Department of Health Outcomes Research and Policy, Harrison School of Pharmacy, Auburn University, Auburn, AL, USA.
Department of Mathematics and Statistics, College of Science and Math, Auburn University, Auburn, AL, USA.
Res Synth Methods. 2014 Dec;5(4):352-70. doi: 10.1002/jrsm.1121. Epub 2014 May 26.
Distributed data networks representing large diverse populations are an expanding focus of drug safety research. However, interpreting results is difficult when treatment effect estimates vary across datasets (i.e., heterogeneity). In a previous study, risk estimates were generated for selected drugs and potential adverse outcomes. Analyses were replicated across eight distributed data sources using an identical analytic structure. To evaluate heterogeneity of risk estimates across data sources, the estimates were combined with summary-level data characterizing the population of each data source. Meta-analysis, meta-regression, and plots of the influence on overall results versus contribution to heterogeneity were examined and used to illustrate an approach to heterogeneity assessment. Heterogeneity, as measured by the I-squared statistic, was high with variability across outcomes. Plots of the relationship between influence on overall results and contribution to heterogeneity suggest that certain datasets and characteristics were influential but there was variability dependent on the drug and outcome being assessed. Exploratory meta-regression identified many possible influential factors, but may be subject to ecological bias and false positive conclusions. Distributed data network drug safety analyses can produce heterogeneous risk estimates that may not be easily explained. Approaches illustrated here can be useful for research that is subject to similar problems with heterogeneity.
代表大型多样化人群的分布式数据网络是药物安全研究的一个扩展焦点。然而,当治疗效果估计在数据集之间(即异质性)存在差异时,解释结果就变得困难了。在之前的一项研究中,针对选定的药物和潜在的不良后果生成了风险估计。使用相同的分析结构在八个分布式数据源中复制了分析。为了评估风险估计在数据源之间的异质性,将这些估计与每个数据源的人群特征的汇总水平数据进行了组合。对荟萃分析、荟萃回归以及对整体结果的影响与异质性贡献的关系进行了分析,并用于说明评估异质性的方法。异质性,由 I 平方统计量衡量,在不同的结果中变化很大。总体结果影响与异质性贡献关系的图表明,某些数据集和特征具有影响力,但存在依赖于评估的药物和结果的可变性。探索性荟萃回归确定了许多可能的影响因素,但可能受到生态偏差和假阳性结论的影响。分布式数据网络药物安全分析可能会产生难以解释的异质性风险估计。此处说明的方法对于容易受到异质性类似问题影响的研究可能很有用。