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 and method are provided for diagnosis of animal respiratory diseases using auscultation techniques. Animal lung sounds are recorded and digitized. Lung sounds are obtained by an electronic digital stethoscope or a wireless audio digital recording unit. The sounds are stored as digital data, and one or more algorithms are applied to the data for producing an output to the user indicative of the health of the animal. The acoustic characteristics of the sound are compared with baseline data in the algorithms. One embodiment includes a digital stethoscope with an integral display. Another embodiment provides a system for gathering information about an animal to include not only auscultation data, but also information from other field devices such as temperature probes or weigh scales. The combined information can be analyzed by system software to generate detailed information to a user to include a diagnosis and recommended treatment options.

Abstract: A surgical instrument having a housing, an outer shaft extending from the housing along a longitudinal axis, an inner shaft extending within the outer shaft along the longitudinal axis, a rotator knob position about the outer shaft, and a tube stop coupling the rotator knob to the outer shaft for collective rotation about the longitudinal axis and fixed within the housing against movement along the longitudinal axis. The tube stop has a pair of bearing surfaces that extend into a pair of longitudinal tracks of the outer shaft, and the rotator knob includes a pair of rails that extend into the pair of tracks of the outer shaft and block the tube stop exiting the tracks. The tube stop is captured between a pair of ribs in the housing to hold the tube stop in place while allowing the rotator knob to rotate the outer shaft.

Abstract: A system comprises processing circuitry and memory comprising program instructions that, when executed by the processing circuitry, cause the processing circuitry to: apply a first set of rules to first patient parameter data for a first determination of whether sudden cardiac arrest of a patient is detected; determine that a one or more context criteria of the first determination are satisfied; and in response to satisfaction of the context criteria, apply a second set of rules to second patient parameter data for a second determination of whether sudden cardiac arrest of the patient is detected. At least the second set of rules comprises a machine learning model, and the second patient parameter data comprises at least one patient parameter that is not included in the first patient parameter data.

Abstract: Automated systems and methods are presented for determining the physiological response of human or suitable animal subjects to physical exertion. The methods and systems can include monitoring sensors that capture the motion of the subject along with corresponding physiological data, and can track such motion for the duration of a period of physical exertion. The system is able to acquire an initial stream of physiological data from the subject during a range of physical exertion activities that are representative of the events intended to be monitored with the proposed method and system, enabling a corresponding dynamic physiological response model to be created. The motion tracking system and physiological response model can then be used to predict the physiological response to physical exertion events under a prescribed framework, including applications during real-time event monitoring.

Abstract: A cardiac physiological parameter measuring method, a device, a terminal and a computer storage medium, comprising: by means of one or more vibration sensors, acquiring vibration information of a subject to be tested that is in a supine state, the vibration sensors being configured to be disposed below the left shoulder of the subject to be tested; generating hemodynamic related information on the basis of the vibration information determining an MC feature point of an MC event on the basis the hemodynamic related information.

Abstract: A swallowing analyzing system (S) includes a swallowing sensor (1) and a swallowing analyzer (30). A piezoelectric film sensor (3) of the swallowing sensor (1) includes a plurality of sensing portions (3A) and (3B) in a longitudinal direction of the neck region. The piezoelectric film sensor (3) is located within a range of movement of thyroid cartilage (103), which occurs along with swallowing, and is attached to skin of an anterior neck region (102). The piezoelectric film sensor (3) individually outputs analog signals (S1a) and (S2a) along with deformation of the plurality of sensing portions (3A) and (3B). A body (20) of the swallowing sensor (1) determines whether the swallowing occurs based on displacement signals that are low frequency components of the analog signals (S1a) and (S2a). The body (20) extracts data on the signals during the swallowing and wirelessly outputs the data to the swallowing analyzer (30).

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: In certain embodiments a light therapy system (e.g., phototherapy device), such as for treatment of Alzheimer's disease, depression, dementia, short-term memory, or for improved learning, improved athletic performance or improved cognitive performance, is provided where the light system comprises a blue light source that operates at a frequency in the range from 20 to 50 Hz (preferably around 40 Hz), whereby the system enables retinal ganglion cells of a human to be exposed in order to stimulate brain waves (gamma oscillations in the human's brain).

Abstract: Provided are a controllably self-deformable optical fiber, a multifunctional laser scalpel and a laser processing device including the same. The controllably self-deformable optical fiber drives the protective layer and the optical fiber to deform through controllable deformation of a deformation portion on an outer surface of the protective layer. In addition, the optical fiber also has multiple functions, and can be applied in the treatment of complex lacunae in medical and other related fields.

Abstract: A controlling method for monitoring a physiological condition of a first user. The method includes: obtaining first sensing data of the first user reported by at least one first sensing device; determining the physiological condition of the first user based on a result derived from the first sensing data and a reference range corresponding to the first sensing data; and upon determining that the physiological condition of the first user is abnormal, sending a control instruction to a second sensing device to switch the second sensing device from the first state to the second state.

Abstract: A medical device is directed to monitoring health parameters of a patient, and includes a main unit and a sensor module. The main unit includes mechanical features, a main array interface, and a processor sub-unit, which includes a processor that has communication drivers, a memory, and a sensor module. The sensor module includes a sensor unit, sensor components, enabling components, and a sensor module array interface that mates with the main array interface. In response to the sensor module being electrically and mechanically coupled to the main unit, the medical device acquires one or more bio-signals of the patient. The bio-signals correspond to an anatomic part of the patient and caries out measurements of health parameters.

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 skin treatment device and a head assembly for the skin treatment device include a cover member that passes light and heat to a user's skin. The cover member presents a comfortable flat surface at its exterior, and includes features that couple to a heating element that surrounds a plurality of visible light LEDs. A heat spreader is used to spread heat generated by infrared LEDs and prevent hot spots.

Abstract: Systems and methods for tracking sympathetic-driven arousal state (SDAS) including nociception under anesthesia is described herein. The method includes obtaining heart rate variability and electrodermal activity of a subject. Point process models are generated for the heart rate variability and the electrodermal activity. A multimodal approach is implemented to determine a state space framework based on these point process models. SDAS can be estimated using the state space framework. In some implementations, an anesthesiologist can modify the dosage of drugs administered to the subject based on this estimation.

Abstract: A manipulation system for microscope applications comprises a micromanipulation tool and a protective device protecting the tool, wherein the tool and the protective device are movable relative to one another between a position protecting the tool in a contactless manner and a position releasing the tool for the manipulation.

Abstract: A method of determining a heart rate of a patient having an implanted blood pump including applying a voltage to a plurality of coils of a stator of the blood pump to produce an electromagnetic force to rotate a rotor in communication with the plurality of coils; displaying a waveform associated with a back electromotive force in the plurality of coils of the blood pump, the waveform being proportional to an axial position of the rotor relative to the stator; determining a time interval between a first alteration in the waveform relative to a baseline and a second alteration in the waveform relative to the baseline; and determining the heart rate of the patient based on the time interval.

Abstract: Methods and devices for an optical assembly for a laser generator comprise: a laser source producing a first beam of light and an optical assembly. The optical assembly comprises a prism. The prism has a bottom surface configured to receive a first beam at an incoming angle of incidence relative to a first surface normal, and a hypotenuse surface configured to transmit, at an exit angle relative to a second surface normal, a second beam having a second aspect ratio. The optical assembly further comprises a plano-convex lens configured to transmit the second beam to a coupler. The coupler comprises a first coupling plane at a first distance from the plano-convex lens and a second coupling plane at a second distance from the plano-convex lens. The combination of the prism and the plano-convex lens is configured to change the beam divergence, so that the first coupling plane has a third aspect ratio and the second coupling plane has a fourth aspect ratio.

Abstract: Embodiments described herein include sensors and sensor systems having probe-off detection features. For example, sensors and physiological monitors described herein include hardware and/or software capable of providing an indication of the integrity of the connection between the sensor and the patient. In various embodiments, the physiological monitor is configured to output an indication of a probe-off condition for an acoustic sensor (or other type of sensor). For example, in an embodiment, a signal from an acoustic sensor is compared with a signal from a second sensor to determine a probe-off condition.