ACS stimulation field may be greater than 1.5 V/m. The ACS may be applied during a preferred excitation phase.

Abstract: The invention is method comprising the use of an external photic stimulator treat and/or prevent pain in a subject, such as migraine headache, dental pain, and/or other sources of cranial pain. The presently disclosed method includes treating the pain externally through the cheek, over the zygomatic arch and area of the trigeminal ganglion. The external photic stimulation is believed to inhibit excessive firing of trigeminal ganglion circuits, preventing the excessive expression of calcitonin gene-related peptides and/or other inflammatory manifestations of the pain.