This document describes automated abdominojugular reflux (AJR) testing. To automate AJR tests, a pressure cuff wrapped around a person's abdomen applies pressure while video of their neck is captured. By way of example, a medical professional wraps a pressure cuff around the person's abdomen and records video of the person's neck using a smartphone, which communicates with the pressure cuff to synchronize the application of pressure with video capture. The video is processed to detect and track the response of jugular venous pulse (JVP), which is compared to AJR test thresholds to determine test results. While determining JVP, and thereby results of AJR tests, from reconstructed videos may not result in data that is as accurate as invasive intra-heart tests, it requires little if any risk to patients and is easy for medical professionals to perform. Further, these techniques enable AJR tests to be performed automatically and without relying on estimates made by skilled medical professionals.

Systems, methods, and interfaces are described herein for noninvasively determining an optimal coronary sinus branch to cannulate for a medical electrical lead. One exemplary method involves applying an electrode apparatus having a plurality of electrodes to a torso of a patient. One of a right ventricular (RV) lead is introduced to a right ventricle or a right atrial (RA) lead is introduced to a right atrium. Noninvasively ultrasonic energy is introduced to a target tissue selected from a set of target tissues. In response to delivering ultrasonic energy to the cardiac tissue, a processing unit receives a torso-surface potential signal from each of a plurality of electrodes distributed on a torso of a patient for the target tissue. Signals are sensed from one of the RA lead and the RV lead in response to delivering ultrasonic energy. For at least a subset of the plurality of electrodes, calculating, with the processing unit, a torso-surface activation time based on the signal sensed from the electrode. Determining whether the tissue site or the another tissue site provides optimal cardiac resynchronization.

Modular, miniaturized cardiovascular sensors, systems, methods, and wearable devices for the non-obtrusive evaluation, monitoring, and high-fidelity mapping of cardiac mechanical and electromechanical forces and central arterial blood pressure are presented herein. The sensor manufacturing process is also presented. Using accelerometers, the sensors register body-surface (preferably torso-surface) movements and vibrations generated by cardiac forces. The sensors may contain single-use or reusable components, which may be exchanged to fit different body sizes, shapes, and anatomical locations; they may be incorporated into clothing, bands, straps, and other wearable arrangements. The invention presents a practical, noninvasive solution for electromechanical mapping of the heart, which is useful for a wide range of healthcare applications, including the remote monitoring of heart failure status and the guidance of cardiac resynchronization therapy. Exercise and cardiovascular fitness tracking applications are also presented.

A first collection of biometric data of a user on a mattress of the bed system is sensed via a sensor of the bed system. The user is instructed to perform an exercise activity. The user is instructed to return to and lay on the mattress after performing the exercise activity. A second collection of biometric data of the user on the mattress of the bed system is sensed via the sensor of the bed system again after the user has performed the exercise activity. A stress test output is generated based on the sensed first biometric data and the sensed second biometric data. The stress test output is displayed to the user.

A modulated physiological sensor is a noninvasive device responsive to a physiological reaction of a living being to an internal or external perturbation that propagates to a skin surface area. The modulated physiological sensor has a detector configured to generate a signal responsive to the physiological reaction. A modulator varies the coupling of the detector to the skin so as to at least intermittently maximize the detector signal. A monitor controls the modulator and receives an effectively amplified detector signal, which is processed to calculate a physiological parameter indicative of the physiological reaction.

Methods and apparatuses are provided for measuring a biometric signal by an electronic device. An object having an animation effect for inhalation and exhalation is displayed. The animation effect includes the object being expanded to guide the inhalation of a user and the object being contracted to guide exhalation of the user. A sensor unit obtains at least one biometric signal related to a heart rate of the user while the object is displayed. A motion of the electronic device is detected having a strength that is greater than or equal to a threshold strength. Based on the motion ceasing before exceeding a predetermined time, display of the object and obtaining of the at least one biometric signal is continued. Based on the motion lasting longer than or equal to the predetermined time, the obtaining of the at least one biometric signal and the displaying of the object is terminated.

A brain activity estimation device includes a facial skin temperature acquisition element and a brain activity estimation element. The acquisition element detects a skin temperature of at least part of a human face, and acquires facial skin temperature data including detected temperature data and location data of a detection region in a time series manner. The estimation element estimates human brain activity based on the facial skin temperature data acquired. The estimation element decomposes the facial skin temperature data into a plurality of components, extracts a component as a determination component, and determines whether the determination component is related to the human brain activity based on a presence or absence of a temperature change in a prescribed region of the human face.

The invention relates to registering changes in vascular tone during and after a functional load, and processing data using spectral analysis methods within the frequency ranges of endothelial (0.0095-0.02 Hz), neurogenic (0.02-0.05 Hz), and myogenic (0.05-0.14 Hz) regulation mechanisms. Furthermore, the temperature of an area of a patient's skin is continuously registered. During the first 1-2 minutes, the temperature of the examined skin surface is increased to 38-42° C., and the heating power is fixed. Temperature fluctuations are registered over the course of 10 minutes The heater is shut-off. Over the course of 10 minutes following the shut-off and a decrease in temperature to 30-32° C., temperature fluctuations continue to be registered, and the obtained values are compared, with coefficients being calculated for the relative change in the amplitudes of the temperature fluctuations, which are then used for determining the existence of a disorder in a vascular tone regulation mechanism.

A measurement device and method for measuring psychology stress index and blood pressure is disclosed. When the measurement device is in the psychology stress measurement mode and a pressurizing motor unit is pressurizing an airbag unit with a variable speed, the micro-processor unit may control the pressurizing motor unit to stop pressurizing the airbag unit after the pressure signal is determined as a pulse signal, and the micro-processor unit may measure the pulse signal to determine the psychology stress index. The psychology stress index is a ratio of SDNN and RMSSD according to interval data of the pulse signal within a period of time.

A monitoring apparatus includes a wearable electronic device having an audio port and a headset having at least one earbud, at least one physiological and/or environmental sensor, and circuitry that processes signals produced by the at least one physiological and/or environmental sensor and transmits the processed signals to the electronic device via the audio port. The headset may include a microphone in audio communication with the electronic device via the audio port, and the circuitry modulates audio signals produced by the microphone and signals produced by the at least one physiological and/or environmental sensor for transmission to the electronic device via the audio port. The circuitry may power the at least one physiological and/or environmental sensor via power supplied by the electronic device through the audio port and may include a processor that coordinates collection, modulation, and/or transmission of signals produced by the at least one physiological and/or environmental sensor.