Abstract: Gamma brain stimulation for preventing or treating Alzheimer's disease or sleeping disorders using light or sound is known. A strobing 40 Hz light source has been shown to cause positive effects due to the stimulation. It is an advantage to know the actual dosage of light that enters the person's eyes in order to understand the relationship between dosage and effectiveness. A camera is used to detect the subject's gaze angle, distance, pupil diameter and any other factors that affect the light power that enters the eye. A target dosage is first determined by a medical worker, such as to determine the effects of the exact same dosage on a group of similar persons, such as Alzheimer's patients. With deviations of gaze angle, distance, and pupil size from the ideal, the effective dosage is decreased. The disclosed system adjusts the actual dosage, such as session duration, based on such factors so that the final dosage received by the person is consistent and meets the target dosage.

Abstract: Methods and apparatus for retracting the dura away from a cutting tool during a laminectomy procedure. The method includes inserting a memory shape surgical sponge (patty) into an initial epidural space between the dura and the tool used to decompress (e.g., drill) the lamina. As the lamina is further decompressed, the patty tends to spring back toward its nominal position, urging the dura away from the decompression and isolating the dura from the drill.

Abstract: The present disclosure pertains to optimizing sleep score parameters. In one embodiment, a first set of vectors is obtained, where each vector includes parameter values of sleep-related parameters for calculating a sleep score. For each vector of the first set, a correlation value indicating a degree of a correlation between the vector and a user-indicated sleep score associated with a set of parameter values representative of a sleep metric of the user is determined. A second set of vectors is generated based on a first subset and a second subset of the first set of vectors satisfying a first and second criteria, respectively. A correlation value associated with each vector of the second set is determined. For each sleep-related parameter, a parameter value of a given vector of the second set is assigned based on the correlation values associated with the second set.

Abstract: User comfort control system having non-invasive bio-patch. In some embodiments, a system for providing comfort of a person can include a wearable patch configured to be attached to a skin of the person and sense a biological condition of the skin, and to transmit information representative of the sensed biological condition. The system can further include a controller configured to receive the information and generate a control signal. The system can further include an adjustment element associated with a furniture item implemented to support and provide comfort for the person. The adjustment element can be in communication with the controller and be configured to adjust a comfort level of the furniture item for the person in response to the control signal.

Abstract: This disclosure pertains to a system configured to control light exposure for circadian phase management and/or light deficient disorders of a subject. The system comprises a user interface, physiological sensors configured to generate output signals conveying physiological data of the subject, and a light control valve configured to block or reduce blue light ambient radiation reaching eyes of the subject. Processors are in communication with the user interface, the physiological sensors, the light control valve, and radiation generators. The processors cause the system to receive physiological goals of the subject, determine a light control plan based on the physiological goals, the physiological data, environmental data, and time data. The system operates the light control valve to block or reduce blue light ambient radiation based on the light control plan, and generate, using the one or more radiation generators, therapeutic light radiation based on the light control plan.

Abstract: The present invention concerns a system for treating cancer or tumors by thermotherapy, comprising an expandable implant device, an excitation catheter and an electric power source, wherein the implant device configured for circumferentially subtending a vessel upon expansion of the implant device in said vessel, the implant device comprising a set of cross-connected conductors forming a circumferential structure with openings in between the conductors, said openings having a minimal opening distance when the implant device is expanded of at least 2 mm, wherein the excitation catheter comprises a longitudinal shaft with a distal end, a proximal end, and a longitudinal body in between, whereby the catheter comprises a longitudinal axis along the longitudinal shaft, and whereby the catheter further comprises an emitter coil at or near the distal end, and whereby the longitudinal body of the catheter further comprises a wiring lumen comprising electrical wiring extending from the distal end to the proximal end,

Abstract: A control circuit accesses information regarding a plurality of pre-existing vetted radiation treatment plans for a variety of patients and uses that information to train at least one model (such as a dose volume histogram estimation model). The control circuit then uses that model to develop estimates for a radiation treatment plan for a particular patient. The control circuit can then use those estimates to develop a candidate radiation treatment plan.

Abstract: An implantable position detecting system is configured to detect a position of an implantable device with respect to a body structure. The system includes at least one proximity measuring transducer configured to be implanted on the body structure a distance from the implantable device, the at least one proximity measuring transducer being configured to receive energy from an external electromagnetic field generated by an external sensing interface, wherein the at least one proximity sensor is configured to emit an emitted signal responsive to the electromagnetic energy and to receive distance information comprising a sensing signal that is responsive to the distance from the implantable device.

Abstract: The invention concerns a device for helping a user fall asleep, comprising a light source designed to emit a substantially monochromatic red or quasi-monochromatic light encouraging the user to fall asleep, characterized in that it comprises a control unit designed to automatically control said light source according to a predefined law according to which the light power emitted by said light source decreases gradually over time in such a way as to change automatically between a maximum power value and a minimum power value, the light power emitted by said light source at a given time always being greater than or equal to the light power emitted at a subsequent time.

Abstract: The present disclosure pertains to a system and method for providing mandibular advancement and sleep positional therapy to a user for a sleep session. The system is formed by a mandibular advancement device for treating obstructive sleep disordered breathing (e.g., obstructive sleep apnea and snoring) that includes an electronics module configured to aid in sleep positional training. The present system and method facilitate advancing a lower jaw of the user into a protruding position relative to an upper jaw of the user to increase a size of an airway of the user, determining whether a posture of the user has breached a posture threshold, and, responsive to a breach, prompting the user to change posture such that the posture of the user no longer breaches the posture threshold.

Abstract: A system to provide circadian-friendly lighting for nighttime hospital care comprising a lighting module and a transmitter tag that interface wirelessly wherein the lighting module comprises red-shifted light spectra, which is proven to be less disruptive to melatonin production than current blue-shifted hospital lighting; wherein the light output of the devices is modulated by the proximity of a tag to the device, with light intensity increasing with closer proximity between these two components and decreasing with increased distance, thereby providing hands-free lighting to caregivers in the specific locations where they need light to perform care tasks.

Abstract: A surgical implant includes a biocompatible member configured for securement to an underlying target surgical site and a radiation source integrated into or onto the biocompatible member. The surgical implant may be one of a clip, pin, or coil and the radiation source includes at least one brachytherapy capsule, or other radioactive material incorporated therein or provided thereon. The radioactive material provides a dose of radiation to the target surgical site. The surgical implant may also be formed from titanium, stainless steel or polymers. A surgical applier is provided for allowing a surgeon to apply the implant to a patient's tissue.

Abstract: Aspects of the present disclosure provide methods, apparatuses, and systems for closed-loop sleep protection and/or sleep regulation. According to an aspect, a biosignal parameter and ambient noise are measured. The biosignal parameter is used to determine sleep condition of a subject. The sleep condition is determined based on one or more of personalized sleep data or historical sleep data collected using a subset of society. Based on the sleep condition, an arousal threshold is determined. Based on the ambient noise and the determined sleep condition, one or more actions are taken to regulate sleep and avoid sleep disruption.

Abstract: Provided are systems and methods for decalcifying aortic valves and/or other valves, blood vessels, and/or cardiac tissues in a mammalian (e.g., a human) patient (e.g., a patient having or suspected of having calcific aortic valve disease (CAVD)). A transcatheter (aortic) valve decalcification system/method can include applying one or more pulsed magnetic fields to the calcium deposit(s) within a valve or other vessel or tissue within the patient. The system can include a catheter having pulsed magnetic field ribbons disposed therein, and the catheter can be provided to the patient.

Abstract: A method for sealing and flushing a delivery member includes sealing one or more lumens and flushing air from the one or more lumens. An interventional device delivery system includes a handle assembly and a delivery member. The handle assembly includes a catheter holder with a passageway therethrough. A flush block is associated with the catheter holder and has a flush port and a flush chamber. The delivery member is associated with the handle assembly and includes a plurality of catheters. At least one of the catheters has a proximal end disposed within the passageway in the catheter holder and is in fluid communication with the flush chamber.

Abstract: A phototherapy or BRT process and apparatus is provided, which, using a pre-recorded bioresonance frequency or compilation of frequencies, causes an EMR emitter to emit within a biological window of a target organism to positively or negatively affect the organism. The EMR may be generated in one or more LEDs by a device connected to a controller of the EMR emitter which device provides the pre-recorded bioresonance frequency or compilation of frequencies to control the LEDs' emitted light in terms of its intensity and/or a frequency or flicker-rate.

Abstract: A method, system and apparatus for a vibration-masking device for use in the bed emits sufficient vibration to mask ambient vibrations and aid in sleep and relaxation. Low frequency vibrations also help reduce the risk of deep vein thrombosis, also referred to as DVT. The apparatus is designed to be cooled so as to avoid overheating when used in the bed or in upholstered furniture.

Abstract: A multi-purpose balloon intra-cavity catheter includes a catheter having a proximal end portion, a central portion and a non-branching distal end portion, a plurality of lumens associated with the catheter extending from the proximal end portion, and a plurality of inflatable balloons positioned in the central portion and/or the non-branching distal end portion. Each of the plurality of inflatable balloons is communicatively associated with a corresponding one of the plurality of lumens, the plurality of inflatable balloons being selectively inflated or deflated to position and stabilize the catheter in a cavity for delivery of a medical treatment. The catheter can include an extraction opening associated with a lumen to remove fluids and materials from the cavity, and a connector associated with a corresponding lumen adapted to selectively receive one or more of a fluid medium or a radioactive isotope provided to a corresponding lumen for delivery of the medical treatment.

Abstract: A method for helping a user awaken from sleep includes receiving information indicating a wake-up time frame; receiving a plurality of biometric readings of the user, each biometric reading including at least one of a heart rate or respiration rate; based on the plurality of biometric readings, determining that the user has had sufficient sleep; and arranging a wake-up sound after entering the wake-up time frame and after determining that the user has had sufficient sleep or at the end of the wake-up timeframe.

Abstract: Typically, high NREM stage N3 sleep detection accuracy is achieved using a frontal electrode referenced to an electrode at a distant location on the head (e.g., the mastoid, or the earlobe). For comfort and design considerations it is more convenient to have active and reference electrodes closely positioned on the frontal region of the head. This configuration, however, significantly attenuates the signal, which degrades sleep stage detection (e.g., N3) performance. The present disclosure describes a deep neural network (DNN) based solution developed to detect sleep using frontal electrodes only. N3 detection is enhanced through post-processing of the soft DNN outputs. Detection of slow-waves and sleep micro-arousals is accomplished using frequency domain thresholds. Volume modulation uses a high-frequency/low-frequency spectral ratio extracted from the frontal signal.