A patient interface for delivering breathable gas to a patient includes a nasal prong assembly including a pair of nasal prongs structured to sealingly communicate with nasal passages of a patient's nose in use and headgear to maintain the nasal prong assembly in a desired position on the patient's face. The headgear includes side straps and rigidizers provided to respective side straps. Each rigidizer includes a first end portion that provides a connector structured to engage a respective end of the nasal prong assembly and an inwardly curved protrusion in the form of a cheek support that curves inwardly of the connector. The cheek support is adapted to follow the contour of the patient's cheek and guide a respective end portion of the side strap into engagement with the patient's cheek to provide a stable cheek support.

A respiratory assistance component is disclosed that changes shape when an electrical charge is provided. The amount of electrical charge that is applied may be based on values, characteristics, or user controlled parameters of the respiratory assistance system. The component may be all or part of a patient interface, a tube, a flow generator, and/or a sleep mat.

Disclosed herein are embodiments describing nonrebreather facemasks for efficiently and comfortably delivering oxygen to patients. One embodiment describes a cup-shaped pliable facemask that is suited to cover and seal a patient's nose, mouth, and cheeks within the cup-shaped facemask. Certain other embodiments describe an inlet tube outwardly extending from the facemask at an angle in line with the pathway of a patient's nostrils to better provide oxygen directly into a patient's nose. Other embodiments envision varying facemask's stiffness for improved comfort and sealing against the patient's face. While other embodiments envision a reduction in dead space of a facemask when worn by a patient to improve oxygen efficiency used by the patient.

A patient interface is disclosed which is comfortable for the user to wear and includes at least in part a moisture permeable or breathable area in the body of the patient interface. In another embodiment the patient interface is a strapless mask that is moulded to fit the contours of a user's face and maximise the mask-to-skin seal. An adhesive material is bonded to the mask cushion and is stamped in place to form substantially the same shape as the cushion such that it fits the facial contours of the user.

A tubing assembly for use with a patient interface device includes a manifold portion structured to be coupled to a conduit carrying a flow of breathing gas and a number of tubular portions. Each tubular portion extends from the manifold portion to a distal end which is structured to be coupled to the patient interface device. Each tubular portion is structured to communicate the flow of breathing gas from the manifold portion to the patient interface device. Each tubular portion comprises an adjustment element which provides for a characteristic of the tubular portion to be selectively varied.

Device, systems, and methods relating to a mask interface are disclosed. For example, a mask interface may include a body and an interface coupled to the body. The body may include a nasal portion including an opening and a mouth portion including an open channel. The interface may be in contact with a subject’s face and may include a flexible material conformable to the subject’s face.

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 nasal ventilation mask having one or more attachment ports located adjacent to and overlying an upper lip of a patient when worn.

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.

Methods and apparatus for automated detection of an airway device coupled to an automatic rescue breathing unit (ARBU) are disclosed. The automatic detection apparatus includes a keying system that utilizes color adapters coupled to specific airway devices to indicate to a controller that the airway device is a particular size and has a particular airway protection classification (e.g., protected or unprotected). The controller may then determine the proper rescue breath rate and volume (e.g., tidal volume) based on knowing the size and classification of the airway device. In some instances, the controller may also receive information on chest compressions applied to the patient. Automatic detection of the size and classification of the airway device, along with chest compressions, may improve the process of providing automated rescue breaths to a patient.