Method of treating a patient having pulmonary hypertension by long term NO therapy
View Patent ↗The invention concerns a nasal cannula assembly ( 10 ) adapted to deliver gases to a patient comprising a first compartment ( 1 ) and a second compartment ( 2 ) separated by a separation wall ( 6 ); a pair of nasal prongs ( 5 ) in fluid communication with the first compartment ( 1 ); the first compartment ( 1 ) comprising a first inlet ( 11 ) for introducing a first gas into said first compartment ( 1 ); the second compartment ( 2 ) comprising a second inlet ( 2 ) for introducing a second gas into said second compartment ( 2 ); and the separation wall ( 6 ) comprising at least one valve element ( 3 ) for controlling the passage of gas from the second compartment ( 2 ) to the first compartment ( 1 ). The invention concerns also a breathing assistance apparatus comprising a source of NO gas, and said nasal cannula assembly ( 10 ) in fluid communication with said source of NO gas.
1. A method for treating pulmonary vasoconstriction in a patient, comprising:
a) providing a nasal cannula assembly ( 10 ) adapted to deliver gases to the patient, the nasal cannula assembly ( 10 ) comprising:
A) a hollow body ( 4 ) configured to be capable of acting as a gas conduct or a gas manifold and comprising an internal chamber ( 7 ) defining a first compartment ( 1 ),
B) the first compartment ( 1 ) and a second compartment ( 2 ) separated by a separation wall ( 6 ),
C) a pair of nasal prongs ( 5 ) in fluid communication with the first compartment ( 1 ),
D) the first compartment ( 1 ) comprising a first inlet ( 11 ) forming a side gases entry in fluid communication with a gas transport conduct and configured to conduct a first gas into said first compartment ( 1 ),
E) the second compartment ( 2 ) having a fully inflated internal volume for a gas of about 0.5 to 5 ml, the second compartment ( 2 ) comprising,
a second inlet ( 12 ) configured to conduct a second gas into said second compartment ( 2 ), and
a deformable wall ( 14 ) having a greater compliance while filling than when the second compartment ( 2 ) is full,
F) the separation wall ( 6 ) comprising two, one-way, duckbill or umbrella valves ( 3 ) a cracking pressure of 0.5 kPa or less which are oriented and arranged in the separation wall ( 6 ) directly opposite the pair of nasal prongs ( 5 ) to thereby be capable of
permitting a passage of gas from the second compartment ( 2 ) to the first compartment ( 1 ) and
preventing or limiting a passage of gas from the first compartment ( 1 ) to the second compartment ( 2 ),
b) providing a source of NO-containing gas having from 1 ppm to 5000 ppm in volume of NO in a balance of nitrogen in fluid communication with the nasal cannula assembly ( 10 ),
c) providing a source of an oxygen-containing gas containing at least 21% (by volume) of O 2 in fluid communication with the nasal cannula assembly ( 10 ), and
d) providing a therapeutically-effective amount of the NO-containing gas to said patient through said nasal cannula assembly for inhalation.
2. The method according to claim 1 , wherein the patient is an adult, an infant or a newborn.
3. The method according to claim 1 , wherein the patient is a newborn and has pulmonary vasoconstriction associated with persistent pulmonary hypertension.
4. The method according to claim 1 , wherein the patient has pulmonary vasoconstriction associated with pulmonary arterial hypertension.
5. The method according to claim 1 , wherein the hollow body ( 4 ) and said pair of nasal prongs ( 5 ) are integrally molded from a soft plastics material.
6. The method according to claim 1 , wherein the pair of nasal prongs ( 5 ) are detachable from said hollow body ( 4 ) and selected from different sized prongs suitable for different sized patient nares.
7. The method according to claim 1 , wherein the nasal cannula assembly does not comprise a sensor configured to detect an onset of patient inspiration.
8. The method according to claim 1 , wherein the pair of nasal prongs ( 5 ) includes an external pillow element ( 8 ) at an end.
9. The method according to claim 8 , wherein the external pillow element ( 8 ) is made of silicone.
10. The method according to claim 1 , wherein the nasal cannula assembly further comprises an expiratory orifice ( 13 ) in the first compartment ( 1 ) defining a fluid communication path from an internal chamber ( 7 ) to an external atmosphere.