A mask system for delivering air pressurized above atmospheric pressure to the airways of a patient to treat sleep disordered breathing (SDB) by continuous positive airway pressure (CPAP) may include a mask having a cushion configured to form a seal with the patient's nose; two inlet conduits, each of the two inlet conduits configured to extend from a position superior to the patient's head and along a corresponding side of the patient's head, and each of the two inlet conduits being in fluid communication with a corresponding side of the mask to deliver pressurized air to the mask; a first vent arrangement configured to be positioned superior to the patient's head in use and configured to discharge gas to atmosphere during therapy; and a second vent arrangement configured to be positioned inferior to the first vent arrangement in use and configured to discharge gas to atmosphere during therapy.

A patient interface for use in delivering a flow of breathable gas to an airway of a patient includes a first seal adapted to contact the patient's face and seal a first space between the patient interface and the patient's face at a first positive pressure; and a second seal adapted to contact the patient's face and seal a second space between the patient interface and the patient's face at a second positive pressure. The first seal also seals the first space from the second space. A leak reducing element may be provided on a seal to reduce and/or diffuse leakage of gas. A vacuum line configured to create a negative pressure may be provided in the second space to remove any gas leaking from the first space to the second space. A seal may be connected to a conduit for delivering the flow of gas that is incorporated into a frame of the patient interface. The seal may be inflatable by the flow of breathable gas to pressurize the seal against the patient's face and include a vent that directs the flow of breathable gas to a space between the patient interface and the patient's face. A cuff may be provided over the seal in the nasal bridge region to direct any leakage of the gas flow from the seal in the nasal bridge region in a direction away from the patient's eyes.

Aspects of the present technology comprise a positioning and stabilising structure to hold a seal-forming structure in a therapeutically effective position on a head of a patient. The seal-forming structure may be constructed and arranged to form a seal with a region of the patients face surrounding an entrance to the patients airways for sealed delivery of a flow of air at a therapeutic pressure of at least 4 cmH2O with respect to ambient air pressure throughout the patients respiratory cycle in use. The positioning and stabilising structure may comprise a front hoop arranged to contact, in use, at least a region of the patients head superior to an otobasion superior of the patients head and a rear strap. The positioning and stabilising structure may comprise an adjustment mechanism for adjustment of the front hoop and the rear strap relative to the patients head, the adjustment mechanism being arranged in a single operation to adjust both the front hoop and rear strap to enable the positioning and stabilising structure to fit different size heads.

A device includes a body defining a respiration passage in fluidic communication with a filter fitting disposed on a first end of the body and a mask fitting disposed on a second end of the body, and a treatment passage in fluidic communication with the mask fitting. A treatment fitting is disposed on the body and is coupleable to a treatment source such that a seal in the treatment fitting transitions from a closed state to an open state to allow fluidic communication between the treatment source and the treatment passage. The device configured to permit (i) inhalation air and/or exhaled breath to be drawn and/or expelled through the filter fitting, the respiration passage, and the mask fitting and (ii) a respiratory therapeutic to be drawn from the treatment source coupled to the treatment fitting, through the treatment passage, and through the mask fitting.

A patient interface includes: a plenum chamber; a seal-forming structure; a positioning and stabilising structure; a plenum chamber insert configured to be positioned and retained within the plenum chamber; and a vent structure; wherein the plenum chamber insert has a plenum chamber insert port; wherein the plenum chamber insert has an exterior surface configured to be positioned adjacent to an interior surface of the plenum chamber; wherein when the plenum chamber insert is positioned and retained within the plenum chamber, a radial channel is formed by the interior surface of the plenum chamber and the exterior surface of the plenum chamber insert such that gas is able to pass between a patient-proximal side plenum chamber insert and a patient-distal side of the plenum chamber insert via the radial channel during use.

Methods and/or apparatus automate setting of a pressure ramp to permit pressure to gradually arrive at a treatment pressure such as in the initial or pre-sleep stages of use of a respiratory therapy pressure device for treatment of a respiratory disorder during sleep (e.g., sleep disordered breathing). In an example, apparatus for treating a respiratory disorder may include a breathable gas pressure generating device. The apparatus may include a controller, including a processor(s). The controller may be configured to collect historic sleep onset parameter(s) concerning timing of a patient falling asleep. The apparatus may determine, based on the historic sleep onset parameter(s), a pre-sleep limit. The apparatus may determine a pre-sleep profile of pressure versus time having a duration spanning the pre-sleep limit and having a plurality of ramping sub-therapeutic pressures. The apparatus may control, upon initiation of treatment, setting of the pressure generating device according to the pre-sleep profile.

A pump interface tubing for use in a peristaltic pump includes a tubular core having an outer surface and a treatment on the outer surface. The treatment reduces static charge buildup on the tubular core during operation of the peristaltic pump, and thereby reduces the noise signal that might otherwise undesirably couple to a signal of interest. Treatments include nitrile layers, heat shrink layers, cotton fiber layers, and anti-static sprays.

A gas washout vent, and a patient interface with the gas washout vent, configured to allow patient-exhaled CO.sub.2 to flow to an exterior of the plenum chamber to minimise rebreathing of exhaled CO.sub.2 by the patient, the gas washout vent including at least one outlet orifice; a diffusing member at least partly covering the outlet orifice; and a blocking member having an air-impermeable material, the blocking member preventing gas exiting from the outlet orifice from flowing straight through the diffusing member.

Device (1) for preventing apnea episodes in infants, which simulates a breathing pattern suitable for synchronizing the infant's breathing and which is provided as a tactile direct stimulus, arranged in contact with the infant's back while sleeping; it comprises a breathing pattern generator means (2) that emits air pulses that reach the infant through transmitter means comprising a flexible conduit (3) that transports the air to an inflatable/deflatable chamber (4).

A ventilation system having a mask, a blowing assembly, and a processor. The mask has a mask body and a pressure sensor operatively associated with the mask body and configured to measure pressure within the mask. The mask body defines an inlet opening and a plurality of leak openings. The blowing assembly is positioned in fluid communication with the inlet opening of the mask body and configured to direct air to the inlet opening of the mask body. The processor is positioned in operative communication with the blowing assembly and the pressure sensor of the mask. The processor is configured to selectively control the blowing assembly based upon at least the measured pressure within the mask.