Study of montelukast for the treatment of respiratory symptoms of post-respiratory syncytial virus bronchiolitis in children

被引:95
作者
Bisgaard, Hans [1 ]
Flores-Nunez, Alejandro [2 ]
Goh, Anne [3 ]
Azimi, Parvin [4 ]
Halkas, Andrew [5 ]
Malice, Marie-Pierre [6 ]
Marchal, Jean-Louis [6 ]
Dass, S. Balachandra [6 ]
Reiss, Theodore F. [6 ]
Knorr, Barbara A. [6 ]
机构
[1] Copenhagen Univ Hosp, Dept Pediat, Danish Pediat Asthma Ctr, DK-2900 Copenhagen, Denmark
[2] Hosp Nino Poblano, Dept Pediat Pulmonol, Puebla, Mexico
[3] KK Womens & Childrens Hosp, Dept Pediat Med, Singapore, Singapore
[4] Childrens Hosp Oakland, Oakland, CA USA
[5] Netcare Krugersdorp Hosp, Johannesburg, South Africa
[6] Merck Res Labs, Rahway, NJ USA
关键词
post-respiratory syncytial virus bronchiolitic asthma symptoms; symptom-free days; wheeze; leukotriene receptor antagonist;
D O I
10.1164/rccm.200706-910OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: A pilot study (Bisgaard H; Study Group on Montelukast and Respiratory Syncytial Virus. A randomized trial of montelukast in respiratory syncytial virus postbronchiolitis. Am J Respir Crit Care Med 2003;167:379-383) reported the efficacy of montelukast in post-respiratory syncytial virus (RSV) bronchiolitic respiratory symptoms. Objectives: To evaluate the efficacy and safety of montelukast, 4 and 8 mg, in treating recurrent respiratory symptoms of post-RSV bronchiolitis in children in a large, multicenter study. Methods: This was a double-blind study of 3- to 24-month-old children who had been hospitalized for a first or second episode of physician-diagnosed RSV bronchiolitis and who tested positive or RSV. Patients (n = 979) were randomized to placebo or to montelukast at 4 or 8 mg/day for 4 weeks (period I) and 20 weeks (period II). The primary end point was percentage symptom-free days (%SFD; day with no daytime cough, wheeze, and shortness of breath, and no nighttime cough). Measurements and Main Results: No significant differences were seen between montelukast and placebo in %SFD over period I: mean +/- SD for placebo and for montelukast at 4 and 8 mg were 37.0 +/- 30.7, 38.6 +/- 30.4, and 38.5 +/- 29.9, respectively. Least-squares mean differences (95% confidence interval) between montelukast (4 mg) and placebo and between montelukast (8 mg) and placebo were 1.9% (-2.9, 6.7) and 1.6% (-3.2, 6.5), respectively. Secondary end points were similar across treatments. Both doses were generally well tolerated. During the first two treatment weeks, average %SFD was approximately 29%. In post hoc analyses of patients (n = 523) with persistent symptoms (%SFD <= 30% over Weeks 1-2), differences in %SFD were seen between montelukast and placebo over Weeks 3-24: difference were 5.7 (0.0, 11.3) for montelukast (4 mg) minus placebo and 5.9 (0.1, 11.7) for montelukast (8 mg) minus placebo. Conclusions: In this study, montelukast did not improve respiratory symptoms of post-RSV bronchiolitis in children.
引用
收藏
页码:854 / 860
页数:7
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