Abstract: An apparatus for assisting a rescuer in performing chest compressions during CPR on a victim, the apparatus comprising a pad or other structure configured to be applied to the chest near or at the location at which the rescuer applies force to produce the chest compressions, at least one sensor connected to the pad, the sensor being configured to sense movement of the chest or force applied to the chest, processing circuitry for processing the output of the sensor to determine whether the rescuer is substantially releasing the chest following chest compressions, and at least one prompting element connected to the processing circuitry for providing the rescuer with information as to whether the chest is being substantially released following chest compressions.

Abstract: Systems and methods for applying enhanced guided active compression decompression cardiopulmonary resuscitation are provided. Exemplary systems include a load cell, a handle, an adhesive pad. The handle and the adhesive pad are configured for magnetic coupling.

Abstract: A system comprising: a wrist-worn device configured to be worn on the wrist of a rescuer performing cardiopulmonary resuscitation (CPR), the wrist-worn device including: one or more sensors coupled with the wrist-worn device, the one or more sensors being configured to sense one or more parameters indicative of a fatigue level of the rescuer; and a sensor interface configured to provide the sensed parameters to one or more external computing devices via an interface; and a wearable computing device configured to be worn by a rescuer, the wearable computing device including: a device interface for receiving information related to CPR; and a display for displaying an indication of the received information.

Abstract: This document describes an automated external defibrillator comprising a control configured to switch between a pediatric operating mode and an adult operating mode, wherein each operating mode comprises a mode-specific energy configuration and a mode-specific user configuration; an indicator configured to provide an indication of the operating mode in use during a resuscitation process; one or more processors configured to switch to the mode-specific energy configuration and the mode-specific user configuration upon a change of operating mode between the pediatric operating mode and the adult operating mode such that the automated external defibrillator delivers a defibrillating shock to a patient based on the mode-specific energy configuration; and an interface of the automated external defibrillator provides resuscitation instructions to a user based on the mode-specific user configuration.

Abstract: An external wearable defibrillator for monitoring a patient for cardiac-related events is provided. The defibrillator includes ECG sensors configured to be disposed about a torso of the patient, therapy electrodes, and at least one motion sensor. The ECG sensors, therapy electrodes, and at least one motion sensor are configured to be worn continuously for an extended period of time. The defibrillator includes a wearable medical device controller including at least one processor configured to receive ECG data, receive motion data, identify at least one of ventricular tachycardia or ventricular fibrillation, initiate a treatment protocol including a defibrillation shock, and, using at least one of the ECG data or the motion data, identify a predetermined pattern for syncope. The predetermined pattern includes bradycardia. The at least one processor is further configured to record the predetermined pattern in a memory and perform an intervening action to address the predetermined pattern.

Abstract: A system for managing responders acquiring medical equipment and responding to an emergency medical event includes mobile devices associated with responders; a computer aided dispatch (CAD), and an equipment/responder management system communicatively coupled to the mobile devices and CAD and configured to receive an event location from the CAD, retrieve medical equipment locations from a database, receive responder locations from the mobile devices, send the event and equipment locations to a first mobile device, generate an activity log for the event including first responder status information based on the responder location, the event and medical equipment locations, send the activity log to the first mobile device, send the event location and the medical equipment locations to a second mobile device, update the activity log with second responder status information based on the responder, event and medical equipment locations, and send the activity log to the mobile devices.

Abstract: A medical device management system comprising a defibrillating apparatus, which comprises a plurality of electrodes configured to monitor ECG signals and deliver a defibrillation shock. The system including a communication unit configured to establish a secured wireless network, automatically generate a first text message upon receipt of a signal indicative of deployment of the defibrillating apparatus, associate the first text message with a unit identifier, automatically send the first text message, automatically generate a second text message comprising defibrillation shock status upon delivery of the defibrillation shock, associate the second text message with the unit identifier, automatically send the second text message; and a handheld device associated with a caregiver and configured to receive the first and second text messages and associate the first and second text messages with the specific defibrillating apparatus based on the unit identifier specific to the defibrillating apparatus.

Abstract: An example of a system for providing emergency care to a patient includes an automated chest compression device configured to engage the patient at the patient's sternum to provide multiple chest compression cycles to the patient's sternum, an automated mechanical ventilation device to induce negative pressure ventilation, and a controller operably coupled to the automated chest compression device and the automated mechanical ventilation device and including one or more processors configured to control the automated chest compression device to cyclically perform chest compressions, and control the automated mechanical ventilation device to cyclically induce the negative pressure ventilation out-of-phase with the chest compressions such that the automated mechanical ventilation device cyclically induces the negative pressure ventilation prior to each compression of the patient's sternum.

Abstract: Methods and devices are described, such as for chest compression depth measurement for CPR performed on infants and for allowing active decompression of a patient's chest during a release phase of a chest compression cycle. An anterior segment of a resilient wrap-around structure may be positioned on the patient's sternum, including a first motion sensor. A posterior segment of the resilient wrap-around structure may be positioned on the patient's back, including a second motion sensor. Chest compressions may be provided such that the first motion sensor moves in fixed relation with the patient's sternum and the second sensor moves in fixed relation with the patient's back. Active decompression may be allowed for, including the resilient wrap-around structure exerting an expansive force on the patient's chest wall during a release phase of a chest compression cycle and hastening expansion of the patient's chest during the release phase.

Abstract: A wearable monitoring and therapeutic device includes at least two sensing electrodes. Each sensing electrode includes a metallic surface integrated in a garment. The device includes at least two therapy electrodes. Each of the at least two therapy electrodes includes a receptacle, and each receptacle includes at least one dose of conductive fluid. The device includes the garment. The garment includes a fabric that is stretchable and that is breathable and/or moisture wicking, and conductive wiring configured to at least partially electrically connect that at least two sensing electrodes to at least one defibrillator component. The device includes the at least one defibrillator component. The at least two therapy electrodes are configured to provide an electric shock to the subject. Prior to the application of the electric shock, each receptacle is configured to release the conductive fluid from the receptacle.

Abstract: Medical techniques include systems and methods for administering a positive pressure ventilation, a positive end expiratory pressure, and a vacuum to a person. Approaches also include treating a person with an intrathoracic pressure regulator so as to modulate or upregulate the autonomic system of the person, and treating a person with a combination of an intrathoracic pressure regulation treatment and an intra-aortic balloon pump treatment.

Abstract: An example of a system for post-case analysis of cardiopulmonary resuscitation (CPR) performance trends includes a ventilation metrics device with sensors configured to generate signals indicative of ventilation treatment data during a medical treatment of a patient, and a patient monitor/defibrillator configured to receive the signals, calculate the ventilation treatment data based on the received signals, and transmit the ventilation treatment data, and a remote computing device configured to communicatively couple with the treatment monitoring system and with an output display device, the computing device including at least one memory and at least one processor communicatively coupled to the memory, the at least one processor configured to receive treatment data from the treatment monitoring system, the treatment data including the ventilation treatment data, and provide case review information at a case review dashboard at the output device, the case review information including time trend plots of the ve

Abstract: Ambulatory medical devices may occasionally improperly administer a therapeutic stimulation pulse to a patient upon an incorrect detection of arrhythmia in the patient. To address these improperly administered therapeutic stimulation pulses, an ambulatory medical device includes processes and systems for verifying an initial declaration of an arrhythmia. The ambulatory medical device described include at least one first sensing electrode and at least one second sensing electrode distinct from the at least one first sensing electrode. First electrocardiogram (ECG) signals detected by the first sensing electrode are analyzed to provide an initial declaration of the arrhythmia condition of the patient. As a treatment protocol is being initiated in response to the analysis of the first ECG signals, second ECG signals detected by the second sensing electrode are analyzed to verify the initial declaration of the arrhythmia.

Abstract: A medical tool kit is provided for packaging, storing, and transporting medical instruments and tools of various types. The medical tool kit is capable of providing continuing sterilization to the medical instruments and tools kept inside the medical tool kit after the tool case is opened during its normal use in a medical procedure. The medical tool kit is further capable of emitting a GPS tracking signal to identify the location of an opened medical tool kit during an emergency as well as creating hands free communication between the user of the medical tool kit and local emergency institutions.

Abstract: A remote alarm for use with a wearable medical device. The remote alarm is configured to receive alarms, voice messages and prompts issued by the wearable medical device and to repeat those alarms, voice messages and prompts in a manner that can more easily be perceived by a patient wearing the wearable medical device or a bystander. The remote alarm can be configured to receive a communication from the wearable medical device, and in response, to identify one or more messages to be provided to the patient or a bystander. The messages may be provided audibly, visually, tactilely or combinations thereof. The remote alarm may further be configured to take certain actions depending upon the content of the communication, such as sending a telephone message to alert emergency personnel to the identity, location and medical condition of the patient, or sending an email.

Abstract: A computer-implemented method for managing medical equipment includes presenting, at a display of a mobile computing device associated with an inspector, an inspection user interface configured to capture one or more user inputs from the inspector, receiving inspection account information via the one or more user inputs, receiving a location of the mobile computing device, providing, at the inspection user interface, identification information for transported medical equipment that is associated with the inspection account information, receiving status information for the transported medical equipment via the one or more user inputs, receiving, at a remote medical equipment database, location information for the transported medical equipment, and updating a maintenance report for the transported medical equipment by storing an inspection information entry in the maintenance report.

Abstract: A system for providing cardiopulmonary resuscitation (CPR) feedback configurable at a point of use is described that includes one or more sensors configured to generate a signal corresponding to motion of the chest during an administration of chest compressions and a defibrillator configured to couple to the one or more sensors, the defibrillator including an input device configured to accept user input indicative of a compression depth goal, one or more processors and a memory, the one or more processors configured to determine chest compression feedback that varies based on the user input and is based at least in part on the motion of the chest during the administration of chest compressions, and a display configured to display the chest compression feedback.

Abstract: A wearable arrhythmia monitoring and treatment device for improving confidence in determined arrhythmias prior to treatment includes a plurality of sensing electrodes, one or more therapy electrodes, and an electrode signal acquisition circuit having a plurality of inputs. The electrode signal acquisition circuit is configured to sense a respective signal provided by each of a plurality of different pairings of the plurality of sensing electrodes. The wearable arrhythmia monitoring and treatment device includes a monitoring and detection circuit including at least one processor configured to analyze the respective signals provided by each of the plurality of different pairings of the plurality of sensing electrodes, change a confidence level in a determined arrhythmia condition based on the respective signals provided by the plurality of different pairings of the plurality of sensing electrodes, and initiate a therapy to the patient via the one or more therapy electrodes based on the confidence level.

Abstract: A system for managing an individualized cardiac rehabilitation plan is provided. The system includes an externally worn device and a server. The server includes a processor configured to receive input regarding the rehabilitation plan; generate one or more plans specifying an individualized set of rehabilitative exercise sessions for a patient, receive electrocardiogram (ECG) and non-ECG physiological information acquired from the patient compare the ECG and/or non-ECG physiological information to predetermined criteria and dynamically adjust the cardiac rehabilitation plan based on the comparison to create an adjusted cardiac rehabilitation plan.

Abstract: A digitally controlled aspirator is provided with a processor that allows the user to select operating conditions including one or more default settings. The processor further includes sensors for sensing operational and environmental conditions and adjusts the operation of the aspirator to reflect the sensed conditions.