Provided/Disclosed is a cardiopulmonary resuscitation (CPR) training apparatus, comprising: a mannequin including a head portion with an airway, and a body portion connected to the head portion; a compression portion provided in the body portion, the compression portion to be pressed in response to a chest compression; an airbag connected to the airway, the airbag configured to enable an artificial ventilation; and a measurer configured to measure a CPR performance state in response to the chest compression and the artificial ventilation performed on the mannequin.

A method for health education, certification, and recordation is disclosed. The method may include obtaining, at a server, a user input from a user interface. The user input may define an interval for a desired CPR certification schedule. The method may include generating, at the server, a CPR certification program. Generating the CPR certification program may include generating at least two task groups. Each task group of the at least two task groups may include a healthcare certification task. The method may include administering, at the server, the CPR certification program. Administering the CPR certification program may include assigning, at the interval defined by the user input, one task group of the at least two task groups to a user enrolled in the CPR certification program, and receiving an indication that the enrolled user has completed the healthcare certification task of the assigned one task group.

A cardiopulmonary resuscitation (CPR) training apparatus for infants is disclosed. The CPR training apparatus for infants includes a body portion, a head portion including a head frame rotatably connected to the body portion, a tunnel portion including a tunnel frame installed on a neck of the body portion, and a lower catching protrusion extending from a lower side of the tunnel frame to an upper side of the tunnel frame, an airway portion including an airway tube installed to be in communication with a mouth of the head portion, and a neutral closure portion connected to an outside of the airway tube so as to be positioned above the lower catching protrusion, and a tube portion configured to connect the airway tube and an artificial lung to each other by passing through the tunnel portion between the lower catching protrusion and the neutral closure portion. The neutral closure portion may be in contact with the lower catching protrusion to close the tube portion when the head portion is in a neutral state with respect to the body portion, and the neutral closure portion may be spaced apart from the lower catching protrusion to open the tube portion when the head portion is tilted at a predetermined angle or more with respect to the body portion.

An airway simulation system includes a simulated airway having a hollow body defining a passageway therein with a first portion and a second portion. The second portion includes a bifurcated section having a left branch section and a right branch section and connects to the first portion at the distal end of the first portion. The simulated airway includes at least one orifice defined along the hollow body and in communication with at least one pressure transducer. One branch of the left branch section and the right branch section is configured to receive airflow from a distal end, and the other of the left branch section and the right branched section includes a cap at a distal end to prevent airflow from being received by the distal end of the capped branch. A method for simulating a human airway is also disclosed.

A method and system of tracking and analyzing data during a medical procedure is provided. A wearable sensor (e.g. EEG system to obtain EEG signals) is worn by a practitioner, where the wearable sensor covers a body part of the practitioner. The practitioner performs a medical procedure on a person. The medical procedure is video recorded. A computer system digitally registers the medical procedure by registering (i) the digital data from the wearable sensor, and (ii) the digital data of the video recording. The computer system synchronizes the registered digital data of (i) and (ii) into a synchronized data set, and sections are then identified for the synchronized data set. The computer system generates sensor data maps from the synchronized data set and the identified sections, which are then useful for the practitioner, colleagues and other learners for feedback and training purposes.

An airway resistance device providing reliable and constant airway resistance for a given position of an occlusion mechanism that may be used in a lung simulator device in order to allow the simulation of a number of medical conditions which impacts the airflow in the airways. The airway resistance device includes one or more laminar flow channels and a variable occlusion mechanism that retains the laminar flow characteristics, such that resistance is constant for a given occlusion configuration.

An external defibrillator system includes one or more compression sensors; one or more physiological sensors; and at least one processor. The at least one processor is configured to: receive and process chest compression signals and physiological signals from the sensors, determine values for chest compression depth and/or chest compression rate based on the received chest compression signals, determine a trend of at least one physiological parameter over a period comprising multiple chest compressions based on the received physiological signals, adjust a target chest compression depth and/or target chest compression rate based on the determined trend of the at least one physiological parameter, compare the determined values for chest compression depth and/or chest compression rate to the adjusted target compression depth and/or the adjusted target compression rate, and provide feedback about the quality of chest compressions performed on the patient.

Described herein are systems and methods of guiding a user to achieve musculoskeletal counterpulsation. A method may include receiving a cardiovascular cycle signal from a first sensor; determining a heart rate of the user based on the cardiovascular cycle signal; receiving a rhythmic musculoskeletal activity timing signal from a second sensor; determining an actual musculoskeletal activity cycle (MSKC) to cardiovascular cycle (CC) timing relationship; comparing the actual MSKC to CC timing relationship to a target MSKC to CC timing relationship; providing a recurrent prompt to the user as a timing indication for performance of a rhythmic musculoskeletal activity to guide the user to achieve a musculoskeletal activity cycle rate (MSKR) that approaches the target MSKC to CC timing relationship; and altering a feature of the recurrent prompt based on a determined alignment between the actual MSKC to CC timing relationship and the target MSKC to CC timing relationship.

Anatomic simulators, assemblies, and related methods are disclosed. In some embodiments, an anatomic simulator may include constraint panels that define a variably sized volume configured to receive an organ model. An elastic member may be configured to provide a restorative force when the constraint panels are moved to an expanded configuration. Alignment apertures in the constraint panels may be configured to permit marking of an organ model and/or visibility of a mark disposed on the organ model to position and orient the organ model in the anatomic simulator. In some embodiments, an anatomic simulation assembly may include an anatomic simulator, a pressure source, pneumatic controls, a pressure sensor, and a processor. In some embodiments, a method of simulating anatomic motion may include flowing a fluid to an organ model, sensing a pressure, and controlling the flow of fluid based on the sensed pressure to maintain a target pressure.

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