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.

A patient interface assembly includes a frame with a central aperture by which a flow of pressurized breathable gas is introduced in use. The frame includes a wall on a central portion of the frame that surrounds the central aperture. A cushion is removably secured to the frame at the wall surrounding the central aperture and is made of a material that is relatively softer than the frame. A headgear assembly includes a pair of strap portions constructed of a flexible fabric material. A pair of yoke portions is positioned between the strap portions and the frame. Each yoke portion has a proximal end adjacent the frame and a distal end having a connector slot that connects to the respective strap portion of the headgear assembly. The yoke portions have a multilayer construction with one layer being a fabric layer. The yoke portions have a degree of flexibility in one direction and are more resistant to bending in another direction generally orthogonal to the one direction to resist vertical rotation of the patient interface assembly.

A patient interface mask for use with a breathing assistance apparatus includes a seal that, in use, circumscribes a nose, mouth, or nose and mouth of a patient and defines an interior space of the mask. The mask includes an inlet into the interior space and an outlet from the interior space. A sensor is positioned outside of the interior space and in the path of exit gases exiting the interior space through the outlet. The sensor detects a parameter of the exit gases, such as temperature, humidity or both.

A patient interface may include: a plenum chamber having an oral portion and a nasal portion, and a positioning and stabilising structure configured to generate a force to hold the seal-forming structure on the patient's head. The plenum chamber may include: a seal-forming structure constructed and arranged to form a seal with the patient's face, said nasal portion of the seal-forming structure having at least one nasal hole, said oral portion of the seal-forming structure having an oral hole, and a shell having one or more plenum chamber inlet ports sized and structured to receive the flow of air at the therapeutic pressure for breathing by a patient throughout the patient's respiratory cycle in use, and the shell supporting the seal-forming structure.

A nasal assembly for delivering breathable gas to a patient includes a frame having lateral connector, a cushion with a pair of nozzles, and a clip to secure the cushion to the frame. The frame includes a vent channel and a plurality of vent holes. The frame/cushion includes structure (lugs/cut outs) to prevent the assembly of an unvented frame with an unvented cushion, for safety purposes. The frame includes cored portions that interface with corner lugs provided on the cushion. A patient interface includes a frame, a cushion (nasal mask, nasal-oro mask, nozzles, etc.) and a vent assembly including a pattern of vent holes including at least two rows.

This invention relates to a patient interface, such as a nasal cannula, comprising a body to be positioned upon a user (preferably such as a user's face), the body including at least one (and preferably a pair of) nasal prong(s), the or each nasal prong including a lumen capable of being fluidly connected thereto for fluid communication with a supply of breathable gas, the or each nasal prong to be in a configuration either inserted into, or to direct a flow of gas toward, a nare or the nares of the user's nose, wherein the body includes at least one element responsive to force(s) or movement(s), or both, experienced by at least a first region of the patient interface.

A sealing arrangement for forming a seal between a patient's face and a patient interface device for use in delivering a flow of a treatment gas to the patient includes a generally planar substrate body having a first side and an opposite second side. The substrate body includes a main portion having an opening defined therethrough that is sized and configured to encompass the mouth and nose of the patient. The sealing arrangement further includes a first adhesive layer disposed on the first side of the substrate body and a second adhesive layer disposed on the second side of the substrate body. The first adhesive layer is sized and configured to adhere to the skin of the patient with a first adherence force and the second adhesive layer is sized and configured to adhere to a cushion of the patient interface device with a lesser second adherence force.

A breathing apparatus includes a first air pathway for receiving ambient air and channeling the air through a portion of the breathing apparatus, a heating section operatively coupled to the first air pathway and configured to elevate a temperature of the ambient air in the first air pathway to a first prescribed temperature, and a cooling section operatively coupled to the first air pathway and configured to reduce the temperature of the ambient air heated by the heating section to a second prescribed temperature, the second prescribed temperature lower than the first prescribed temperature. A breathing circuit is coupled to the first air pathway and configured to provide the cooled air to a user.

A device for providing a known concentration of blended air and oxygen, or oxygen, to an individual which incorporates a face mask inside a hood, thereby preventing aerosolization of potentially harmful exhaled gases and controlling condensation issues within the hood while under pressurized conditions. The air tight seal required to allow placement and removal of the hood on the individual will be manufactured using injection molded elastomers to over-mold injection molded rigid plastic components.

A patient interface assembly having an improved support for use in securing a patient interface device to the head of a patient overcomes the shortcomings of conventional headgear. The improved support provides a self-adjusting anchor point situated anterior to the ear of the patient that provides enhanced stability in mounting the patient interface device to the patient.