Plotnick L H, Ducharme F M
Division of Pediatric Emergency Medicine, Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, Quebec H3H 1P3, Canada.
BMJ. 1998 Oct 10;317(7164):971-7. doi: 10.1136/bmj.317.7164.971.
To estimate the therapeutic and adverse effects of addition of inhaled anticholinergics to beta2 agonists in acute asthma in children and adolescents.
Systematic review of randomised controlled trials of children and adolescents taking beta2 agonists for acute asthma with or without the addition of inhaled anticholinergics.
Hospital admission, pulmonary function tests, number of nebulised treatments, relapse, and adverse effects.
Of 37 identified trials, 10 were relevant and six of these were of high quality. The addition of a single dose of anticholinergic to beta2 agonist did not reduce hospital admission (relative risk 0.93, 95% confidence interval 0.65 to 1.32). However, significant group differences in lung function supporting the combination treatment were observed 60 minutes (standardised mean difference -0.57, -0.93 to -0.21) and 120 minutes (-0.53, -0.90 to -0.17) after the dose of anticholinergic. In contrast, the addition of multiple doses of anticholinergics to beta2 agonists, mainly in children and adolescents with severe exacerbations, reduced the risk of hospital admission by 30% (relative risk 0.72, 0.53 to 0.99). Eleven (95% confidence interval 5 to 250) children would need to be treated to avoid one admission. A parallel improvement in lung function (standardised mean difference -0.66, -0.95 to -0.37) was noted 60 minutes after the last combined inhalation. In the single study 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.
Adding multiple doses of anticholinergics to beta2 agonists seems safe, improves lung function, and may avoid hospital admission in 1 of 11 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 and adolescents with severe asthma exacerbation.
评估在儿童和青少年急性哮喘治疗中,在β2激动剂基础上加用吸入性抗胆碱能药物的治疗效果及不良反应。
对使用β2激动剂治疗急性哮喘的儿童和青少年进行随机对照试验的系统评价,这些试验中有的加用了吸入性抗胆碱能药物,有的未加用。
住院情况、肺功能测试、雾化治疗次数、复发情况及不良反应。
在检索到的37项试验中,10项与之相关,其中6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减少住院率(相对危险度0.93,95%置信区间0.65至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-0.57,-0.93至-0.21)和120分钟(-0.53,-0.90至-0.17)时,观察到联合治疗组在肺功能方面存在显著差异。相比之下,在β2激动剂基础上加用多剂量抗胆碱能药物(主要用于重度急性发作的儿童和青少年)可使住院风险降低30%(相对危险度0.72,0.53至0.99)。每治疗11名(95%置信区间5至250)儿童可避免1例住院。在最后一次联合吸入后60分钟,观察到肺功能有类似改善(标准化均数差-0.66,-0.95至-0.37)。在一项不论哮喘严重程度,每次吸入β2激动剂时均系统性加用抗胆碱能药物的研究中,对于少数可用的观察指标未发现组间差异。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。
在β2激动剂基础上加用多剂量抗胆碱能药物似乎是安全的,可改善肺功能,并且每11例接受此类治疗的患者中可能有1例可避免住院。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急性发作的学龄儿童和青少年中使用。