Rossetti L, Marchetti I, Orzalesi N, Scorpiglione N, Liberati A
Online J Curr Clin Trials. 1993 Nov 11;Doc No 100:[6512 words; 199 paragraphs].
The aim of this study was to assess critically the published literature concerning medical treatment of primary open-angle glaucoma (POAG), and to see whether trial methodologic quality was related to a clinically relevant outcome measure.
We identified and reviewed the methodologic quality of 102 published randomized clinical trials (RCTs) on treatment of POAG using an explicit protocol and explored the association between selected aspects of design and conduct and the studies' clinical relevance.
Our analysis revealed serious methodologic problems with the trials reviewed. Areas of major concern were: use of unsatisfactory or unspecified methods of randomization (89% of the trials reported no information), exclusion of some patients from the analysis (53% of the studies), failure to provide evidence of having estimated the number of patients needed to detect a prespecified treatment difference (96% failed to provide such an estimate), and incomplete description of patient characteristics (in 39% of the RCTs information on this item was insufficient). Within this generally unsatisfactory picture we found, however, that those studies adopting a double-masked design and those not excluding patients after randomization followed patients for longer periods of time and assessed treatment effectiveness using a clinically relevant outcome (that is, visual field changes) compared to other studies.
For clinicians to make use of the results of clinical trials, future studies must be adequately designed and conducted. In particular, proper method of randomization, masking of the observers, and inclusion of all randomized patients in the analysis must be used. Of perhaps even greater importance is the need for trials to measure clinically relevant outcomes.
本研究旨在严格评估已发表的有关原发性开角型青光眼(POAG)药物治疗的文献,并探讨试验方法学质量与临床相关结局指标之间是否存在关联。
我们使用明确的方案,识别并回顾了102项已发表的关于POAG治疗的随机临床试验(RCT)的方法学质量,并探讨了设计与实施的选定方面与研究的临床相关性之间的关联。
我们的分析揭示了所审查试验存在严重的方法学问题。主要关注的领域包括:使用不令人满意或未明确说明的随机化方法(89%的试验未报告相关信息)、将部分患者排除在分析之外(53%的研究)、未能提供估计检测预定治疗差异所需患者数量的证据(96%未提供此类估计)以及对患者特征的描述不完整(39%的RCT在此项目上信息不足)。然而,在这一总体不尽人意的情况中,我们发现,与其他研究相比,那些采用双盲设计且随机分组后不排除患者的研究随访时间更长,并使用临床相关结局(即视野变化)评估治疗效果。
为了临床医生能够利用临床试验的结果,未来的研究必须进行充分的设计与实施。特别是,必须采用适当的随机化方法、对观察者进行盲法处理,并将所有随机分组的患者纳入分析。或许更为重要的是,试验需要测量临床相关结局。