An air delivery conduit includes first and second conduit portions that cooperate to form the conduit, each conduit portion including an inner layer of a film laminate that forms an interior surface of the conduit and an outer layer of a textile that forms an exterior surface of the conduit.

An apparatus is disclosed that includes an aircraft or repurposed aircraft or fuselage having a cabin capable of pressurization, a way to pressurize the cabin whether by built in machinery or external apparatus, a way to deliver oxygen to a plurality of persons in the cabin, a source of hyperbaric oxygen, a pressure gauge or regulator configured to measure or regulate a pressure of the hyperbaric oxygen or the aircraft, a plurality of face or head coverings configured to provide the hyperbaric oxygen to persons or patients in need thereof, and an optional exhaust system configured to remove gas(es) from the face or head coverings without releasing the gas(es) into the cabin. Each of the face or head coverings includes a gas inlet, a gas outlet, and one or more seals adapted to contain oxygen in the face or head covering at a pressure greater than 1 atm. A related kit and a related method of treating persons with hyperbaric oxygen are also disclosed.

A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways comprising: a cushion member that includes a retaining structure and a seal-forming structure permanently connected to the retaining structure; a frame member attachable to the retaining structure; and a positioning and stabilising structure attachable to the frame member.

A molded breathing appliance for supporting a nasal oxygen tube having an upper bite rim, a lower bite rim, a moldable material disposed within the upper bite rim and lower bite rim for conforming to a patient's maxillary bite impression and mandibular bite impression, respectively, an L-shaped member extending outwardly perpendicular to the upper bite rim, and a transverse support disposed on the L-shaped member and configured with a plurality of sets of oxygen tube finger clamps to retain a nasal oxygen tube in proximity with a patient's nostrils.

An apparatus including a tubular channel having a pathway extending between a proximal end and a distal end of the tubular channel. The proximal end is configured to connect directly or indirectly to an end tidal CO.sub.2 monitor. The distal end has an opening. The apparatus further includes a detection member including a chamber disposed in fluid communication with the pathway of the tubular channel such that gas entering the tubular channel via the opening on the distal end passes into the chamber. A detection element is disposed within the chamber and includes a component that is sensitive to one or more systemic biomarkers such that, upon exposure to a predetermined concentration level of the one or more systemic biomarkers contained in the gas, a state of the detection element experiences a permanent alteration and the detection member indicates that the predetermined concentration level of the one or more systemic biomarkers is present in the gas.

Nasal cannula apparatus, includes in an inlet tubular fitting sized and configured to directly endwise connect to a source of oxygen, or oxygen and air. The fitting defines an inlet flow passage area A, having a 15 mm external diameter. A pair of tubular prongs is operatively connected with the inlet fitting, and receivable in an infant's nostrils to deliver oxygen, or oxygen and air flow to the infant, the prongs each having flow passing area A.sub.3, and A.sub.1>>A.sub.3.

Apparatus and methods for delivering a heated and humidified mixture of oxygen and air are provided. The apparatus includes an air compressor and oxygen concentrator enclosed in the housing of a vapor transfer system. The air compressor supplies air at a first pressure to a gas inlet. The oxygen concentrator provides oxygen at a second pressure to the gas inlet. The oxygen concentrator and the air compressor are in fluid communication and are configured such that the first pressure of the compressed air and the second pressure of the oxygen are about equal. The apparatus includes a vapor transfer system having a gas passage, a liquid passage having heated liquid and vapor, and a membrane that separates the gas passage and liquid passage. The membrane is positioned to transfer vapor from the liquid passage to the gas passage.

In one embodiment, a method for accurate leak estimation in a flow generation system includes measuring a total flow through the flow generation system, measuring a pressure in in the primary flow circuit of the flow generation system, determining when the measured pressure is within a predetermined threshold of EPAP, and calculating an intentional leak flowrate and an unintentional leak flowrate based on the relationship Q.sub.FS(t)=Q.sub.IL(t)+Q.sub.UL(t) when the measured pressure is within the predetermined threshold. In another embodiment, a flow generation system includes in one embodiment an airflow generator connected in-line to a flow sensor, a pressure sensor and a patient interface connection by a first gas flow circuit, and a controller electrically coupled to the airflow generator, the flow sensor and the pressure sensor. The controller sends a control signal to the airflow generator based on a first flow value measured from the flow sensor and an unintentional leak flow value that is derived from a proportional relationship with an intentional leak flow value.

The ingestible compositions system includes the co-production of orally-ingestible compositions usable as inhalable respiratory agents including delivery apparatus and related methods.

A ventilator (100) ventilates a patient (102) by a high-flow oxygen therapy via a tube system (104). The ventilator has at least one sensor element (110), at least one actuatable inhalation valve or exhalation valve (120) and a control unit (130). The sensor element is arranged and configured to determine and to output a measured variable (112) within the tube system. The measured variable indicates a gas flow within the tube system. The actuatable inhalation valve or exhalation valve is arranged and configured to make possible a flow of a breathing gas from a ventilation circuit (107) of the ventilator. The control unit regulates a ventilation pressure provided by the ventilator via the at least one sensor element and the at least one inhalation valve or exhalation valve such that a predefined maximum pressure is not exceeded in a predefined area (140) of the tube system.