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DC Field | Value | Language |
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dc.contributor.author | Torpong Thongngarm | en_US |
dc.contributor.author | Chamard Wongsa | en_US |
dc.contributor.author | Phichayut Phinyo | en_US |
dc.contributor.author | Paraya Assanasen | en_US |
dc.contributor.author | Pongsakorn Tantilipikorn | en_US |
dc.contributor.author | Mongkhon Sompornrattanaphan | en_US |
dc.date.accessioned | 2021-01-27T03:59:34Z | - |
dc.date.available | 2021-01-27T03:59:34Z | - |
dc.date.issued | 2020-01-01 | en_US |
dc.identifier.issn | 22132198 | en_US |
dc.identifier.other | 2-s2.0-85095764896 | en_US |
dc.identifier.other | 10.1016/j.jaip.2020.09.057 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85095764896&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/71625 | - |
dc.description.abstract | © 2020 American Academy of Allergy, Asthma & Immunology Background: Using intranasal corticosteroid (INCS) regularly is recommended for treating perennial allergic rhinitis. However, no studies have evaluated “as-needed” use. Objective: To compare the efficacy between as-needed and regular use of INCS in patients with moderate to severe perennial allergic rhinitis. Methods: In a 6-week randomized controlled trial, participants were assigned to either fluticasone furoate (FF) nasal spray, (27.5 μg) 2 sprays once daily for 1 week, followed by as-needed use (FF-as-needed) for 5 more weeks or 2 sprays once daily for 6 weeks (FF-regular). The primary outcome was a change in the total nasal symptom score (TNSS). The secondary outcomes were the change in nasal peak inspiratory flow, Rhinoconjunctivitis Quality of Life-36 Questionnaire score, and cumulative FF dose. Results: In total of 108 patients, 53 and 55 patients were randomized to the FF-as-needed and FF-regular group, respectively. The difference in mean change in TNSS between the 2 groups was not significant at week 6 (1.21 points; 95% CI, −0.08 to 2.49; P = .066). The FF-regular group tended toward a greater improvement in TNSS. The FF-regular group had a higher mean change in nasal peak inspiratory flow than the FF-as-needed group at week 6 (−19.21 L/min; 95% CI, −33.54 to −4.89; P = .009). Both groups had similar improvement in Rhinoconjunctivitis Quality of Life-36 Questionnaire. The mean cumulative FF dose in the FF-as-needed group was 51% that of the FF-regular group. Conclusions: Both as-needed and regular use of INCS had similar improvement in TNSS and RCQ-36 score in patients with perennial allergic rhinitis. As-needed use had half of INCS exposure of the regular use. | en_US |
dc.subject | Medicine | en_US |
dc.title | As-Needed Versus Regular Use of Fluticasone Furoate Nasal Spray in Patients with Moderate to Severe, Persistent, Perennial Allergic Rhinitis: A Randomized Controlled Trial | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of Allergy and Clinical Immunology: In Practice | en_US |
article.stream.affiliations | Faculty of Medicine, Siriraj Hospital, Mahidol University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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