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Inhaled glucocorticoids versus leukotriene receptor antagonists as single agent asthma treatment: systematic review of current evidence

机译:吸入糖皮质激素与白三烯受体拮抗剂作为单药治疗哮喘:当前证据的系统评价

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摘要

Objective To compare the safety and efficacy of anti-leukotrienes and inhaled glucocorticoids as monotherapy in people with asthma. Design Systematic review of randomised controlled trials comparing anti-leukotrienes with inhaled glucocorticoids for 28 days or more in children and adults. Main outcome measure Rale of exacerbations that required treatment with systemic glucocorticoids. Results 13 trials (12 in adults, one in children) met the inclusion criteria; all were in people with mild and moderate asthma. Leukotrienc receptor antagonists were compared with inhaled glucocorticoids at a daily dose equivalent to 400-450 μg beclometasone dipropionate. Patients treated with leukotriene receptor antagonists were 60% more likely to suffer an exacerbation requiring systemic glucocorticoids (relative risk 1.6, 95% confidence interval 1.2 to 2.2; number needed to treat 27, 13 to 81). A 130 ml greater improvement (80 ml to 170 ml) in forced expiratory volume in one second and a 19 l/min greater increase (14 l to 24 l) in morning peak expiratory How rate were noted in favour of inhaled glucocorticoids. Differences in favour of inhaled glucocorticoids were also observed for nocturnal awakenings, use of rescue β_2 agonists, and days without symptoms. Risk of side effects was no different between groups, but leukotriene receptor antagonists were associated a 2.5-fold increase risk of withdrawals due to poor asthma control (relative risk 2.5, 1.8 to 3.5). Conclusions Inhaled glucocorticoids doses equivalent to 400 μg/day beclometasone are more effective than leukotriene receptor antagonists in the treatment of adults with mild or moderate asthma. There is insufficient evidence to conclude on the efficacy of anti-leukotrienes in children.
机译:目的比较抗白三烯和吸入糖皮质激素作为哮喘单一疗法的安全性和有效性。在儿童和成人中比较抗白三烯和吸入糖皮质激素治疗28天或更长时间的随机对照试验的设计系统评价。主要结局指标需加全身糖皮质激素治疗的急性发作。结果13项试验(成人12项,儿童1项)符合纳入标准。所有人都患有轻度和中度哮喘。将白三烯受体拮抗剂与吸入的糖皮质激素进行比较,每日剂量相当于400-450μg倍氯米松二丙酸酯。用白三烯受体拮抗剂治疗的患者加重需要全身性糖皮质激素的可能性高60%(相对危险度1.6,95%置信区间1.2至2.2;需要治疗的人数27、13至81)。一秒内强迫呼气量增加了130 ml(从80 ml到170 ml),早晨峰值呼气速率增加了19 l / min(从14 l到24 l)增加了,这表明吸入糖皮质激素是有利的。在夜间觉醒,使用抢救性β_2激动剂和无症状的日子中,还观察到吸入糖皮质激素的支持率存在差异。两组之间的副作用风险没有差异,但是由于哮喘控制不佳,白三烯受体拮抗剂的戒断风险增加了2.5倍(相对风险为2.5,1.8至3.5)。结论吸入糖皮质激素相当于400μg/天倍氯米松的剂量在治疗轻度或中度哮喘的成年人中比白三烯受体拮抗剂更有效。没有足够的证据得出抗白三烯在儿童中的功效的结论。

著录项

  • 来源
    《British Medical Journal》 |2003年第7390期|p.621-623|共3页
  • 作者

    Francine M Ducharme;

  • 作者单位

    Department of Paediatrics, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

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