A heart monitoring system for a person includes one or more wireless nodes; and wearable appliance in communication with the one or more wireless nodes, the appliance monitoring vital signs.

The present invention relates to devices, systems, and methods for controlling the concentration of potassium in dialysate in a closed loop potassium control system. The devices, systems, and methods can be compatible with any dialysis system including sorbent-based dialysis systems, single pass dialysis systems, or other multi-pass dialysis systems. The systems can use closed loop potassium control over potassium concentration in the dialysate to reduce the probability of patient arrhythmias. The potassium concentration can be controlled and personalized to a patient using certain predetermined patient parameters. Related systems, algorithms, and control systems are contemplated for optimizing the potassium concentration in the dialysate.

An object information acquiring apparatus is used which has an irradiating unit irradiating an object with light with a first wavelength at a first irradiation frequency, an element receiving an acoustic wave generated by the object irradiated with the light to output an electric signal, a processing unit acquiring characteristic information on the object using the electric signal, a scanning unit changing position of the irradiating unit relative to the object, and a controlling unit controlling movement of the scanning unit. The controlling unit controls the scanning unit such that an amount of light to which an identical area of the object is exposed is larger than a smallest value of a maximum permissible exposure at the first irradiation frequency.

A communicative water bottle includes communication logic and wireless transmission logic technology electronically connected with a variety of sensors either on the water bottle or located remote from the water bottle. The sensors on the bottle create digital data associated with amount of fluid in the bottle and change thereof. The sensors remote from the bottle, which can be on an activity tracker, create digital data associated with an activity being performed by a user, such as running, or the absence of activity, such as remaining sedentary. A display on the bottle can indicate to the user the amount of fluid consumed or a reminder that fluid should be consumed. The fluid consumption data syncs with other remote devices such as mobile applications executable on smartphones.

The present invention relates to a method and to an apparatus for predicting one or more parameters characteristic for the outcome of a blood treatment, wherein the blood treatment is a treatment in which the blood of the patient has fluid removed via at least one membrane, wherein the parameters are the allowed drinking volume, the hyperhydration or hypohydration of the patient, the clearance of large molecules and/or the allowed salt intake, wherein the prediction of the allowed drinking volume and the prediction of the hyperhydration or hypohydration are carried out on the basis of the planned weight loss due to ultrafiltration, of the drinking quantity during the treatment, of the rinseback volume and of residual diuresis data, and/or wherein the prediction of the clearance of large molecules is carried out on the basis of the urea clearance, and/or wherein the prediction of the allowed salt intake takes place based on the sodium ion quantity removed by ultrafiltration and by diffusion from the blood.

An apparatus for detecting conductance parameter of high protein body fluid sample is provided. The apparatus includes at least one liquid collection element, and at least two electrodes horizontally aligned in the liquid collection element. Also provided are methods for detecting dehydration in a subject, comprising the steps of measuring the conductance parameter of the saliva of the subject.

A device (100) for measuring the amount of water in a subject's body includes a main body part (110) formed in a linear shape and an insertion part (120) extending in a curved shape from one end of the main body part (100). The insertion part (120) includes a tip side insertion part (120-2) having a tip surface (122) to which a sensor unit (121) is fixed and a base end side insertion part (120-1), wherein the sensor unit (121) is brought into contact with a body surface of a subject through a slide mechanism. A protective member (651) liquid-tightly covers the slide mechanism between the tip side insertion part (120-2) and a base end side insertion part (120-1). The protective member (651) smoothly connects the outer peripheral surface of the tip side insertion part (120-2) and the outer peripheral surface of the base end side insertion part (120-1).

A system, method and device are described for biometric analysis using a wearable device. The device can be removeably securable to a user's skin surface and can include a plurality of electrodes positioned to acquire electrical signals from the skin surface. The device can also include an electromyography acquisition module and skin impedance acquisition module. A processing unit can use the electrodes to capture a plurality of electrical signals including at least one electromyography signal. The processing unit can generate calibration data based on a subset of the captured electrical signals and process the electromyography signals using the calibration data to determine a biometric for the user.

An athletic wear includes at least one of an athlete garment, a helmet, a glove, a wristband, a headband, a mouth guard, and a pad. A plurality of sensors and at least one camera are integrated into the at least one of the athlete garment, the helmet, the glove, the wristband, the headband, the mouth guard, and the pad. A processor is in signal communication with the plurality of sensors and the at least one camera for receiving, analyzing, and transmitting data signals obtained by the plurality of sensors and the at least one camera. The plurality of sensors are configured to obtain a wearer's physiological data, position data and movement data.

Novel tools and techniques are provided for assessing, predicting and/or estimating a probability that a patient is bleeding, in some cases, noninvasively. In various embodiments, tools and techniques are provided for implementing rapid detection of bleeding of the patient or implementing assessment, prediction, or estimation of a probability of bleeding of the patient following injury, in some instances, in real-time before, during, and after fluid resuscitation. According to some embodiments, one or more sensors might monitor physiological data of the patient before, during, and after resuscitation following injury. A computer system might receive and analyze the physiological data, and might estimate a probability that the patient is bleeding, based at least in part on the analyzed physiological data. An indication of at least one of an assessment, prediction, or estimate of a probability that the patient is bleeding may then be displayed on a display device.