A rescue tube comprising a tube having a first and second end, a one-way valve and a ported double swivel elbow; wherein the one-way valve and ported double swivel elbow are connected to one another, and the one-way valve is attached to the tube.

In various embodiments, an apparatus to aid in cardiopulmonary resuscitation (CPR), may include: a support structure (200, 300, 400) shaped to support a head and neck of a patient at respective positions suitable for opening an airflow of the patient during performance of CPR on the patient; one or more electromagnetic radiation sources (208, 308, 408) mounted on the support structure to emit electromagnetic radiation having a wavelength within a predetermined frequency range of wavelengths onto skin of the patient; and one or more electromagnetic or optical sensors (210, 310, 410) mounted on the support structure to detect electromagnetic radiation within the predetermined frequency range that is reflected from or transmitted into the patient's skin.

A CPR training assembly for instructing a person to perform CPR or choking rescue on an infant, a child or an adult includes a housing and an audio unit that is coupled to the housing. The audio unit emits audio outwardly from the housing to audibly alert a user. The audio unit stores data pertaining to audible instructions for performing CPR or choking rescue on infants, children and adults. A control unit is coupled to the housing and the control unit is electrically coupled to the audio unit to select the audible instructions for a respective one of the infants, children and adults. In this way the user can choose to receive audible instructions that correspond to whether an infant, a child or an adult needs CPR or choking rescue.

Devices and methods for delivering air to a patient are provided. A device includes a first portion having a first airflow inlet and a first impeller configured to move in response to airflow from the first airflow inlet contacting the first impeller, the first portion defining a first airflow path; a second portion having a second airflow inlet, a second impeller, and an outlet for communicating airflow to a patient, the second portion defining a second airflow path; and means for coupling the first portion and the second portion, such that movement of the first impeller causes corresponding movement of the second impeller, wherein the second impeller is configured to impel air through the second airflow inlet and out of the outlet to the patient, upon movement of the second impeller and wherein the first and second airflow paths are not in fluid communication.

A stabilizer arm for a BVM resuscitator and method of use is disclosed. The stabilizer arm provides the necessary support to the reservoir bag to enable the user to exert downward pressure on the BVM resuscitator while simultaneously squeezing the reservoir bag, and creates force that is focused, directed, and realized at the mask of the assembly. Due to the presence of the stabilizer arm, this pressure pushes the facial mask downward to assist in forming a tight mask to face seal. The stabilizer arm may be internal, external or integrated into the reservoir bag wall of the BVM resuscitator and may be retro-fitted or original equipment manufactured. The external stabilizer arm may be designed to engage the outlet port neck of the BVM resuscitator with an open collar or a closed collar. The internal stabilizer arm may be configured to fit BVM resuscitators having single piece or multiple piece outlet valve design.

An electrode assembly includes a first surface to be placed adjacent a person's skin and a second surface including a plurality of reservoirs of conductive gel. The plurality of reservoirs of conductive gel are disposed on sections of the electrode assembly that are at least partially physically separated and may move at least partially independently of one another to conform to contours of a body of a patient. The electrode assembly is configured to dispense an amount of the electrically conductive gel onto the first surface in response to an activation signal and to provide for a defibrillating shock to be applied to the patient through the amount of the electrically conductive gel.

A stabilizer arm for a BVM resuscitator and method of use is disclosed. The stabilizer arm provides necessary support to the reservoir bag to enable the user to exert downward pressure on the BVM resuscitator while simultaneously squeezing the reservoir bag, and creates force that is focused, directed, and realized at the mask of the assembly. Due to presence of stabilizer arm, this pressure pushes the facial mask downward to assist in forming a tight mask to face seal. The stabilizer arm may be internal, external or integrated into the reservoir bag wall of the BVM resuscitator and may be retro-fitted or original equipment manufactured. The external stabilizer arm may be designed to engage the outlet port neck of the BVM resuscitator with an open collar or a closed collar. The internal stabilizer arm may be configured to fit BVM resuscitators having single piece or multiple piece outlet valve design.

A device for administering cardiopulmonary resuscitation to a mammalian animal of the type having a front leg and a snout. The device includes an overlay configured to overlay a side chest area of the animal, the overlay including a front leg opening for the front leg of the animal, and indicium or indicia or both for guiding the administration of cardiopulmonary resuscitation; and a muzzle configured for positioning over the snout of the animal.

An electrode assembly includes a first surface to be placed adjacent a person's skin and a second surface including a plurality of reservoirs of conductive gel. The plurality of reservoirs of conductive gel are disposed on sections of the electrode assembly that are at least partially physically separated and may move at least partially independently of one another to conform to contours of a body of a patient. The electrode assembly is configured to dispense an amount of the electrically conductive gel onto the first surface in response to an activation signal and to provide for a defibrillating shock to be applied to the patient through the amount of the electrically conductive gel.

A capnograph system may be used together with a ventilation system for a patient. The capnograph system may include a capnography module with a carbon dioxide detector, which may generate a carbon dioxide signal responsive to an amount of carbon dioxide detected within an air path of the ventilation system. A monitoring circuit may further detect a pressure within the air path. A processing component within the capnography module may generate a pressure signal responsive to the pressure detected in the air path. The pressure signal, alone or in combination with other signals such as the carbon dioxide signal, may be used to detect spontaneous breaths of the patient.