Wilson A J, Gibson P G, Coughlan J
Department of Respiratory and Sleep Medicine, John Hunter Hospital, Locked Bag 1, Hunter Mail Centre, Newcastle, NSW, Australia, 2310.
Cochrane Database Syst Rev. 2000(2):CD001281. doi: 10.1002/14651858.CD001281.
Theophylline and long acting beta2-agonists are bronchodilators used for the management of persistent asthma symptoms, especially nocturnal asthma. They represent different classes of drug with differing side-effect profiles.
To assess the comparative efficacy, safety and side-effects of long-acting beta-agonists and theophylline in the maintenance treatment of asthma.
Randomised, controlled trials (RCTs) were identified using the Cochrane Airways Group register. The register was searched using the following terms: asthma and theophylline and long acting beta-agonist or formoterol or foradile or eformoterol or salmeterol or bambuterol or bitolterol. Titles and abstracts were then screened to identify potentially relevant studies. The bibliography of each RCT was searched for additional RCTs. Authors of identified RCTs were contacted for other relevant published and unpublished studies.
All included studies were RCTs involving adults and children with clinical evidence of asthma. These studies must have compared oral sustained release and/or dose adjusted theophylline with an inhaled long-acting beta-agonist.
Potentially relevant trials, identified by screening titles and/or abstracts, were obtained. Two reviewers independently assessed full text versions of these trials to decided whether the trial should be included in the review, and assessed its methodological quality. Where there was disagreement between reviewers, this was resolved by consensus, or reference to a third party. Data were extracted by two independent reviewers. Inter-rater reliability was assessed by simple agreement. Study authors were contacted to clarify randomisation methods, provide missing data, verify the data extracted and identify unpublished studies. Relevant pharmaceutical manufacturers were also contacted.
Six trials met the inclusion criteria. Five used salmeterol and one, biltoterol. They were of varying quality. There was a trend for salmeterol to improve FEV1 more than theophylline in three studies and salmeterol use was associated with more symptom free nights. Bitolterol, used in only one study, was reported to be less effective than theophylline. Subjects taking salmeterol experienced fewer adverse events than those using theophylline (Relative Risk 0.38; 95%Confidence Intervals 0.25, 0.57). Significant reductions were reported for central nervous system adverse events (Relative Risk 0.51; 95%Confidence Intervals 0.30, 0.88) and gastrointestinal adverse events (Relative Risk 0.32; 95%Confidence Intervals 0.17, 0.59).
REVIEWER'S CONCLUSIONS: Salmeterol may be more effective than theophylline in reducing asthma symptoms including night waking and improving lung function. More adverse events occurred in subjects using theophylline when compared to salmeterol.
茶碱和长效β2受体激动剂是用于治疗持续性哮喘症状,尤其是夜间哮喘的支气管扩张剂。它们代表不同类别的药物,副作用情况不同。
评估长效β受体激动剂和茶碱在哮喘维持治疗中的相对疗效、安全性和副作用。
使用Cochrane Airways Group登记册识别随机对照试验(RCT)。使用以下术语检索该登记册:哮喘、茶碱、长效β受体激动剂、福莫特罗、奥西那林、依替福莫特罗、沙美特罗、班布特罗、双甲苯丙醇。然后筛选标题和摘要以识别潜在相关研究。检索每个RCT的参考文献以查找其他RCT。联系已识别RCT的作者以获取其他相关的已发表和未发表研究。
所有纳入研究均为涉及有哮喘临床证据的成人和儿童的RCT。这些研究必须将口服缓释和/或剂量调整的茶碱与吸入长效β受体激动剂进行比较。
获取通过筛选标题和/或摘要识别出的潜在相关试验。两名评审员独立评估这些试验的全文版本,以决定该试验是否应纳入综述,并评估其方法学质量。评审员之间存在分歧时,通过共识或参考第三方解决。数据由两名独立评审员提取。通过简单一致性评估评分者间信度。联系研究作者以澄清随机化方法、提供缺失数据、核实提取的数据并识别未发表研究。还联系了相关制药制造商。
六项试验符合纳入标准。五项使用沙美特罗,一项使用双甲苯丙醇。它们的质量各不相同。在三项研究中,沙美特罗使第一秒用力呼气量(FEV1)改善的趋势大于茶碱,且使用沙美特罗与更多无症状夜间相关。仅在一项研究中使用的双甲苯丙醇据报道比茶碱效果差。服用沙美特罗的受试者比使用茶碱的受试者经历的不良事件更少(相对危险度0.38;95%置信区间0.25,0.57)。据报道中枢神经系统不良事件(相对危险度0.51;95%置信区间0.30,0.88)和胃肠道不良事件(相对危险度0.32;95%置信区间0.17,0.59)有显著减少。
沙美特罗在减轻包括夜间觉醒在内的哮喘症状和改善肺功能方面可能比茶碱更有效。与沙美特罗相比,使用茶碱的受试者发生更多不良事件。