首页> 外文期刊>Clinical trials: journal of the Society for Clinical Trials >Statistical analysis and design for estimating accuracy in clinical-center classification of cause-specific clinical events in clinical trials.
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Statistical analysis and design for estimating accuracy in clinical-center classification of cause-specific clinical events in clinical trials.

机译:统计分析和设计,用于估计临床试验中特定原因的临床事件的临床中心分类的准确性。

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BACKGROUND: When cause-specific clinical events (for instance, hospitalization for cardiac disease) are used as the primary or key secondary outcomes, it is important to assess how accurately these events have been classified and estimate the error-corrected treatment effects to ensure validity. However, it may not be feasible to verify cause classification for every event in large clinical trials. PURPOSE: We present statistical methods for the design and analysis of outcome-classification accuracy and for estimating error-corrected treatment effects. METHODS: Using the Hemodialysis (HEMO) Study, in which primary causes were designated for all 7822 hospitalizations by the 15 participating clinical centers - but only two subsets were audited by the Outcome Committee - we applied existing methods to obtain unbiased estimates of the sensitivity and specificity of clinical-center classifications. The multiple imputation method was used to correct for the misclassification of events. We then examined how trial results were affected by three methods of event classification: unaudited, imputed, and adjudicated. RESULTS: We applied a three-step procedure to extend the results for the two subsets of audited events to estimate the sensitivity and specificity for the complete set. Finite population sample size formulas were developed for designing the quality control sample. Based on the HEMO analysis, the estimate of the intervention effect using the unaudited outcome was biased; the bias was reduced using the outcome corrected by imputation. LIMITATIONS: The methods are limited to situations in which there are clinical-center classifications for all clinical events but only partial availability of reference standard classifications, and the verification process does not depend on the true event cause or other unobserved information. CONCLUSIONS: Designing a quality control study to estimate the accuracy of outcome classification is important. The multiple imputation method can be used to correct for errors in outcome classification and to estimate the error-corrected treatment effect. Trial results need to be reexamined using the error-corrected outcome.
机译:背景:将特定原因的临床事件(例如,心脏病住院)用作主要或次要结局指标时,评估这些事件的分类准确度并评估经错误校正的治疗效果以确保有效性非常重要。但是,在大型临床试验中为每个事件验证原因分类可能并不可行。目的:我们提出了统计方法,用于设计和分析结果分类的准确性,并估计误差校正后的治疗效果。方法:使用血液透析(HEMO)研究,其中15个参与临床中心确定了所有7822例住院的主要病因-但结果委员会仅审核了两个子集-我们应用了现有方法来获得敏感性和敏感性的无偏估计。临床中心分类的特异性。多重插补方法用于纠正事件的错误分类。然后,我们研究了三种事件分类方法对试验结果的影响:未经审核,估算和裁决。结果:我们应用了一个三步过程来扩展两个审计事件子集的结果,以估计整个过程的敏感性和特异性。开发了有限的样本数量公式来设计质量控制样本。根据HEMO分析,使用未经审计的结果对干预效果的估计是有偏差的;使用归因校正后的结果可减少偏差。局限性:该方法仅限于以下情况:所有临床事件均具有临床中心分类,但参考标准分类仅部分可用,并且验证过程不取决于真实事件原因或其他未观察到的信息。结论:设计质量控制研究以评估结果分类的准确性非常重要。多重插补方法可用于校正结局分类中的错误并估计经过错误校正的治疗效果。必须使用错误更正的结果重新检查试验结果。

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