An oral appliance for the treatment of sleep disorder breathing in a patient has a U shaped appliance body with a front section and two arms. The appliance body has an inner wall and an outer wall, and a web interconnects the inner and outer walls forming an upper dental arch receiving channel. The front section of the body has an air inlet opening for taking in air during inhalation. The oral appliance also has an air outlet member with an air outlet and an air flow passageway connecting the air inlet opening with the air outlet.

The present specification is directed a method manufacturing a patient interface for treatment of sleep disordered breathing using air pressure by delivery of air to a patient's airway. The method includes locating a shell, a first sub section of a seal forming structure, and a first section of the seal forming structure in a tool. The first sub section includes a groove. The first section is constructed from a thermoformable material. The method further includes introducing a moulding material to the tool and overmolding the shell, the first sub section, and the first section. The moulded material forms a second sub section of the seal forming structure that connects the first sub section to the shell and fully encloses the first section within the groove.

Techniques for improved machine learning are provided. A set of two-dimensional images of a user is accessed. A three-dimensional mesh depicting a head of the user is generated based on processing the set of two-dimensional images using a machine learning model, where the three-dimensional mesh is scaled to a size of the head of the user. The three-dimensional mesh is modified to remove one or more facial expressions. A set of facial measurements is determined based on the modified three-dimensional mesh, and a user interface is selected for the user based on the set of facial measurements.

Techniques for improved machine learning are provided. A set of two-dimensional images of a user is accessed. A three-dimensional mesh depicting a head of the user is generated based on processing the set of two-dimensional images using a machine learning model, where the three-dimensional mesh is scaled to a size of the head of the user. The three-dimensional mesh is modified to remove one or more facial expressions. A set of facial measurements is determined based on the modified three-dimensional mesh, and a user interface is selected for the user based on the set of facial measurements.

A system for concentrating oxygen inside a mask with filters is provided. The system comprising a mask body having a contoured shape that fits above the patient's nose and mouth; filters which allow gasses but not contaminants to pass through; a port with detachable cap for gas sampling; an inlet port connected which can be open to room air or attached to standard oxygen tubing or a ventilator circuit. The mask may be worn with or without an oxygen source. The mask body is firmly sealed against the patient's face with the filters functioning to prevent microbial contamination of the environment while concentrating oxygen within the lumen of the mask.

A method of manufacturing a patient interface for sealed delivery of a flow of air at a continuously positive pressure with respect to ambient air pressure to an entrance to the patient's airways includes collecting anthropometric data of a patient's face. Anticipated considerations are identified from the collected anthropometric data during use of the patient interface. The collected anthropometric data is processed to provide a transformed data set based on the anticipated considerations, the transformed data set corresponding to at least one customised patient interface component. At least one patient interface component is modelled based on the transformed data set.

A system for reducing airway obstructions of a patient may include a ventilator, a control unit, a gas delivery circuit with a proximal end in fluid communication with the ventilator and a distal end in fluid communication with a nasal interface, and a nasal interface. The nasal interface may include at least one jet nozzle, and at least one spontaneous respiration sensor in communication with the control unit for detecting a respiration effort pattern and a need for supporting airway patency. The system may be open to ambient. The control unit may determine more than one gas output velocities. The more than one gas output velocities may be synchronized with different parts of a spontaneous breath effort cycle, and a gas output velocity may be determined by a need for supporting airway patency.

A positioning and stabilising structure for a full-face mask of a patient interface comprises a superior strap portion, an inferior strap portion, and two anterior strap portions. Each anterior strap portion having a generally triangular surface with a first width and a second width that is less than the first width and disposed more anterior while in use. The superior strap portion and the inferior strap portion are each connected to or formed integrally with each anterior strap portion at a respective corner of the generally triangular surface. Each anterior strap portion is connected or connectable to a connection portion that engages the plenum chamber. The connection portion is releasably engageable from the plenum chamber. The superior strap portion and the inferior strap portion are joined to the anterior strap portions anterior to the patient's ears, when in use.

A positioning and stabilising structure for a full-face mask of a patient interface comprises a superior strap portion, an inferior strap portion, and two anterior strap portions. Each anterior strap portion having a generally triangular surface with a first width and a second width that is less than the first width and disposed more anterior while in use. The superior strap portion and the inferior strap portion are each connected to or formed integrally with each anterior strap portion at a respective corner of the generally triangular surface. Each anterior strap portion is connected or connectable to a connection portion that engages the plenum chamber. The connection portion is releasably engageable from the plenum chamber. The superior strap portion and the inferior strap portion are joined to the anterior strap portions anterior to the patient's ears, when in use.

The present specification is directed a method manufacturing a patient interface for treatment of sleep disordered breathing using air pressure by delivery of air to a patient's airway. The method includes locating a shell, a first sub section of a seal forming structure, and a first section of the seal forming structure in a tool. The first sub section includes a groove. The first section is constructed from a thermoformable material. The method further includes introducing a moulding material to the tool and overmolding the shell, the first sub section, and the first section. The moulded material forms a second sub section of the seal forming structure that connects the first sub section to the shell and fully encloses the first section within the groove.