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在成人和儿童复发性和/或慢性哮喘管理中,抗白三烯药物与吸入性糖皮质激素的比较

Anti-leukotriene agents compared to inhaled corticosteroids in the management of recurrent and/or chronic asthma in adults and children.

作者信息

Ng D, Salvio F, Hicks G

出版信息

Cochrane Database Syst Rev. 2004(2):CD002314. doi: 10.1002/14651858.CD002314.pub2.

Abstract

BACKGROUND

Anti-leukotrienes agents are currently being studied as alternative first line agents to inhaled corticosteroids in mild to moderate chronic asthma.

OBJECTIVES

To compare the safety and efficacy of anti-leukotriene agents with inhaled glucocorticoids (ICS) and to determine the dose-equivalence of anti-leukotrienes to daily dose of ICS.

SEARCH STRATEGY

We searched MEDLINE (1966 to Aug 2003), EMBASE (1980 to Aug 2003), CINAHL (1982 to Aug 2003), the Cochrane Airways Group trials register, and the Cochrane Central Register of Controlled Trials (August 2003), abstract books, and reference lists of review articles and trials. We contacted colleagues and international headquarters of anti-leukotrienes producers.

SELECTION CRITERIA

Randomised controlled trials that compared anti-leukotrienes with inhaled corticosteroids during a minimal 30-day intervention period in asthmatic patients aged 2 years and older.

DATA COLLECTION AND ANALYSIS

Two reviewers independently assessed the methodological quality or trials and extracted trial data. The primary outcome was the rate of exacerbations requiring systemic corticosteroids. Secondary outcomes included lung function, indices of chronic asthma control, adverse effects and withdrawal rates.

MAIN RESULTS

27 trials (including 1 trial testing two protocols) met the inclusion criteria; 13 were of high methodological quality; 20 are published in full-text. All trials pertained to patients with mild to moderate persistent asthma. Only 3 trials focused on children and adolescents. Trial duration varied from 4 to 37 weeks. In most trials, daily dose of ICS was 400 mcg of beclomethasone or equivalent. Patients treated with anti-leukotrienes were 65% more likely to suffer an exacerbation requiring systemic steroids [Relative Risk 1.65; 95% Confidence Interval (CI) 1.36 to 2.00]. Twenty six (95% CI: 17 to 47) patients must be treated with anti-leukotrienes instead of inhaled corticosteroids to cause one extra exacerbation. Significant differences favouring ICS were noted in secondary outcomes where()the improvement in FEV(1) reached 130 mL [13 trials; 95% CI: 50, 140 mL ]. Other significant benefits of ICS were seen for symptoms, nocturnal awakenings, rescue medication use, symptom-free days, and quality of life. Anti-leukotriene therapy was associated with 160% increased risk of withdrawals due to poor asthma control. Twenty nine (95% CI 20 to 48) patients must be treated with anti-leukotrienes instead of inhaled corticosteroids to cause one extra withdrawal due to poor control. Risk of side effects was not different between groups.

REVIEWERS' CONCLUSIONS: Inhaled steroids at a dose of 400 mcg/day of beclomethasone or equivalent are more effective than anti-leukotriene agents given in the usual licensed doses. The exact dose-equivalence of anti-leukotriene agents in mcg of ICS remains to be determined. Inhaled glucocorticoids should remain the first line monotherapy for persistent asthma.

摘要

背景

目前正在研究抗白三烯药物,以作为轻度至中度慢性哮喘患者吸入性糖皮质激素的替代一线药物。

目的

比较抗白三烯药物与吸入性糖皮质激素(ICS)的安全性和疗效,并确定抗白三烯药物与ICS日剂量的等效剂量。

检索策略

我们检索了MEDLINE(1966年至2003年8月)、EMBASE(1980年至2003年8月)、CINAHL(1982年至2003年8月)、Cochrane气道组试验注册库以及Cochrane对照试验中央注册库(2003年8月)、摘要书籍以及综述文章和试验的参考文献列表。我们还联系了抗白三烯药物生产商的同事和国际总部。

选择标准

在年龄2岁及以上的哮喘患者中,在至少30天的干预期内比较抗白三烯药物与吸入性糖皮质激素的随机对照试验。

数据收集与分析

两名评价者独立评估试验的方法学质量并提取试验数据。主要结局是需要全身使用糖皮质激素的加重发作率。次要结局包括肺功能、慢性哮喘控制指标、不良反应和退出率。

主要结果

27项试验(包括1项测试两种方案的试验)符合纳入标准;13项方法学质量高;20项全文发表。所有试验均涉及轻度至中度持续性哮喘患者。仅3项试验关注儿童和青少年。试验持续时间从4周至37周不等。在大多数试验中,ICS的日剂量为400微克倍氯米松或等效剂量。接受抗白三烯药物治疗的患者发生需要全身使用糖皮质激素加重发作的可能性高65%[相对危险度1.65;95%可信区间(CI)1.36至2.00]。必须用抗白三烯药物而非吸入性糖皮质激素治疗26名(95%CI:17至47)患者,才会多发生1次加重发作。在次要结局方面发现显著有利于ICS的差异,其中第1秒用力呼气量(FEV₁)的改善达到130毫升[13项试验;95%CI:50,140毫升]。ICS在症状、夜间觉醒、急救药物使用、无症状天数和生活质量方面也有其他显著益处。抗白三烯治疗因哮喘控制不佳导致退出的风险增加160%。必须用抗白三烯药物而非吸入性糖皮质激素治疗29名(95%CI 20至48)患者,才会因控制不佳多发生1次退出。两组间副作用风险无差异。

评价者结论

每日剂量为400微克倍氯米松或等效剂量的吸入性糖皮质激素比常用许可剂量的抗白三烯药物更有效。抗白三烯药物以ICS微克计的确切等效剂量仍有待确定。吸入性糖皮质激素应仍然是持续性哮喘的一线单一疗法。

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