Seddon P, Bara A, Ducharme F M, Lasserson T J
Royal Alexandra Hospital for Sick Children, Dyke Road, Brighton, Sussex, UK, BN1 3JN.
Cochrane Database Syst Rev. 2006 Jan 25;2006(1):CD002885. doi: 10.1002/14651858.CD002885.pub2.
Xanthines have been used in the treatment of asthma as a bronchodilator, though they may also have anti-inflammatory effects. The current role of xanthines in the long-term treatment of childhood asthma needs to be reassessed.
To determine the efficacy of xanthines (e.g. theophylline) in the maintenance treatment of paediatric asthma.
A search of the Cochrane Airways Group Specialised Register was undertaken with predefined search terms. Searches are current to May 2005.
Randomised controlled trials,lasting at least four weeks comparing a xanthine with placebo, regular short-acting beta-agonist (SABA), inhaled corticosteroids (ICS), cromoglycate (SCG), ketotifen (KET) or leukotriene antagonist, in children with diagnosed with chronic asthma between 18 months and 18 years old.
Two reviewers independently selected each study for inclusion in the review and extracted data. Primary outcome was percentage of symptom-free days.
Thirty-four studies (2734 participants) of adequate quality were included. Xanthine versus placebo (17 studies): The proportion of symptom free days was larger with xanthine compared with placebo (7.97% [95% CI 3.41, 12.53]). Rescue medication usage was lower with xanthine, with no significant difference in symptom scores or hospitalisations. FEV1 , and PEF were better with xanthine. Xanthine was associated with non - specific side-effects. Data from behavioural scores were inconclusive. Xanthine versus ICS (four studies) : Exacerbations were less frequent with ICS, but no significant difference on lung function was observed. Individual studies reported significant improvements in symptom measures in favour of steroids, and one study reported a difference in growth rate in favour of xanthine. No difference was observed for study withdrawal or tremor. Xanthine was associated with more frequent headache and nausea. Xanthine versus regular SABA (10 studies): No significant difference in symptoms, rescue medication usage and spirometry. Individual studies reported improvement in PEF with beta-agonist. Beta-agonist treatment led to fewer hospitalisations and headaches. Xanthine was associated with less tremor. Xanthine versus SCG (six studies ): No significant difference in symptoms, exacerbations and rescue medication. Sodium cromoglycate was associated with fewer gastro-intestinal side-effects than xanthine. Xanthine versus KET (one study): No statistical tests of significance between xanthine and ketotifen were reported. Xanthine + ICS versus placebo + same dose ICS (three studies) : Results were conflicting due to clinical/methodological differences, and could not be aggregated.
AUTHORS' CONCLUSIONS: Xanthines as first-line preventer alleviate symptoms and reduce requirement for rescue medication in children with mild to moderate asthma. When compared with ICS they were less effective in preventing exacerbations. Xanthines had similar efficacy as single preventative agent compared with regular SABA and SCG. Evidence on AEs (adverse effects) was equivocal: there was evidence for increased AEs overall, but no evidence that any specific AE (including effects on behaviour and attention) occurred more frequently than with placebo. There is insufficient evidence from available studies to make firm conclusions about the effectiveness of xanthines as add-on preventative treatment to ICS, and there are no published paediatric studies comparing xanthines with alternatives in this role. Our data suggest that xanthines are only suitable as first-line preventative asthma therapy in children when ICS are not available. They may have a role as add-on therapy in more severe asthma not controlled by ICS, but further studies are needed to examine this, and to define the risk-benefit ratio compared with other agents.
黄嘌呤类药物作为支气管扩张剂已用于哮喘治疗,尽管它们可能也具有抗炎作用。黄嘌呤类药物在儿童哮喘长期治疗中的当前作用需要重新评估。
确定黄嘌呤类药物(如茶碱)在小儿哮喘维持治疗中的疗效。
使用预定义的检索词对Cochrane气道组专业注册库进行检索。检索截至2005年5月。
随机对照试验,持续至少四周,比较黄嘌呤类药物与安慰剂、常规短效β-激动剂(SABA)、吸入性糖皮质激素(ICS)、色甘酸(SCG)、酮替芬(KET)或白三烯拮抗剂,纳入18个月至18岁诊断为慢性哮喘的儿童。
两名评价员独立选择每项研究纳入评价并提取数据。主要结局为无症状天数的百分比。
纳入了34项质量合格的研究(2734名参与者)。黄嘌呤类药物与安慰剂(17项研究):与安慰剂相比,黄嘌呤类药物组的无症状天数比例更大(7.97% [95% CI 3.41, 12.53])。黄嘌呤类药物组的急救药物使用量更低,症状评分或住院率无显著差异。黄嘌呤类药物组的第1秒用力呼气容积(FEV1)和呼气峰值流速(PEF)更好。黄嘌呤类药物与非特异性副作用相关。行为评分数据尚无定论。黄嘌呤类药物与ICS(4项研究):ICS组的病情加重频率更低,但肺功能方面未观察到显著差异。个别研究报告称,症状指标方面使用类固醇有显著改善,一项研究报告称生长速率方面使用黄嘌呤类药物有差异。在研究退出或震颤方面未观察到差异。黄嘌呤类药物组的头痛和恶心更频繁。黄嘌呤类药物与常规SABA(10项研究):症状、急救药物使用和肺功能测定方面无显著差异。个别研究报告称β-激动剂可改善PEF。β-激动剂治疗导致的住院和头痛更少。黄嘌呤类药物组的震颤更少。黄嘌呤类药物与SCG(6项研究):症状、病情加重和急救药物方面无显著差异。色甘酸钠的胃肠道副作用比黄嘌呤类药物少。黄嘌呤类药物与KET(1项研究):未报告黄嘌呤类药物与酮替芬之间的显著性统计学检验。黄嘌呤类药物 + ICS与安慰剂 + 相同剂量ICS(3项研究):由于临床/方法学差异,结果相互矛盾,无法汇总。
黄嘌呤类药物作为一线预防药物可缓解症状,并减少轻度至中度哮喘儿童的急救药物需求。与ICS相比,它们在预防病情加重方面效果较差。与常规SABA和SCG相比,黄嘌呤类药物作为单一预防药物的疗效相似。关于不良反应(AE)的证据不明确:总体上有证据表明AE增加,但没有证据表明任何特定的AE(包括对行为和注意力的影响)比安慰剂更频繁发生。现有研究中没有足够的证据就黄嘌呤类药物作为ICS附加预防治疗的有效性得出确凿结论,也没有已发表的儿科研究比较黄嘌呤类药物与其他药物在这一作用中的效果。我们的数据表明,当无法使用ICS时,黄嘌呤类药物仅适用于儿童哮喘的一线预防治疗。它们可能在ICS无法控制的更严重哮喘中作为附加治疗发挥作用,但需要进一步研究来检验这一点,并确定与其他药物相比的风险效益比。