A trauma scene monitoring system includes a medic-worn illumination device, a casualty-worn informatics system, and a remote monitoring station. The illumination device includes a frame with boom-mounted light sources positioned below the wearer's eyes near the zygomatic bones, thus orienting the light sources to project light in the direction of the wearer's view. Also included are audio/video means to capture audio/video information from a scene attended by the medic, and a telemetry unit to transmit that information to the remote monitoring station. The casualty-worn informatics system is integrated within a headband worn by a monitored individual. The informatics system includes sensors to provide the monitored individual's vital statistics and a telemetry unit to transmit data concerning the monitored individual to the remote monitoring station. At the remote monitoring station, receiving and presentation stations provide views of the data concerning the monitored individual and audio/video data from the medic-worn illumination device.

A defibrillator and method for using a defibrillator which adopts an ECG analysis algorithm that can detect a cardiac arrhythmia in the presence of noise artifact induced by cardio pulmonary resuscitation (CPR) compressions. The apparatus and method offers guidance throughout a cardiac rescue protocol involving both defibrillation shocks and CPR that improves the effectiveness of the rescue, resulting in more CPR “hands-on” time, better treatment of refibrillation, and reduced transition times between CPR and electrotherapy.

Techniques for wireless component monitoring are described herein. The techniques may include entering a low power mode to associate a radio frequency identification (RFID) component with a patient monitoring device within a first range. The techniques also include entering a high power mode wherein the patient monitoring device is to detect the RFID component within a second range of the patient monitoring device, wherein the second range is larger than the first range.

The present disclosure describes a closed-loop fluid resuscitation and/or cardiovascular drug administration system that uses continuous measurements and adaptive control architecture. The adaptive control architecture uses a function approximator to identify unknown dynamics and physiological parameters of a patient to compute appropriate infusion rates and to regulate the endpoint of resuscitation.

A cardiopulmonary resuscitation (CPR) cerebral monitoring device including a measurement probe having one or more optical emitters, and one or more optical detectors, and including an optical instrument having an optical source, and an optical detector. Also included is a controller configured to control the optical instrument to emit multi-spectral light through the one or more optical emitters to illuminate a tissue, control the optical detector to detect multi-spectral light emitted from the illuminated tissue, compare the emitted multi-spectral light to the detected multi-spectral light, compute a plurality of cerebral tissue parameters based on the comparison, determine CPR procedures based on the plurality of cerebral tissue parameters, and control a user output device to instruct a user to perform the CPR procedures, and/or control an automated CPR device to perform the CPR procedures.

A computing system (118) includes a computer readable storage medium (122) with computer executable instructions (124), including a biophysical simulator (126) and an electrocardiogram signal analyzer (128). The computing system further includes a processor (120) configured to execute the electrocardiogram signal analyzer determine myocardial infarction characteristics from an input electrocardiogram and to execute the biophysical simulator to simulate a fractional flow reserve or an instant wave-free ratio index from input cardiac image data and the determined myocardial infarction characteristics.

A process for measuring heart beats fiducial points and classifying heart beats includes sampling a raw ECG signal,—providing a first filtered signal,—providing a second filtered signal, detecting left and right limits data for the beats in said second filtered signal, and receiving the first filtered signal and receiving said left and right limits data, sampling and storing ECG curve data of beats from said first filtered signal synchronized by said left and right limits data and extracting fiducial points of said beats from said ECG curve data, said fiducial points including at least the QRS points values of the beats, and classifying each of said beats in classes based on a correlation of its ECG curve data with respect to average ECG curves data of classes of previously averaged classified beats.

Technologies and implementations for a wearable healthcare system, which may be worn by a person. The wearable healthcare systems may include one or more motion sensors. A motion analysis modules may be included in the wearable healthcare system, which may be configured to determine physical activities and intensity of the physical activities of the person.

A system for carbon dioxide (CO2) removal from a circulatory system of a patient includes a medical device providing extracorporeal lung assist (ECLA) treatment to the patient through extracorporeal removal of CO2 from the patient's blood; at least one control unit controlling the operation of the medical device so as to control a degree of CO2 removal obtained by the ECLA treatment; and a bioelectric sensor detecting a bioelectric signal indicative of the patient's efforts to breathe. The at least one control unit is configured to control the operation of the medical device based on the detected bioelectric signal.

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.