Ducharme Francine M
Department of Paediatrics, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
BMJ. 2003 Mar 22;326(7390):621. doi: 10.1136/bmj.326.7390.621.
To compare the safety and efficacy of anti-leukotrienes and inhaled glucocorticoids as monotherapy in people with asthma.
Systematic review of randomised controlled trials comparing anti-leukotrienes with inhaled glucocorticoids for 28 days or more in children and adults.
Rate of exacerbations that required treatment with systemic glucocorticoids.
13 trials (12 in adults, one in children) met the inclusion criteria; all were in people with mild and moderate asthma. Leukotriene receptor antagonists were compared with inhaled glucocorticoids at a daily dose equivalent to 400-450 microg 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 flow rate were noted in favour of inhaled glucocorticoids. Differences in favour of inhaled glucocorticoids were also observed for nocturnal awakenings, use of rescue beta2 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).
Inhaled glucocorticoids doses equivalent to 400 microg/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.
比较抗白三烯药物与吸入性糖皮质激素单药治疗哮喘患者的安全性和有效性。
对随机对照试验进行系统评价,比较抗白三烯药物与吸入性糖皮质激素在儿童和成人中治疗28天或更长时间的效果。
需要全身使用糖皮质激素治疗的加重发作率。
13项试验(12项针对成人,1项针对儿童)符合纳入标准;所有试验对象均为轻、中度哮喘患者。白三烯受体拮抗剂与吸入性糖皮质激素进行比较,吸入性糖皮质激素的日剂量相当于400 - 450微克二丙酸倍氯米松。接受白三烯受体拮抗剂治疗的患者发生需要全身使用糖皮质激素的加重发作的可能性高60%(相对风险1.6,95%置信区间1.2至2.2;需治疗人数27,13至81)。吸入性糖皮质激素组一秒用力呼气量改善幅度更大(80毫升至170毫升),晨间呼气峰值流速增加更多(14升/分钟至24升/分钟),增加幅度为19升/分钟。在夜间觉醒、使用急救β2激动剂和无症状天数方面也观察到有利于吸入性糖皮质激素的差异。两组间副作用风险无差异,但白三烯受体拮抗剂因哮喘控制不佳导致停药的风险增加2.5倍(相对风险2.5,1.8至3.5)。
日剂量相当于400微克倍氯米松的吸入性糖皮质激素在治疗轻度或中度哮喘成人患者方面比白三烯受体拮抗剂更有效。尚无足够证据得出抗白三烯药物对儿童有效性的结论。