Vent system for CPAP patient interface used in treatment of sleep disordered breathing
View Patent ↗A vent assembly for use with a mask assembly includes a first vent, a second vent and a selector to switch the flow of exhaled gas from a patient between the first and second vents.
1. A patient interface for delivery of a flow of pressurized, breathable gas generated by a flow generator at a treatment pressure that is continuously positive with respect to ambient air pressure, while a patient is sleeping, to an entrance to the patient's airways to ameliorate sleep disordered breathing, said patient interface comprising:
a patient contacting portion configured to seal against an area surrounding the patient's nostrils to deliver the flow of pressurized, breathable gas to the patient's airways;
a cavity bounded at least partly by the patient contacting portion, the cavity configured to be pressurized at the treatment pressure by the flow of pressurized, breathable gas;
a swivel elbow configured to be connected to an air delivery conduit to receive the flow of pressurized, breathable gas generated by the flow generator; and
a vent assembly comprising:
a first vent having a plurality of first holes configured to allow a first flow of gas to pass through the plurality of first holes; and a second vent having at least one second hole configured to allow a second flow of gas to pass through the at least one second hole,
wherein the first vent has a first vent characteristic and the second vent has a second vent characteristic that is different from the first vent characteristic, and
wherein the vent assembly is configured to allow the first flow of gas to exit through the plurality of first holes to atmosphere and to allow the second flow of gas to exit through the at least one second hole to atmosphere, the first flow of gas and the second flow of gas exiting from the vent assembly to atmosphere simultaneously.
2. The patient interface of claim 1 , wherein the swivel elbow includes the first vent.
3. The patient interface of claim 1 , wherein the first vent characteristic is a dimension of each of the plurality of first holes and the second vent characteristic is a dimension of the at least one second hole.
4. The patient interface of claim 1 , wherein the first vent characteristic is a combined cross-sectional area of the plurality of first holes and the second vent characteristic is a combined cross-sectional area of the at least one second hole.
5. The patient interface of claim 4 , wherein the combined cross-sectional area of the plurality of first holes is greater than the combined cross-sectional area of the at least one second hole.
6. The patient interface of claim 4 , wherein the combined cross-sectional area of the at least one second hole is greater than the combined cross-sectional area of the plurality of first holes.
7. The patient interface of claim 1 , wherein each of the plurality of first holes is smaller than the at least one second hole.
8. The patient interface of claim 1 , wherein each of the plurality of first holes has a diameter less than 0.5 millimeters.
9. The patient interface of claim 1 , wherein each of the plurality of first holes has a diameter less than 0.1 millimeters.
10. The patient interface of claim 1 , wherein the patient contacting portion is constructed from silicone.
11. The patient interface of claim 1 , wherein the patient contacting portion is configured to seal against the patient's upper lip such that the flow of pressurized, breathable gas is not delivered to the patient's mouth.
12. The patient interface of claim 1 , further comprising a rigid frame that at least partly bounds the cavity.
13. The patient interface of claim 1 , wherein at least one of the first vent and the second vent is configured to allow gas to pass from the cavity to an exterior of the patient interface to minimise rebreathing of exhaled carbon dioxide by the patient.
14. The patient interface of claim 1 , wherein the at least one second hole of the second vent is configured to allow gas to pass from the cavity to an exterior of the patient interface to minimise rebreathing of exhaled carbon dioxide by the patient.
15. The patient interface of claim 1 , wherein:
each of the plurality of first holes is smaller than the at least one second hole,
the patient contacting portion is constructed from silicone, and
the patient contacting portion is configured to seal against the patient's upper lip such that the flow of pressurized, breathable gas is not delivered to the patient's mouth.
16. The patient interface of claim 15 , wherein the first vent characteristic is a combined cross-sectional area of the plurality of first holes and the second vent characteristic is a combined cross-sectional area of the at least one second hole.
17. The patient interface of claim 16 , wherein the combined cross-sectional area of the plurality of first holes is greater than the combined cross-sectional area of the at least one second hole, or the combined cross-sectional area of the at least one second hole is greater than the combined cross-sectional area of the plurality of first holes.
18. The patient interface of claim 15 , wherein the first vent characteristic is a dimension of each of the plurality of first holes and the second vent characteristic is a dimension of the at least one second hole.
19. The patient interface of claim 15 , wherein each of the plurality of first holes has a diameter less than 0.5 millimeters.
20. The patient interface of claim 15 , wherein the swivel elbow includes the first vent.
21. The patient interface of claim 15 , wherein at least the plurality of first holes of the first vent are configured to allow the first flow of gas to pass from the cavity to an exterior of the patient interface to allow carbon dioxide washout, and
wherein the second vent is configured to allow the second flow of gas to pass through the at least one second hole to atmosphere during use.
22. The patient interface of claim 1 , wherein at least the plurality of first holes of the first vent are configured to allow the first flow of gas to pass from the cavity to an exterior of the patient interface to allow carbon dioxide washout, and
wherein the second vent is configured to allow the second flow of gas to pass through the at least one second hole to atmosphere during use.