Department of Clinical Neurosciences, University of Edinburgh, Western General Hospital, Edinburgh, UK.
Trials. 2010 Apr 22;11:43. doi: 10.1186/1745-6215-11-43.
We assessed the prevalence, and potential impact of, trials of pharmacological agents for acute stroke that were completed but not published in full. Failure to publish trial data is to be deprecated as it sets aside the altruism of participants' consent to be exposed to the risks of experimental interventions, potentially biases the assessment of the effects of therapies, and may lead to premature discontinuation of research into promising treatments.
We searched the Cochrane Stroke Group's Specialised Register of Trials in June 2008 for completed trials of pharmacological interventions for acute ischaemic stroke, and searched MEDLINE and EMBASE (January 2007 - March 2009) for references to recent full publications. We assessed trial completion status from trial reports, online trials registers and correspondence with experts.
We identified 940 trials. Of these, 125 (19.6%, 95% confidence interval 16.5-22.6) were completed but not published in full by the point prevalence date. They included 16,058 participants (16 trials had over 300 participants each) and tested 89 different interventions. Twenty-two trials with a total of 4,251 participants reported the number of deaths. In these trials, 636/4251 (15.0%) died.
Our data suggest that, at the point prevalence date, a substantial body of evidence that was of relevance both to clinical practice in acute stroke and future research in the field was not published in full. Over 16,000 patients had given informed consent and were exposed to the risks of therapy. Responsibility for non-publication lies with investigators, but pharmaceutical companies, research ethics committees, journals and governments can all encourage the timely publication of trial data.
我们评估了已完成但未全文发表的急性脑卒中药物试验的发生率及其潜在影响。试验数据未能发表是不可取的,因为这违背了参与者同意接受实验性干预风险的利他主义精神,可能会对治疗效果的评估产生偏差,并可能导致对有前途的治疗方法的研究过早终止。
我们于 2008 年 6 月在 Cochrane 卒中组的专门试验注册库中搜索了急性缺血性脑卒中药物干预的完成试验,并在 MEDLINE 和 EMBASE(2007 年 1 月至 2009 年 3 月)中搜索了最近的全文出版物。我们根据试验报告、在线试验登记册和与专家的通信来评估试验完成情况。
我们确定了 940 项试验。其中,125 项(19.6%,95%置信区间 16.5-22.6)已完成但未在截止日期前全文发表。它们包括 16058 名参与者(16 项试验每项都有超过 300 名参与者),共测试了 89 种不同的干预措施。22 项共涉及 4251 名参与者的试验报告了死亡人数。在这些试验中,636/4251(15.0%)名患者死亡。
我们的数据表明,在截止日期时,大量与急性脑卒中临床实践和该领域未来研究都相关的证据尚未全文发表。超过 16000 名患者已获得知情同意,并暴露于治疗风险之下。未能发表的责任在于研究者,但制药公司、研究伦理委员会、期刊和政府都可以鼓励及时发表试验数据。