Methods and systems that analyze electrocardiogram (ECG) data to identify whether it would be beneficial for a caregiver to administer an electric shock to the heart in an effort to get the heart back into a normal pattern and a consistent, strong beat. By conducting a running check for conditions that are pre-validated by a comprehensive patient database to have high predictive value (e.g., with a low false-positive rate), a shockable rhythm can be identified fast (e.g., less than 6 seconds, less than 3 seconds, possibly in less than a second) and without having to analyze ECG data for longer time segments than would otherwise be required using conventional methods.

A medical device for providing therapy to a patient comprises at least one processor configured to receive a first patient biometric signature from at least one first sensor interface. The at least one processor is further configured to record the first patient biometric signature in a patient encounter record in at least one memory. The at least one processor is further configured to receive patient information from an external source, the patient information comprising a second patient biometric signature. The at least one processor is further configured to make a determination that the second patient biometric signature corresponds to the first patient biometric signature. The at least one processor is further configured to, in response to making the determination, merge the patient information and the patient encounter record into a merged record for a patient encounter.

A method for computing fractional flow reserve (FFR), including receiving geometrical parameters of a blood vessel segment including a proximal end and a distal end, the geometrical parameters including a first geometrical parameter, a second geometrical parameter and a third geometrical parameter; and with the proximal end as a reference point, deriving a reference lumen diameter function and a geometrical parameter difference function based on the geometrical parameters and the distance from the position along the segment of blood vessel to the reference point. Derivatives of the geometrical parameter difference function are calculated in multiple scales. FFR is computed as a ratio of a second blood flow pressure at the first location of the blood vessel to a first blood flow pressure at the proximal end of the segment based on the multiple scales of derivative difference functions and the maximum mean blood flow velocity.

A defibrillator (AED) using an ECG analysis model or algorithm which can function in two different modes. The ECG analysis model is particularly suited for analysis during periods of CPR. Both modes of operation reach a shock decision in essentially the same way, where one or more ECG data segments indicate a shockable cardiac condition. In one mode of operation, the shock decision is irreversible once made. In another mode of operation, the shock decision is reversible if one or more subsequent ECG data segments indicate a no-shock decision. Improved specificity of the model is obtained without undue degradation of sensitivity to shockable ECG.

Systems, devices, and methods for monitoring and treating a patient on route to a medical facility are disclosed. The system comprises a critical care unit; at least one patient monitoring device coupled to the critical care unit, wherein the critical care unit obtains physiological data about the patient from each patient monitoring device; at least one patient treatment device coupled to the critical care unit, wherein the critical care unit provides treatment instructions to each patient treatment device; a two way communications device coupled to the critical care unit; and a remote communications terminal in communication with the two way communications device. The critical care unit preferably sends the physiological data to the remote communications terminal and receives the treatment instructions from the remote communications terminal via the two way communications device.

There are provided systems and methods for performing mean arterial pressure (MAP) derived prediction of future hypotension. Such a system includes a hardware unit including a hardware processor and a system memory, a hypotension prediction software code stored in the system memory, and a sensory alarm. The hardware processor is configured to execute the hypotension prediction software code to receive MAP data of the living subject, and to transform the MAP data to one or more parameters predictive of a future hypotension event of the living subject. The hardware processor is further configured to execute the hypotension prediction software code to determine a risk score of the living subject corresponding to the probability of the future hypotension event based on at least some of the one or more parameters, and to invoke the sensory alarm if the risk score of the living subject satisfies a predetermined risk criteria.

Medical diagnostic devices and related methods of use are described in which one or multiple coils in a sensor, each coil connected with an RLC circuit and frequency counter, are held against a patient's head at predetermined cranial locations. Frequencies of the RLC circuit are measured and compared against those taken from known, control heads, to determine whether there is a medical problem and what type of problem. In some instances, too high of frequencies can reveal pooled blood in the head, a sign of hemorrhagic stroke, while too low of frequencies imply lack of blood supply, a sign of ischemic stroke. A head-mountable frame can assist a first responder in securing and guiding the coils and, along with fiducials, allow for automatic comparison of frequencies with the correct control data.

A system for assisting a user in providing chest compressions to a patient includes: a first motion sensor configured for measuring motion of a first region of a thorax of the patient; and a first housing physically coupled with the first motion sensor. The first housing includes: a first frame for holding the first motion sensor in place, and a textured padding for receiving at least a portion of at least one hand of the user during chest compressions. The textured padding covers the first frame and the first motion sensor. The textured padding comprises an exterior having a plurality of raised surface features. The system also includes: a second motion sensor configured for measuring motion of a second region of the thorax of the patient; and a second housing physically coupled with the second motion sensor and having a second frame for holding the first motion sensor in place.

A system for providing a visual summary of a condition of a patient when traumatic brain injury (TBI) is suspected or diagnosed includes at least one patient condition sensor configured to sense data representative of a patient condition parameter of interest for a TBI patient; at least one airflow sensor configured to sense data representative of ventilations provided to the patient; at least one visual display for providing the visual summary to a user; and at least one controller. The at least one controller is configured to cause the visual display to provide the visual summary. The visual summary can include at least one visual representation of at least one patient condition parameter for each time interval of a plurality of time intervals, at least one visual representation of ventilation information, and a visual indication of when at least one patient condition parameter is outside of a target range.

A medical device including a probe configured to be orally inserted into a lumen extending into the thorax of the subject, a plurality of electrodes, and a control circuit. The probe includes a first electrode. The plurality of electrodes includes at least one second electrode and at least one third electrode configured to be disposed externally on the thorax of the subject on a first side of a sternum of the subject and a second side of the sternum of the subject, respectively, the second side opposite the first side. The control circuit is electrically coupled to the first electrode and the at least one second and third electrodes and configured to measure an impedance between the first electrode and each of the at least one second and third electrodes and determine a ratio of arterial blood volume relative to venous blood volume based upon the measured impedance.