孟鲁司特在2 - 14岁儿童哮喘中的应用

Richard B R Muijsers, Stuart Noble
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引用次数: 10

摘要

未标记:孟鲁司特是一种半胱氨酸白三烯受体拮抗剂,用于>或=2岁患者的持续性哮喘的预防性治疗。在一项为期8周的随机双盲试验中,在6至14岁的儿童中,孟鲁司特(5mg /天)治疗导致FEV1(1秒用力呼气量,主要临床结局)显著增加。此外,在一系列评估症状、加重率、β激动剂使用和生活质量的次要终点上观察到显著改善。与布地奈德加安慰剂相比,同时服用孟鲁司特(5mg /天)和吸入布地奈德(200微克,每日两次)导致FEV1有增加的趋势(p=0.06,主要终点),并且在按需使用β -受体激动剂和哮喘发作天数百分比方面均有统计学意义上的显著降低。两组患者哮喘相关生活质量无显著差异。在临床试验中,通常在2至14岁持续性哮喘儿童开始治疗后1天内观察到肺功能的改善和按需使用β 2激动剂的减少。一项针对6- 11岁儿童的随机、非盲试验以及该试验延长6个月的数据表明,孟鲁司特的治疗依从性和患者满意度都高于吸入色甘酸钠(色甘酸钠)或吸入倍氯米松。此外,患者和家长更喜欢口服孟鲁司特而不是色胺酸钠。在2- 5岁的持续性哮喘儿童中,孟鲁司特(4mg /天)治疗导致一系列结局的显着改善,例如按需使用β 2激动剂,症状评分和哮喘症状天数百分比,主要用于评估耐受性的随机双盲试验评估。来自小型随机双盲试验的数据表明,孟鲁司特可减少6- 14岁儿童运动性支气管收缩。孟鲁司特通常耐受性良好。孟鲁司特治疗的所有年龄段儿童的不良事件发生频率与接受安慰剂治疗的儿童相当。结论:在2至14岁儿童的临床试验中,口服孟鲁司特已显示出作为哮喘预防治疗的有效性。在依从性和便利性方面,该药比吸入色胺酸钠和奈多克罗米等更标准的治疗方法有好处。此外,当加入吸入皮质类固醇时,该药具有显著的益处(根据次要终点)。孟鲁司特为儿童哮喘患者提供了一种有效、耐受性良好且方便的治疗选择。
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Spotlight on montelukast in asthma in children 2 to 14 years of age.

Unlabelled: Montelukast is a cysteinyl leukotriene receptor antagonist which is used as a preventive treatment for persistent asthma in patients > or =2 years of age. In children aged 6 to 14 years montelukast (5 mg/day) treatment resulted in a significant increase in FEV1 (forced expiratory volume in 1 second, primary clinical outcome) during an 8-week randomized, double-blind trial. Moreover, significant improvements were observed for a range of secondary endpoints assessing symptoms, exacerbation rates, beta-agonist usage and quality of life. Concomitant administration of montelukast (5 mg/day) and inhaled budesonide (200 microg twice daily) resulted in a trend towards an increase in FEV1 (p=0.06, primary endpoint) and a statistically significant reduction in both as-needed beta2-agonist usage and the percentage of days with asthma exacerbations compared with budesonide plus placebo. No significant differences were observed in asthma-related quality of life between the two groups. During clinical trials both improvements in lung function and reductions in as-needed beta2-agonist usage were generally observed within 1 day after initiation of therapy in children 2 to 14 years of age with persistent asthma. Data from a randomized, nonblind trial in 6- to 11-year-old children and a 6-month extension to this trial suggest that both compliance to therapy and patient satisfaction are greater for montelukast than for either inhaled cromolyn sodium (sodium cromoglycate) or inhaled beclomethasone. In addition, patients and parents preferred oral montelukast over cromolyn sodium. In 2- to 5-year-old children with persistent asthma, montelukast (4 mg/day) treatment resulted in significant improvements in a range of outcomes, such as as-needed beta2-agonist usage, symptom scores and percentage of days with asthma symptoms, as assessed during a randomized, double-blind trial primarily designed to assess tolerability. Data from small randomized, double-blind trials suggest that montelukast reduces exercise-induced bronchoconstriction in 6- to 14-year-old children. Montelukast is generally well tolerated. The frequency of adverse events in montelukast-treated children of all ages was comparable to that in patients receiving placebo.

Conclusion: Oral montelukast has shown efficacy as a preventive treatment for asthma during clinical trials in children aged 2 to 14 years. The drug offers benefits over more standard therapies such as inhaled cromolyn sodium and nedocromil in terms of compliance and convenience. In addition, the drug offers significant benefits when added to inhaled corticosteroids (according to secondary endpoints). Montelukast offers an effective, well tolerated and convenient treatment option for children with asthma.

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