A breathing arrangement includes a patient interface, at least one inlet conduit, and a headgear assembly. The patient interface includes a mouth covering assembly including a cushion structured to sealingly engage around exterior of a patient's mouth in use, a nozzle assembly including a pair of nozzles structured to sealingly engage within nasal passages of a patient's nose in use, and a flexible element connecting the mouth covering assembly and the nozzle assembly. The at least one inlet conduit is structured to deliver breathable gas into at least one of the mouth covering assembly and the nozzle assembly for breathing by the patient. The headgear assembly is removably connected to at least one of the mouth covering assembly and the nozzle assembly so as to maintain the mouth covering assembly and the nozzle assembly in a desired position on the patient's face.

The present disclosure describes a pressure support therapy device valve that enables a subject to safely supplement therapy pressure support with low flow oxygen while using a heated (or non-heated) tube. The valve conducts a pressurized flow of breathable gas and the low flow oxygen to the heated tube. The valve includes electrical components configured to pass power from the pressure support therapy device to the heated tube, and a plunger biased to close a flow path from the pressure support therapy device when a pressurized flow of breathable gas is not provided (or is below a predetermined pressure threshold). Closing the flow path stops oxygen gas from flowing back through the valve toward the pressurized gas source.

A respiratory treatment device includes a housing, an inlet configured to receive air into the housing, an outlet configured to permit air to exit the housing, and a flow path defined between the inlet and the outlet. A restrictor member positioned along the flow path that is configured to move between a closed position, where the flow of air along the flow path is restricted, and an open position, where the flow of air along the flow path is less restricted. A vane in communication with the flow path rotatable in response to the flow of air along the flow path is configured to move the restrictor member between the closed position and the open position. A protrusion extends in to the housing to limit movement of the restrictor member from the closed position to the open position.

A patient interface includes a plenum chamber, a seal-forming structure, and a positioning and stabilising structure to provide a force to hold the seal-forming structure in a therapeutically effective position on a patient's head. The positioning and stabilizing structure includes a superior strap portion, an inferior strap portion, and a posterior connecting strap portion connected to or formed integrally with the superior strap portion and the inferior strap portion. The posterior connecting strap portion is constructed from a mesh material that is different than the material used to construct the superior strap portion and the inferior strap portion. The posterior connecting strap portion has a greater stretch capability than the superior strap portion and a lesser stretch capability than the inferior strap portion. The stretch capabilities allow the positioning and stabilizing structure to be removable from the patient's head when the loop engages the connection portion.

A patient interface comprises a seal-forming structure including a textile membrane and a support structure to support the textile membrane. The seal-forming structure may have a varying construction in order to accommodate different regions and the varying contours of the patients face to ensure a robust and comfortable seal. An air impermeable layer of the textile membrane may have a thickness that varies in different portions of the textile membrane and/or different regions of the cushion assembly. Further, the seal-forming structure may include an underlying cushion, and an arrangement of the textile membrane and the underlying cushion and/or the configuration of the underlying cushion may vary in different regions of the cushion assembly to optimize patient comfort and the effectiveness of the seal in different regions of the patients face.

A patient interface including a seal-forming structure having a mouth portion that forms at least part of the mouth plenum and is configured to seal around the patient's mouth and a nasal portion that is configured to seal with the patient's nares. The nasal portion includes a nasal plenum positioned to receive pressurized gas from the mouth plenum. The seal-forming structure also includes a clip configured to connect the mouth plenum to the nasal plenum and act as a conduit for the flow of the pressurized gas from the mouth plenum to the nasal plenum. The clip includes a mouth portion end configured to engage the mouth portion, a nasal portion end configured to engage the nasal portion, and a pair of wings protruding from the nasal portion end into an interior of the nasal plenum so that the wings engage an interior surface of the nasal plenum.

Methods and systems are provided for delivering anesthetic agent to a patient. In one embodiment, an anesthetic vaporizer includes a sump configured to hold a liquid anesthetic agent; an ultrasonic transducer coupled to a bottom of the sump and at least partially disposed within the sump; a vaporizing chamber fluidically coupled to the sump; and a heating element coupled to the vaporizing chamber and configured to increase a temperature of a surface disposed within the vaporizing chamber.

An aspect provides a ventilation manifold for a ventilator, the manifold comprising a fluid flow path, the flow path comprising: bifurcated end paths, a constriction path and a compressed breathable gas chamber fluidly coupled to a compressed breathable gas source, the manifold having a manifold axis defined by the constriction path; a source path of the bifurcated ends coupled to an outlet conduit for a ventilator to present the compressed breathable gas at a source angle to one side of the manifold axis; and a vent path at a vent angle to the manifold axis for an exhaust flow, the vent path acting to provide a fluid pressure valve upon an inlet compressed breathable gas from the constriction path to urge flow towards the source path and a by-pass for returned outlet spent gas flow from the source path against the inlet compressed breathable gas at the constriction path, the fluid pressure valve and the by-pass dependent upon the relative magnitudes of the source angle and the vent angle to the manifold axis and/or each other along with the configuration of the constriction path and/or the configuration of the source path and/or the vent path.

The present invention is generally related to a device and method for sanitizing a medical instrument with ozone, in particular the invention relates to a system, method and a device for sanitizing a continuous positive airway pressure (CPAP) device. The device has an ozone compartment, an ozone operating system and one or more ozone distribution lines that distribute ozone to a continuous positive airway pressure device. The device may further include a heater adapter unit to connect heating systems in CPAP devices while distributing ozone to sanitize the CPAP device in accordance with the present invention.

A tracheal tube (e.g., an endotracheal tube) includes an inserting cannula (that may be able to swivel), and wherein the inserting cannula is connected to an elbow adaptor through a Bayonet Neill-Concelman (BNC) connection. The BNC connection may provide more secure connection of the corresponding components and may be able to withstand greater amounts of force exerted on them without becoming detached from each other. The elbow adapter may further be coupled to a pressure release valve that will alleviate pressure buildup within the tracheal tube.