Abstract: 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.

Abstract: A respiratory mask for continuous positive airway pressure treatment includes a cushion adapted to be positioned against the face of a patient. The cushion is configured in a gasket arrangement around an entrance to the airways of the patient. The cushion is constructed from a polyurethane foam and has a thickness of greater than about 5 mm.

Abstract: A patient interface system for delivering a flow of breathable gas to a patient includes a patient interface structure configured to sealingly engage the face of the patient and a retaining element configured for application to the patient. The retaining element is configured to support the patient interface structure in sealing engagement with the face of the patient. The retaining element includes an adhesive and/or at least one strap. In addition, the patient interface structure is configured to be released from and re-engaged with the retaining element for re-positioning of the patient interface structure relative to the patient's face in a plurality of positions while the retaining element remains supported by the patient.

Abstract: An adjustable mask system (100) includes a cushion with a seal (130) having the ability to change size and/or shape. The seal is preferably a one-piece, continuous member without interruptions. To effect adjustment of the size and/or shape of the seal, an actuator may be provided, which may take the form of a dial (190).

Abstract: Aspects of the present technology comprise a positioning and stabilising structure to hold a seal-forming structure in a therapeutically effective position on a head of a patient. The positioning and stabilising structure may comprise at least one gas delivery tube to deliver the flow of air to the entrance of a patient's airways via the seal-forming structure. The at least one gas delivery tube may be constructed and arranged to contact, in use, at least a region of the patient's head superior to an otobasion superior of the patient's head. The positioning and stabilising structure may comprise an adjustment mechanism for adjustment of a length of the at least one gas delivery tube to enable the positioning and stabilising structure to fit different size heads.

Abstract: An apparatus for delivering a flow of breathable gas to a patient for the treatment of Sleep Disordered Breathing (SDB) that is less obtrusive includes a nasal cannula, cannulae (2a, 2b), prongs, or pillows and may be sealed or unsealed with the nares of the patient in use. The cannula, pillows or prongs may be positioned on the face of the patient by a headgear (6). The cannula, pillows or prongs may be smaller, lighter, and/or less visible than other nasal cannula, cannulae, pillows or prongs and may therefore be less obtrusive to the patient.

Abstract: A respiratory mask for continuous positive airway pressure treatment includes a cushion adapted to be positioned against the face of a patient. The cushion is configured in a gasket arrangement around an entrance to the airways of the patient. The cushion is constructed from a polyurethane foam and has a thickness of greater than about 5 mm.

Abstract: A patient interface is configured to deliver a flow of pressurized breathable gas to a patient's airways. The patient interface includes a central portion with an opening configured to deliver the pressurized breathable gas to the patient's nares. A first stabilizing portion extends from the central portion and is structured to engage an outer side of a respective one of the patient's nostrils. A second stabilizing portion is opposite the first stabilizing portion and extends from the central portion. In addition, the second stabilizing surface is structured to engage an outer side of a respective one of the patient's nostrils. The central portion, the first stabilizing portion and the second stabilizing portion cooperate to form a U-shape configured to cradle the patient's nose so that the tip of the patient's nose remains exposed when the patient interface is mounted on the patient's face.

Abstract: A patient interface for delivering breathable gas to a patient includes a foam interfacing portion adapted to provide a nasal interface to contact under and around the patient's nose in use and including an orifice adapted to surround both the patient's nares in use, and a positioning and stabilizing structure to support the foam interfacing portion in an operative position on the patient's face. The positioning and stabilizing structure is structured to provide a range of rotational, axial, and/or lateral movement to the foam interfacing portion while maintaining a sufficient interface and resisting the application of tube drag and/or headgear tension to the foam interfacing portion.

Abstract: An apparatus for delivering a flow of breathable gas to a patient for the treatment of Sleep Disordered Breathing (SDB) that is less obtrusive includes a nasal cannula, cannulae (2a, 2b), prongs, or pillows and may be sealed or unsealed with the nares of the patient in use. The cannula, pillows or prongs may be positioned on the face of the patient by a headgear (6). The cannula, pillows or prongs may be smaller, lighter, and/or less visible than other nasal cannula, cannulae, pillows or prongs and may therefore be less obtrusive to the patient.

Abstract: A cushion assembly for a patient interface includes a foam cushion and an elastomeric support portion configured to support the foam cushion. The foam cushion is more compliant in a nasal bridge region than other regions of the cushion assembly, the nasal bridge region being a region configured to engage the patient's nasal bridge when the cushion assembly is mounted on the patient's face.

Abstract: A cushion assembly for a patient interface including an elastomeric support portion and an elastomeric seal-forming structure supported by the elastomeric support portion that is more rigid than the elastomeric seal-forming structure. The elastomeric seal-forming structure includes a first compliant region and a second compliant region separated from the first compliant region by a support region that is more rigid than the first and second compliant regions. The more rigid support region extends to and is anchored by the elastomeric support portion. In addition, for every point in the rigid support region, the inner surface has a negative curvature when the outer surface has a positive curvature and the inner surface has a positive curvature when the outer surface has a negative curvature.

Abstract: A cushion assembly for a patient interface includes an elastomeric seal-forming portion that includes a dome-shaped superior region (3180A); a saddle-shaped inferior region (3180G); a first support region (3180E) having a consistent wall thickness, preferably 2 mm, that is greater than the wall thickness of the dome-shaped superior and the saddle-shaped inferior regions, preferably 0.3 mm; a second support region (3180D) having a varied wall thickness and is bounded by the first support region (3180E) on a proximal side and having a distal side opposite the proximal side. In claim 1, the wall thickness in the second support region (3180D) increases from the distal side to the proximal side, preferably 2 to 1.3 mm. Preferably, wall thickness of a third support region (3180F) is 1.3 mm, a compliant region (3180C) is 0.85 mm and a flap (3180H) is 0.5 mm. Preferably flap (3180H) moves independently of a loop connection (3110).

Abstract: One form of the present technology includes a sealing structure to seal against a user's face around the user's airways. The sealing structure includes a flap or membrane that extends inward towards the user's airways and includes a structure that prevents an inner boundary of the flap or membrane from being blown outwards (e.g., folded backwards upon itself) due to internal pressurization.

Abstract: A PAP system includes a PAP device to generate a supply of pressurized air, a patient interface adapted to form a seal with the patient's face, air delivery tubing to interconnect the patient interface and the PAP device, and a cover that substantially encloses at least a portion of the PAP device and a portion of the air delivery tubing. The cover allows the PAP device to be carried by and/or supported on the patient's head.

Abstract: A retractable tube for use in a respiratory apparatus for delivering a pressurized flow of breathable gas to a patient has an internal diameter of about 30 mm or less, a weight of about 500 g/m or less, and an unextended length of about 2 m or less. The retractable tube includes a portion that is extensible in a range of about 40%-400% in response to force applied to the tube, and the extensible portion is configured to return the tube to its unextended length in the absence of force applied to the tube. A respiratory apparatus for delivering a flow of pressurized breathable gas includes a flow generator to generate the flow and a patient interface to deliver the flow to the patient's airways. The flow generator and the patient interface are connected by a retractable tube. A method of delivering a flow of pressurized breathable gas includes connecting the flow generator and the patient interface using a retractable tube.

Abstract: A PAP system includes a PAP device to generate a supply of pressurized air, a patient interface adapted to form a seal with the patient's face, air delivery tubing to interconnect the patient interface and the PAP device, and a cover that substantially encloses at least a portion of the PAP device and a portion of the air delivery tubing. The cover allows the PAP device to be carried by and/or supported on the patient's head.

Abstract: A retractable tube for use in a respiratory apparatus for delivering a pressurized flow of breathable gas to a patient has an internal diameter of about 30 mm or less, a weight of about 500 g/m or less, and an unextended length of about 2 m or less. The retractable tube includes a portion that is extensible in a range of about 40%-400% of its unextended length in response to force applied to the tube, and the extensible portion is configured to return the tube to its unextended length in the absence of force, or reduced force, applied to the tube.

Abstract: A patient interface system for delivery of a supply of air at positive pressure to the entrance of a patient's airways for treatment of sleep disordered breathing includes an air delivery tube connected to a flexible portion of a plenum; a vent structure having sufficient rigidity to support its own weight under gravity and/or not to block or fold under tube movement or tube drag; and a patient interface structure. The patient interface structure includes a seal forming structure arranged on a top portion of the plenum; and a seal positioning and stabilizing structure connected to a flexible portion of the plenum. The seal-forming structure is substantially decoupled from a tube drag force.