Plotnick L H, Ducharme F M
The Montreal Childrens' Hospital, Room C538E, 2300 Tupper Street, Montreal, Quebec, CANADA, H3H 1P3.
Cochrane Database Syst Rev. 2000(4):CD000060. doi: 10.1002/14651858.CD000060.
Several randomized controlled trials have examined, with conflicting results, the efficacy of the addition of anticholinergics to beta2 agonists in acute pediatric asthma. The pooling for a larger number of randomized controlled trials may provide not only greater power for detecting group differences and also provide better insight into the influence of patients' characteristics and treatment modalities on efficacy.
The aims of this study were to estimate the therapeutic and adverse effects attributable to the addition of inhaled anticholinergics to beta2 agonists in acute pediatric asthma.
We searched Medline (1966 to April 2000), Embase (1980 to April 2000), Cinahl (1982 to April 2000) and reference lists of studies. We also contacted drug manufacturers and trialists.
Randomised trials comparing the combination of inhaled anticholinergics and beta2 agonists with beta2 agonists alone in children aged 18 months to 17 years with acute asthma.
Assessments of trial quality and data extraction were done by two reviewers independently.
Of the 40 identified trials, 13 were relevant and eight of these were of high quality. The addition of a single dose of anticholinergic to beta2 agonists did not reduce hospital admission [RR=0.93 (95% CI: 0.65, 1.32)]. However, significant group differences in lung function supporting the combination of anticholinergics and beta2-agonists were observed 60 minutes [SMD=0.57 (95% CI:0.21, 0.93)] and 120 minutes [SMD=0.53 (95% CI: 0.17, 0.90)] after the dose of anticholinergic. In contrast, the addition of multiple doses of anticholinergics to beta2 agonists reduced the risk of hospital admission by 25% [RR=0.75 (95% CI: 0.62,0.89)] in children with predominantly moderate and severe exacerbations. Twelve (95% CI: 8, 32) children would need to be treated to avoid one admission. When restricting this strategy to children with severe exacerbations, seven (95% CI: 5, 20) children need to be treated to avoid an admission. At 60 minutes after the last anticholinergic inhalation, a weighted mean group difference of 9.68 in change in % predicted FEV1 [95% CI:5.70, 13.68] favored anticholinergic use. In the two studies where anticholinergics were systematically added to every beta2 agonist inhalation, irrespective of asthma severity, no group differences were observed for the few available outcomes. There was no increase in the amount of nausea, vomiting or tremor in patients treated with anticholinergics.
REVIEWER'S CONCLUSIONS: A single dose of an anticholinergic agent is not effective for the treatment of mild and moderate exacerbations and is insufficient for the treatment of severe exacerbations. Adding multiple doses of anticholinergics to beta2 agonists appears safe, improves lung function and would avoid hospital admission in 1 of 12 such treated patients. Although multiple doses should be preferred to single doses of anticholinergics, the available evidence only supports their use in school-aged children with severe asthma exacerbation. There is no conclusive evidence for using multiple doses of anticholinergics in children with mild or moderate exacerbations.
多项随机对照试验研究了在小儿急性哮喘中,β2 激动剂联合使用抗胆碱能药物的疗效,结果相互矛盾。汇总更多的随机对照试验不仅可以提高检测组间差异的效能,还能更好地洞察患者特征和治疗方式对疗效的影响。
本研究旨在评估在小儿急性哮喘中,β2 激动剂联合吸入抗胆碱能药物的治疗效果及不良反应。
我们检索了 Medline(1966 年至 2000 年 4 月)、Embase(1980 年至 2000 年 4 月)、Cinahl(1982 年至 2000 年 4 月)以及相关研究的参考文献列表。我们还联系了药品制造商和试验者。
比较吸入抗胆碱能药物与β2 激动剂联合使用和单独使用β2 激动剂治疗 18 个月至 17 岁急性哮喘儿童的随机试验。
由两名审阅者独立进行试验质量评估和数据提取。
在确定的 40 项试验中,13 项相关,其中 8 项质量较高。在β2 激动剂基础上加用单剂量抗胆碱能药物并未降低住院率[相对危险度(RR)=0.93(95%可信区间:0.65,1.32)]。然而,在给予抗胆碱能药物剂量后 60 分钟[标准化均数差(SMD)=0.57(95%可信区间:0.21,0.93)]和 120 分钟[SMD=0.53(95%可信区间:0.17,0.90)]时,观察到肺功能存在显著组间差异,支持抗胆碱能药物与β2 激动剂联合使用。相比之下,在主要为中度和重度加重的儿童中,在β2 激动剂基础上加用多剂量抗胆碱能药物可使住院风险降低 25%[RR=0.75(95%可信区间:0.62,0.89)]。每 12 名(95%可信区间:8,32)接受治疗的儿童中,可避免 1 例住院。若将此策略仅限于重度加重的儿童,每 7 名(95%可信区间:5,20)接受治疗的儿童中,可避免 1 例住院。在最后一次吸入抗胆碱能药物后 60 分钟,预测第 1 秒用力呼气容积(FEV1)变化的加权平均组间差异为 9.68[95%可信区间:5.70,13.68],支持使用抗胆碱能药物。在两项研究中,无论哮喘严重程度如何,在每次吸入β2 激动剂时均系统性地加用抗胆碱能药物,在少数可用结局方面未观察到组间差异。接受抗胆碱能药物治疗的患者恶心、呕吐或震颤的发生率未增加。
单剂量抗胆碱能药物对轻度和中度加重无效,对重度加重治疗不足。在β2 激动剂基础上加用多剂量抗胆碱能药物似乎安全,可改善肺功能,每 12 名接受此类治疗的患者中可避免 1 例住院。虽然多剂量抗胆碱能药物应优于单剂量,但现有证据仅支持在重度哮喘加重的学龄儿童中使用。对于轻度或中度加重的儿童,尚无确凿证据支持使用多剂量抗胆碱能药物。