Abstract: A system for delivering a pressurized flow of breathable gas to a patient includes a patient interface and a flow generator mounted on the patient interface. The patient interface is configured to contact the patient's head and includes a frame and a cushion supported by the frame and configured to sealingly connect the patient interface to the patient's face and form a chamber between the frame and the patient's face. An inlet port in the frame is configured to receive the pressurized flow of breathable gas. The flow generator is configured to generate the pressurized flow and is capable of creating a pressure of about 2-40 cm H2O in the chamber. In addition, a pressure sensor assembly spans from an outlet port of the flow generator to the inlet port of the patient interface.

Abstract: A water reservoir includes a reservoir base configured to hold a predetermined maximum volume of water to be used for humidification of pressurized breathable air, a reservoir lid pivotally connected to the reservoir base to allow the water reservoir to be movable between an open position and a closed position, the reservoir lid comprising an inlet and an outlet, and a seal configured to sealingly engage the reservoir lid and the reservoir base when the water reservoir is in the closed position, wherein the reservoir base includes an overfill protection element having an egress path for water at a predetermined location.

Abstract: A patient interface comprises a support structure and a seal-forming structure. The support structure is arranged to support the sealing portion and is configured to connect to the frame. The sealing portion comprises textile and is attached to the support structure along an outer perimeter of the sealing portion such that in use the sealing portion may be in tension due to reactive stress of the support structure and/or a resilient stretch characteristic of the textile such that the sealing portion exerts a force against the patient's face.

Abstract: A humidifier tub includes a first side having an air inlet opening configured to receive the pressurized flow of respiratory gas. A second side opposes the first side. An air outlet opening is configured to discharge the pressurized flow of respiratory gas with added humidity. An inlet passage extends from the air inlet opening toward the second side so that the pressurized flow of respiratory gas travels through the inlet passage in a first direction. A guidance structure is located between the first and second sides and positioned so that a traveling direction of the pressurized flow of respiratory gas changes from the first direction to a second direction upon the pressurized flow of respiratory gas engaging the guidance structure. The guidance structure extends downward from a lid. In addition, the first direction is a lateral direction and the second direction is a downward direction.

Abstract: A head-mounted display system includes a head-mounted display unit and a positioning and stabilising structure structured and arranged to hold the head-mounted display unit in an operational position over a user's face in use. The positioning and stabilising structure includes a rear support structure adapted to contact posterior regions of a user's head and a forehead support connector, which includes a forehead support strap, which extends generally along and in the direction of the sagittal plane and connects the rear support structure to a superior edge region of the head-mounted display unit. The forehead support connector further includes a forehead support rigidiser that provides rigidification to a portion of the forehead support connector.

Abstract: A flow regulating valve for a respiratory treatment system is disclosed, as well as a vent arrangement comprising the flow regulating valve. The flow regulating valve may include an inlet, an outlet, and a variable conduit in fluid communication with the inlet and the outlet. The variable conduit may include a movable portion that may move to vary an impedance of the variable conduit, thereby regulating a flow rate of the air travelling through the variable conduit. Advantageously, the flow regulating valve may thus reduce wastage of air (e.g. humidified air) that is exhausted from a respiratory treatment system, while maintaining sufficient washout of air.

Abstract: A patient interface assembly includes an elastomeric piece configured to receive a flow of pressurized respiratory gas and sealingly engage the patient's face. The elastomeric piece forms a plenum and includes a mouth sealing portion, a nasal sealing portion, and an anterior surface with an air inlet opening configured to be coupled to a connector and/or an air delivery tube. The patient interface assembly also includes a stiffening structure that is attached to the anterior surface of the elastomeric piece. The stiffening structure comprises a central aperture that is sized so that the air inlet opening and a portion of the anterior surface surrounding the air inlet opening remain exposed through the central aperture. The stiffening structure is configured so that the entirety of the stiffening structure is inferior to the patient's nose in use.

Abstract: A server is provided and is programmed to automatically determine, based on the identification data that uniquely identifies a patient device, whether there is an upgrade to the code or data (e.g., software or firmware) stored in the electronic memory of the patient device that can be applied thereto. In response to determination that there is an upgrade that can be applied, a data package is delivered to the patient device via the first wireless transceiver, the data package to be automatically applied to the electronic memory of the patient device.

Abstract: The present technology relates to a tub for a humidifier comprising a container made of a first material, a heating element, and a lining made of a second, preferably biocompatible, material different from the first material, wherein the container comprises a base and a side wall defining a reservoir for a supply of liquid to be evaporated, the heating element is provided on the base of the container, and the lining covers the heating element and a substantial portion of the inner surface of the side wall of the container.

Abstract: Apparatus for generating a supply of air at positive pressure for the amelioration or treatment of a respiratory disorder includes a first chamber, a second chamber, at least one inlet tube structured and configured to allow ambient air to enter the first chamber, at least one flow tube structured and configured to allow air to pass from the first chamber to the second chamber, and a blower structured and configured to produce a flow of air at positive pressure. The blower is positioned in the first chamber and structured and configured to receive air from the second chamber. The blower includes a housing structured and configured to sealingly separate air flow through an interior of the housing from the first chamber. The at least one inlet tube is axially spaced from the at least one flow tube.

Abstract: A headgear or headgear segments are manufactured to shape thereby producing little or no waste material. Techniques such as knitting, braiding, crocheting, and 3D printing can be used produce the headgear.

Abstract: A personal entertainment respiratory apparatus provides air to a user to provide a fully immersive entertainment experience. The personal entertainment system may comprise a flow generator for providing the flow of air. A personal spatial respiratory interface may be coupled to the flow generator. The personal spatial respiratory interface may comprise an outlet for the flow generator. The personal spatial respiratory interface may further be configured to direct the flow of air within an ambient breathing proximity of a user. The personal entertainment respiratory apparatus may further comprise a controller and a sensory particle dispenser. The controller and sensory particle dispenser may be configured to selectively activate release of a sensory particle from the dispenser into the directed flow of air in response to an entertainment triggering signal.

Abstract: A positive airway device is configured to deliver a pressurized flow of humidified respiratory gas to a patient's airways and includes a flow generator with a blower portion and a docking portion laterally adjacent to the blower portion. The docking portion is separated from the blower portion by a divider and comprises a cavity configured to laterally receive a humidifier tub. The humidifier tub comprises a first tub subsection with an air inlet opening and an air outlet opening and a second tub subsection. A flange extending outwardly from an outer surface of the humidifier tub forms a transition between the first and second tub subsections. The humidifier tub is configured so that when the humidifier tub is fully received by the docking portion, the first tub subsection is enclosed within the cavity and the second tub subsection remains outside the cavity.

Abstract: A gas-washout vent includes a housing with a first wall with one or more passages through the wall configured to provide fluid communication with a portion of the patient interface system exposed to a therapy pressure. The passages include respective first openings on a first surface of the first wall. The housing at least partially defines a second opening in communication with ambient atmosphere. A diffusing material is located at least partially within the housing to be adjacent the first surface. A surface of the diffusing material facing the first surface is spaced away from the first surface by a gap that extends to provide a fluid communication between all of the first openings and between all of the first openings and the second opening. The housing is configured so that air is prevented from flowing out of the housing at all areas directly opposite each of the first openings.

Abstract: An impeller for use in a centrifugal blower, the impeller includes a hub defining an axis of rotation for the impeller; a plurality of inclined blades, the plurality of inclined blades extending away from the hub; and a plurality of reverse inclined blades, the plurality of reverse inclined blades extending away from the hub. Each of the plurality of inclined blades are joined to an adjacent inclined blade at least in part by a reverse inclined blade.

Abstract: A patient interface including a seal-forming structure with a textile membrane that has at least one hole such that the flow of air at a therapeutic pressure is delivered to at least an entrance to the patient's nares and/or an entrance to the patient's mouth. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in a cavity of a plenum chamber throughout the patient's respiratory cycle, in use. The textile membrane includes a first portion that is held in a relaxed state and a second portion that is held in a taut state. The taut state of the second portion is configured to allow the seal-forming structure to include a three-dimensional shape that has multiple curvatures.

Abstract: An apparatus for generating and providing a pressurized breathable gas to a patient's airways includes a respiratory pressure therapy (RPT) device having an engagement port pneumatically and electrically coupled to the RPT device, and an air delivery tube configured to engage the engagement port so as to pass a flow of breathable gas to a patient interface. The air delivery tube includes electric contacts associated with a heating and/or a sensing arrangement. The air delivery tube includes a locking collar rotatably movable between (1) an unlocked position to allow connection/disconnection of the air delivery tube to/from the engagement port, and (2) a locked position to releasably lock the air delivery tube to the engagement port. The air delivery tube is structured and arranged to, when the locking collar is rotated into the locked position, pneumatically connect to the engagement port and define an operational configuration of the apparatus.

Abstract: A patient interface to deliver of a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways including at least the entrance of a patient's nares while the patient is sleeping, to ameliorate sleep disordered breathing, includes a seal-forming structure, a positioning and stabilising structure, and a connector assembly adapted to connect to an air circuit. The connector assembly includes a ring member configured to be removably and releasably secured in the patient interface and an elbow assembly configured to connect to the air circuit. The elbow assembly is repeatedly connectable to and disconnectable from the ring member. The elbow assembly includes an elbow member and a clip member that includes a separate and distinct structure from the elbow member, and the clip member is configured and arranged to connect to the elbow member.

Abstract: A cushion/frame assembly for a patient interface includes a cushion frame and a cushion. The cushion frame includes a cushion frame material, an annular wall portion having an opening that extends along a cushion frame longitudinal axis, and a projection extending radially with respect to the opening. The cushion frame is configured to snap fit with an outer frame having headgear attachment points and being configured to engage an inlet conduit. The cushion is connected to the cushion frame. The cushion is structured to form a seal with the patient and includes a cushion material that is more flexible than the cushion frame material.