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首页> 外文期刊>BMC Pediatrics >A systematic review of the reporting of Data Monitoring Committees' roles, interim analysis and early termination in pediatric clinical trials
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A systematic review of the reporting of Data Monitoring Committees' roles, interim analysis and early termination in pediatric clinical trials

机译:系统地审查了数据监测委员会在儿科临床试验中的作用,中期分析和提前终止的报告

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Background Decisions about interim analysis and early stopping of clinical trials, as based on recommendations of Data Monitoring Committees (DMCs), have far reaching consequences for the scientific validity and clinical impact of a trial. Our aim was to evaluate the frequency and quality of the reporting on DMC composition and roles, interim analysis and early termination in pediatric trials. Methods We conducted a systematic review of randomized controlled clinical trials published from 2005 to 2007 in a sample of four general and four pediatric journals. We used full-text databases to identify trials which reported on DMCs, interim analysis or early termination, and included children or adolescents. Information was extracted on general trial characteristics, risk of bias, and a set of parameters regarding DMC composition and roles, interim analysis and early termination. Results 110 of the 648 pediatric trials in this sample (17%) reported on DMC or interim analysis or early stopping, and were included; 68 from general and 42 from pediatric journals. The presence of DMCs was reported in 89 of the 110 included trials (81%); 62 papers, including 46 of the 89 that reported on DMCs (52%), also presented information about interim analysis. No paper adequately reported all DMC parameters, and nine (15%) reported all interim analysis details. Of 32 trials which terminated early, 22 (69%) did not report predefined stopping guidelines and 15 (47%) did not provide information on statistical monitoring methods. Conclusions Reporting on DMC composition and roles, on interim analysis results and on early termination of pediatric trials is incomplete and heterogeneous. We propose a minimal set of reporting parameters that will allow the reader to assess the validity of trial results.
机译:背景技术根据数据监测委员会(DMC)的建议,有关中期分析和临床试验的早期停止的决定对试验的科学有效性和临床影响具有深远的影响。我们的目的是评估有关DMC组成和作用,中期分析和儿科试验的早期终止的报告的频率和质量。方法我们对2005年至2007年发表的4篇普通和4篇儿科期刊的随机对照临床试验进行了系统回顾。我们使用全文数据库来确定报告DMC,中期分析或提前终止的试验,其中包括儿童或青少年。提取了有关一般试验特征,偏倚风险以及有关DMC组成和作用,中期分析和提前终止的一组参数的信息。结果该样本的648例儿科试验中有110例(占17%)通过DMC或中期分析或早期停止进行了报道,并包括在内。普通期刊68篇,儿科期刊42篇。在110项纳入试验中,有89项报告了DMC的存在(81%); 62篇论文,包括有关DMC的89篇论文中的46篇(占52%),也介绍了有关中期分析的信息。没有论文能充分报告所有DMC参数,并且有九个(15%)报告了所有中期分析细节。在32项提前终止的试验中,有22项(69%)没有报告预定的停止指南,有15项(47%)没有提供统计监测方法的信息。结论关于DMC的组成和作用,中期分析结果以及儿科试验的提前终止的报告不完整且异质。我们提出了一套最少的报告参数,使读者可以评估试验结果的有效性。

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