An external defibrillator system is provided. The system includes: a graphical display; one or more sensors for obtaining data regarding chest compressions performed on a patient; and a controller configured to display on the graphical display numeric values for depth and/or rate of the chest compressions based upon the data from the one or more sensors. A method for using an external defibrillator including the steps of: obtaining data regarding chest compressions perforated on a patient; and displaying on a graphical display screen of the defibrillator numeric values for depth and/or rate of the chest compressions based upon the data is also provided.

An external defibrillator system is configured with at least two different algorithms for determining the duration of a shock administered to a patient being treated and selects the algorithm based on one or more patient parameters such as, for example, the patient's TTI. The patient's TTI can be measured prior to or while the shock is being administered to the patient. The shock can be, for example, a multiphasic defibrillation or a multiphasic cardioversion shock. The charge voltage of the system's energy storage device can additionally be varied depending on the one or more patient parameters. For example, the system may charge the energy storage device so that the charge voltage is higher or lower than a nominal charge voltage responsive to the patient's TTI is higher or lower compared to an average TTI, respectively.

In some examples, a system can be used for delivering cardiac resynchronization therapy (CRT). The system may include a pacing device configured to be implanted within a patient. The pacing device can include a plurality of electrodes, signal generation circuitry configured to deliver ventricular pacing via the plurality of electrodes, and a sensor configured to produce a signal that indicates mechanical activity of the heart. Processing circuitry can be configured to identify one or more features of a cardiac contraction within the signal, and determine whether the contraction was a fusion beat based on the one or more features.

A device for supporting determination of return of spontaneous circulation, ROSC, during an associated cardiopulmonary resuscitation, CPR, procedure which is being performed on an associated patient. A sensor is used to sense a physiological signal of the patient. Frequency analysis of the signal is carried out to extract dominant fundamental frequency components in the signal. From this analysis it is possible to determine that there has been a potential ROSC.

A modular medical system employing a bedside patient monitor (20), a portable patient monitor (40), a monitor docking station (50), a therapy applicator (30) and a therapy docking station (60). In operation, the portable patient monitor (40) is docked to the bedside patient via the monitor docking station (50) whereby the bedside patient monitor (20) and the portable patient monitor (40) measure patient parameters (e.g., ECG, Sp O2, pulse rate, NIBP, Et CO2, etc.) upon the portable patient monitor (40) being coupled to a patient. Alternatively, the portable patient monitor (40) is docked to the therapy applicator (30) via the therapy docking station (60) whereby the therapy applicator (30) conditionally delivers the electrical therapy (e.g., defibrillation shock, synchronized conversion, transcutaneous pacing, etc.) to the patient upon the portable patient monitor (40) being coupled to the patient.

Systems and methods related to the field of cardiac resuscitation, and in particular to devices for assisting rescuers in performing cardio-pulmonary resuscitation (CPR).

A novel optogenetic system, including constructs and methods, is provided based on the interaction of Rhodopseudomonas palustris BphP1 and Rhodopseudomonas palustris PpsR2 or a non-dimerizing variant thereof.

Devices and methods for CPR chest compression with active decompression.

An ambulatory medical device that can communicate with a vehicle is described. An example of the ambulatory medical device includes one or more sensing electrodes configured to sense cardiopulmonary signals of a patient, a network interface, and one or more processors configured to receive signals from one or more vehicle occupancy sensors, detect usage of the ambulatory medical device in a vehicle based on the received signals from the one or more vehicle occupancy sensors, detect at least one of a medical event and a medical premonitory event of the patient based on the sensed cardiopulmonary signals, and provide driving control information to the vehicle, via the network interface, based at least in part on the detected usage of the ambulatory medical device in the vehicle and the detected medical event or medical premonitory event of the patient.

A method for determining quality of a communications link between an external instrument (EI) and an implantable medical device (IMD) is provided. The method includes receiving, with a receiver of an EI, data packets sent at intervals from an IMD and determining, with a processor of the EI, an expected time interval between a first data packet and a second data packet. The processor of the EI determines a difference between the expected time interval between the first data packet and the second data packet and an actual time interval between the first data packet and the second data packet. The processor of the EI also provides a time variant communication quality indicator based on the difference between the expected time interval between the first data packet and the second data packet and the actual time interval between the first data packet and the second data packet.