Allergy & Respiratory Center, 4048 Dressler Road NW, Canton, OH 44718, USA.
Am J Rhinol Allergy. 2010 Nov-Dec;24(6):444-50. doi: 10.2500/ajra.2010.24.3534.
Fluticasone furoate nasal spray (FFNS), an intranasal corticosteroid, has been shown to be effective in perennial allergic rhinitis in randomized, double-blind, placebo-controlled studies but has been less extensively studied in perennial allergic rhinitis than seasonal allergic rhinitis. This study was designed to evaluate the efficacy and safety of FFNS in perennial allergic rhinitis in adolescents and adults ≥12 years of age.
In this randomized, double-blind, placebo-controlled, parallel-group study (FFU111439), patients ≥12 years old with perennial allergic rhinitis received FFNS, 110 micrograms (n = 160), or placebo (n = 155) q.d. for 4 weeks.
Over the entire treatment period, FFNS was significantly (p < 0.05) more effective than placebo with respect to mean changes from baseline in daily reflective total nasal symptoms (primary end point), morning and evening reflective total nasal symptoms, daily reflective individual nasal symptoms, morning predose instantaneous total and individual nasal symptoms, and morning and evening peak nasal inspiratory flow. FFNS did not show a statistically significant difference from placebo in comparisons of ocular symptom measures. Clinically meaningful improvement versus placebo was observed on the Rhinoconjunctivitis Quality of Life Questionnaire with Standardised Activities overall score. Adverse events reported in >3% of patients in a treatment group and reported more frequently with FFNS than placebo were epistaxis (15% FFNS, 8% placebo) and nasopharyngitis (5% FFNS, 1% placebo).
Once-daily FFNS was well tolerated and more effective than placebo at improving nasal symptoms of perennial allergic rhinitis in adolescents and adults ≥12 years of age.
氟替卡松糠酸酯鼻喷雾剂(FFNS)是一种鼻腔皮质类固醇,在随机、双盲、安慰剂对照研究中已被证明对常年性变应性鼻炎有效,但在常年性变应性鼻炎中的研究不如季节性变应性鼻炎广泛。本研究旨在评估 FFNS 在 12 岁及以上青少年和成人常年性变应性鼻炎中的疗效和安全性。
在这项随机、双盲、安慰剂对照、平行组研究(FFU111439)中,12 岁及以上的常年性变应性鼻炎患者接受 FFNS,110 微克(n=160)或安慰剂(n=155)qd 治疗 4 周。
在整个治疗期间,FFNS 在从基线的平均变化方面显著(p<0.05)优于安慰剂,包括每日反射性总鼻症状(主要终点)、早晚反射性总鼻症状、每日反射性个体鼻症状、早晨预给药瞬间总鼻和个体鼻症状以及早晨和晚上的最大鼻吸气流量。FFNS 在眼部症状测量方面与安慰剂相比没有统计学上的显著差异。使用标准化活动总体评分, Rhinoconjunctivitis 生活质量问卷在临床上有意义的改善优于安慰剂。在治疗组中报告发生率超过 3%且报告频率高于安慰剂的不良事件是鼻出血(15%FFNS,8%安慰剂)和鼻咽炎(5%FFNS,1%安慰剂)。
每天一次的 FFNS 耐受性良好,在改善 12 岁及以上青少年和成人常年性变应性鼻炎的鼻症状方面优于安慰剂。