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外科随机对照试验的报告质量:一项系统评价。

The reporting quality of randomised controlled trials in surgery: a systematic review.

作者信息

Agha Riaz, Cooper Derek, Muir Gordon

机构信息

International Journal of Surgery, Surgical Associates Ltd, 167 Earls Court Road, London SW5 9RF, UK.

出版信息

Int J Surg. 2007 Dec;5(6):413-22. doi: 10.1016/j.ijsu.2007.06.002. Epub 2007 Oct 29.

Abstract

OBJECTIVES

In order to examine the reporting quality of urological RCTs, the initial objectives of this study were to evaluate the degree to which RCTs involving urological surgical techniques (as the intervention) published in the years 2000-2003 complied with the CONSORT statement, and to assess trends and patterns of compliance. Following our initial findings in urology, we extended the methodology to a number of other specialties to assess whether our findings in urology could be generalised to other surgical disciplines.

METHODS

The Royal Society of Medicine (RSM) Library was commissioned to search the Medline and Cochrane databases for RCTs in compliance with the study inclusion criteria below. Additional analyses of five other specialties (non-urological trials: cardiovascular, gastrointestinal, hepatic, orthopaedic and vascular) were also made. For the non-urological trials, 15 English language trials (from each specialty) were randomly picked from a blast search conducted by the RSM for the year 2003. The RCTs were given a score out of 22, reflecting how many of the 22 CONSORT items were complied with (with each item being given equal weighting), this score was termed the "CONSORT score".

RESULTS

Urology trials: In total 122 RCT abstracts were identified which met the inclusion criteria for this study. From these, 32 were excluded as they were follow-up studies, involved a virtual procedure or were a cost analysis, leaving 90 RCTs published across 35 different journals which were analysed (68.2%, 90/122). The average score of 11.1 for urological trials indicates that RCTs in our sample do not comply with the CONSORT statement. No trials reported how they implemented their randomisation process. Only 46% of RCTs stated that they had permission from an ethics review board, 20% had declared their sources of funding, 14% stated whether there were any conflicts of interest and only 1.1% stated their trial registry number. For non-urological studies, an average CONSORT score of 11.2 was obtained.

CONCLUSION

Clinical research teams conducting RCTs in urology and other surgical disciplines demonstrate poor compliance with the CONSORT statement. We would recommend that trials should be registered at their outset and that urological and other surgical journals to consider supporting the CONSORT statement and to have compliance 'hard-wired' into their submission, editorial and peer-review processes. Since it seems the best researchers are unable to produce an RCT results which enable surgical techniques to be critically assessed, there is a need for education about the CONSORT statement and its importance at all levels of surgical training. We believe that an open debate is needed on the possible role of other research designs, such as tracker studies. Whether this study actually raises the question of how appropriate RCTs are to surgical techniques, we leave to the reader.

摘要

目的

为了检验泌尿外科随机对照试验(RCT)的报告质量,本研究最初的目的是评估2000 - 2003年间发表的涉及泌尿外科手术技术(作为干预措施)的随机对照试验符合CONSORT声明的程度,并评估其依从性的趋势和模式。基于我们在泌尿外科的初步研究结果,我们将该方法扩展到其他一些专业领域,以评估我们在泌尿外科的研究结果是否可以推广到其他外科学科。

方法

委托皇家医学学会(RSM)图书馆在Medline和Cochrane数据库中检索符合以下研究纳入标准的随机对照试验。还对其他五个专业领域(非泌尿外科试验:心血管、胃肠、肝脏、骨科和血管)进行了额外分析。对于非泌尿外科试验,从RSM在2003年进行的一次快速检索中随机抽取15项英文试验(每个专业领域)。这些随机对照试验根据22项CONSORT条目得到一个分数(反映在22项条目中符合的数量,每项权重相等),该分数称为“CONSORT分数”。

结果

泌尿外科试验:共识别出122篇符合本研究纳入标准的随机对照试验摘要。其中,32篇因是随访研究、涉及虚拟手术或为成本分析而被排除,剩下90篇发表在35种不同期刊上的随机对照试验进行了分析(90/122,68.2%)。泌尿外科试验的平均分数为11.1,表明我们样本中的随机对照试验不符合CONSORT声明。没有试验报告其随机化过程是如何实施的。只有46%的随机对照试验表明他们获得了伦理审查委员会的许可,20%声明了其资金来源,14%说明了是否存在利益冲突,只有1.1%声明了其试验注册号。对于非泌尿外科研究,CONSORT平均分数为11.2。

结论

在泌尿外科和其他外科学科进行随机对照试验的临床研究团队对CONSORT声明的依从性较差。我们建议试验应在开始时进行注册,泌尿外科和其他外科期刊应考虑支持CONSORT声明,并将依从性“硬性要求”纳入其投稿、编辑和同行评审过程。由于似乎最优秀的研究人员也无法得出能够对手术技术进行严格评估的随机对照试验结果,因此在所有外科培训层面都需要开展关于CONSORT声明及其重要性的教育。我们认为需要就其他研究设计(如追踪研究)的可能作用展开公开辩论。至于这项研究是否实际上提出了随机对照试验对手术技术是否合适的问题,我们留给读者思考。

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