A patient interface assembly has a patient interface and a securement system for the patient interface and/or patient interface tubing. The patient interface has a body and at least one nasal prong extending from the body. The at least one nasal prong has a gas inlet for fluid communication with a supply of breathable gas, and a gas outlet configured to direct a flow of gas towards a nare of the user's nose. The at least one nasal prong further includes an exterior surface, at least a portion of the exterior surface is a sealing surface configured to seal the nare of the user's nose. The securement system has a two-part releasable attachment or connection arrangement, the arrangement comprising a first patch and a second patch.

Methods and system for treating obstructive sleep apnea and snoring are disclosed. The system generally comprises a mask for delivering pressurized air to patient's breathing orifice, a sensing mechanism for continuously assessing the state of patient's breathing and a pressure generator for generating the pressurized air in the mask. The pressurized air is applied to the breathing orifice only during selected portions of the breathing cycle, when such pressure might be required to prevent occlusion of the airway or to restore patency of the airway after such occlusion occurs.

A patient interface structure for delivery of respiratory therapy to a patient includes a front plate configured to conform to the shape of the patient's face; a mouth cushion defining a breathing chamber and provided to the front plate and configured to seal around the patient's mouth; and a nasal cushion configured to seal the patient's nasal airways. The nasal cushion is supported by the mouth cushion, does not contact a bridge of the patient's nose in use, and extends at least partially into the breathing chamber. A patient interface system includes a patient interface structure and a patient interface structure positioning system configured to position, stabilize and secure the patient interface structure in sealing engagement with the patient's face.

Methods or systems (7000) are implemented for treatment with or monitoring use of respiratory pressure therapy device(s). The device may be for a respiratory disorder. A processor, such as a processor of a server communicating with the therapy device, may analyse data relating to respiratory therapy delivered by the device. The processor may generate data in the processor representing a prediction, such as compliance prediction(s), about progress of therapy based on the analysis. The processor may select an action to improve therapy based on data representing the prediction. The processor may take or prompt selected action to improve the therapy. In some cases, a processor may analyse usage data concerning a period of days with a therapy device and generate compliance prediction indicators based on the analysis. The indicators indicate whether compliance will be likely. The processor may recommend engagement action to improve compliance based on evaluation of the indicators.

A headgear, for use in combination with a breathing apparatus, has a plastic or elastomer core and a fabric or textile casing. The headgear, or portions thereof, may also include a length adjustment arrangement that permits adjustment of a length of a section of the headgear. The length adjustment arrangement can comprise overlapping strap portions of the headgear. In some configurations, the overlapping strap portions can be covered by a sleeve. The sleeve can be secured to the headgear by overmolded end caps. A nasal respiratory interface can include a frame having a front surface, a rear surface, and an aperture extending from the front surface to the rear surface. The frame can have an oval form with a truncated height portion. The interface can also include a seal for a nasal pillow. The seal can be attached to the frame.

A patient interface is configured to deliver breathable gas to a patient. The patient interface includes a cushion configured to form a seal with the patient's face and a frame with an elongated body comprising a central bore and a circumferential channel. The circumferential channel is configured to receive a rim of the cushion. Headgear is attachable to the frame and is configured to support the cushion and the frame on the patient's head. The headgear includes a left rigidizer attached to a left front strap and a right rigidizer attached to a right front strap. The left and right rigidizers are arranged to have different flexibilities in different directions so that a stiffness of the left and right rigidizers in a first direction resist a vertical rotation of the patient interface.

A patient interface comprising a plenum chamber configured to receive in use a flow of air at the therapeutic pressure for breathing by a patient, a seal-forming structure configured to form a seal with or around the patient's nose and/or mouth, a positioning and stabilising structure configured to hold the seal-forming structure in a sealing position, and at least one inflatable body. In one form, an inflatable body is provided to a portion of the positioning and stabilising structure. In another form the inflatable body is provided to a hoop structure. In another form, the patient interface comprises a lever arrangement, wherein an inflatable body is provided to the lever arrangement. In yet another form, the seal-forming structure comprises an inflatable body. The patient interface may be configured to limit or prevent mouth leak or mandible movement during CPAP therapy, adjust the fit of the positioning and stabilising structure on the patient's head, and/or improve the seal formed with patient's face in use.

A shroud for a mask system includes a retaining portion structured to retain a frame, a pair of upper headgear connectors each including an elongated arm and a slot at the free end of the arm adapted to receive a headgear strap, and a pair of lower headgear connectors each adapted to attach to a headgear strap. The retaining portion, the upper headgear connectors, and the lower headgear connectors are integrally formed as a one piece structure.

Disclosed is a nasal ventilation mask having separate ports to monitor end-tidal CO.sub.2 expulsion integrated into the mask in order to monitor end-tidal CO.sub.2 expelled nasally or orally. Also disclosed is a CPR mask for nose-to-mouth and/or mouth-to-mouth resuscitation, having a body shaped to cover the nose and/or mouth of a victim, the mask including a CO.sub.2 absorber for eliminating at least in part rescuer's exhaled CO.sub.2 delivered to the victim.

A seal-forming structure for a patient interface may include a patient-contacting surface configured to engage the patient’s facial skin to form a seal; a posterior opening formed in the patient-contacting surface, the posterior opening configured to provide the flow of air at said therapeutic pressure to the patient’s nares; and a support structure extending from the patient contacting surface to an interior surface of the seal-forming structure, the support structure and the interior surface forming a continuous loop, wherein the patient interface is configured to allow the patient to breath from ambient through their mouth in the absence of a flow of pressurised air through the plenum chamber inlet port, or the patient interface is configured to leave the patient’s mouth uncovered.