An electronic device and a method for controlling the same are provided. The electronic device includes a communicator including circuitry, a first sensor configured to detect movement information of the electronic device, a memory including a first determination module configured to determine whether a user carries the electronic device and a second determination module configured to determine a detecting method for detecting a user location, and a processor configured to identify whether a user of the electronic device carries the electronic device based on the movement information of the electronic device obtained by the first sensor by using the first determination module, and determine a detecting method for detecting location information of the user according to whether the user carries the electronic device by using the second determination module.

Methods and systems for imaging and analysis are described. Accurate pressure ulcer measurement is critical in assessing the effectiveness of treatment. However, the traditional measuring process is subjective. Each health care provider may measure the same wound differently, especially related to the depth of the wound. Even the same health care provider may obtain inconsistent measurements when measuring the same wound at different times. Also, the measuring process requires frequent contact with the wound, which increases risk of contamination or infection and can be uncomfortable for the patient. The present application describes a new automatic pressure ulcer monitoring system (PrUMS), which uses a tablet connected to a 3D scanner, to provide an objective, consistent, non-contact measurement method. The present disclosure combines color segmentation on 2D images and 3D surface gradients to automatically segment the wound region for advanced wound measurements.

An orthopedic system configured for use in a pre-operative, intra-operative, and post-operative assessment. The orthopedic system comprises a first screw, a second screw, a first device, a second device, and a computer. The first device and the second device are respectively coupled to a first bone and a second bone of a musculoskeletal system. The first and second devices each include electronic circuitry, one or more sensors, and an IMU. A bracket, wrap, or sleeve can be used to hold the first and second devices to the musculoskeletal system. The first and second devices are configured to send measurement data to a computer. The first and second devices each have an antenna system. Electronic circuitry in the first or second devices are configured to harvest energy from a received radio frequency signal to recharge a battery to maintain operation.

An ultrasound diagnostic apparatus includes: an image generator that generates ultrasound image data based on a reception signal received from an ultrasound probe that sends and receives ultrasound waves; a fastener that attaches the ultrasound probe to a subject and fastens the ultrasound probe on the subject such that a pressure applied to the subject to which the ultrasound probe is attached is adjustable; and a hardware processor. The hardware processor controls driving of the fastener, based on difference information between before fastening the ultrasound probe and during/after fastening the ultrasound probe, the difference information being on at least one of positional information on a position of an observation target of the subject, angle information on an angle of the observation target, and pressure information on a pressure applied to the subject.

The blood glucose (BG) detector (BGD) stores baseline BG data therein. The BGD has a housing with legs forming a U-shaped sensing channel for a finger web or ear antihelix. The sensory channel limits insertion of the web/antihelix. A positional light sensor subsystem audibly and/or visually indicates a test-to-test detection position. A BG sensor on the legs uses IR 1550 bandwidth light to detect BG by transmission through the web/antihelix ro generate a detected BG signal. A comparator (in processor-memory system) compares detected BG signal to baseline BG data and generates a displayable BG level to the user via a display module. Alternatively, a leg-to-leg distance sensor may be used. A keypad enables upload of the BD baseline data (or an I/O port).

According to certain embodiments, a wearable electronic device comprises: a housing; a first electrode and a second electrode disposed on the housing; an A/D converter connected to the first electrode and the second electrode; a pulse generator connected to the first electrode and the second electrode; and a processor operatively connected to the A/D converter and the pulse generator; wherein the processor is configured to: control the pulse generator to output a series of pulse waves to the first electrode when an external object is in contact with the first electrode; and controlling the A/D converter to obtain biometric information from the first electrode and second electrode in response to outputting the series of pulse waves.

Optoelectronic modules operable to measure proximity independent of object surface reflectivity and, in some implementations, operable to measure characteristics (such as surface reflectivity or absorptivity) of stationary or moving objects are disclosed. The optoelectronic modules are operable to determine, for example, pulse rate, peripheral blood circulation, and/or blood oxygen levels of moving objects, such as the appendage of a user, in some instances. The optoelectronic modules can be used to measure peripheral blood circulation, for example, when a user of the optoelectronic module is engaged in physical activity, such as walking, running or cycling.

Systems and methods are presented for monitoring brain pulsatility. A change in volume of the brain is estimated based at least in part on an output of a non-contact, surface measuring sensor (e.g., a distance sensor or a camera). A metric indicative of brain pulsatility is then calculated based at least in part on a ratio of the estimated change in volume of the brain relative to a change in arterial blood pressure.

This invention is a smart bra for optical scanning of breast tissue which has light emitters which transmit light into breast tissue, light receivers which receive the light after it has been transmitted through the breast tissue, and expandable components which selectively move light emitters and/or receivers closer to the surface of a breast where there are air gaps.

The present disclosure provides methods and apparatus for evaluating tissue structure in damaged or healing tissue. The present disclosure also provides methods of identifying a patient at the onset of risk of pressure ulcer or at risk of the onset of pressure ulcer, and treating the patient with anatomy-specific clinical interventions selected, based on spectral imaging (SI). The present disclosure also provides methods of stratifying groups of patients based on risk of wound development and methods of reducing incidence of tissue damage in a care facility. The present disclosure also provides methods to analyze trends of SI intensities to detect tissue damage before it is visible, and methods to compare bisymmetric SI intensities to identify damaged tissue.