Episodic use of an inhaled corticosteroid or leukotriene receptor antagonist in preschool children with moderate-to-severe intermittent wheezing

被引:210
|
作者
Bacharier, Leonard B. [1 ]
Phillips, Brenda R. [2 ]
Zeiger, Robert S. [3 ,4 ]
Szefler, Stanley J. [5 ]
Martinez, Fernando D. [6 ]
Lemanske, Robert F., Jr. [7 ,8 ]
Sorkness, Christine A. [9 ]
Bloomberg, Gordon R.
Morgan, Wayne J. [6 ]
Paul, Ian M. [2 ]
Guilbert, Theresa [10 ]
Krawiec, Marzena [5 ]
Covar, Ronina [5 ]
Larsen, Gary [5 ]
Mellon, Michael [3 ,4 ]
Moss, Mark H. [7 ,8 ]
Chinchilli, Vernon M. [2 ]
Taussig, Lynn M. [5 ]
Strunk, Robert C.
机构
[1] Washington Univ, St Louis Childrens Hosp, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[2] Penn State Univ, Dept Publ Hlth Sci, Hershey, PA USA
[3] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[4] Kaiser Permanente So Calif, Dept Allergy, San Diego, CA USA
[5] Natl Jewish Med & Res Ctr, Dept Pediat, Denver, CO USA
[6] Univ Arizona, Arizona Resp Ctr, Tucson, AZ USA
[7] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Madison, WI 53706 USA
[8] Univ Wisconsin, Sch Med & Publ Hlth, Dept Pediat, Madison, WI 53706 USA
[9] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
[10] Univ Wisconsin, Sch Med, Dept Pediat, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
Wheezing; preschool children; montelukast; budesonide;
D O I
10.1016/j.jaci.2008.09.029
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Acute wheezing illnesses in preschoolers require better management strategies to reduce morbidity. Objectives: We sought to examine the effectiveness of episodic use of an inhaled corticosteroid and a leukotriene receptor antagonist in preschoolers with intermittent wheezing. Methods: In a randomized, double-blind, placebo-controlled 12-month trial, 238 children aged 12 to 59 months with moderate-to-severe intermittent wheezing received 7 days of either budesonide inhalation suspension (1 mg twice daily), montelukast (4 mg daily), or placebo in addition to albuterol with each identified respiratory tract illness (RTI). Proportion of episode-free days (EFDs) during the 12-month trial was the primary outcome. Results: The 3 treatment groups did not differ in proportions of EFDs, with adjusted mean EFDs of 76% (95% CI, 70% to 81%)for budesonide, 73% (95% CI, 66% to 79%) for montelukast, and 74% (95% CI, 65% to 81%) for conventional therapy (P = .66). The 3 groups did not differ in oral corticosteroid use, health care use, quality of life, or linear growth. However, during RTIs, budesonide and montelukast therapy led to modest reductions in trouble breathing (38% [P = .003] and 37% [P = .003], respectively) and interference with activity scores (32% [P =.01] and 40% [P =.001], respectively) that were most evident in those with positive asthma predictive indices. Conclusions: In preschool children with moderate-to-severe intermittent wheezing, episodic use of either budesonide or montelukast early in RTIs, when added to albuterol, did not increase the proportion of EFDs or decrease oral corticosteroid use over a 12-month period. However, indicators of severity of acute illnesses were reduced, particularly in children with positive asthma predictive indices. (J Allergy Clin Immunol 2008; 122:1127-35.)
引用
收藏
页码:1127 / 1135
页数:9
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