A device includes a body defining a respiration passage in fluidic communication with a filter fitting disposed on a first end of the body and a mask fitting disposed on a second end of the body, and a treatment passage in fluidic communication with the mask fitting. A treatment fitting is disposed on the body and is coupleable to a treatment source such that a seal in the treatment fitting transitions from a closed state to an open state to allow fluidic communication between the treatment source and the treatment passage. The device configured to permit (i) inhalation air and/or exhaled breath to be drawn and/or expelled through the filter fitting, the respiration passage, and the mask fitting and (ii) a respiratory therapeutic to be drawn from the treatment source coupled to the treatment fitting, through the treatment passage, and through the mask fitting.

A patient interface comprises a plenum chamber and a seal-forming structure. The seal-forming structure comprises a support structure arranged to support a sealing portion that is adapted to sealing engage the patient's face in use. The seal-forming structure may also include a seal biasing portion configured to inflate under pressurization within the cavity in the cushion assembly in use to extend the reach of the sealing portion and decouple the sealing portion from external forces.

A system and method configured to control pressure during enhanced cough flow of a subject are provided. A pressure regulator is operated such that during an individual exhalation of the subject, the pressure regulator is toggled between a first mode in which a subject interface is closed such that substantially no gas is communicated with the airway of the subject there through and a second mode in which the subject interface is opened to cause a series of exsufflation events for the individual exhalation of the subject. The pressure relief valve is associated with the subject interface and configured to open and release gas out of the subject interface, responsive to pressure within the subject interface exceeding a predetermined threshold value so as to maintain the pressure within the subject interface within a predetermined pressure range during the enhanced cough flow.

An inhalation device (1) comprising a compressor (2), an aerosol generator (3) and a pressure relief valve (4), wherein the compressor (2) is configured to provide a compressed gas for the aerosol generator (3) and the pressure relief valve (4) is configured to limit a pressure in the inhalation device (1).

A device for providing a known concentration of blended air and oxygen, or oxygen, to an individual which incorporates a face mask inside a hood, thereby preventing aerosolization of potentially harmful exhaled gases and controlling condensation issues within the hood while under pressurized conditions. The air tight seal required to allow placement and removal of the hood on the individual will be manufactured using injection molded elastomers to over-mold injection molded rigid plastic components.

The present invention provides systems, methods, and apparatus for applying a hyperoxic therapy delivery system to a patient; administering hyperoxic gas to the patient according to an oxygen dose-response model; and adjusting the administration of the hyperoxic gas to the patient based upon monitored parameters related to a condition of the patient. Numerous additional features are disclosed.

A surgical humidification system includes a source of gas flow and a humidifier that receives the gas flow and outputs a humidified gas to a delivery conduit. The delivery conduit has an outlet and a suitable interface, such as a diffuser, is connected to the outlet. The interface can be positioned near or within an open surgical cavity of a patient to supply the humidified gas to the cavity. The system also includes a pressure relief arrangement that operates to relieve pressure from the system above a normal operating pressure. The pressure relief arrangement can be located in a non-sterile portion of the system, such as upstream from the humidifier, for example.

A leak control system (26) for an evacuation system (12) of an insufflation system (1), for controlling leakage of insufflating gas from a vessel (5) of a subject being insufflated. An evacuation conduit (20) connects a Venturi vacuum creating device (14) to the vessel (5) through a pressure relief valve (27) operable from a closed state to an open state in response to a pressure drop across the pressure relief valve (27) in the direction of the arrow A exceeding a predefined pressure drop value. The vacuum creating device (14) is operable in response to a signal from a pressure sensor (10) detecting pressure in the cavity (5) exceeding a predefined pressure value for applying a vacuum to the evacuating conduit (20) to increase the pressure drop across the pressure relief valve (27) to the predefined pressure drop value, for in turn operating the pressure relief valve (27) into the open state. On the pressure in the vessel (5) being reduced below the predefined pressure value, the vacuum creating device (14) is deactivated, and the pressure relief valve (27) transitions into the closed state, thereby preventing further leakage of insufflating gas though the Venturi vacuum creating device (14).

The present disclosure describes systems and apparatuses related to a bronchial isolation tube, a laryngeal mask or similar device, and/or adapters and connectors for use with the same, as well as methods for using the same. In an exemplary airway device, the device may comprise a mask portion being defined at a distal end of the airway device, and may be configured and dimensioned to be positioned in a hypopharyngeal area of a patient to cover and seal around a glottis of the patient; and a channel portion extending from a proximal end of the airway device to the mask portion. The channel portion may include first and second channels, wherein the second channel may obliquely merge with the first channel proximate to an opening of the first channel. In an exemplary embodiment, a third channel may form a combined pharyngeal-gastric access channel.

Apparatus to permit a delivery of a flow of breathable gas to a patient's airways. In one version, a coupler extension may include a seat portion to permit use of a mask with a nasal cannula. In some versions, the coupler extension is configured to conduct the flow of gas to prongs of a nasal cannula. The seat portion can receive and seal with a cushion of a respiratory mask and may have a sealing bevel to promote sealing between the cushion of the respiratory mask and a facial contact surface of a user. In some versions, a conduit adapted to communicate a flow of gas may comprise a slit valve formed by a portion of the wall material of the conduit. In some versions, a nasal interface may include naris pillows to seal with and conduct a flow of breathable gas into a nares of a user. Each naris pillow may include a nasal projection to conduct a further flow of gas. The nasal projection may extend within the naris beyond the seal of the naris pillow.