US2007039615A1PendingUtilityA1
Methods and apparatus for treating rhinitis
Est. expiryNov 8, 2019(expired)· nominal 20-yr term from priority
A61M 15/0065A61K 33/00A61M 15/009A61P 11/00A61M 37/00A61M 2202/0225A61H 2033/145A61H 33/14A61M 15/0083A61M 15/0041A61K 45/06A61M 2202/064
47
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Apparatus and methods deliver treatment agents simultaneously with capnic gases. The capnic gases can enhance the effectiveness of the treatment agent for treating rhinitis, lower the dosage of drug or concentration of agent necessary to achieve a therapeutic result, or both. Exemplary capnic gases include carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases.
Claims
exact text as granted — not AI-modified1 . A method for treating a patient, said method comprising:
administering a treatment agent selected to treat rhinitis to the patient; and delivering a capnic gas to a nasal, oral, auricular, or ocular membrane of the patient; wherein the systemic treatment agent and capnic gas are administered and delivered simultaneously.
2 . A method as in claim 1 , wherein the treatment agent is selected from the group consisting of antihistamines, corticosteroids, leukotriene receptor antagonists, mast cell stabilizers, and decongestants (e.g., alpha-adrenergic agonists).
3 . A method as in claim 2 , wherein the treatment agent comprises an antihistamine.
4 . A method as in claim 2 , wherein the treatment agent comprises an H1 receptor antagonist selected from the group consisting of fexofenadine, cetirizine, loratidine, desloratadine, and azelastine.
5 . A method as in claim 2 , wherein the treatment agent comprises a corticosteroid selected from the group consisting of fluticasone, mometasone, budesonide, triamcinolone, and flunisolide.
6 . A method as in claim 2 , wherein the treatment agent comprises montelukast, a leukotriene receptor antagonist.
7 . A method as in claim 2 , wherein the treatment agent comprises ipratropium, an anticholonergic agent.
8 . A method as in claim 2 , wherein the treatment agent comprises cromolyn, a mast cell stabilizer.
9 . A method as in claim 2 , wherein the treatment agent comprises a decongestant selected from the group consisting of oxymetazoline and pseudoephedrine.
10 . A method as in claim 2 , wherein the treatment agent comprises an alpha-adrenergic agonist.
11 . A method as in claim 1 , wherein the capnic gas is delivered to a nasal or oral mucosa while the patient refrains from inhaling the capnic gas.
12 . A method as in claim 11 , wherein the capnic gas is infused through a nostril and exits through a nostril and/or the mouth.
13 . A method as in claim 11 , wherein the capnic gas is infused through the mouth and exits through at least one nostril and/or the mouth.
14 . A method as in any one of claims 11 to 13 , wherein the capnic gas comprises carbon dioxide at a concentration of at least 50% by volume and is delivered at a controlled flow rate in the range from 0.5 cc/sec to 30 cc/sec.
15 . A method as in claim 1 , wherein the gas is selected from the group consisting of carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases.
16 . A method as in claim 15 , wherein the gas comprises carbon dioxide.
17 . A method as in claim 16 , wherein the carbon dioxide is present at a concentration of at least 50% by volume.
18 . A method as in claim 17 , wherein the carbon dioxide is substantially pure.
19 . A method for treating a patient for rhinitis, said method comprising:
administering a treatment agent selected to treat rhinitis in the patient; and delivering a capnic gas to a nasal, oral, auricular, or optical membrane of the patient; wherein the rhinitis medication and the capnic gas are administered and delivered within sixty minutes of each other.
20 . A method as in claim 19 , wherein the treatment agent is selected from the group consisting of antihistamines, corticosteroids, leukotriene receptor antagonists, mast cell stabilizers, and decongestants.
21 . A method as in claim 20 , wherein the treatment agent comprises an antihistamine.
22 . A method as in claim 20 , wherein the treatment agent comprises an H1 receptor antagonist selected from the group consisting of fexofenadine, cetirizine, loratidine, desloratadine, and azelastine.
23 . A method as in claim 20 , wherein the treatment agent comprises a corticosteroid selected from the group consisting of fluticasone, mometasone, budesonide, triamcinolone, and flunisolide.
24 . A method as in claim 20 , wherein the treatment agent comprises montelukast, a leukotriene receptor antagonist.
25 . A method as in claim 20 , wherein the treatment agent comprises ipratropium, an anticholonergic agent.
26 . A method as in claim 20 , wherein the systemic treatment gent comprises cromolyn, a mast cell stabilizer.
27 . A method as in claim 20 , wherein the treatment agent comprises a decongestant selected from the group consisting of oxymetazoline and pseudoephedrine.
28 . A method as in claim 20 , wherein the treatment agent comprises an alpha-adrenergic agonist.
29 . A method as in claim 19 , wherein the capnic gas is delivered to a nasal or oral mucosa while the patient refrains from inhaling the capnic gas.
30 . A method as in claim 29 , wherein the capnic gas is infused through a nostril and exits through a nostril and/or the mouth.
31 . A method as in claim 29 , wherein the capnic gas is infused through the mouth and exits through at least one nostril and/or the mouth.
32 . A method as in claim 29 , wherein the capnic gas comprises carbon dioxide at a concentration of at least 50% by volume and is delivered at a controlled flow rate in the range from 0.5 cc/sec to 30 cc/sec.
33 . A method as in claim 19 , wherein the capnic gas is selected from the group consisting of carbon dioxide, nitric oxide, nitrous oxide, and dilute acid gases.
34 . A method as in claim 33 , wherein the gas comprises carbon dioxide.
35 . A method as in claim 34 , wherein the carbon dioxide is present at a concentration of at least 50% by volume.
36 . A method as in claim 35 , wherein the carbon dioxide is substantially pure.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.