An electrode sensor kit for establishing electrical contact with skin comprises at least one contact element and a preparation comprising a mixture of water and at least one lipid for enhancing electrical contact properties between said contact element and the skin, wherein said mixture forms an emulsion, in particular a water-in-oil or an oil-in-water emulsion, having a conductivity of less than 3 mS/cm. An electrode assembly for electrical impedance tomography which comprises said kit is characterized in that (a) said at least one contact element forms an electrode or sensor plate, and (b) said at least one contact element comprises a layer of said preparation.

In electrocardiography (ECG) system, a patient cable connecting one or more electrodes to a processing device for processing ECG signals may include one or more electrode connectors mechanically keyed to respective electrodes and/or a device connector mechanically and/or electronically keyed to a cable connector of the processing device. In some embodiments, keying between the cable and electrode is achieved, for example, with an electrode including a hollow-post portion that defines a bore in conjunction with a post protruding from an arm of the electrode connector that is sized to fit within the bore.

An ECG monitoring system includes two or more active electrodes, each active electrode having an electrode pad fixable to a patient to sense physiological potentials from the patient, a common connection port, and a wireless transmitter. The system further includes a common connector electrically connected to the common connector port of each of the two or more active electrodes to provide a comparator signal to each of the active electrodes. Each of the active electrodes compares the physiological potentials sensed at the electrode pad against the comparator signal to generate a cardiac signal, and then wirelessly transmits the cardiac signal with the wireless transmitter.

An adjustable ECG sensor is attachable to a patient to sense cardiac signals and includes an adjustable leadwire having a flexible substrate, a conductor extending along the flexible substrate, and a connector end connectable to a receiver associated with an ECG monitor. The adjustable ECG sensor further includes an electrode having an electrode pad, a clip connected to the electrode pad and attachable to any one of multiple locations on the adjustable leadwire, and a pin that punctures the flexible substrate and electrically connects to the conductor of the adjustable leadwire. The adjustable ECG sensor is fitted to the patient by attaching the clip of the electrode to one of the multiple locations on the adjustable leadwire.

Aspects of the disclosure can provide a method and device for detecting EEG signals of a first person in proximity to the device. The device can include a non-contact EEG directional circuit having non-contact sensors, the non-contact EEG directional circuit being configured to detect the EEG signals produced by a brain of the first person without making contact with the first person. The device can further include a processor coupled to the non-contact EEG directional circuit that is configured to analyze the EEG signals to detect patterns in the EEG signals that correspond to a state of the first person in proximity to the non-contacting sensor and feedback device that is configured to provide a second person with an indication of the state of the first person in proximity to the non-contacting sensor. Additionally, the device can include a contact EEG circuit having sensors that are in contact with the second person and that is configured to detect second EEG signals produced by a brain of the second person, wherein the processor is coupled to the contact EEG circuit and is configured to analyze the second EEG signals to detect patterns in the second EEG signals that correspond to a state of second the person.

A wearable cardioverter defibrillator (WCD) (10) and method (60) comprise a set of electrodes (12) for placement on a subject (14), a mechanism for electrically engaging (16) the set of electrodes to the subject's skin, and at least one non-invasive physiologic sensor (18, 20) configured for placement on the subject. A controller (24) monitors an output of the non-invasive physiologic sensor (18, 20) for detecting a change in a health parameter of the subject being indicative of one or more of a change in subject condition that may be a precursor to potential cardiac arrhythmia or a simultaneously occurring cardiac arrhythmia. Responsive to detecting the change, the controller (24) activates an alarm (26) for requesting a response from the subject (14) within a predetermined time. Responsive to receiving the subject's response within the predetermined time, the controller (24) inhibits the mechanism (16) from electrically engaging the set of electrodes (12) to the subject's skin. Responsive to not receiving the subject's response, the controller (24) initiates the mechanism (16) for electrically engaging the set of electrodes (12) to the subject's skin.

Disclosed herein are devices, methods and systems for monitoring and detection of adverse events in a subject. In an embodiment, an insulin delivery device includes an insulin injection device in communication with a controller for controlling the insulin injection device. The controller is configured to receive a heart signal from one or more heart sensors, and a blood glucose signal from one or more blood glucose sensors. The controller is further configured to analyze changes in the heart rhythm of the subject based on the heart signal and determine, based on the changes in the heart rhythm and the blood glucose signal, whether the subject is and/or will be experiencing an adverse event. Upon determination that the subject is or will be experiencing an adverse event, the controller determines one or more parameters of delivery of insulin to be delivered to the subject. Finally, the controller is configured to control the injection device to deliver insulin to the subject in accordance with the determined one or more parameters of delivery.

provided is an automotive key device connected, in the form of a holder, to a mechanism of opening or shutting an automotive door or merged with the mechanism of opening or shutting the automotive door. The automotive key device includes an electrocardiogram (ECG) sensor having a first body signal electrode and a second body signal electrode and a contact terminal electrically connected to the ECG sensor. The contact terminal is configured to serve as a passage for electrical connection with devices within a vehicle. A steering wheel docking station and a system configured to include the steering wheel docking station and the automotive key device are also provided.

A patient monitoring device includes reusable and disposable portions. The disposable portion includes two or more electrodes for coupling to the skin of the patient, a battery, and a first set of electrical contacts. The reusable portion includes a processor, memory, a second set of electrical contacts, and sensing circuitry coupled to the at least two electrodes, wherein the reusable portion is mechanically coupleable to the disposable portion and wherein the reusable portion is electrically coupleable to the disposable portion through the first and second electrical contacts. The sensing circuitry and the processor are powered from the battery through the coupled first and second electrical contacts, and wherein when the reusable portion and the disposable portion are mechanically uncoupled after having been mechanically coupled, the disposable portion is rendered unusable by the process of mechanically uncoupling the reusable portion and the disposable portion.

A wearable sensing band is presented that generally provides a non-intrusive way to measure a person's cardiovascular vital signs including pulse transit time and pulse wave velocity. The band includes a strap with one or more primary electrocardiography (ECG) electrodes which are in contact with a first portion of the user's body, one or more secondary ECG electrodes, and one or more pulse pressure wave arrival (PPWA) sensors. The primary and secondary ECG electrodes detect an ECG signal whenever the secondary ECG electrodes make electrical contact with the second portion of the user's body, and the PPWA sensors sense an arrival of a pulse pressure wave to the first portion of the user's body from the user's heart. The ECG signal and PPWA sensor(s) readings are used to compute at least one of a pulse transit time (PTT) or a pulse wave velocity (PWV) of the user.