A positioning and stabilising structure comprising at least one gas delivery tube to receive the flow of air from a connection port on top of the patient's head and to deliver the flow of air to the entrance of the patient's airways via the seal-forming structure, the at least one gas delivery tube comprising a tube wall having an extendable concertina structure comprising a plurality of folds in the tube wall alternatingly forming a plurality of ridges and a plurality of grooves, the folds able to be at least partially unfolded to increase a separation of the ridges to elongate the extendable concertina structure; and one or more ridge connecting portions provided to the tube wall, each of the one or more ridge connecting portions connecting two or more adjacent ridges of the plurality of ridges and being configured to resist the separation of the ridges.

A positioning and stabilising structure comprising at least one gas delivery tube to receive the flow of air from a connection port on top of the patient's head and to deliver the flow of air to the entrance of the patient's airways via the seal-forming structure, the at least one gas delivery tube comprising a tube wall having an extendable concertina structure comprising a plurality of folds in the tube wall alternatingly forming a plurality of ridges and a plurality of grooves, the folds able to be at least partially unfolded to increase a separation of the ridges to elongate the extendable concertina structure; and one or more ridge connecting portions provided to the tube wall, each of the one or more ridge connecting portions connecting two or more adjacent ridges of the plurality of ridges and being configured to resist the separation of the ridges.

The present invention relates to a sleep-inducing system using carbon dioxide. The sleep-inducing system includes a mixed gas generation unit which generates a mixed gas of which a carbon dioxide concentration is within a preset range by mixing provided carbon dioxide and air, an emission unit which sprays the mixed gas from a position spaced apart from a user's face, a concentration sensing sensor which measures the carbon dioxide concentration of the sprayed mixed gas, and a control unit which controls the carbon dioxide concentration of the mixed gas generated by the mixed gas generation unit to be within the preset range on the basis of the measured carbon dioxide concentration.

A patient interface may include a plenum chamber pressurisable to a therapeutic pressure; a seal-forming structure constructed and arranged to form a seal with a region of the patient's face; a positioning and stabilising structure to provide an elastic force to hold the seal-forming structure on the patient's head, the positioning and stabilising structure may include a tie; a vent structure; a decoupling structure configured to provide a fluid connection between the plenum chamber and an air circuit for the flow of air at the therapeutic pressure for breathing by the patient; and a frame having at least one tie attachment structure to receive the tie, wherein the frame is configured to be resiliently movable in any direction having at least one of a component parallel to the patient's sagittal plane, a component parallel to the patient's coronal plane, a component parallel to the patient's Frankfort horizontal plane.

A patient interface may include a plenum chamber pressurisable to a therapeutic pressure; a seal-forming structure constructed and arranged to form a seal with a region of the patient's face; a positioning and stabilising structure to provide an elastic force to hold the seal-forming structure on the patient's head, the positioning and stabilising structure may include a tie; a vent structure; a decoupling structure configured to provide a fluid connection between the plenum chamber and an air circuit for the flow of air at the therapeutic pressure for breathing by the patient; and a frame having at least one tie attachment structure to receive the tie, wherein the frame is configured to be resiliently movable in any direction having at least one of a component parallel to the patient's sagittal plane, a component parallel to the patient's coronal plane, a component parallel to the patient's Frankfort horizontal plane.

Gas recirculation systems for use in endoscopic surgical procedures including a gas recirculation pump are disclosed. The gas recirculation pump may work in conjunction with an insufflator used to inflate a patient's peritoneal cavity during surgery. The gas recirculation system may recirculate a flow of gas from and to the patient, based on a detected amount of smoke in the gas, while filtering particulate matter out of the gas and while maintaining an adequate moisture content in the gas. A controller may adjust the speed of a pump motor based on the detected amount of smoke, and may also open a suction exhaust path to vent gas and smoke if the amount of smoke detected exceeds a threshold.

A respiratory mask includes a frame and a cushion module. The frame can include a front wall having a vent and/or a gas inlet opening and a collar extending away from the front wall. The collar surrounds the vent and/or the gas inlet opening. The cushion module comprises a cushion and a housing, which is made of a material more rigid than the cushion. The housing defines a connection opening. A friction coupling selectively couples the cushion module to the frame and comprises an elastomeric friction member coupled to a portion of the housing that defines the connection opening. In some arrangements, an outer surface of the friction member is exposed when the cushion module is coupled to the frame. In some arrangements, the housing extends through the peripheral surface.

A respiratory mask includes a frame and a cushion module. The frame can include a front wall having a vent and/or a gas inlet opening and a collar extending away from the front wall. The collar surrounds the vent and/or the gas inlet opening. The cushion module comprises a cushion and a housing, which is made of a material more rigid than the cushion. The housing defines a connection opening. A friction coupling selectively couples the cushion module to the frame and comprises an elastomeric friction member coupled to a portion of the housing that defines the connection opening. In some arrangements, an outer surface of the friction member is exposed when the cushion module is coupled to the frame. In some arrangements, the housing extends through the peripheral surface.

The invention relates to a connection member configured to connect an air circuit to a patient interface to convey a flow of pressurised breathable gas. The connection member comprises: first and second tube portions configured to connect to a patient interface and air circuit respectively; an anti-asphyxia valve (AAV); and a vent for venting gas exhaled by the patient to the ambient air. The vent is formed between the first and second tube portions. The first tube portion may have a substantially straight first longitudinal central axis and the second tube portion may have a substantially straight second longitudinal central axis that is substantially straight, the first tube portion and the second tube portion being arranged with the first longitudinal central axis substantially parallel to the second longitudinal central axis. The AAV is located in a position on the connection member closer to the patient interface than the vent.

The invention relates to a connection member configured to connect an air circuit to a patient interface to convey a flow of pressurised breathable gas. The connection member comprises: first and second tube portions configured to connect to a patient interface and air circuit respectively; an anti-asphyxia valve (AAV); and a vent for venting gas exhaled by the patient to the ambient air. The vent is formed between the first and second tube portions. The first tube portion may have a substantially straight first longitudinal central axis and the second tube portion may have a substantially straight second longitudinal central axis that is substantially straight, the first tube portion and the second tube portion being arranged with the first longitudinal central axis substantially parallel to the second longitudinal central axis. The AAV is located in a position on the connection member closer to the patient interface than the vent.