Abstract: A triboelectric energy generator includes a substrate, a first triboelectric member disposed on the substrate in a first partial region of a top face of the substrate, a second triboelectric member disposed on the substrate in a second partial region of the top of the substrate, a third triboelectric member disposed above and spaced from the first triboelectric member and the second triboelectric member. The first triboelectric member, the second triboelectric member, and the third triboelectric member are made of different materials. When an ultrasonic wave is applied to a top face of the third triboelectric member, the third triboelectric member is constructed to alternately contact and non-contact both the first triboelectric member and the second triboelectric member, thereby to generate triboelectricity.

Abstract: Embodiments of the invention provide a dental network including a portable dental laser station controllable within a remote access system. The dental laser station can include a dental laser, and a dental handpiece assembly coupled to or including the at least one dental laser. Some embodiments include a processor and a non-transitory computer-readable storage medium including a dental laser management process to exchange dentistry-related parameters between the dental laser station or components and a remote network. Some embodiments include a handpiece assembly structured so that any beam size on the output window or surface is greater than any beam size exiting at the input window or surface. Some embodiments include a laser power supply combination with at least one high voltage (HV) power supply, a coupled or integrated simmer supply, a direct current (DC) supply, and at least one laser configured with a power supply.

Abstract: Methods for treating eating disorders and for reducing a risk associated with developing an eating disorder in patients via therapeutic renal neuromodulation and associated systems. Renal sympathetic nerve activity can be attenuated to improve a patient's eating disorder status or risk of developing an eating disorder. The attenuation can be achieved, for example, using an intravascularly positioned catheter carrying a therapeutic assembly configured to modulate the renal sympathetic nerve.

Abstract: Methods, apparatus, and systems for medical procedures are disclosed herein and include sensing a plurality of tissue electrical potentials at an organ area of an organ, by one or more electrodes on a catheter, determining a number of peak electrical potentials from the plurality of first tissue electrical potentials such that the a peak electrical potential exceeds a potential threshold, determining a first visual characteristic based on the number of peak electrical potential and displaying a rendering of the organ comprising the organ area such that the rendering of the first organ area comprises the first visual characteristic.

Abstract: Contraction stimulation therapy can treat myriad diseases, including lymphedema using a skin patch or implantable stimulator that includes a multiplicity of electrodes, a processor, a stimulation circuit, one or more sensors and programming for a patient interface unit, wherein the processor is programmed to control selection of a subset of the multiplicity of electrodes and of operation of the stimulation circuit responsive to an indication of an adverse physiologic response. The indication of patient discomfort may be determined by monitoring a physiologic parameter of the subject using the one or more sensors, by direct input from the subject via the patient interface unit programming, or a combination thereof. The devices, systems and methods also provide for automatically optimizing the stimulation parameters applied by the stimulation circuit responsive to feedback from the one or more sensors and/or by using direct input from the subject.

Abstract: An implantable apparatus for providing tumor treating fields to a target site is disclosed. The implantable apparatus includes an inflatable body having a longitudinal axis and a plurality of stimulation zones coupled to the inflatable body. The stimulation zones are configured to produce an electric field. Inflation of the body causes elongation of the body along the longitudinal axis.

Abstract: A ceiling artificial intelligence (AI) health monitoring system, includes a monitoring device provided on a ceiling of a space to acquire health information from a patient, and a medical management device configured to apply the health information of the patient acquired to an artificial intelligence-based learning model to determine health condition information of the patient and provide the determination result to a doctor monitor. The medical management device is configured to provide remote medical diagnosis information from the doctor monitor to a user terminal.

Abstract: The present invention discloses a method for determining a maximum value of a heart rate data of a user performing a physical activity. Acquire first heart rate data in a first duration of the physical activity performed by the user. Acquire motion data in the first duration of the physical activity performed by the user. Calculate second heart rate data based on the motion data in the first duration of the physical activity performed by the user by a mathematical model and estimate the maximum value of the heart rate data of the user based on a comparison between the first first heart rate data and the second heart rate data.

Abstract: Apparatuses, systems, and methods for more accurate remote monitoring of a user's body to stabilize the user during fall events and to thereby prevent the user from falling. In some embodiments, a wearable device comprising a power source, one or more sensors configured to monitor a user's COG (COG), at least one plurality of electrodes, a communications interface and a control device is provided. The wearable device is configured to apply electrical pulses according to defined electrical pulse stimulation protocols via the electrodes to target muscle groups of the user's body, causing those target muscle groups to contract and thereby stabilize the user's body during a fall event.

Abstract: Various embodiments of an interface control subsystem may be used between an electrode terminal and a recording terminal of a neurostimulation and neurorecording system. The interface control subsystem may operate in three modes. In a disable mode, a first transistor and a second transistor disposed between the electrode terminal and the recording terminal may operate in a cutoff region and generate a high impedance. In an active mode, the first transistor and the second transistor may operate in a saturation region and generate a low impedance. In a stimulation mode, the first transistor and the second transistor operate in a triode region and generate an impedance between the high impedance of the disable mode and the low impedance of the active mode. The interface control subsystem may further limit voltage at the recording terminal in response to a detected overvoltage condition.

Abstract: A wearable physiological signal detecting device includes a device main body and a telescopic structure. The device main body has a strap which surrounds to form a wearable space. The telescopic structure is disposed in the strap and has first surfaces and second surfaces. Each of the first surfaces faces the corresponding second surface. Each of the first surfaces and the corresponding second surface continuously move close and contact each other to assume a first state. The strap can be forced so that each of the first surfaces and the corresponding second surface move away from each other and have an angle to assume a second state. The size of the wearable space when the first surface and the corresponding second surface assume the second state is greater than the size of the wearable space when the first surface and the corresponding second surface assume the first state.

Abstract: A joint movement monitoring device includes a joint pad that fits over a joint. The joint pad has a primary section placed over a first side of the joint and has an opposing section placed over a second side of the joint. A plurality of three-dimensional (3D) magnetic sensors are incorporated into the primary section of the joint pad. The 3D magnetic sensors are separated by a known distance. A magnet is incorporated into the opposing section of the joint pad. A controller obtains signals from the plurality of 3D magnetic sensors. The signals are used to detect magnet rotation angles related to 3D magnetic sensors within the plurality of 3D magnetic sensors. The detected magnet rotation angles are used to monitor joint position of the joint.

Abstract: A stimulation apparatus for a patient may include an external system configured to transmit transmission signals and an implantable system configured to receive the transmission signals from the external system. The implantable system may include at least one implantable lead, a first implantable device for connecting to the implantable lead during a first time period, and a second implantable device for subsequently connecting to the implantable lead for a second time period.

Abstract: A system for clinical decision support for a caregiver during a clinical encounter involving respiratory distress includes a defibrillator-patient monitor including sensors configured to gather patient physiological data, a user interface device, a memory, and a processor communicatively coupled to the defibrillator-patient monitor, the memory, and the user interface device and configured to control the user interface device to display diagnosis and treatment pathways (DTPs) including a respiratory distress DTP, receive a user selection of the respiratory distress DTP, control the user interface device to provide at least a portion of the physiological data in response to the user selection of the respiratory distress DTP, provide a suggested respiratory distress diagnosis at the user interface device based on the physiological data and the user selection of the respiratory distress DTP, and provide a respiratory distress treatment protocol at the user interface device based on the suggested respiratory distr

Abstract: Assessing a likelihood of a person experiencing a fatigue event when the person tasked with monitoring a vehicle operating in an autonomous driving mode may include receiving a set of response times for a psychomotor vigilance test administered to the person. The test may include a plurality of trials which involve a person lifting a finger from a user input device. Whether the person passed or failed each trial of the set of trials may be determined. A model trained using data from prior psychomotor vigilance tests administered to the person may be identified for the person. Results of the determinations of whether the person passed or failed each trial of the set of trials may be input into the model in order to determine a value representative of a likelihood of a fatigue event. An intervention response may be initiated based on the value.

Abstract: A method of blocking a nerve or neuron by applying an electrical stimulation to the nerve or neuron, wherein the electrical stimulation is of an intensity below the excitation threshold of the nerve or neuron for a length of time sufficient to produce a block of nerve conduction or neuron excitation.

Abstract: An auscultation device includes an electrocardiogram (ECG) device, a sound receiver device, a synchronization device and a processor. The ECG device is configured to receive an ECG signal. The sound receiver device is configured to receive a heart sound signal. The synchronization device is configured to transmit a synchronization signal to the ECG device and the sound receiver device, so that the ECG device starts to receive the ECG signal and the sound receiver device starts to receive the heart sound signal in time synchronization. Moreover, the processor is configured to generate an ECG according to the ECG signal, generate a heart sound diagram according to the heart sound signal, and generate a synchronization timing diagram according to the ECG and the heart sound diagram.

Abstract: A device is presented herein that is configured to be located underneath an eyelid and worn by a user for treating dry eye. The device includes a first surface configured to face a portion of a sclera of the eye, and a second surface configured to face an eyelid and to be completely covered by the eyelid. In some embodiments, the device further includes a plurality of stimulation electrodes proximal to the first surface, wherein the plurality of stimulation electrodes is configured to stimulate the sclera. The device further includes an energy storage element coupled to the plurality of stimulation electrodes. The energy storage element is configured to supply power to the plurality of stimulation electrodes. The device further includes a processor configured to control a supply of energy from the energy storage element to the plurality of stimulation electrodes to stimulate the sclera.

Abstract: A method for generating sleep apnea information for a portion of body sensor data. The method of generating sleep apnea information is made dependent upon a determined presence or absence of arrhythmia within the portion of body sensor data. A first sleep apnea detection methodology is used in response to an absence of arrhythmia being detected within the portion of body sensor data.

Abstract: In one example in accordance with the present disclosure, an emitter system is described. The emitter system includes an array of emitters. Each emitter emits waves towards a target surface. The emitter system also includes a control system. The control system includes a sensing system to determine whether emitters in the array are properly positioned relative to the target surface. A controller of the control system adjusts emitter sets of the array of emitters based on an output of the sensing system.