Intranasal Mometasone Furoate Alleviates the Ocular Symptoms Associated with Seasonal Allergic Rhinitis: Results of a Post Hoc Analysis

被引:17
作者
Anolik, Robert [1 ]
Nathan, Robert A. [2 ]
Schenkel, Eric [3 ]
Danzig, Melvyn R. [4 ]
Gates, Davis [4 ]
Varghese, Santosh [5 ]
机构
[1] PC, Allergy & Asthma Specialists, Blue Bell, PA 19422 USA
[2] PC, Asthma & Allergy Associates, Colorado Springs, CO USA
[3] Valley Clin Res Ctr, Easton, PA USA
[4] Schering Plough Res Inst, Kenilworth, NJ USA
[5] Schering Plough Corp, Kenilworth, NJ 07033 USA
关键词
Mometasone furoate nasal spray; Seasonal allergic rhinitis; Ocular symptoms;
D O I
10.1159/000144040
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Burdensome symptoms of allergic rhinitis ( AR) include nasal and ocular symptoms such as itching, tearing and redness. Intranasal corticosteroids are efficacious in the treatment of nasal symptoms of AR. Objective: It was the aim of this study to determine the efficacy of the intranasal corticosteroid mometasone furoate nasal spray ( MFNS) in relieving ocular symptoms associated with seasonal AR ( SAR). Methods: Ocular symptom data were analyzed for subjects >= 12 years of age, randomized to MFNS 200 mu g q.d. ( n = 176) or placebo ( n = 177) in a placebo-controlled, double-blind clinical trial. Post hoc efficacy analysis assessed the mean change from baseline in subject-reported total ocular symptom scores ( TOSS) averaged over the treatment period. Results: Mean baseline TOSS was 4.91 for the MFNS group and comparable ( 5.05) for the placebo group - combined average for individual symptoms such as itching, tearing and redness ranged from 0 ( no symptoms) to 9 ( all symptoms, severe). Mean change from baseline in TOSS averaged over days 1 - 15 was - 1.42 for the MFNS group and - 0.94 for the placebo group ( p = 0.02), for an observed treatment difference of 0.49 ( statistical data rounded to 2 decimal positions). Improvement in individual symptoms ( eye itching, tearing and redness) contributed to this treatment effect; the greatest improvement occurred with tearing, which decreased - 0.52 from the baseline score 1.59 in the MFNS group and - 0.31 from 1.67 in those receiving placebo ( p < 0.01), for an observed treatment difference of 0.21. Treatment with MFNS was safe and well tolerated. Conclusion: MFNS is effective in reducing ocular symptoms of SAR, in addition to its established efficacy in reducing nasal symptoms of SAR. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:323 / 330
页数:8
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