A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patients face surrounding the entrance to the patients airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.

A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patients face surrounding the entrance to the patients airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.

Methods and systems for capturing capnography data during high-flow oxygen therapy (HFOT) are disclosed. An example method includes delivering HFOT by delivering breathing gases at an operational flow rate and an operational oxygen concentration level; initiating a temporary flow-reduction function for a set duration, wherein breathing gases are delivered at a temporary flow rate for the set duration, the temporary flow rate being less than the operational flow rate; capturing capnography data for exhaled air during the set duration; and upon expiration of the set duration, resuming HFOT delivery.

Methods and systems for capturing capnography data during high-flow oxygen therapy (HFOT) are disclosed. An example method includes delivering HFOT by delivering breathing gases at an operational flow rate and an operational oxygen concentration level; initiating a temporary flow-reduction function for a set duration, wherein breathing gases are delivered at a temporary flow rate for the set duration, the temporary flow rate being less than the operational flow rate; capturing capnography data for exhaled air during the set duration; and upon expiration of the set duration, resuming HFOT delivery.

Interfaces for positive pressure therapy having a mask assembly, a headgear assembly and a connection port assembly are disclosed herein. The connection port assembly has a ball joint connection with the mask assembly and includes a quick release button for easily disconnecting the gases source conduit from the mask assembly. The mask assembly may include a bias flow vent that is formed separately and attached to the mask assembly. The headgear assembly encircles the rear region of the user’s head and may include at least some portions that are substantially non-stretchable.

Interfaces for positive pressure therapy having a mask assembly, a headgear assembly and a connection port assembly are disclosed herein. The connection port assembly has a ball joint connection with the mask assembly and includes a quick release button for easily disconnecting the gases source conduit from the mask assembly. The mask assembly may include a bias flow vent that is formed separately and attached to the mask assembly. The headgear assembly encircles the rear region of the user’s head and may include at least some portions that are substantially non-stretchable.

A patient interface assembly includes a cushion assembly, and air delivery tube, and a connector assembly. The cushion assembly includes a flexible cushion including a base and a pair of nasal pillows that extend from the base and a frame that is more rigid than the flexible cushion. The connector assembly connects the air delivery tube to the cushion assembly and includes and elbow with a second end with a part spherical ball shape and a gas washout vent with a plurality of vent openings. The connector assembly also includes an elbow connector positioned in the frame. The elbow connector forms a part spherical socket shape that engages the part spherical ball shape of the elbow. The elbow connector includes an anchoring flange, which is configured to secure the flexible cushion to the elbow connector by way of the anchoring flange being inserted into the flexible cushion through a central opening in the flexible cushion.

A patient interface assembly includes a cushion assembly, and air delivery tube, and a connector assembly. The cushion assembly includes a flexible cushion including a base and a pair of nasal pillows that extend from the base and a frame that is more rigid than the flexible cushion. The connector assembly connects the air delivery tube to the cushion assembly and includes and elbow with a second end with a part spherical ball shape and a gas washout vent with a plurality of vent openings. The connector assembly also includes an elbow connector positioned in the frame. The elbow connector forms a part spherical socket shape that engages the part spherical ball shape of the elbow. The elbow connector includes an anchoring flange, which is configured to secure the flexible cushion to the elbow connector by way of the anchoring flange being inserted into the flexible cushion through a central opening in the flexible cushion.

A patient interface includes a positioning and stabilising structure having a knitted headgear strap comprising physical properties and/or characteristics that vary across the headgear strap. The entire headgear strap or portions thereof may be knitted as a single piece of material directly into its final shape. The variations in physical properties and/or characteristics may be provided by different knit structures and/or textile compositions.

A patient interface includes a positioning and stabilising structure having a knitted headgear strap comprising physical properties and/or characteristics that vary across the headgear strap. The entire headgear strap or portions thereof may be knitted as a single piece of material directly into its final shape. The variations in physical properties and/or characteristics may be provided by different knit structures and/or textile compositions.