Comparative nasal airflow with loratadine-pseudoephedrine and fluticasone nasal spray for allergic rhinitis

被引:8
作者
Ng, Charlene C. [1 ]
Romaikin, Daniel [1 ]
Steacy, Lisa M. [2 ]
Stevens, David A. [1 ]
Walker, Terry J. [2 ]
Adams, Daniel E. [2 ]
Ellis, Anne K. [2 ,3 ,4 ]
机构
[1] Bayer US LLC, Consumer Hlth Med Affairs, Whippany, NJ USA
[2] Kingston Hlth Sci Ctr, Allergy Res Unit, Kingston Gen Hosp Site, 76 Stuart St,Watkins 1D, Kingston, ON K7L 2V7, Canada
[3] Queens Univ, Dept Med, Div Allergy & Immunol, Kingston, ON, Canada
[4] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON, Canada
关键词
ENVIRONMENTAL EXPOSURE UNIT; INSPIRATORY FLOW; DOUBLE-BLIND; 120; MG; EFFICACY; ONSET; PLACEBO; SINGLE; SYMPTOMS; PATENCY;
D O I
10.1016/j.anai.2021.05.001
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Although it is known that oral antihistamine-pseudoephedrine combination tablets have a faster onset than intranasal corticosteroid sprays in the treatment of allergic rhinitis after the first dose, the magnitude of change has not been measured in a comparative manner. Furthermore, the sensation of sprayed liquid in the nose may lead patients to mistakenly believe that intranasal steroid sprays work instantly. Objective: To evaluate, numerically, nasal airflow changes provided by a single dose of loratadine-pseudoephedrine tablet (LP) and fluticasone propionate nasal spray (FP) in participants experiencing allergic rhinitis symptoms, including nasal congestion. Methods: This single-center, double-blinded, placebo-controlled, crossover study evaluated objective nasal airflow changes in patients with a documented sensitivity to ragweed pollen. Participants were randomized to receive 1 of 4 treatment sequences, and their peak nasal inspiratory flow (PNIF) was measured in a span of 4 hours after pollen exposure in an environmental exposure unit. Results: Average change in PNIF was 31% with LP in the course of the study, significantly greater than with placebo and FP (12% and 15%, respectively; P <.001). Nevertheless, FP did not produce a significant change compared with its placebo. At hour one post-dose, LP had a clinically significant 31% increase in PNIF, whereas FP only yielded an 8.6% increase (P <.001). Measurable nasal airflow improvements are associated with the opening of nasal passages, allowing congested patients to breathe more freely. Conclusion: A single dose of LP quickly and significantly (P <.001) improved nasal airflow after ragweed pollen challenge in an environmental exposure unit. Comparatively, FP did not display this same benefit. (C) 2021 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc.
引用
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页码:342 / +
页数:9
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