A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways includes a frame member, a cushion assembly provided to the frame member, and an anterior wall member repeatedly engageable with and disengageable from the cushion assembly. The frame member includes connectors operatively attachable to a positioning and stabilizing structure. The cushion assembly includes a seal-forming structure and a void defined by an anterior surface of the cushion assembly. The anterior wall member has a predetermined surface area to seal the void of the cushion assembly and form a gas chamber when the anterior wall member and the cushion assembly are engaged. The void of the cushion assembly is sized such that the patient's nose and/or mouth is substantially exposed when the anterior wall member is disengaged from the cushion assembly thereby improving breathing comfort of the patient.

A ventilator includes a bidirectional breath detection airline and a flow outlet airline. The flow outlet airline includes an airline outlet. The flow outlet airline is configured to be connected to an invasive ventilator circuit or a noninvasive ventilator circuit. The breath detection airline includes airline inlet. The airline inlet is separated from the airline outlet of the flow outlet airline. The ventilator further includes a pressure sensor in direct fluid communication with the breath detection airline. The pressure sensor is configured to measure breathing pressure from the user and generate sensor data indicative of breathing by the user. The ventilator further includes a controller in electronic communication with the pressure sensor. The controller is programmed to detect the breathing by the user based on the sensor data received from the pressure sensor.

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 of the plenum chamber insert and a patient-distal side of the plenum chamber insert via the radial channel during use.

An adapter (1) for establishes a flow channel (2) between a breathing gas supply and a patient connection piece. A set (20) and a system (30) for ventilation or respiratory support, each include the adapter (1). The adapter (1) includes a first connection structure (3) configured to connect to the breathing gas supply and a second connection structure (4) configured to connect to a patient connection piece. A bypass channel (5) branches off from the flow channel (2) and is provided with an extraction opening (7) which can be closed at least temporarily by a safety valve (6). The safety valve (6) is configured such that the extraction opening (7) is closed when a ventilation pressure prevailing in the flow channel (2) is lower than a pressure prevailing on a side of the safety valve facing away from the flow channel (2).

An adjustable tracheostoma valve is disclosed. The adjustable tracheostoma valve includes a passageway for connecting the trachea with the surroundings. A valve disk is provided in the passageway. The disk is moveable to allow for inhalation and exhalation through the passageway and is configured to close in response to pressure to direct air to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx.

A patient interface for sealed delivery of a flow of air to ameliorate sleep disordered breathing may include: a seal-forming structure to form a pneumatic seal with the entrance to the patient's airways; a positioning and stabilising structure to maintain the seal-forming structure in sealing contact with an area surrounding the entrance to the patient's airways; a plenum chamber pressurised at a pressure above ambient pressure in use; a connection port for the delivery of the flow of breathable gas into the patient interface; and a device positioned within a breathing chamber defined, at least in part, by the seal-forming structure and the plenum chamber, wherein the device divides the breathing chamber into a posterior chamber and an anterior chamber, and wherein the device comprises a plurality of apertures such that turbulence of the air in the posterior chamber is less than turbulence in the air in the anterior chamber.

A sedation device (1) has a housing (2) having a ventilator chamber (3) and an associated patient chamber (4) in communication with the ventilator chamber (3). A filter (5) is mounted between the ventilator chamber (3) and the patient chamber (4) and forms a common gas-permeable dividing wall between the ventilator chamber (3) and the patient chamber (4). An inlet port (6) is provided on the ventilator chamber (3) for connection via a Y-piece to a ventilator. An outlet port (9) of the patient chamber (4) connects via a patient breathing tube (10) with a patient. An associated pair of inserts are provided, namely a first insert (14) fixedly mounted in the ventilator chamber (3) and a second insert (15) fixedly mounted in the patient chamber (4). One or both of these inserts (14, 15) are mounted within the housing (2) to vary the internal volume of the housing (2) as required to suit different patients. The inserts (14, 15) are nestably engageable with an inner wall of the housing (2).

A ventilator includes a ventilation body, the ventilation body includes a ventilation cavity and an air inlet end and an air outlet end communicating with the ventilation cavity, the ventilation body further includes an annular shell configured to form the ventilation cavity, the annular shell is formed with an annular cavity inside, an air inlet and an air outlet communicating with the annular cavity are disposed on the annular shell, the air outlet is communicated with the annular cavity and the ventilation cavity, the air outlet has a slit shape extending along a circumferential direction of the annular shell and is disposed to be capable to guide gas flows out towards the air outlet end. The ventilator may greatly increase the ventilation volume and the gas pressure, by using the ventilation body as mentioned above.

Apparatus and methods automate selection of patient interface(s). Image data captured by an image sensor may contain facial feature(s) of a user. The facial features may be captured in association with a predetermined reference feature of known dimension(s) such as with a user interface display that is generated with a sequence of icons that are activated for directing and tracking movement within the interface for desired image capture. The user's facial feature(s) and the reference feature may be detected in the captured image data. The image may be processed to measure an aspect of the detected facial feature(s) based on the reference feature. A patient interface size may be detected from standard patient interface sizes based on a comparison between the measured aspect of the facial feature(s) and a data record relating sizing information of the standard patient interface sizes and the measured aspect of the facial feature(s).

A respiratory delivery system providing a bi-level pressure airflow. The system includes respiratory and pneumatic circuits. The respiratory circuit includes a respiratory gas supply, a patient interface, and a bi-level pressure regulator. The respiratory gas supply supplies a respiratory gas to the patient interface via a first conduit. The bi-level pressure regulator is coupled to the patient interface via a second conduit and is configured to cyclically alternate the respiratory gas passing through the bi-level pressure regulator between a low-pressure level and a high-pressure level. The pneumatic circuit includes a pneumatic gas supply and a pneumatic cycler configured to output a cycling pressure level. The cycler is coupled to the bi-level pressure regulator via a third conduit. The bi-level pressure regulator cyclically alternates the pressure level of the respiratory gas between the low-pressure level and the high-pressure level with the timing defined by the cycling of the pneumatic gas.