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Impact and modulation of nasal obstruction
Author(s) -
Horak F.
Publication year - 2002
Publication title -
allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.363
H-Index - 173
eISSN - 1398-9995
pISSN - 0105-4538
DOI - 10.1034/j.1398-9995.57.s75.5.x
Subject(s) - desloratadine , medicine , placebo , allergen , rhinomanometry , anesthesia , crossover study , randomized controlled trial , antihistamine , allergy , gastroenterology , nose , surgery , pharmacology , immunology , pathology , alternative medicine
Nasal obstruction, the leading symptom of allergic rhinitis, results from the combined activity of early‐ and late‐phase allergic reactions. Desloratadine inhibits both early‐ and late‐phase inflammatory mediators in vitro . Thus, double‐blind, placebo‐controlled, randomized, crossover trials were conducted to assess the efficacy of desloratadine against nasal obstruction, measured objectively and subjectively, during controlled exposure of patients with seasonal allergic rhinitis to allergen. Positive results were obtained in three single‐dose studies; desloratadine 5 mg resulted in a greater improvement from baseline than did placebo in the total symptom score and the nasal obstruction symptom score ( P ≤ 0.02). Desloratadine was more effective than placebo in a multiple‐dose study; desloratadine 5 mg was given once daily for 7 days, and a 6‐h allergen challenge was administered at the end of treatment compared with placebo. Desloratadine treatment was associated with less deterioration from baseline in the mean nasal airflow ( P < 0.05) and in the mean severity score for the symptom of nasal obstruction ( P < 0.03). Desloratadine significantly reduces the severity of nasal obstruction in patients with seasonal allergic rhinitis.