A ventilator uses teeth of gear to operate up to eight or more bellows. A common drive shaft can be used to operate a stack of multiple such gears, which collectively operate up to 40 or more bellows. Valves can be used to control flow from different ones of the bellows to individual recipients.

A flow generator for a CPAP system configured to deliver a pressurized flow of respiratory gas to a patient's airways includes a housing and a motorized fan positioned within the housing. The motorized fan is configured to pressurize the flow of respiratory gas. In addition, an outlet port is provided in the housing. The outlet port is configured to connect to a humidifier or an air delivery tube and is in communication with an outlet of the motorized fan. The flow generator further includes a water collection receptacle in communication with the outlet port and the motorized fan outlet. The water collection receptacle is configured to collect water entering the flow generator through the outlet port before the water reaches the motorized fan outlet.

A manually actuated, self-inflating bag valve mask provides users with a positive pressure ventilation device that reliably provides a proper tidal volume to the patient and controls the rate of ventilation of the patient. The bag valve mask is lightweight, compact, durable, and quickly deployable in the field. The device is preferably operable with one hand and can be configured for use in low-light environments.

A breathing circuit system for delivering gas from a fresh source to a user through a face mask. The system includes a cylindrical housing and a resiliently-biased valve supported substantially centrally within the housing. In the default or “off” position, the resilient bias causes the valve to be seated on a valve seat shutting off axial flow of gas through the valve housing. When the patient or user breathes, negative pressure is applied to one side of the valve effective to sufficiently overcome the resilient bias imposed on the valve to move the valve off the valve seat axially (or otherwise open in another direction) within the housing, thereby allowing flow of gas through both the valve seat and the valve housing, and into the breathing circuit connected thereto. When the patient's breathing pauses and begins to exhale, the valve bias returns the valve to its default or off condition shutting off flow of gas through the valve.

Resuscitation apparatuses and methods for assisted ventilation are described herein. The apparatuses may include functional elements that allow the manual delivery of a prescribed volume to an adult or an infant lung. Furthermore, the apparatuses may inform and assure an emergency worker that an appropriate volume is being delivered and therefore lessen the possibility of barotrauma from over-delivery, or ventilatory distress from under-delivery. In some embodiments, the apparatuses include biomechanical and ergonomic functional elements that allow an adult hand to hold it in place during operation, while at the same time, allowing the user to actuate the apparatus to deliver only the necessary amount of volume suitable for an infant lung. In other embodiments, a volume-controlled design is applied to pediatric and adult resuscitation.

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.

A patient interface for delivering breathable gas to a patient includes a sealing portion including a nose tip engagement portion adapted to form a seal with the patient's nose tip, an upper lip engagement portion adapted to form a seal with the patient's upper lip and/or base of the patient's nares, and nostril engagement flaps adapted to form a seal with the patient's nares. The nose tip engagement portion, the upper lip engagement portion, and the nostril engagement flaps are all structured to extend or curve outwardly from a supporting wall defining an air path.

A patient interface for delivering breathable gas to a patient includes a sealing portion including a nose tip engagement portion adapted to form a seal with the patient's nose tip, an upper lip engagement portion adapted to form a seal with the patient's upper lip and/or base of the patient's nares, and nostril engagement flaps adapted to form a seal with the patient's nares. The nose tip engagement portion, the upper lip engagement portion, and the nostril engagement flaps are all structured to extend or curve outwardly from a supporting wall defining an air path.

The oxygen delivery device is a portable structure. The oxygen delivery device contains a plurality of oxygen canisters. The plurality of oxygen canisters contain oxygen under pressure. The oxygen delivery device stores the plurality of oxygen canisters. The oxygen delivery device dispenses the oxygen contained in the plurality of oxygen canisters. The oxygen delivery device comprises a housing, a distribution apparatus and the plurality of oxygen canisters. The housing contains the plurality of oxygen canisters and the distribution apparatus. The housing: a) stores the plurality of oxygen canisters; and, b) forms a fluidic connection between the plurality of oxygen canisters and the distribution apparatus. The distribution apparatus delivers the oxygen received from the plurality of oxygen canisters for consumption.

The present ventilator system, for detecting and treating concurrent chronic obstructive pulmonary disease (COPD) and obstructive sleep apnea (OSA event(s)) overlap syndrome, comprises a pressure generator for generating a pressurized flow of breathable gas for delivery to an airway of a subject; sensor(s) for generating output signals conveying information related to breathable gas parameters; and processor(s) operatively connected to the sensor(s) and the pressure generator, configured to: detect presence of OSA event(s) and/or expiratory flow limitation (EFL) in the subject based on the output signals. Responsive to detecting concurrent presence of OSA event(s) and EFL, the processors are configured to determine OSA EVENT(S) therapy parameters for treating the detected OSA event(s) in the subject; determine EFL therapy parameters for treating the detected EFL in the subject; determine a priority treatment based on a comparison between the OSA event(s) therapy parameters and the EFL therapy parameters; and control the pressure generator to deliver the determined priority treatment.