Nasal cannula without nostril prongs

1. A nasal cannula for an oxygen delivery system, comprising:

a tube configured to connect to an oxygen supply; and

a fitting configured to connect to the tube and configured to rest below a nose of a patient, wherein the fitting includes a main body including a proximal surface configured to rest against an area superior to an upper lip of the patient, and a superior surface including a first discharge port and a second discharge port spaced apart by a bridge section;

wherein the first and second discharge ports are configured to be situated inferior to and aligned with, respectively, a first and a second nostril of the patient;

wherein the bridge section includes an inferior-most portion of the superior surface and laterally-outermost edges of the superior surface are at a superior location relative to the inferior-most portion;

wherein the main body portion includes a first prong projecting laterally from a first side of the main body portion and a second prong projecting laterally from a second side of the main body portion, the first and second prongs including, respectively, a first inlet port and a second inlet port;

wherein the first inlet port is fluidly coupled to the first discharge port via a first internal passageway within the first prong and the main body portion, and the second inlet port is fluidly coupled to the second discharge port via a second internal passageway within the first second prong and the main body portion;

wherein the first and second internal passageways are separate, discrete passageways configured such that fluid within one of the first and second internal passageways does not intermix with fluid in the other of the first and second internal passageways; and

wherein the fitting does not include nostril prongs, and no portion of the fitting is configured to project from the superior surface towards the nose of the patient.

2. The nasal cannula as recited in claim 1 , wherein, when the nasal cannula is worn by the patient, the fitting is configured to be spaced-apart from the nose of the patient.

3. The nasal cannula as recited in claim 1 , wherein an inferior surface of the main body portion is convex when viewed from below.

4. The nasal cannula as recited in claim 3 , wherein a ratio between a length of the main body portion and a maximum height of the main body portion is about 2.2:1.

5. The nasal cannula as recited in claim 1 , wherein:

a distal surface of the main body portion is substantially convex when viewed from a position in front of the main body portion, and

the proximal surface of the main body portion is substantially flat.

6. The nasal cannula as recited in claim 5 , wherein a ratio between a length of the main body portion to a distance between the distal surface and the proximal surface is about 2.2:1.

7. The nasal cannula as recited in claim 1 , wherein:

a first portion of the tube is configured to fit over the first prong, and

a second portion of the tube is configured to fit over the second prong.

8. The nasal cannula as recited in claim 1 , wherein:

the first internal passageway includes a straight section within the first prong and a curved section within the main body portion between the straight section and the first discharge port, and

the second internal passageway includes a straight section within the second prong and a curved section within the main body portion between the straight section and the second discharge port.

9. The nasal cannula as recited in claim 1 , wherein the fitting is integrally formed as a one-piece structure.

10. The nasal cannula as recited in claim 9 , wherein the fitting is provided by an integrally molded piece of plastic.

11. The nasal cannula as recited in claim 1 , wherein the fitting further includes a distal surface opposite the proximal surface, the superior surface configured to extend distally from the patient from the proximal surface to the distal surface.

12. The nasal cannula as recited in claim 11 , wherein the proximal surface is configured to face in a proximal direction towards the patient and the distal surface faces in a distal direction opposite the proximal direction.

13. The nasal cannula as recited in claim 1 , wherein the superior surface is configured to face in a superior direction and the proximal surfaces is configured to face in a proximal direction towards the patient, the proximal direction normal to the superior direction.

14. The nasal cannula as recited in claim 1 , wherein, when the nasal cannula is worn by the patient, the superior surface is configured to contact the nose of the patient.

15. The nasal cannula as recited in claim 1 , wherein the first and second discharge ports each include an opening that is at a superior location relative to the inferior-most portion.

16. The nasal cannula as recited in claim 1 , wherein the first internal passageway is symmetrical with the second internal passageway about a centerline of the main body portion.

17. A system, comprising:

a nasal cannula including a tube and a fitting connected to the tube an oxygen supply connected to the tube and including a blower and a sensor, wherein the blower is configured to deliver oxygen to the tube when information from the sensor indicates a change in pressure corresponding to either an inhale or exhale of a patient, wherein the blower is configured to deliver oxygen to the tube when information from the sensor indicates a change in pressure as low as 0.05 cm H 2 O;

wherein the fitting is configured to rest below a nose of the patient and includes a main body including a proximal surface configured to rest against an area superior to an upper lip of the patient, and a superior surface including a first discharge port and a second discharge port spaced apart by a bridge section;

wherein the first and second discharge ports are configured to be situated inferior to and aligned with, respectively, a first and a second nostril of the patient;

wherein the bridge section includes an inferior-most portion of the superior surface and laterally-outermost edges of the superior surface are at a superior location relative to the inferior-most portion;

wherein the main body portion includes a first prong projecting laterally from a first side of the main body portion and a second prong projecting laterally from a second side of the main body portion, the first and second prongs including, respectively, a first inlet port and a second inlet port;

wherein the first inlet port is fluidly coupled to the first discharge port via a first internal passageway within the first prong and the main body portion, and the second inlet port is fluidly coupled to the second discharge port via a second internal passageway within the first second prong and the main body portion;

wherein the fitting does not include nostril prongs, an no portion of the fitting is configured to project from the superior surface towards the nose of the patient; and

wherein the fitting is formed as a one-piece structure and provided by an integrally molded piece of plastic.

18. The system as recited in claim 17 , wherein the blower is configured to deliver oxygen to the tube when information from the sensor indicates a change in pressure within a range of 0.05 cm H 2 O and 0.3 cm H 2 O.

19. A nasal fitting, comprising:

a main body including a proximal surface configured to rest against an area superior to an upper lip of a patient, and a superior surface including a first discharge port and a second discharge port spaced apart by a bridge section;

wherein the first and second discharge ports are configured to be situated inferior to and aligned with, respectively, a first and a second nostril of the patient;

wherein the superior surface is concave when viewed from above such that the bridge section includes an inferior-most portion of the superior surface and the first and second discharge ports each include an opening that is at a superior location relative to the inferior-most portion;

wherein the nasal fitting does not include nostril prongs, and no portion of the fitting is configured to project from the superior surface towards the nose of the patient; and

wherein the nasal fitting is formed as a one-piece structure and provided by an integrally molded piece of plastic.

20. The nasal fitting as recited in claim 19 , wherein:

the main body portion includes a first prong projecting laterally from a first side of the main body portion and a second prong projecting laterally from a second side of the main body portion, the first and second prongs including, respectively, a first inlet port and a second inlet port;

the first inlet port is fluidly coupled to the first discharge port via a first internal passageway within the first prong and the main body portion, and the second inlet port is fluidly coupled to the second discharge port via a second internal passageway within the second prong and the main body portion; and

the first and second internal passageways are separate, discrete passageways configured such that fluid within one of the first and second internal passageways does not intermix with fluid in the other of the first and second internal passageways.