A wearable breath analysis device is disclosed that may be worn, for example, around the neck or wrist of a user. The wearable device may be a stand-along device (in which case it may include a display that provides a user interface), or may operate in conjunction with a smartphone or other command device. The wearable device may include auditory and/or vibratory notice and communications features or capabilities, for example, such as a reminder or notice to conduct a breath analyte measurement, instructions to the user in the course of conducting the measurement, and notice of the breath analyte measurement results. The auditory or vibratory notice may be provided at the wearable, and/or at the command device where a command device is used. Related methods also are provided.

A method for identifying a change associated with a state of health of a user. In one embodiment, the method includes at least one computer processors receiving monitoring data associated with monitoring a user, where the monitoring data is generated by one or more sensors. The method further includes determining a state of health of the monitored user by analyzing the monitoring data utilizing one or more models. The method further includes determining a level of urgency based, at least in part, upon the determine state of health of the monitored user. The method further includes transmitting one or more respective notifications to one or more devices based, at least in part, on the determined state of health of the user and the corresponding level of level of urgency, and where a notification includes a determined state of health and the corresponding determined state of urgency associated with the monitored user.

A device (10) for converting a movement of a user into a voltage comprises a neck cord (20), a piezoelectric sensor (30) and a printed circuit board (40). The neck cord is coupled to the piezoelectric sensor and provides in use a pulling force that acts on the piezoelectric sensor in a first direction. The printed circuit board is electrically and mechanically coupled to the piezoelectric sensor. The weight of the printed circuit board cause in use a gravity force to act on the piezoelectric sensor in a second direction, which differs from the first direction such that the movement of the user (5) wearing the neck cord causes a change in the shape of the piezoelectric sensor which in response thereto generates the voltage. The voltage may be used as a supply source for an electrical component (41) mounted on the PCB, or may be used as a wake-up signal for an electrical component such as a processor (41) or an accelerometer.

A system for diverting emboli within a patient can include a device that detects a presence of emboli in a first blood vessel of a patient. A compression member can be aligned with a second blood vessel of the patient when a collar supporting the compression member is positioned at least partially around a portion of the patient. In response to the detection device, a controller can actuate the compression member, when the presence of emboli is detected, from an unactuated state to an actuated state in which at least a portion of the compression member (i) is closer to the second blood vessel than while in the unactuated state and (ii) compresses and limits blood flow through the second blood vessel.

A motion of a model including a joint, at least one body part that rotates with respect to the joint, and a plurality of inertial sensors attached to each body part and measuring a rotational motion of the body part is tracked by obtaining a rotational matrix of a sensor coordinate system fixed to each of the inertial sensors with respect to an inertial coordinate system fixed to ground, by using a signal measured by the inertial sensor attached to each body part; obtaining a rotational matrix of the sensor coordinate systems with respect to a body part coordinate system fixed to each body part, by using an obtained rotational matrix value of the sensor coordinate system; obtaining a rotational matrix of each body part coordinate system with respect to the inertial coordinate system, by using a calculated rotational matrix of the sensor coordinate systems; and calculating a joint variable with respect to each body part, by using a calculated rotational matrix of the body part coordinate system.

A wearable electronic device, a system and methods of monitoring with a wearable electronic device. The device includes a hybrid wireless communication module with wireless communication sub-modules to selectively acquire location data from both indoor and outdoor sources, as well as a wireless communication sub-module to selectively transmit an LPWAN signal to provide location information based on the acquired data. The device may also include one or more sensors to collect one or more of environmental data, activity data and physiological data. The device may transmit some or all of its acquired data to a larger system, including a cloud-based server to, in addition to providing location-based data, be used as a part of a predictive health care protocol to correlate changes in acquired data to salient indicators of the health of a wearer of the device. In one form, the predictive health care protocol uses a machine learning model.

The present disclosure provides a device for measuring jugular venous pressure of a patient. The device comprises a body defining a longitudinal enclosure and having a window along a length of the longitudinal enclosure to allow light to exit the longitudinal enclosure, and a beam generator comprising an array of light emitters. The beam generator is configured to direct light out the window to generate a beam of light along a plane perpendicular to a longitudinal direction and at an adjustable position along the longitudinal direction. The device has an adjustment mechanism for adjusting the position of the beam of light relative to the body along the longitudinal direction, and a readout indicating the position of the beam of light along the longitudinal direction.

A local coil apparatus for performing a magnetic resonance (MR) scanning on a local part of a subject is provided. The local coil apparatus may include at least one receiving system for receiving the local part. The at least one receiving system may each include an activation member, a receiving member assembly, and a driving mechanism. The receiving member assembly may include one or more receiving members. Each of the one or more receiving members may include a first coil assembly configured to receive MR signals during the MR scanning. The driving mechanism may be physically connected to the one or more receiving members. When the local part is placed on the activation member, the activation member may cause the driving mechanism to drive the receiving member assembly to change from a first configuration to a second configuration to reduce a distance between at least a portion of the first coil assembly and a portion of the local part so that the first coil assembly conforms to the local part.

The invention provides a neck-worn sensor (referred to herein as the ‘necklace’) that is a single, body-worn system that measures the following parameters from an ambulatory patient: heart rate, pulse rate, pulse oximetry, respiratory rate, temperature, thoracic fluid levels, stroke volume, cardiac output, and a parameter sensitive to blood pressure called pulse transit time. From stroke volume, a first algorithm employing a linear model can estimate the patient's pulse pressure. And from pulse pressure and pulse transit time, a second algorithm, also employing a linear algorithm, can estimate systolic blood pressure and diastolic blood pressure. Thus, the necklace can measure all five vital signs along with hemodynamic parameters. It also includes a motion-detecting accelerometer, from which it can determine motion-related parameters such as posture, degree of motion, activity level, respiratory-induced heaving of the chest, and falls.

A device (10) for assessing a patient's absolute and/or relative risk of cognitive decline and/or dementia, the device (10) comprising: a probe (12) configured to be placed adjacent to a patient's common carotid artery, internal carotid artery or external carotid artery, at least two sensors (101, 102, 104, 106, 108, 110) associated with the probe (12), the sensors being configured to measure one or more of: wave intensity of carotid pulse; wave power of carotid pulse; and pressure waveform of carotid pulse, pulse wave velocity, artery compliance, artery stiffness, artery diameter; micro-emboli count; Heart rate variability; and changes to the eye or retina.