Division of General Internal Medicine, University Hospital of Bern, 3010 Bern, Switzerland.
Division of General Internal Medicine, University Hospital of Bern, 3010 Bern, Switzerland.
J Clin Epidemiol. 2014 Mar;67(3):278-84. doi: 10.1016/j.jclinepi.2013.09.011. Epub 2013 Nov 28.
Although the use of an adjudication committee (AC) for outcomes is recommended in randomized controlled trials, there are limited data on the process of adjudication. We therefore aimed to assess whether the reporting of the adjudication process in venous thromboembolism (VTE) trials meets existing quality standards and which characteristics of trials influence the use of an AC.
We systematically searched MEDLINE and the Cochrane Library from January 1, 2003, to June 1, 2012, for randomized controlled trials on VTE. We abstracted information about characteristics and quality of trials and reporting of adjudication processes. We used stepwise backward logistic regression model to identify trial characteristics independently associated with the use of an AC.
We included 161 trials. Of these, 68.9% (111 of 161) reported the use of an AC. Overall, 99.1% (110 of 111) of trials with an AC used independent or blinded ACs, 14.4% (16 of 111) reported how the adjudication decision was reached within the AC, and 4.5% (5 of 111) reported on whether the reliability of adjudication was assessed. In multivariate analyses, multicenter trials [odds ratio (OR), 8.6; 95% confidence interval (CI): 2.7, 27.8], use of a data safety-monitoring board (OR, 3.7; 95% CI: 1.2, 11.6), and VTE as the primary outcome (OR, 5.7; 95% CI: 1.7, 19.4) were associated with the use of an AC. Trials without random allocation concealment (OR, 0.3; 95% CI: 0.1, 0.8) and open-label trials (OR, 0.3; 95% CI: 0.1, 1.0) were less likely to report an AC.
Recommended processes of adjudication are underreported and lack standardization in VTE-related clinical trials. The use of an AC varies substantially by trial characteristics.
尽管推荐在随机对照试验中使用裁决委员会(AC)进行结局评估,但有关裁决过程的资料有限。因此,我们旨在评估静脉血栓栓塞(VTE)试验中裁决过程的报告是否符合现有质量标准,以及哪些试验特征会影响 AC 的使用。
我们系统地检索了 MEDLINE 和 Cochrane 图书馆,从 2003 年 1 月 1 日至 2012 年 6 月 1 日,以获取关于 VTE 的随机对照试验。我们提取了关于试验特征和质量以及裁决过程报告的信息。我们使用逐步向后逻辑回归模型来确定与使用 AC 独立相关的试验特征。
我们纳入了 161 项试验。其中,68.9%(111/161)报告使用了 AC。总体而言,使用 AC 的 111 项试验中有 99.1%(110/111)使用了独立或盲法 AC,14.4%(16/111)报告了 AC 内部如何做出裁决决定,4.5%(5/111)报告了裁决的可靠性是否进行了评估。在多变量分析中,多中心试验[比值比(OR),8.6;95%置信区间(CI):2.7,27.8]、使用数据安全监测委员会(OR,3.7;95% CI:1.2,11.6)和 VTE 作为主要结局(OR,5.7;95% CI:1.7,19.4)与使用 AC 相关。无随机分组隐匿(OR,0.3;95% CI:0.1,0.8)和开放性试验(OR,0.3;95% CI:0.1,1.0)不太可能报告使用 AC。
推荐的裁决过程报告不足,且在与 VTE 相关的临床试验中缺乏标准化。AC 的使用因试验特征而异。