A wearable bladder monitoring device is disclosed (1) comprising securing means (27, 29) for securing the device to a subject's (40) body; a phased array (11) of ultrasound transducers (10) having configurable output frequencies; a configurable phased array controller (13) adapted to control the phased array to direct ultrasound beams (30, 30′, 30″) into the subject's body under a plurality of discrete beam angles and to collect echo signals (31, 31′, 31″) of said ultrasound beams, wherein the phased array controller (13) is adapted to direct a set of ultrasound beams (30, 30′, 30″) into the subject's body for at least a subset of said discrete beam angles in response to a configuration instruction defining the respective output frequencies of the ultrasound beams in said set; and a device communication module (21) for communicating data pertaining to said echo signals to a remote device (5) to facilitate the remote processing of said data and to receive said configuration instruction from the remote device. Also disclosed is a wearable bladder monitoring system adapted to generate such a configuration instruction for the estimation of the degree of turbidity of urine contained in the monitored bladder with the wearable bladder monitoring device, as well as a computer-implemented method and computer program product for facilitating such urine turbidity estimation.

A system includes a processing circuit configured to receive signals corresponding ultrasound data, extract a blood flow waveform from the signals, the blood flow waveform corresponds to a single pulse of the signals, determine a curvature characteristic of the blood flow waveform based on a plurality of local curvature parameters, and identify a medical condition for the blood flow waveform using the blood flow waveform. Each of the plurality of local curvature parameters indicates a degree to which the blood flow waveform deviates from a straight line at a location on the blood flow waveform.

Techniques for automated titration of CPAP device for a subject include receiving multiple ultrasound images representing a cross section of an airway in a neck of the subject at corresponding different times. Multiple different positive pressure values imposed by a device on the airway of the subject are also received at each of the corresponding times. For each of the ultrasound images, a mask of pixels associated with an air-tissue interface is automatically formed, and a value of a statistic of pixels within the mask is automatically determined. A titration pressure for a continuous positive airway pressure (CPAP) device is automatically determined based on the positive pressures and the value of the statistic for each of the ultrasound images. Output data that indicates the titration pressure for the CPAP device is presented on a display device, such as by operating the CPAP device itself at the titration pressure.

A wearable, open and adjustable MRI head coil system having an assembly of support members, panels, or portions defining one or more access openings. The support members, panels, or portions can support, house, or otherwise include radiofrequency receiver antennae or imaging coils such that the assembly is positionable or wearable by a patient for MRI scanning. The radiofrequency receiver antennae or imaging coils, and other devices can be simultaneously in contact with a patient's head, thereby enabling use during diagnostic, therapeutic, surgical, or other interventional procedures.

Systems and methods for stroke detection in accordance with embodiments of the invention are illustrated. One embodiment includes a system for detecting strokes, including a processor, a first ultrasound transmitter located on a patient's head in communication with the processor, a first ultrasound receiver located on the patient's head in communication with the processor, a memory in communication with the processor, including a stroke diagnostics application, where the stroke diagnostics application directs the processor to transmit a first ultrasound signal from the first ultrasound transmitter across a patient's brain, the brain comprising a first and second hemisphere, receive the first ultrasound signal using the first ultrasound receiver, where the ultrasound signal is affected during transit by harmonics generated by microbubbles in the blood of the patient stimulated by the first ultrasound signal, and detect that a stroke has occurred based on the harmonic effects on the first received ultrasound signal.

Ultrasonic energy is used for treating degenerative dementia. A focal point of an ultrasonic transducer beam is directed at a target area of the brain to promote removal of substances that accumulate in the interstitial pathways that are at least partially responsible for the degenerative dementia. In one example, the target area of the brain may comprise the hippocampus and the degenerative dementia may be Alzheimer's disease. The ultrasonic beam may stimulate brain tissue at a frequency that corresponds to a naturally occurring deep sleep burst frequency of neurons and subsequent astrocyte activation patterns that drive a convective process responsible for brain solute disposal. For example, the transducer may generate a burst frequency of between 1-4 hertz to stimulate deep sleep brain functions that help remove amyloid plaque.

Described herein are devices and methods useful in automating ultrasound imaging. The device include a base coupled with soft robotics, which may be attached to an ultrasound transducer probe in order to robotically manipulate the probe to perform an ultrasound scan. The device has an adjustable structure configured to hold the probe on a walking soft robot. The device can be configured to be attached to, or worn by, the patient. With soft robotic actuation and locomotion, the holder can move and position the probe during a real time ultrasound scanning procedure. Furthermore, the holder may be equipped with sensors to sense and map pressure and location. The position of the holder can be robotically monitored and controlled so as to achieve consistency and reproducibility between ultrasound scans. Due to the wearable nature of the holder, the scans may be conducted while the patient is in motion, thereby providing a portable solution for ultrasonic imaging. The holder is cost effective and may be used in conjunction with various ultrasound probes.

A patient monitoring system includes: a biomedical sensor including: a transducer configured to produce a signal corresponding to a biological function; a sensor converter configured to convert the signal to a converted signal; and a transmitter configured to produce a communication, based on the converted signal, that is indicative of one or more values of the biological function, and to send the communication wirelessly; and a base station including: a receiver configured to receive the communication wirelessly and to produce a receiver output signal; a base station interface configured to produce a base station output signal indicative of the one or more values of the biological function; and at least one output port to receive the base station output signal and configured to be hard-wire connected to a display that is configured to display information indicative of the biological function.

Systems and methods can include a system for positioning an ultrasound probe proximal to anatomy of a patient on a radiation couch including a substantially planar base including engagement features to directly or indirectly index the substantially planar base to the radiation couch and a centrally located guide extending longitudinally along a top side of the base, a probe holder, configured to be coupled to, to translate longitudinally, and to be user-accessed and user-controlled from within, a central region of the substantially planar base, a clamp, configured to localize the probe holder at a specified location along a translation path in the central region of the substantially planar base, leg supports shaped to accommodate a patient's legs from behind, the pair of leg supports being shaped and arranged to provide a space therebetween that can accommodate an ultrasound probe holder.

Aspects of the technology described herein related to monitoring fetal heartbeat and uterine contraction signals. An ultrasound system may be configured to sweep a volume to collect ultrasound data, detect a fetal heartbeat and/or uterine contraction signal in the ultrasound data, and automatically steer an ultrasound beam to monitor the fetal heartbeat and/or uterine contraction signal. The ultrasound system may be further configured to determine a location where the fetal heartbeat and/or uterine contraction signal is detectable or detectable at a highest quality. The ultrasound system may include a wearable ultrasound device, such as an ultrasound patch coupled to a subject. The wearable ultrasound device may have a two-dimensional array of ultrasonic transducers capable of steering ultrasound beams in three dimensions.