A connector is described that may be configured to connect between a first tube and a second tube. The connector has an internal component and an external component. The external component has a first end and a second end. The first end has an external taper and an internal coupling face that may be configured to interact with the first tube and the second end may be configured to interact with the second tube. The internal component may be configured to rotate independently to the external component. The external component has a gripping region to aid the user in disconnection of the connector. An attachment mechanism may attach the second tube to the internal component.

A breathing device includes a first and second nasal insert for each nostril of a user. Each insert includes an opening and a valve provided at the opening for selectively restricting or allowing the passage of air through the opening. The breathing device also includes a controller adapted to control each of the valves so that the passage of air is restricted at one of the nasal inserts and allowed at the other.

Systems and methods for providing respiratory therapy are disclosed. The system includes a nebulizer operable to aerosolize a medicament, a cylindrical mixing chamber, an impacting cap and a recirculation tube. The mixing chamber has an inlet port, an outlet port, an aerosol port in fluid communication with the nebulizer, and a drainage port. The inlet port receives a flow of breathing gas. The mixing chamber receives the aerosol via the aerosol port, entrains aerosol into the flow of breathing gas, and delivers the breathing gas entrained with aerosol to the outlet port. The impacting cap receives and coalesces a portion of the aerosol into droplets within the space defined by the mixing chamber and the impacting cap. The mixing chamber is also configured to direct rain-out resulting from the droplets to the drainage port. The system also includes a recirculation tube to return the rain-out to the nebulizer.

A system of breathing arrangements for delivering breathable gas to a patient includes at least first and second cushion components, e.g., full-face, nasal, nasal prongs, nose tip, and/or a combination of any of the above, including a nasal or full-face cushion and nasal prongs/nozzles combination, etc., that are different from one another in at least one aspect, and a common frame assembly configured to support each of the first and second cushion components. Various embodiments are directed to a full-face or nasal mask used with a frame having lateral connector portions having a stiffening member. The mask assembly may include a nose height adjustment device for the height of the cushion, or a cushion adjustment member by which the position of the cushion may be adjusted relative to the frame. The mask assembly may include a chin strap assembly.

An automatic positive airway pressure (AutoPAP) therapy device can be configured such that the minimum and/or maximum pressures deliverable by the device can automatically change. The minimum and/or maximum pressures can change as a function of pressures delivered over the course of the current therapy session and/or over the course of prior therapy sessions. The minimum and/or maximum pressures can also change as a function of the presence, absence, type, severity, or length of sleep disordered breathing events (SDBE) detected by the device over the course of the current therapy session and/or over the course of prior therapy sessions.

A nasal plug includes a first tube having a first wall forming a first lumen of a first diameter. The first tube has a first tube proximal end in a proximal plane and a distal end in a distal plane. The nasal plug further includes a second tube that includes a second wall forming a second lumen of a second diameter, the second diameter smaller than the first diameter. A channel is formed by the second lumen and extends from the first tube proximal end into the first lumen of the first tube. The second tube also includes a flexible wall having a free end within the first lumen. The flexible wall is movable within the first lumen and has a length sufficient to touch a surface of the first lumen and fluidically seal the first lumen between the flexible wall and the surface of the first lumen. The second tube includes a channel proximal end in a channel proximal end plane. The channel proximal end plane is at an angle with respect to the distal plane of the first tube.

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.

A patient interface assembly includes a patient interface configured to deliver breathing gases to the airway of a patient. A headgear is configured to support the patient interface on the head of a patient. The headgear can include a tab on each side configured to overlie the patient's cheek and forming a portion or an entirety of an attachment region for the patient interface. The tab can be angled relative to an adjacent portion of the headgear. In some configurations, the headgear includes a rear portion having a first degree of stretch and/or a front portion having a second degree of stretch. In some configurations, the headgear also includes a chinstrap having a third degree of stretch. In some configurations, the third degree of stretch is greater than the first degree of stretch and the second degree of stretch.

The invention relates to systems for securing a tube (e.g. feeding tube) and/or a patient interface or a dermal patch to a user. One embodiment comprises a holder, an interface side of the holder attachable to the patient interface or the dermal patch for securing a feeding tube to the patient interface or the patch, the holder comprising at least a first channel or recess for receiving the feeding tube to couple the feeding tube to the patient interface. Another embodiment comprises a patient interface itself comprising a backing for positioning on a patient's face, a dermal patch having a patient side and an interface side, the patient side of the patch attachable to the user, the patch comprising at least a first flap portion attachable to the tube for affixing the tube to the patch, a two-part releasable connection arrangement for releasably securing the patient interface to the patch.

A universal respiratory detector for detecting a respiratory gas. The universal respiratory detector may include a plurality of layers with a visual indicator to quickly and reversibly change color to detect a respiratory gas parameter such as carbon dioxide. The color change may be visible from both sides of the detector. In some examples, the respiratory detector may be a biocompatible and conformable sticker for mounting on a person’s face or an oxygen delivery device.