Abstract: A method includes providing one or more instructions to perform a first action associated with administration of a medication; obtaining first data representing a capture of a patient performing the first action based on the one or more instructions as output by the output device; extracting information about movements of the patient from the first data; presenting an image configured to induce an emotional response in the patient; obtaining second data representing capture of the patient performing one or more microexpressions in response to presentation of the image; obtaining additional data including one or more of demographic information of the patient, information of a disease associated with the patient, or one or more characteristics of the medication; and based on the extracted information about the movements, the one or more microexpressions, and the additional data, determining a medical outcome including a progression of the disease in the patient.

Abstract: A blood pump system including a blood pump, an intravascular flow cannula, and a pressure sensor. The intravascular flow cannula is in flow communication with the blood pump and has a distal end portion distally from the blood pump and a proximal end portion closer to the blood pump. The intravascular flow cannula has at least one blood flow through opening at its distal end portion for blood to enter or exit the flow cannula. The blood flow through opening has a borderline surrounding the through opening. The pressure sensor is configured radially within the flow cannula and borders a proximal portion of the borderline.

Abstract: A catheter system includes a power source, a controller, and a light guide. The power source generates a plurality of energy pulses. The controller controls the power source so that the plurality of energy pulses cooperate to produce a composite energy pulse having a composite pulse shape. The light guide receives the composite energy pulse. The light guide emits light energy in a direction away from the light guide to generate a plasma pulse away from the light guide. The power source can be a laser and the light guide can be an optical fiber. Each of the energy pulses has a pulse width, and the energy pulses are added to one another so that the composite energy pulse has a pulse width that is longer than the pulse width of any one of the energy pulses. At least two of the energy pulses can have the same wavelength as or a different wavelength from one another.

Abstract: A device for providing augmented reality may include a support frame supporting at least one transparent lens, an image display module displaying augmented reality content through the at least one transparent lens, a blood-pressure information detector connected to the support frame to detect at least one blood-pressure related information including a blood-pressure, a heart rate, and oxygen saturation in case that a skin of the user touches the blood-pressure information detector, a skin information detector connected to the support frame to detect at least one skin related information including a moisture level and an oil level of the user's skin in case that the user's skin touches the skin information detector, and a control module that controls the image display module to display the at least one blood-pressure related and the at least one skin related information as augmented reality contents.

Abstract: A device used for neurostimulation includes a plurality of electrodes. In order to improve therapeutic efficacy when using a group of N electrodes equal to or larger than 3, the device is configured to deliver a number of N+1 electrical phases during one cycle via the electrodes such that during N electrical phases of the cycle each electrode of the group delivers alternating a therapeutic electric phase and a number of N?1 charge balancing electric phases. One electrode of the group delivers its specific therapeutic electric phase and the other electrodes of the group deliver a charge balancing phase having an opposite polarity of the therapeutic electric phase delivered, and such that during an additional electrical phase each electrode of the plurality of electrodes delivers an electrical phase with an amplitude that establishes charge neutrality for residual charge on each respective electrode based on phases of the N other electrical.

Abstract: A method comprises driving, by a motor, a camshaft of a transmission of a telesurgically operated instrument to a first rotational state of a plurality of rotational states. The camshaft defines a longitudinal axis and rotates about the longitudinal axis. The method further comprises engaging, in the first rotational state, a first input gear of a first effector drivetrain of the transmission with a first gear of the first effector drivetrain via a first power cam of the camshaft. The method further comprises disengaging, in the first rotational state, a first locker arm of the first effector drivetrain from the first gear via a first locker cam of the camshaft.

Abstract: The present disclosure provides systems and methods relating to neuromodulation. In particular, the present disclosure provides systems and methods for evaluating the efficacy of neuromodulation therapy using evoked potential (EPs). The systems and methods disclosed herein facilitate the evaluation of both parameter-dependent and system-dependent changes in EPs as indicators of therapeutic efficacy.

Abstract: A network-hosted product selection system includes a first server having at least one connected data repository, the first server including a non-transitory medium coupled thereto, the non-transitory medium including instructions for the first server to accept a digitally coded patient state diagnosis model from a connected input device, parse said diagnosis model for information, compare results with information derived from individual ones of product data models, the product data models including parse able tags weighing efficacy in treatment of one or more medical conditions and or symptoms derived from the patient state diagnosis model, select one or more product data models weighing high in efficacy based on at least collective tag weight and displaying products and associated transactional data and product consumption recommendation data.

Abstract: An electronic device, method, and computer-readable recording medium execute a customizable physiological measurement schedule for measuring one or more physiological parameters of a patient. A display displays information related to the patient including physiological data, and a memory is configured to store one or more programs. The one or more processors execute the one or more programs to provide a graphical user interface (“GUI”) on the display including a customizable measurement schedule. An input is received directed to one or more measurement times and corresponding measurement intervals of the one or more physiological parameters to the customizable measurement schedule using a first selection. When the customizable measurement schedule is executed, the one or more programs when executed by the one or more processors provide a first visible indication as each measurement time and corresponding measurement interval of the customizable measurement schedule is completed.

Abstract: The various implementations described herein include methods and systems for monitoring biometric information. In one aspect, a method includes (i) capturing, via an inward-facing camera of an artificial-reality headset, a plurality of images of a region of a face of the user, the region including an eye of the user, where (a) a first image of the plurality of images includes a first position of a pupil in the eye, and (b) a second image of the plurality of images includes a second position of the pupil in the eye, the second position different than the first position; and (ii) determining heart rate information based on the plurality of images.

Abstract: An apparatus and method for subject monitoring and diagnosing with non-invasive measures are disclosed.

Abstract: A device for non-invasive light delivery to a subject. The device includes a controller disposed in the housing, the controller being electrically connected to the power source; at least one waveform electronics assembly; a plurality of laser diodes disposed in the housing, the plurality of laser diodes being configured to operate in a super-pulsed regime, the controller being configured to operate the plurality of laser diodes with a Megahertz (MHz) modulation and peak power in milliwatts (mW), the plurality of laser diodes including at least one near-infrared laser diode, at least one mid-infrared laser diode, at least one far-infrared laser diode, and at least one visible-range laser diode; a plurality of optical fibers bundled into at least one fiber bundle, a distal end of the at least one fiber bundle being arranged and configured for delivering light from the plurality of optical fibers to the subject.

Abstract: In certain embodiments, a surgical contact lens system for ophthalmic treatment with a laser beam includes a patient contact lens and a surgical contact lens. The patient contact lens reduces one or more refractive errors of the eye and has a concave surface and a convex surface. The concave surface is to be disposed outwardly from a cornea of an eye. The surgical contact lens has an eye end to be disposed outwardly from the convex surface of the patient contact lens. The surgical contact lens includes a frame and an optical component coupled to the frame. The patient contact lens reduces pressure from the surgical contact lens to reduce corneal folding of a posterior surface of the cornea. The optical component of the surgical contact lens and the patient contact lens transmit the laser beam to treat the eye.

Abstract: Certain exemplary embodiments can provide an apparatus wearable by a user. The apparatus can comprise a biometric sensor constructed to generate signals based upon measurements of the user. The apparatus can comprise a processor constructed to determine a significant detrimental change in the user via an algorithm based upon the signals.

Abstract: An electrical stimulation method is provided. The electrical stimulation method is applied to an electrical stimulation device. The steps of the electrical stimulation method include obtaining a target energy value; providing an electrical stimulation signal to a target area; calculating a total energy value according to an energy value transmitted from the electrical stimulation signal to the target area; and determining whether the total energy value has reached the target energy value.

Abstract: A medical system can include a foot pedal assembly that includes one or more pedals configured to be foot operated for controlling various function of the system. A dynamic indicator can be associated with a first pedal of the one or more pedals. The dynamic indicator can be configured to provide a first indication when the medical system is in a first state, and provide a second indication when the medical system is in a second state. The system can further be configured to determine a state of the medical system, cause the dynamic indicator to provide the first indication in response to the determined state comprising the first state, and cause the dynamic indicator to provide the second indication in response to the determined state comprising the second state.

Abstract: Systems and methods for closed-loop control of electrostimulation based on signal features derived from evoked neural activities are disclosed. A system comprises an electrostimulator to deliver a stimulation therapy, a sensing circuit to sense an evoked response induced by the stimulation therapy, and a controller circuit to identify, from a plurality of candidate signal features, a target signal feature that satisfies a performance criterion for distinguishing a first stimulation effect according to a first stimulation setting from a second stimulation effect according to a different second stimulation setting. The target signal feature can be identified based on evaluations of a discrimination metric for each of the candidate signal features. The controller circuit can determine a value of the target signal feature from the sensed evoked response, and control the electrostimulator to adjust the stimulation therapy based on the value of the target signal feature.

Abstract: A transducer apparatus for delivering tumor treating fields to a subject's body, the transducer apparatus including: a plurality of electrode elements; wherein the plurality of electrode elements comprises a first electrode element and a second electrode element, wherein the first electrode element and the second electrode element are substantially located in a plane of the transducer apparatus; and when viewed from a direction perpendicular to the plane, the first electrode element and the second electrode element have edges located adjacent each other without any other electrodes between them, wherein the edges of the first electrode element and the second electrode element extend parallel to each other along their length.

Abstract: Provided is a digital stethoscope capable of outputting a heart sound data and/or a therapeutic data. The digital stethoscope includes a housing, a physiological data acquisition unit configured to acquire the heart sound data, a therapeutic data unit providing the therapeutic data and an output unit configured to output heart sound data and/or therapeutic data, wherein the physiological data acquisition unit and the therapeutic data unit are provided within the housing.

Abstract: Respiratory function can be preserved and/or enhanced in patients with a respiratory insufficiency using a photoceutical applied by a photoceutical medical device to at least one primary inspiratory muscle and/or a lung. At least one site on a body of a patient can be selected for delivery of the photoceutical to the muscle(s); and the photoceutical can be applied at the at least one site by the photoceutical medical device for a time period from a first start time to a first end time to treat the at least one primary inspiratory muscle and/or the lung of the patient to preserve and/or enhance the respiratory function. The photoceutical can include a light signal with at least one delivery scheme (e.g., superpulsed, pulsed. and/or continuous) and one or more wavelengths.