Abstract: The present invention relates to a member (14, 24, 26) of a patient interface (10) for providing a flow of breath-able gas to a self-ventilating patient (12). The member (14, 24, 26) includes a wear-out indicator (32) for indicating a wear-out of the member (14, 24, 26) to the patient (12). The wear-out indicator (32) includes an elastic structure (34) that appears in a first colour in an unstressed condition and is configured to re-versibly change its apparent colour when being stretched and re-turned to its unstressed condition again. The elastic structure (34) is configured to indicate a wear-out of the member (14, 24, 26) by appearing in a second colour in its unstressed condition when the structure (34) has lost at least a part of its elasticity, wherein the second colour is different from the first colour.

Abstract: A back strap for a patient interface device having a headgear component including a first strap member and a second strap member attached to the first strap member and structured to wraparound a back of the patient's head. The back strap member includes a first portion having a first attachment mechanism structured to couple the first portion to the second strap member, a connecting portion extending from the first portion, and a second portion having a second attachment mechanism structured to couple the second portion to at least one of the first strap member, a patient sealing assembly, or skin, hair, neck or clothing of the patient in a manner wherein the back strap member is configured to hold the second strap member and prevent it from riding up on a head of the patient during use.

Abstract: A respiratory interface device is provided. The respiratory interface device includes a patient interface device, a patient circuit, and a pressure generating assembly. Pressure generating assembly includes a first pressure generating device and a second pressure generating device. Patient circuit includes a reduced conduit.

Abstract: A cushion member (10) is for use in a pressure support system (2) for delivering a flow of breathing gas to an airway of a patient. The cushion member includes an annular body (12) comprising a first end (14) and a second end (16) disposed opposite the first end, the body defining a passage (18) therethrough; a sealing portion (20) extending from the second end of the body into the passage, the sealing portion having an outer surface (21) structured to sealingly engage about the airway of the patient and an inner surface (23) disposed opposite the outer surface; and a support portion (22,24) extending from the second end of the body into the passage and terminating at a distal end (26,28). The distal end of the support portion engages a portion of the body at or about the second end.

Abstract: A cushion member (10) for use in a pressure support system (2) for delivering a flow of breathing gas to an airway of a patient, the cushion member comprising:—a body portion (12) comprising a first end (14) and a second end (16) disposed opposite the first end, the body portion defining a passage (18) therethrough; and—a sealing portion (20) structured to sealingly engage about the airway of the patient, the sealing portion extending radially inwardly from the first end to an edge portion (22), the sealing portion having a notched portion (30) defined therein which extends outward from the edge portion.

Abstract: A pressure support device for providing pressure support therapy to a patient includes an airflow generator structured to generate pressure to provide pressure compensation to the patient via a patient circuit, one or more sensors structured to gather data related to effectiveness of the pressure compensation, and a processing unit structured to analyze outputs of the sensors while pressure support therapy is provided to the patient to determine if the pressure compensation provided to the patient is improper and to initiate action to confirm whether components of the patient circuit have been changed in response to determining that the pressure compensation provided to the patient is improper.

Abstract: A patient interface device that overcomes the shortcomings of conventional patient interface devices is provided. One embodiment of the patient interface device provides a cushion for a patient interface device that includes a first end portion structured to contact a portion of a patient's face. The first end portion includes an inner, first surface, an outer, second surface and at least one pocket disposed between the first end portion first surface and the first end portion second surface.

Abstract: A component—such as a respitratory mask—for use in a user circuit for delivering a flow of a treatment gas to the airway of a patient includes a housing. The housing includes an exterior portion having a number of exterior surfaces positioned to be exposed to a surrounding environment. The housing further includes an interior portion having a number of interior surfaces (30) defining a passageway through the housing. The exterior portion has a first heat capacity and the interior portion has a second heat capacity which is less than the first heat capacity.

Abstract: A method of obtaining a 3D scan of a patient's face includes receiving a request for a 3D scanner from the patient, sending the 3D scanner to the patient, receiving the 3D scan of the patient's face obtained from the 3D scanner from the patient, receiving the 3D scanner from the patient, and using the 3D scan of the patient's face to make, select, or customize a patient interface device for the patient.

Abstract: A method of improving delivery of a pressure support therapy provided by a pressure support device to a patient via a patient interface device includes begins by receiving current data regarding details of one or more of the patient and the delivery of the pressure support therapy. The current data is then compared to stored data. If a change is determined between the current data and the stored data which is indicative of a poor mask fitment, an indication is provided of a need for a new patient interface device fitting for the patient.

Abstract: A method of determining facial metrics of a person includes: receiving a request that the person requires a mask; navigating an autonomously operable vehicle to the person using at least one imaging device; capturing a number of images of the person using the at least one imaging device; and determining facial metrics of the person from the number of images. The method may be further employed in a method for identifying a mask for the person which further includes determining a mask for the user from the facial metrics; and identifying the mask to the person.

Abstract: A method of determining facial metrics of a patient includes: capturing a first image of the patient with an image capturing device positioned in a first known position with the assistance of a positioning device, capturing a second image of the patient with the image capturing device positioned in a second known position different that the first known position with the assistance of the positioning device, and determining facial metrics of the patient by analyzing the first image and the second image.

Abstract: An apparatus for use with an electronic device in capturing facial metrics of a user of the electronic device, wherein the electronic device has a front facing camera facing the user and a rear facing camera facing away from the user. The apparatus includes a frame structured to be coupled to the electronic device and a number of reflective surfaces mounted to the frame. The number of reflective surfaces are positioned and structured such that the front facing camera may capture a first image of the user and the rear facing camera may capture a second image of the user simultaneously with the first image.

Abstract: A sealing arrangement (20) for use in a patient interface device (18). The assembly includes a flexible member (30) having a sealing surface (30A) structured to engage a surface of the patient at or about the airway, a first magnetic material disposed in or on the flexible member, and a second magnetic material (36) positioned in one or more of a carrier member structured to be removably positioned on, in, or about the patient, and a portion of the patient interface device. The first and second magnetic materials are positioned and structured to magnetically interact in a manner which urges the sealing surface toward the surface of the patient when the flexible member is disposed at or about the airway and the second magnetic material is disposed at a corresponding position.

Abstract: A cushion is for use in a pressure support system for delivering a flow of breathing gas to an airway of a patient. The cushion includes a body having a first end and a second end located opposite the first end. The body defines a space therein. The cushion further includes a sealing portion defining a single opening into the space. The single opening is adapted to surround both a first nostril and a second nostril of a patient. The sealing portion is located between the first end and the second end. The sealing portion includes a first protruding portion and a second protruding portion each extending outwardly from the body and being adapted to sealingly engage against an interior surface of a corresponding one of the first nostril and the second nostril.

Abstract: A coupling for use in a system (2) for communicating a flow of gas from a pressure generating device (4) to an airway of a patient includes a first portion (16, 16?, 16?) adapted to be coupled in fluid communication with the pressure generating device and a second portion (10) selectively coupled to the first portion. The second portion is adapted to be coupled in fluid communication with the airway of the patient. At least one of the first portion and the second portion includes an illuminated portion (18, 20), the illuminated portion being adapted to be visible to a patient when the first and second portions are uncoupled and adapted to be not visible to a user when the first and second portions are coupled. The illuminated portion assists a user in locating and recoupling the first and second portions of the coupling in a darkened room.

Abstract: A respiratory interface device is provided. The respiratory interface device includes a cushion structured to be coupled to a faceplate that includes a peripheral end and a coupling assembly. The faceplate peripheral end includes a formable material and a portion of faceplate peripheral end is a customized contoured end. Cushion is coupled to faceplate adjacent faceplate customized contoured end, cushion conforming to faceplate customized contoured end.

Abstract: A cushion assembly (16) for use in a patient interface device (10) includes a cushion member having a sealing flap (24) adapted to sealing engage a user's face about at least one of an oral orifice or nasal orifices of the user. The cushion member defines a cavity (30) therein accessible via an opening generally defined by the sealing flap. The cushion assembly further includes a stabilizing member (16b) having a first end and an opposite second end, the first end and the second end being selectively coupled to the sealing flap such that the stabilizing member spans across at least a portion of the opening.

Abstract: A pressure support system includes a gas flow generator; a patient interface device structured to be secured to a patient; a gas delivery conduit structured to couple the gas flow generator to the patient interface device; and a passive noise system provided on at least one of the gas flow generator, the patient interface device, and the gas delivery conduit, the passive noise system being structured to utilize a flow of gas to alter a base audible output of the pressure support system.

Abstract: A patient interface device is for use in a pressure support system delivering a flow of breathing gas to an airway of a patient. The patient interface device includes a sealing apparatus having a cushion structured to sealingly engage about the airway of the patient and defining a passage therethrough which is structured to receive the flow of breathing gas. A first magnetic material is coupled to the cushion, and a second magnetic material coupled to the cushion or another element of the sealing apparatus. The second magnetic material and the first magnetic material are configured such that there is a repulsive magnetic force therebetween. The coupling of the first magnetic material and the second magnetic material provides an adjustable coupling that provides selective adjustment of the magnitude of the repulsive magnetic force.