Abstract: Systems and methods for speech-controlled or speech-enabled health monitoring of a subject are described. A device includes a substrate configured to support a subject, a plurality of non-contact sensors configured to capture acoustic signals and force signals with respect to the subject, an audio interface configured to communicate with the subject, and a processor in connection with the plurality of sensors and the audio interface. The processor configured to determine biosignals from one or more of the acoustic signals and the force signals to monitor a subject's health status, and detect presence of speech in the acoustic signals. The audio interface configured to interactively communicate with at least one of the subject or an entity associated with the subject based on at least one of an action needed due to the subject's health status and a verbal command in detected speech.

Abstract: A system for providing exercise incentives and/or providing massage is disclosed herein. The system includes a pair of shoes to be worn by a user during exercise; a software application downloadable to an electronic device and configured to wirelessly communicate with the pair of shoes; and a server in communication with the software application. In some embodiments, the pair of shoes includes massage pads and cooling/warming elements. The system is primarily useful for providing a monetary incentive to exercise and secondarily useful for providing relief to a user's feet via massage.

Abstract: The present disclosure provides alert implants that comprise a medical device and an implantable reporting processor (IRP), where one example of such a medical device includes a component for a total knee arthroplasty (TKA) such as a tibial extension, a femoral component for hip replacements, a breast implant, a distal rod for arm or leg breakage repair, a scoliosis rod, a dynamic hip screw, a spinal interbody spacer, and tooling and methods that may be used to form the alert implant, and uses of such alert implants in the health maintenance of patients who receive the implant.

Abstract: Methods and systems for providing neuromodulation therapy are disclosed. The systems include an Implantable Pulse Generator (IPG) or External Trial Stimulator (ETS) that is capable of sensing an Evoked Compound Action Potential (ECAP), and (perhaps in conjunction with an external device) is capable of adjusting a stimulation program while based on the sensed ECAP. The stimulation program may include a pre-pulse component that may be adjusted based on the sensed ECAP. Moreover, stimulation may be applied to neural elements timed to coincide with the arrival of ECAPs at those neural elements. The stimulation may enhance or suppress activation of those neural elements.

Abstract: A monitoring device configured to be attached to a body of a subject includes a physiological sensor configured to detect and/or measure physiological information from the subject, an activity sensor configured to sense physical activity information from the subject, an actuator configured to adjust stability of the monitoring device relative to the body of the subject, and a processor in communication with the activity sensor and the actuator. The processor is configured to process the physical activity information to detect a change in the physical activity of the subject and to control the at least one actuator to adjust the stability of the monitoring device relative to the body of the subject in response to detecting that a change in the physical activity of the subject has occurred.

Abstract: An electronic device may determine whether a user wears the electronic device by means of at least one sensor; measure a first bio-signal of the user by means of the at least one sensor while the user wears the electronic device; drive an RF sensor included in a charging device while the electronic device is connected to the charging device including the RF sensor through an interface, thereby measuring a second bio-signal of the user that is generated by the RF signal oscillated from the RF sensor; receive at least one of electric power for charging the battery from the charging device and the second bio-signal through the interface; generate health information of the user on the basis of at least the first bio-signal and the second bio-signal; and display the generated health information on a display.

Abstract: A device is provided for accurately mapping a tumor embedded in healthy tissue by using a probe ion that emits detectable light in response to the probe ion being bound to the tumor. An exciting laser beam is cleansed of light frequencies that excite the probe ion bound to the healthy tissue by using intracavity quenching that eliminates the wavelengths that excite the probe ion bound to the healthy tissue. A resulting emission from the probe ions bound to the tumor is photo-detected to illuminate the tumor and the periphery of the tumor. In one embodiment, the illumination of the tumor and its periphery is used to guide a surgical laser to accurately excise the tumor with a minimal loss of healthy tissue.

Abstract: A wearable cardioverter defibrillator monitor case includes a housing configured to surround a defibrillator electronics assembly, a front cover removably attachable to the housing, and a rear cover removably attachable to the housing. The wearable cardioverter defibrillator case has a shock indicator positioned on the housing at an interface between the housing and the front cover.

Abstract: Devices and methods for assisting blood flow are provided. The device includes a housing with an inlet and an outlet, and a fluid barrier separating the housing into a first section containing the inlet and outlet, and a second section. The device also includes an impeller shaft coupled to an impeller and a first magnet in the first section of the housing, and a drive shaft coupled to a second magnet in the second section of the housing. The first and second magnets are arranged such that rotation of the drive shaft rotates the second magnet causing rotation of the first magnet, which drives the impeller.

Abstract: A method and apparatus for the treatment of Sleep Apnea events and Hypopnea episodes wherein one embodiment comprises a wearable, belt like apparatus containing a microphone and a plethysmograph. The microphone and plethysmograph generate signals that are representative of physiological aspects of respiration, and the signals are transferred to an imbedded computer. The embedded computer extracts the sound of breathing and the sound of the heart beat by Digital Signal Processing techniques. The embedded computer has elements for determining when respiration parameters falls out of defined boundaries for said respiration parameters. This exemplary method provides real-time detection of the onset of a Sleep Apnea event or Hypopnea episode and supplies stimulation signals upon the determination of a Sleep Apnea event or Hypopnea episode to initiate an inhalation. In one embodiment, the stimulus is applied to the patient by a cutaneous rumble effects actuator and/or audio effects broadcasting.

Abstract: A method includes collecting a set of user information, determining a user current performance by: determining a sleep score or debt, measuring the user's previous physical activity, heart rate, or body temperature, calculating weights for the sleep score and the sleep debt, the measured previous physical activity, heart rate, or body temperature, calculating a weighted sum of the weighted sleep score, the weighted sleep debt, the weighted user's previous physical activity, weighted heart rate, or weighted body temperature, setting a user target level of performance, measuring a circadian rhythm and a user's duration of sleep or sleep cycle, comparing the circadian rhythm, the duration of sleep or sleep cycle, the current performance level, and current time zone information over days to determine a separate user performance level, comparing the target level of performance to the separate user performance level, and providing an alert and feedback user related to the comparison.

Abstract: An adapter assembly is provided and includes a housing for connection with a surgical device and for operative communication with at least one rotatable drive shaft of the surgical device; an outer tube having a proximal end supported by the housing and a distal end for connection with a selected end effector, wherein the distal end of the outer tube is in operative communication with each of the at least one force receiving drive member of the end effector; at least one drive transmitting/converting assembly for interconnecting a respective one of the at least one rotatable drive shaft of the surgical device and one of the at least one force receiving drive member of the end effector; and a circuit board supported in the housing and storing at least one of operating parameters and life cycle information which are unique to the adapter assembly.

Abstract: The present disclosure pertains to a system and method for monitoring and for facilitating pulmonary and systemic hemodynamics in the treatment and/or prevention of cardiac arrhythmias or structural cardiac changes, caused by altered preload. The system comprises: a pressure generator; a first sensor configured to generate output signals conveying information related to venous blood accumulation during cardiac preload in the subject; a second sensor configured to generate output signals conveying information related to systemic arterial circulation in the subject; and one or more hardware processors configured by machine-readable instructions to control the pressure generator to adjust the pressure levels of the flow of breathable gas during one or both of inhalation and exhalation to facilitate the pulmonary and systemic circulation based on the output signals from the first sensor and the second sensor.

Abstract: Disclosed are a deep body spread microwave hyperthermia device for personal uses and an operation method thereof. The operating method may include generating a control signal to control patches attached to the skin of a user, dividing the control signal into a first signal and a second signal having a phase different from a phase of the first signal, transmitting the first signal and the second signal to patches attached to different positions, among the patches, and producing hyperthermia in a body of the user by radiating radio waves based on the first signal or the second signal received by each of the patches.

Abstract: Described herein are methods and systems for monitoring acoustical activity from the abdominal region to guide the optimal timing of food ingestion. According to one embodiment of the method, the rate of intestinal digestion events, as well as the change in the rate across specific time periods, is analyzed to guide ingestion behavior in a way that improves health. The result of guidance may be to reduce weight in people who are obese, to improve performance in athletes seeking to balance energy availability and energy expenditure, or to increase caloric intake in people who are undernourished. The method can be applied using a smartphone application to provide contextually appropriate and specific user guidance about whether, when, and how much to eat in a manner that aligns with the physiologic patterns of intestinal activity.

Abstract: A pigment treatment system includes a handheld apparatus to receive a sub-nanosecond laser beam with a wavelength of about 480 nm to about 550 nm and output a sub-nanosecond laser beam with a wavelength of about 700 nm to about 740 nm. The handheld apparatus includes a monolithic crystal with a first surface coating and a second surface coating to facilitate the change in wavelength of the laser beam through the crystal.

Abstract: Disclosed herein is an implantable pulse generator for administering electrotherapy via an implantable lead. The pulse generator includes a housing and a header connector assembly coupled to the housing. The header connector assembly includes a connector assembly and a header enclosing the connector assembly. The connector assembly includes a support and a connector receptacle. The support extends at least partially about the connector receptacle and is at least partially responsible for having prevented injection molding material from entering the connector receptacle when the injection molding material was injection molded about the connector assembly in forming the header.

Abstract: A method for modifying a refractive property of ocular tissue in an eye by creating at least one optically-modified gradient index (GRIN) layer in the corneal stroma and/or the crystalline by continuously scanning a continuous stream of laser pulses having a focal volume from a laser having a known average power along a continuous line having a smoothly changing refractive index within the tissue, and varying either or both of the scan speed and the laser average power during the scan. The method may further involve determining a desired vision correction adjustment, and determining a position, number, and design parameters of gradient index (GRIN) layers to be created within the ocular tissue to provide the desired vision correction.

Abstract: A biometric monitoring system comprises a substrate with a first surface having a length and a width. A first transmitting antenna is coupled to the first surface at a first end of the length of the first surface. A second transmitting antenna is coupled to the first surface at a second end of the length of the first surface. The first and second transmitting antennas extend across the width of the first surface. A plurality of receiving antennas are coupled to the first surface, each of which extends across the width of the substrate and is spaced apart from an adjacent receiving antenna along the length by a predetermined distance. A controller is configured to supply a first signal to the first transmitting antenna and sequentially measure a transmission coefficient or voltage of the first signal at the plurality of receiving antennas until an attenuation in the transmission coefficient or voltage exceeds a threshold.

Abstract: The present disclosure provides an oral data collection device comprising a mouthguard and at least two sensors, a medical analytics system comprising the device, and methods of using the device and system to provide a personalized treatment protocol, stage a health condition, measure a response to therapy, phenotype for selection to participate in drug trials, measure stability of an anatomical structure, or predict a rate of change of a health condition in a subject in need thereof.