Castro-Rodriguez Jose A, Rodrigo Gustavo J
Department of Pediatrics and Family Medicine, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Pediatrics. 2009 Mar;123(3):e519-25. doi: 10.1542/peds.2008-2867.
To compare the efficacy of inhaled corticosteroids in infants and preschoolers with recurrent wheezing or asthma.
Randomized, prospective, controlled trials published January 1996 to March 2008 with a minimum of 4 weeks of inhaled corticosteroids versus placebo were retrieved through Medline, Embase, and Central databases. The primary outcome was wheezing/asthma exacerbations; secondary outcomes were withdrawal caused by wheezing/asthma exacerbations, changes in symptoms score, pulmonary function (peak expiratory flow and forced expiratory volume in 1 second), or albuterol use.
Of eighty-nine studies identified, 29 (N = 3592 subjects) met the criteria for inclusion. Patients who received inhaled corticosteroids had significantly less wheezing/asthma exacerbations than those on placebo (18.0% vs 32.1%); posthoc subgroup analysis suggests that this effect was higher in those with a diagnosis of asthma than wheeze but was independent of age (infants versus preschoolers), atopic condition, type of inhaled corticosteroid (budesonide metered-dose inhaler versus fluticasone metered-dose inhaler), mode of delivery (metered-dose inhaler versus nebulizer), and study quality (Jadad score: <4 vs >/=4) and duration (<12 vs >/=12 weeks). In addition, children treated with inhaled corticosteroids had significantly fewer withdrawals caused by wheezing/asthma exacerbations, less albuterol use, and more clinical and functional improvement than those on placebo.
Infants and preschoolers with recurrent wheezing or asthma had less wheezing/asthma exacerbations and improve their symptoms and lung function during treatment with inhaled corticosteroids.
比较吸入性糖皮质激素对反复喘息或哮喘婴幼儿及学龄前儿童的疗效。
通过检索Medline、Embase和Central数据库,获取1996年1月至2008年3月发表的随机、前瞻性对照试验,这些试验中吸入性糖皮质激素治疗至少4周,与安慰剂进行对比。主要结局为喘息/哮喘加重;次要结局包括因喘息/哮喘加重导致的撤药、症状评分变化、肺功能(呼气峰值流速和1秒用力呼气量)或沙丁胺醇使用情况。
在检索到的89项研究中,29项(N = 3592名受试者)符合纳入标准。接受吸入性糖皮质激素治疗的患者喘息/哮喘加重情况明显少于接受安慰剂治疗的患者(18.0%对32.1%);事后亚组分析表明,这种效果在诊断为哮喘的患者中比喘息患者更高,但与年龄(婴儿与学龄前儿童)、特应性状况、吸入性糖皮质激素类型(布地奈德定量气雾剂与氟替卡松定量气雾剂)、给药方式(定量气雾剂与雾化器)、研究质量(Jadad评分:<4对≥4)和疗程(<12周对≥12周)无关。此外,与接受安慰剂治疗的儿童相比,接受吸入性糖皮质激素治疗的儿童因喘息/哮喘加重导致的撤药明显更少,沙丁胺醇使用更少,临床和功能改善更多。
反复喘息或哮喘的婴幼儿及学龄前儿童在吸入性糖皮质激素治疗期间喘息/哮喘加重情况减少,症状和肺功能得到改善。