A non-invasive sensor unit, such as a glove or pad, is adapted to be placed over the chest of an injured person who may be in need of CPR and/or AED. The sensor unit includes a plurality of electrodes for detecting one or more ECG voltages of the person. A controller processes the ECG voltages and displays them on a display, thereby enabling the user to assess whether CPR and/or AED is needed. The sensor unit is adapted to continue to provide ECG data while the user is applying chest compressions to the person. The sensor unit may include accelerometers for reducing artifacts from the ECG voltages that arise from the movement of the user while applying chest compressions. The electrodes are, in some embodiments, capacitive sensors that enable ECG voltages to be detected without requiring direct contact with the skin of the person.

A newborn respiration monitoring system includes a flow sensor that measures a gas flow and a CO.sub.2 sensor that measures a CO.sub.2 within the breathing circuit for an infant. The system further includes a resuscitation module executable on a processor of a computing system to receive the flow measurement and the CO.sub.2 measurement and determine respiratory information for the infant. A digital display is communicatively connected to the computing system and displays the respiratory information.

Embodiments herein include a method for detecting a brain condition in a subject. The method can include obtaining a breath sample from the subject and contacting it with a chemical sensor element, where the chemical sensor element includes a plurality of discrete graphene varactors. The method can include sensing and storing capacitance of the discrete graphene varactors to obtain a sample data set and classifying the sample data set into one or more preestablished brain condition classifications. Other embodiments are also included herein.

This document provides methods and materials for improving the training on the use of tourniquets. For example, methods and devices for confirming the proper pressure of a tourniquet using a tourniquet training device are provided.

The technologies described herein are generally directed to facilitating operation of a health network control system. In accordance with one or more embodiments, systems described herein can include a processor, and a memory that can store executable instructions that, when executed by the processor, can facilitate performance of operations that can include facilitating receiving, from transceiver of a second device, a first signal that can describe an event related to treatment of the treatment subject. Further, the operations can include, based on an analysis of the subject information, the event information and facility information representative of a group of treatment facilities, selecting a treatment facility that can perform the treatment of the treatment subject, resulting in a selected treatment facility, and facilitating communicating via a second signal to the transceiver of the second device, selected facility information corresponding to the selected treatment facility.

A system for facilitating resuscitation includes: a first electrode assembly having a therapy side and a first motion sensor; a second electrode assembly having a therapy side and a second motion sensor; processing circuitry operatively connected to and programmed to receive and process signals from the first and second motion sensors to estimate at least one of a chest compression depth and rate during administration of chest compressions and to compare the chest compression depth or rate to a desired range; and an output device for providing instructions to a user to administer chest compressions based on the comparison of the estimated chest compression depth or rate to the desired range. One or both of the electrode assemblies may be constructed so that the conductive therapeutic portion is able to maintain substantial conformance to the anatomy of the patient when coupled thereto. For example, at least a portion of the flexible electrode pad may be able to flex from a more rigid sensor housing, or the sensor housing itself may be relatively small compared to the flexible electrode pad so as not to cause lift off of the therapeutic side from the patient.

A flow sensor system for ventilation treatment comprises a flow conduit configured to allow gas flow between a first region and a second region, the flow conduit defining a lumen for the gas flow; a flow restrictor disposed within the lumen of the flow conduit between the first region and the second region; a first absolute pressure sensor disposed adjacent to the first region of the flow conduit and configured to measure a pressure of the gas flow at the first region of the flow conduit; and a second absolute pressure sensor disposed adjacent to the second region of the flow conduit and configured to measure pressure of the gas flow at the second region of the flow conduit.

A lifesaving device and a lifesaving control method are provided. Wherein, the lifesaving device includes: at least one first detection module (200) configured for detecting human body biological characteristic information, a lifesaving device body (100) capable of being worn on a body of a user, and at least one first gasbag module (300) arranged on the lifesaving device body (100); after the first gasbag module (300) is activated, a lifesaving gasbag (1) can be popped up; the first detection module (200) is in signal connection with the first gasbag module (300) and is configured for activating the first gasbag module (300) when the biological characteristic information detected meets a first preset condition.

Electrodes for use in electroencephalographic recording, including consciousness and seizure monitoring applications, have novel features that speed, facilitate or enforce proper placement of the electrodes, including any of alignment indicators, tabs and juts, color coding, and an insulating bridge between reference and ground electrodes which ensures a safe application distance between the conductive regions of the two electrodes in the event of cardiac defibrillation. A method of using a set of at least four such electrodes is also disclosed.

The present disclosure describes systems, apparatus, and methods for collecting biometric data from a patient. In some cases, this biometric data can be collected during the course of an emergency encounter using a medical device. The medical device can also perform other functions, such as monitor patient vital signs, receive and record notes and textual information, communicate with other devices, and/or deliver a therapeutic treatment. The medical device can also be configured to record and/or maintain a patient record, and to embed the patient biometric data into the patient record for use in later confirming and/or determining an identity of the patient. Some embodiments can also collect biometric data relating to one or more caregivers of the patient, and to embed the caregiver biometric data into the patient record. This caregiver biometric data can be used to confirm and/or identify one or more caregivers in a patient record.