A system is provided for resuscitative therapy to a patient by delivering active chest compression decompressions. The system may include an ACD device configured to be coupled to the patient's chest and constructed for a rescuer to press and pull on the ACD device to administer active compression decompression therapy. Additionally, the ACD device may include at least one sensor for sensing at least one active compression decompression parameter, processing circuitry configured to process the at least one active compression decompression parameter and provide an output based on the at least one parameter, a first communication circuit configured to transfer data related to the processed output of the at least one parameter, and a second communication circuit capable of being removably coupled to either the electrode assembly or the ACD device.

A method for performing cardiopulmonary resuscitation (CPR) includes elevating the heart of an individual to a first height relative to a lower body of the individual. The lower body may be in a substantially horizontal plane. The method may also include elevating the head of the individual to a second height relative to the lower body of the individual. The second height may be greater than the first height. The method may further include performing one or more of a type of CPR or a type of intrathoracic pressure regulation while elevating the heart and the head. The first height and the second height may be determined based on one or both of the type of CPR or the type of intrathoracic pressure regulation.

A method for performing cardiopulmonary resuscitation (CPR) includes elevating the heart of an individual to a first height relative to a lower body of the individual. The lower body may be in a substantially horizontal plane. The method may also include elevating the head of the individual to a second height relative to the lower body of the individual. The second height may be greater than the first height. The method may further include performing one or more of a type of CPR or a type of intrathoracic pressure regulation while elevating the heart and the head. The first height and the second height may be determined based on one or both of the type of CPR or the type of intrathoracic pressure regulation.

This disclosure describes a solution to enable more useful and responsive methods for a person's wishes for resuscitation actions to be canceled or discontinued in the event of a medical event. In this solution, a person can record their do not resuscitate (DNR) wishes with more specificity. For instance, they can specify conditions for treatment or non-treatment in the event of a medical emergency that would otherwise call for live-saving procedures or the use of an automated external defibrillator (AED) device. Conditional DNR data can be recorded in an electronic device (e.g., emergency pendant or smart watch, or in an electronic device) implanted within or on the person's body. This data can also be stored in a database accessible via a network.

A portable medical treatment apparatus and interactive application that leads a user through a medically acceptable query flow for treating medical emergencies, including cardiac or pulmonary medical emergencies that can be treated with electrotherapy and other medical emergencies.

A respiration device (1) supports cardio-pulmonary resuscitation (CPR) and a method for operating a respiration device (1) supports cardio-pulmonary resuscitation (CPR). The respiration device (1) has a control and regulation unit (7) in order to actuate an expiratory metering unit (3), and an inspiratory metering unit (2) such that, in a first phase, a current value of pressure is increased relative to a first pre-defined value (16) and such that, in a second phase, the current value of the pressure is reduced relative to the first pre-defined value (16).

A system for monitoring performance of a resuscitation activity on a patient by an acute care provider is provided. The system includes: a first wearable sensor configured to sense movement of a first portion of an acute care provider's hand; a second wearable sensor configured to sense movement of a second portion of the acute care provider's hand; and a controller. The controller is configured to: receive and process signals representative of performance of a resuscitation activity from the first sensor and the second sensor; identify from the processed signals information indicative of at least one of a relative distance, a relative orientation, a change in relative distance and a change in relative orientation between the first sensor and the second sensor during performance of the resuscitation activity; and determine at least one resuscitation activity parameter based, at least in part, on the identified information.

The present invention relates to a multi-part device for generating a clearly audible sound when an external force is applied onto a first force-transmission means that acts, via a spring system, on a base plate in an apparatus for controlled cardiopulmonary resuscitation of the human body in the event of cardiac arrest, and is characterised in that the external geometric dimensions and shapes are adapted to the anatomical conditions of the pectoral-adjacent thorax, in particular the spring system generating a signal that acts on at least one oscillatable element, the spring system being arranged between the first force-transmission means and the base plate, which spring system consists substantially of at least one spring element and one planar spring element, in particular the spring element also being a conical spring element.

A cardiopulmonary resuscitation assisting apparatus including: an acceleration sensor (13); a magnetic sensor (19); a first calculation section (233A) which obtains a relational expression (N) between a compression depth Da and the coil-to-coil distance AD; a determination section (234) which differentiates the relational expression (N) with respect to an output value of the magnetic sensor (19) and compares a resulting differentiated value of the relational expression (N) with a predetermined threshold to thereby determine whether notification for assistance of cardiopulmonary resuscitation is necessary or not; and a voice generating section (25) which performs the notification for assistance of cardiopulmonary resuscitation.

A compression device may include a compression plunger in operable communication with a fulcrum assembly and housing assembly in operable communication with a stepper assembly. The compression device may be constructed and arranged to allow a user to administer CPR to a patient by stepping on a portion of the stepper assembly to generate hydraulic power that may be utilized to move the compressor plunger to apply compressive force to the patient's chest. The compression device may include a housing assembly and fulcrum assembly constructed and arranged to provide for variable height and width such that patients of varying sizes can be accommodated and may receive CPR.