Textile patient interface
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 including at least entrance of a patient's nares to ameliorate sleep disordered breathing may include a seal-forming structure comprising a foam undercushion and a textile membrane for contact with the patient's face; a positioning and stabilising structure to maintain the seal-forming structure in sealing contact with an area surrounding an entrance to the patient's airways while maintaining a therapeutic pressure at the entrance to the patient's airways; and a plenum chamber pressurised at a pressure above ambient pressure in use.
1. 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 a patient's airways including at least the patient's nares, wherein the patient interface is configured to maintain a therapy pressure in a range of about 4 cmH2O to about 30 cmH2O above ambient air pressure in use, throughout the patient's respiratory cycle, while the patient is sleeping, to ameliorate sleep disordered breathing, said patient interface comprising:
a seal forming structure comprising:
a foam undercushion; and
an air-impermeable textile membrane configured to contact the patient's face during use, the air impermeable textile membrane having an outer periphery that is joined to the foam undercushion by an airtight bond and an inner portion that lies freely on the foam undercushion such that the inner portion of the air-permeable textile membrane is separable from the foam undercushion by the flow of air in use;
a positioning and stabilizing structure configured to maintain the seal-forming structure in sealing contact with an area of the patient's face surrounding an entrance to the patient's airways while maintaining a therapeutic pressure at the entrance to the patient's airways; and
a plenum chamber configured to be pressurized by the flow of air at a pressure above ambient pressure in use, the plenum chamber being attached to the foam undercushion.
2. The patient interface according to claim 1 , wherein the air-impermeable textile membrane is constructed from a textile material that is coated to be air impermeable.
3. The patient interface according to claim 1 , wherein the seal-forming structure is integrally formed with the positioning and stabilising structure.
4. The patient interface according to claim 1 , further comprising an air delivery tube substantially made from a textile and that is air impermeable.
5. The patient interface according to claim 1 , wherein the foam undercushion includes an outer periphery, the outer periphery of the air-impermeable textile membrane being joined to the outer periphery of the foam undercushion.
6. The patient interface according to claim 5 , wherein the foam undercushion includes an interior surface bounded by the outer periphery of the foam undercushion and the air-impermeable textile membrane includes an interior surface bounded by the outer periphery of the air-impermeable textile membrane and formed on the inner portion, and
wherein the interior surface of the foam undercushion is adjacent to the interior surface of the air-impermeable textile membrane such that the interior surfaces are separable from one another by the flow of air in use while the outer periphery of the air-impermeable textile membrane remains joined to the outer periphery of the foam undercushion.
7. The patient interface according to claim 6 , wherein the air-impermeable textile membrane includes a sealing surface opposite the interior surface of the air-impermeable textile membrane, the sealing surface being configured to contact the patient's face in use.
8. 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 a patient's airways including at least the patient's nares, wherein the patient interface is configured to maintain a therapy pressure in a range of about 4 cmH2O to about 30 cmH2O above ambient air pressure in use, throughout the patient's respiratory cycle, while the patient is sleeping, to ameliorate sleep disordered breathing, comprising:
a plenum chamber configured to be pressurized at a pressure above ambient pressure in use by the flow of air; and
a seal forming structure including:
an undercushion constructed from a foam material and structured to releasably engage with the plenum chamber; and
an air-impermeable textile membrane configured to contact the patient's face during use, the air-impermeable textile membrane having an outer periphery that is joined to the undercushion by an airtight bond and an inner portion that lies freely on the undercushion such that the inner portion of the air-impermeable textile membrane is separable from the undercushion by the flow of air in use;
wherein the plenum chamber is structured to deform the foam material to impart a predetermined shape to the foam material of the undercushion.
9. The patient interface according to claim 8 , wherein the predetermined shape of the foam material is V-shaped.
10. The patient interface according to claim 9 wherein the foam material comprises alar sealing regions configured to engage the patient's face proximate to the corners of the patient's nose.
11. The patient interface according to claim 8 , wherein the air-impermeable textile membrane is constructed from a textile material that is coated to be air impermeable.
12. The patient interface according to claim 8 , wherein the air-impermeable textile membrane is constructed from a textile material that is laminated to be air impermeable.
13. The patient interface according to claim 8 , wherein the foam material is air impermeable.
14. The patient interface according to claim 8 , wherein the foam material has a substantially uniform thickness.
15. The patient interface according to claim 8 , wherein the foam material has a variable thickness.
16. The patient interface according to claim 8 , wherein the foam material has at least one opening to permit pressurised air to enter the patient's nares.
17. The patient interface according to claim 16 , wherein the at least one opening is tapered at a peripheral edge to reduce distortion of the shape of the at least one opening in use.
18. The patient interface according to claim 8 , wherein the plenum chamber further comprises a connection port, and
wherein a tube is releasably connected to the plenum chamber at the connection port.
19. The patient interface according to claim 8 , further comprising a textile positioning and stabilising structure operatively connected to the plenum chamber.
20. The patient interface according to claim 8 , wherein the plenum chamber further comprises a vent.
21. The patient interface according to claim 8 , wherein the air-impermeable textile membrane is constructed from a textile material that is inflatable in use to engage with the underside of the patient's nose.
22. The patient interface according to claim 8 , wherein the undercushion includes an outer periphery, the outer periphery of the air-impermeable textile membrane being joined to the outer periphery of the undercushion.
23. The patient interface according to claim 22 , wherein the undercushion includes an interior surface bounded by the outer periphery of the undercushion and the air-impermeable textile membrane includes an interior surface bounded by the outer periphery of the air-impermeable textile membrane and formed on the inner portion, and
wherein the interior surface of the undercushion is adjacent to the interior surface of the air-impermeable textile membrane such that the interior surfaces are separable from one another by the flow of air while the outer periphery of the air-impermeable textile membrane remains joined to the outer periphery of the undercushion.
24. The patient interface according to claim 23 , wherein the air-impermeable textile membrane includes a sealing surface opposite the interior surface of the air-impermeable textile membrane, the sealing surface being configured to contact the patient's face in use.