Abstract: A humidifier heater base assembly has a heater plate with a thermally conductive portion and a perimeter portion around a perimeter of the heater plate. A resilient member has an inner part attached to the perimeter portion and an outer part adapted to provide a resilient perimeter flange around at least part and preferably the whole of the perimeter portion. The resilient member fixes the heater base to the humidifier by the resilient perimeter flange such that the heater plate and the inner part can move relative to the humidifier in a direction substantially transverse to the general plane of the heater plate. At least a portion of the resilient perimeter flange remains stationary relative to the humidifier.

Abstract: An apparatus for oxygenation and/or CO2 clearance of a patient. The apparatus comprising: a flow source or a connection for a flow source for providing a gas flow, a gas flow modulator, a controller to control the gas flow. The controller is operable to: receive input relating to heart activity and/or trachea gas flow of the patient, and control the gas flow modulator to provide a varying gas flow with at least two oscillating components. One oscillating component has a frequency based on the heart activity and/or trachea flow of the patient. One oscillating component has a frequency to: promote bulk gas flow movement, or promote mixing.

Abstract: A gases delivery system for medical use is disclosed that has a container configured to house a metal-organic framework material within at least one section of the container. An activation mechanism may be associated with the container. The metal-organic framework material may contain one or more substances such that the one or more substances may be released from the metal-organic framework material when energy is applied to the container via the activation mechanism. The activation mechanism may be a heating mechanism. One or more containers housing metal-organic framework materials may be used in a gases recirculation system.

Abstract: A catheter mount is configured to be attached to a respiratory apparatus. The catheter mount includes a plurality of ports in fluid communication with each other. The plurality of ports include an interface port configured to connect to an interface tube, a conduit port configured to connect to a conduit tube, and at least one suction port configured to allow insertion of a suction catheter. The at least one suction port can be positioned to allow the suction catheter, when inserted, access to both the interface port and conduit port.

Abstract: A patient interface, including a mask assembly and a headgear assembly, provides improved facial sealing and improved ease of use. The mask assembly includes an inflating or ballooning seal. The seal can be secured between two portions of a snap-fit exoskeleton. The headgear assembly connects to the mask assembly with flexible straps during course fitting and with more rigid straps following course fitting. The straps include holes that fit over a tapering post on the mask assembly.

Abstract: A surgical humidification system includes a source of gas flow and a humidifier that receives the gas flow and outputs a humidified gas to a delivery conduit. The delivery conduit has an outlet and a suitable interface, such as a diffuser, is connected to the outlet. The interface can be positioned near or within an open surgical cavity of a patient to supply the humidified gas to the cavity. The system also includes a pressure relief arrangement that operates to relieve pressure from the system above a normal operating pressure. The pressure relief arrangement can be located in a non-sterile portion of the system, such as upstream from the humidifier, for example.

Abstract: A breathing assistance apparatus and method of controlling a breathing assistance apparatus is disclosed. Particularly, the breathing assistance apparatus is controlled such that it has a drying cycle to enable drying of the tubing that supplies gases to a user and prevent the harbouring of pathogens within the tube. The drying cycle is preferably operated automatically by internal controllers in the apparatus. However, it may be manually activated by pressing a button on the apparatus. The drying cycle is preferably activated at the end of a user's treatment session.

Abstract: A patient interface of a respiratory therapy system is provided, and includes a mask body; a mask seal secured to the mask body and configured to form a seal with the user's face, at least around the user's mouth; the mask body and mask seal being arranged to define an interior breathing chamber of the patient interface; and an inlet to the breathing chamber configured to receive a flow of breathable gases into the breathing chamber. To assist in allowing a user to speak clearly whilst wearing/using the patient interface, a user actuatable speech valve is provided on the patient interface and is operable to selectively occlude and open a speech flow path from the breathing chamber to atmosphere when the user wishes to speak.

Abstract: A respiratory assistance apparatus includes a conduit connecting a flow generator and an outlet. The conduit includes a venture formation. The apparatus further includes an oxygen inlet in fluid communication or selective fluid communication with an oxygen outlet. The oxygen outlet is directed into the conduit and toward a mouth of the venture formation. The flow generator provides a flow path for air to enter the conduit when the flow generator is not operating.

Abstract: A respiratory mask for providing positive pressure therapy having ball jointed elbow, one or more detachable forehead pieces and headgear comprising a spacer fabric region is disclosed herein. The elbow is configured to be removable when oriented to a predetermined position. The forehead pieces are provided in one or more sizes. The spacer fabric region comprises two or more layers wherein the raw edges are turned to the inside of the layers. The seal comprises features that improves seal performance and accommodates a wider variety of facial geometries.

Abstract: A connector is used to connect a gases supply to a user. The user can be fitted with an interface, such as a cannula, while the gases supply can include a conduit. The connector interfaces between the conduit and the interface. The connector has a female assembly and a male assembly that connect together, such as by push fit. The male assembly includes an inner portion sized and configured to mate with a first female connector and an outer portion sized and configured to alternatively mate with a second female connector.

Abstract: A pressure regulating device for use with a breathing assistance and/or resuscitation apparatus, which conveys gases along a gases pathway to a patient, includes a mounting for connecting the pressure regulating device to a first outlet in fluid communication with the gases pathway. The mounting holds a valve member that selectively blocks, at least in part, the first outlet. A control member can be manipulated to adjust a property of the valve member. The valve member at least partially blocks the first outlet when the pressure of gases in the pathway is below a selected level, and allows at least a portion of the gases to flow out of the first outlet when the pressure of said gases is above the selected level. The property includes a selected level of pressure whereby manipulation of the control member adjusts the level of pressure between a maximum level and a minimum level.

Abstract: A respiratory mask includes a frame and a cushion module including a housing and a cushion that seals on a user's face in use. The housing includes a first connector, for example, a female connector, and the frame includes a second connector, for example, a male connector. The first and second connectors are coupled together in use. The housing includes one or more fasteners that secure the male connector to the female connector. Each fastener includes a base portion coupled to the housing and a moveable portion pivotally connected to the base portion. To assemble the mask, the male connector is inserted into the female connector such that the male connector engages the fasteners. Advancement of the male connector into the female connector causes the fasteners to change orientation from a neutral position to a toggled position and compress. The compressed fasteners apply a retention force to the male connector.

Abstract: A respiratory assistance apparatus includes a flow generator and a humidifier. The humidifier includes a humidification chamber. The humidification chamber comprises a water tub that is configured to receive a volume of water. A lid is hingedly coupled to the water tub for enclosing a volume contained within the water tub.

Abstract: A respiratory system includes a first patient interface for delivery of a flow of gases to a patient, a second patient interface for delivery of a second flow of gases to the patient, and a device that switches the system between a first respiratory mode and a second respiratory mode. In the first respiratory mode, the flow of gases are delivered to an outlet of the first patient interface when the second patient interface is absent from the patient. In the second respiratory mode the device reduces or stops delivery of the first flow of gases to the outlet of the first patient interface when the second patient interface is located together with the first patient interface upon the patient.

Abstract: Positive airway pressure (“PAP”) systems and methods are provided which supply a patient with a range of pressures for treatment when the patient is determined to be asleep, and an awake pressure for use when the patient is determined to be awake, the awake pressure configured for the comfort of the patient. The awake pressure is configured to be lower than the lower bound of the pressure range and can be a therapeutic or sub-therapeutic pressure. The PAP systems and methods disclosed herein advantageously allow for the pressure range to be tailored for effective treatment of sleep disordered breathing while allowing the awake pressure to be set for the comfort of the patient. This can advantageously increase both the efficacy of the treatment of SDB and patient compliance with the treatment.

Abstract: A respiratory mask includes a housing and a cushion or seal that seals on a user's face in use. An upper portion of the seal that is disposed on a user's nasal bridge in use can roll toward and/or over the outer surface of the housing to form a rolling bridge feature that adjusts to different nose sizes. As the rolling bridge rolls, an apex of the seal moves away from the user's face to adjust to larger nose sizes. The apex does not move downward and can move upward relative to a location of the apex in a neutral position of the seal.