Nayak Anjuli S, Philip George, Lu Susan, Malice Marie-Pierre, Reiss Theodore F
University of Illinois, College of Medicine at Peoria, USA.
Ann Allergy Asthma Immunol. 2002 Jun;88(6):592-600. doi: 10.1016/S1081-1206(10)61891-1.
Histamine and cysteinyl leukotrienes seem to be important mediators of allergic rhinitis.
This multicenter, randomized, double-blind, parallel-group, placebo-controlled trial evaluated the effectiveness and tolerability of montelukast, loratadine, and combination therapy with montelukast and loratadine for treating patients with fall seasonal allergic rhinitis.
After a 1-week, single-blind, placebo run-in period, 907 male and female patients aged 15 to 82 years were randomized to 1 of 4 treatments: montelukast 10 mg (n = 155), loratadine 10 mg (n = 301), combination montelukast 10 mg and loratadine 10 mg (n = 302), or placebo (n = 149), administered once daily at bedtime for 2 weeks. The primary endpoint was the daytime nasal symptoms score (mean of congestion, rhinorrhea, pruritus, and sneezing).
Mean symptom scores at baseline were similar for the four treatment groups. For each of the three active treatments, the difference was significant for the mean change from baseline compared with placebo (P < or = 0.001). However, the effect of montelukast/loratadine compared with loratadine alone, the primary comparison, was not significantly different. Differences for each therapy alone compared with placebo were also significant for most secondary endpoints, including nighttime symptom scores, eye symptoms scores, and rhinitis-specific quality of life. Differences for montelukast/loratadine compared with each therapy alone generally showed numerical superiority, and a few endpoints showed differences that were statistically significant. All active treatments showed a safety profile generally similar to placebo.
Montelukast alone or in combination with loratadine is well tolerated and provides clinical and quality-of-life benefits for patients with seasonal allergic rhinitis.
组胺和半胱氨酰白三烯似乎是变应性鼻炎的重要介质。
这项多中心、随机、双盲、平行组、安慰剂对照试验评估了孟鲁司特、氯雷他定以及孟鲁司特与氯雷他定联合治疗秋季季节性变应性鼻炎患者的有效性和耐受性。
在为期1周的单盲、安慰剂导入期后,907名年龄在15至82岁的男性和女性患者被随机分为4种治疗组之一:孟鲁司特10毫克(n = 155)、氯雷他定10毫克(n = 301)、孟鲁司特10毫克与氯雷他定10毫克联合用药(n = 302)或安慰剂(n = 149),于睡前每日给药1次,持续2周。主要终点为日间鼻部症状评分(鼻塞、流涕、瘙痒和打喷嚏的平均值)。
四个治疗组的基线平均症状评分相似。对于三种活性治疗中的每一种,与安慰剂相比,从基线的平均变化差异均具有显著性(P≤0.001)。然而,主要比较的孟鲁司特/氯雷他定与单独使用氯雷他定相比,差异无显著性。单独每种治疗与安慰剂相比,在大多数次要终点上的差异也具有显著性,包括夜间症状评分、眼部症状评分和鼻炎特异性生活质量。孟鲁司特/氯雷他定与单独每种治疗相比,差异通常显示出数值上的优势,少数终点显示出具有统计学显著性的差异。所有活性治疗的安全性概况总体上与安慰剂相似。
单独使用孟鲁司特或与氯雷他定联合使用耐受性良好,可为季节性变应性鼻炎患者带来临床和生活质量方面的益处。