A cushion assembly for a patient interface includes an elastomeric seal-forming portion with a dome-shaped superior region that is intersected by the sagittal plane in the vicinity of a superior tangent point. The seal-forming portion further including a saddle-shaped inferior region that is intersected by the sagittal plane and includes an inferior tangent point. A first support region is located on one side of the sagittal plane between the inferior region and the superior region, the exterior surface of the elastomeric seal forming portion at the first support region being cylinder-shaped and/or saddle-shaped. In addition, a blowout prevention system is configured to counter a force acting on the unsupported edge of the elastomeric seal-forming portion due to a pressure within the chamber, the blowout prevention system being attached to the elastomeric seal-forming portion at the first support region of the elastomeric seal-forming portion.

A device and method of generating an enriched gas within a nasal vestibule of a patient includes a housing, a chamber, a chamber inlet, a pump, a molecular sieve bed, a release outlet, and a breath duct. The chamber is configured to be received within the nasal vestibule. The pump is configured to direct an ambient air from an ambient environment into the chamber. The molecular sieve bed is positioned within the chamber and configured to collect a predetermined molecule from the ambient air thereby generating the enriched gas. The release outlet is configured to discharge the enriched gas from the chamber into the nasal vestibule. The breath duct longitudinally extends through the housing such that the breath duct is configured to fluidly communicate a fluid flow through the housing for nasal breathing by the patient while the chamber is positioned within the nasal vestibule.

The present invention relates to a device to urge the mouth closed during sleep to reduce snoring and/or treat sleep disorders such as sleep apnea. In one aspect, the device includes a jaw-blocking object that is secured beneath the chin of a user and also contacting the clavicular region of the upper chest area. In another aspect, a device of the invention includes a jaw-blocking object in combination with a CPAP mask and headgear for use with a CPAP system.

The present invention relates to a device to urge the mouth closed during sleep to reduce snoring and/or treat sleep disorders such as sleep apnea. In one aspect, the device includes a jaw-blocking object that is secured beneath the chin of a user and also contacting the clavicular region of the upper chest area. In another aspect, a device of the invention includes a jaw-blocking object in combination with a CPAP mask and headgear for use with a CPAP system.

Embodiments of an adaptor for delivering diffused aromatic agents to a user of a CPAP machine is disclosed in this document. The adaptor may include a connector body, a diffuser pad disposed within the connector body, and at least one coupling mechanism on the connector body coupling the connector body within the air supply and positioning the diffuser pad within the airflow of a CPAP machine. The adaptor may be configured to couple directly to a CPAP mask. Similarly, the adaptor may be configured to be placed in the airflow between the CPAP air generator and the mask. The adaptor may be configured such that no modification of the existing CPAP hose, machine, or mask is required.

Embodiments of an adaptor for delivering diffused aromatic agents to a user of a CPAP machine is disclosed in this document. The adaptor may include a connector body, a diffuser pad disposed within the connector body, and at least one coupling mechanism on the connector body coupling the connector body within the air supply and positioning the diffuser pad within the airflow of a CPAP machine. The adaptor may be configured to couple directly to a CPAP mask. Similarly, the adaptor may be configured to be placed in the airflow between the CPAP air generator and the mask. The adaptor may be configured such that no modification of the existing CPAP hose, machine, or mask is required.

A patient interface may include a plenum chamber and a positioning and stabilising structure. The plenum chamber may include a seal-forming structure and a fascia portion. At least a medial portion of the fascia portion is flexible. In embodiments, the patient interface may include a rigidiser to control flexing of the fascia portion.

A patient interface may include a plenum chamber and a positioning and stabilising structure. The plenum chamber may include a seal-forming structure and a fascia portion. At least a medial portion of the fascia portion is flexible. In embodiments, the patient interface may include a rigidiser to control flexing of the fascia portion.

A patient interface includes a frame assembly including connectors operatively attachable to headgear, a cushion assembly provided to the frame assembly and including a seal-forming structure structured to form a seal with the patient's nose and/or mouth, and an air delivery connector provided to the frame assembly and operatively connected to an air delivery tube for supplying the air at positive pressure along an air flow path. The cushion assembly is structured to releasably connect to the frame assembly independently of the air delivery connector. The air delivery connector is structured to releasably connect to the frame assembly independently of the cushion assembly.

A diagnostic tool and methods of using the tool are provided to quantify an amount of nasal collapse in a patient. The diagnostic tool includes a mask with an endoscope port and an opening to allow air flow, an endoscope with a camera adapted to take an image of the nasal valve, and an air flow sensor adapted to measure an inhalation rate of the patient. The diagnostic tool can quantify a size difference between the nasal valve during inhalation and zero flow by calculating a percentage difference in an area or one or more dimensions of the nasal valve during inhalation and zero flow.