Patient interface with seal-forming structure
A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways comprising: a cushion member that includes a retaining structure and a seal-forming structure permanently connected to the retaining structure; a frame member attachable to the retaining structure; and a positioning and stabilising structure attachable to the frame member.
1. A patient interface to deliver pressurized gas to a patient to treat sleep disordered breathing, the patient interface comprising:
a seal-forming structure in the form of a nasal cradle cushion and having a pair of naris ports separated by a nasal sling, each of the naris ports being configured to provide pressurized gas to a corresponding one of the patient's nares, the seal-forming structure forming, at least in part, a gas chamber, the seal-forming structure being configured to prevent the patient's nose from entering the gas chamber, the seal-forming structure being configured to seal against an inferior periphery of the patient's nose and at or near the patient's pronasale, and the seal-forming structure being structured so as not to enter the nostrils of the patient in use;
a plenum chamber formed in one piece with the seal-forming structure, the plenum chamber including a plenum connection region, and the plenum chamber forming, at least in part, the gas chamber;
a frame attached to the plenum chamber at the plenum connection region, the frame having a connection port; and
wherein the seal-forming structure comprises a pair of protruding ends, each of the protruding ends being positioned on a corresponding lateral side of the seal-forming structure, and each of the protruding ends being configured to engage a region of the patient's face between the corresponding ala of the patient's nose and the patient's corresponding nasolabial sulcus,
wherein the seal-forming structure comprises a pair of protruding end support sections cantilevered from an interior surface of the seal-forming structure such that each of the protruding end support sections extends into the gas chamber in a medial direction to contact and support a corresponding one of the protruding ends when the corresponding protruding end is deformed by contact with the patient's face,
wherein the seal-forming structure includes a recessed portion configured to engage the tip of the patient's nose during use, and
wherein the seal-forming structure comprises a compliant region located above the recessed portion, the compliant region being thinner and more flexible than a remainder of the seal-forming structure.
2. The patient interface of claim 1 , wherein the seal-forming structure comprises foam, gel, soft plastic, thermoplastic elastomer, and/or low durometer silicone.
3. The patient interface of claim 1 , wherein the seal-forming structure has a varied thickness around the naris ports.
4. The patient interface of claim 1 , wherein a lower portion of the seal-forming structure is concave in a relaxed state and configured to seal against the patient's upper lip and configured to follow a curvature of the patient's upper lip.
5. The patient interface of claim 1 , wherein the seal-forming structure is configured such that a posterior-facing surface of each of the protruding end support sections is spaced away from a corresponding one of the protruding ends when the protruding ends are not deformed.
6. The patient interface of claim 1 , further comprising a retaining structure at the plenum connection region, the retaining structure being configured to repeatably engage with and disengage from the frame.
7. The patient interface of claim 6 , wherein the seal-forming structure and the plenum chamber are moulded from a first material and the retaining structure is moulded from a second material that has different mechanical characteristics from the first material such that the retaining structure is more rigid than the seal-forming structure and the plenum chamber.
8. The patient interface of claim 7 , wherein the first material is silicone and the second material is silicone with a higher durometer than the first material.
9. The patient interface of claim 1 , wherein the plenum chamber further comprises a sealing lip configured to engage the frame such that an increase in air pressure within the plenum chamber causes a sealing force between the sealing lip and the frame to increase.
10. The patient interface of claim 1 , further comprising a gas delivery tube joined to the frame at the connection port,
wherein the frame is overmolded to the gas delivery tube.
11. The patient interface of claim 1 , wherein the seal-forming structure has a single wall and no undercushion.
12. The patient interface of claim 1 , wherein the seal-forming structure consists of the pair of protruding ends and the pair of protruding end support sections.
13. The patient interface of claim 1 , wherein each of the protruding end support sections has a surface that faces a corresponding one of the protruding ends, the surface being curved such that each of the protruding ends substantially conforms to the corresponding protruding end support section when each of the protruding ends contacts the corresponding protruding end support section.
14. The patient interface of claim 1 , wherein a cross-sectional area of each of the protruding end support sections decreases as each of the protruding end support sections extends away from the interior surface of the seal-forming structure.
15. The patient interface of claim 1 , wherein the seal-forming structure further comprises a pair of thickened sections extending from the interior surface of the seal-forming structure, each of the pair of thickened sections being positioned on a corresponding lateral side of the patient interface so as to be proximal to the patient's corresponding nasolabial sulcus when the seal-forming structure engages the patient's face, and the thickened sections being configured to provide additional support for the seal-forming structure when the seal-forming structure is in sealing engagement with the nose and the face of the patient.
16. The patient interface of claim 15 , wherein the thickened sections are located on the interior surface of the seal-forming structure such that when the seal-forming structure engages the patient's nose and face, the thickened sections are, at least partially, urged against corresponding ones of the protruding end support sections.
17. The patient interface of claim 1 , wherein the frame is constructed from a relatively rigid material such that the frame is more rigid than the seal-forming structure and the plenum chamber.
18. The patient interface of claim 1 , further comprising:
a gas delivery tube joined to the frame at the connection port; and
a retaining structure at the plenum connection region, the retaining structure being configured to repeatably engage with and disengage from the frame,
wherein the seal-forming structure has a varied thickness around the naris ports,
wherein a lower portion of the seal-forming structure is concave in a relaxed state and configured to seal against the patient's upper lip and configured to follow a curvature of the patient's upper lip,
wherein the seal-forming structure is configured such that a posterior-facing surface of each of the protruding end support sections is spaced away from a corresponding one of the protruding ends when the protruding ends are not deformed,
wherein the seal-forming structure and the plenum chamber are moulded from a first material and the retaining structure is moulded from a second material that has different mechanical characteristics from the first material such that the retaining structure is more rigid than the seal-forming structure and the plenum chamber,
wherein the plenum chamber further comprises a sealing lip configured to engage the frame such that an increase in air pressure within the plenum chamber causes a sealing force between the sealing lip and the frame to increase,
wherein the seal-forming structure has a single wall and no undercushion,
wherein the frame is overmolded to the gas delivery tube,
wherein the seal-forming structure further comprises a pair of thickened sections extending from the interior surface of the seal-forming structure, each of the pair of thickened sections being positioned on a corresponding lateral side of the patient interface so as to be proximal to the patient's corresponding nasolabial sulcus when the seal-forming structure engages the patient's face, and the thickened sections being configured to provide additional support for the seal-forming structure when the seal-forming structure is in sealing engagement with the nose and the face of the patient,
wherein the seal-forming structure is configured to seal with the patient's nose below the bridge of the nose, and
wherein each of the protruding end support sections has a cross-sectional profile, as the protruding end support section extends from the interior surface of the seal-forming structure to a free end, that is U-shaped.
19. The patient interface of claim 1 , wherein each of the protruding end support sections has a cross-sectional profile, as the protruding end support section extends from the interior surface of the seal-forming structure to a free end, that is U-shaped.
20. The patient interface of claim 1 , wherein each of the protruding end support sections has a cross-sectional profile, as the protruding end support section extends from the interior surface of the seal-forming structure to a free end, that is circular, elliptical, or oval-shaped.
21. The patient interface of claim 1 , wherein the seal-forming structure is configured to seal with the patient's nose below the bridge of the nose.
22. A patient interface to deliver pressurized gas to a patient to treat sleep disordered breathing, the patient interface comprising:
a seal-forming structure in the form of a nasal cradle cushion and having a pair of naris ports separated by a nasal sling, each of the naris ports being configured to provide pressurized gas to a corresponding one of the patient's nares, the seal-forming structure forming, at least in part, a gas chamber, the seal-forming structure being configured to prevent the patient's nose from entering the gas chamber, the seal-forming structure being configured to seal against an inferior periphery of the patient's nose and at or near the patient's pronasale, and the seal-forming structure being structured so as not to enter the nostrils of the patient in use;
a plenum chamber formed in one piece with the seal-forming structure, the plenum chamber including a plenum connection region, and the plenum chamber forming, at least in part, the gas chamber;
a frame attached to the plenum chamber at the plenum connection region, the frame having a connection port; and
wherein the seal-forming structure comprises a pair of protruding ends, each of the protruding ends being positioned on a corresponding lateral side of the seal-forming structure, and each of the protruding ends being configured to engage a region of the patient's face between the corresponding ala of the patient's nose and the patient's corresponding nasolabial sulcus,
wherein the seal-forming structure comprises a pair of protruding end support sections cantilevered from an interior surface of the seal-forming structure such that each of the protruding end support sections extends into the gas chamber in a medial direction to contact and support a corresponding one of the protruding ends when the corresponding protruding end is deformed by contact with the patient's face,
wherein each of the protruding end support sections has a cross-sectional profile, as the protruding end support section extends from the interior surface of the seal-forming structure to a free end, that is U-shaped.