首页> 外文期刊>JAMA: the Journal of the American Medical Association >Montelukast for chronic asthma in 6- to 14-year-old children: a randomized, double-blind trial. Pediatric Montelukast Study Group (see comments)
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Montelukast for chronic asthma in 6- to 14-year-old children: a randomized, double-blind trial. Pediatric Montelukast Study Group (see comments)

机译:孟鲁司特治疗6至14岁儿童的慢性哮喘:一项随机双盲试验。儿科孟鲁司特研究组(查看评论)

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CONTEXT: Leukotrienes are important mediators of asthma by causing bronchoconstriction, mucous secretion, and increased vascular permeability. Studies using compounds that block leukotrienes have demonstrated improvement in asthma control in adults and adolescents, but children younger than 12 years, for whom asthma is the most common chronic disease, have not been studied. OBJECTIVE: To determine the clinical effect of montelukast, a leukotriene receptor antagonist, in 6- to 14-year-old children with asthma. DESIGN: Eight-week, multicenter, randomized, double-blind study. SETTING: Forty-seven outpatient centers at private practices and academic medical centers in the United States and Canada. PATIENTS: A total of 336 children with forced expiratory volume in 1 second (FEV1) between 50% to 85% of the predicted value, at least 15% reversibility after inhaled beta-agonist administration, a minimal predefined level of daytime asthma symptoms, and daily beta-agonist use. Concomitant inhaled corticosteroids at a constant daily dose were used by 39% of patients receiving montelukast and 33% receiving placebo. INTERVENTION: After a 2-week placebo run-in period, patients received either montelukast (5-mg chewable tablet) or matching-image placebo once daily at bed-time for 8 weeks. MAIN OUTCOME MEASURE: Morning FEV1 percent change from baseline. RESULTS: Mean morning FEV1 increased from 1.85 L to 2.01 L in the montelukast group and from 1.85 L to 1.93 L in the placebo group. This represents an 8.23% (95% confidence interval [CI], 6.33% to 10.13%) increase from baseline in the montelukast group and a 3.58% (95% CI, 1.29% to 5.87%) increase from baseline in the placebo group (P<.001 for montelukast vs placebo). CONCLUSION: Montelukast improves morning FEV1 in 6- to 14-year-old children with chronic asthma.
机译:背景:白三烯通过引起支气管收缩,粘液分泌和血管通透性增加,是哮喘的重要介质。使用阻断白三烯的化合物进行的研究表明,成人和青少年的哮喘控制有所改善,但是尚未研究哮喘是最常见的慢性疾病的12岁以下儿童。目的:确定白三烯受体拮抗剂孟鲁司特在6至14岁哮喘儿童中的临床效果。设计:八周,多中心,随机,双盲研究。地点:美国和加拿大的47个私人诊所门诊中心和学术医疗中心。患者:总共336名儿童在1秒内的强迫呼气量(FEV1)在预测值的50%至85%之间,吸入β-受体激动剂后可逆性至少为15%,白天哮喘症状的最低预定水平,以及每日使用β-激动剂。 39%接受孟鲁司特的患者和33%接受安慰剂的患者以固定的每日剂量同时吸入皮质类固醇。干预:安慰剂进入2周后,患者每天在睡前接受孟鲁司特(5 mg咀嚼片)或匹配图像安慰剂,每天一次,共8周。主要观察指标:早晨FEV与基线相比有1%的变化。结果:孟鲁司特组的平均早晨FEV1从1.85 L增加到2.01 L,安慰剂组从1.85 L增加到1.93L。孟鲁司特组比基线增加了8.23%(95%置信区间[CI],6.33%至10.13%),安慰剂组比基线增加了3.58%(95%CI,1.29%至5.87%)(对于孟鲁司特与安慰剂,P <.001)。结论:孟鲁司特改善了6至14岁慢性哮喘儿童的早晨FEV1。

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