Phillips Carl V
University of Texas School of Public Health, Houston 77225, USA.
Epidemiology. 2003 Jul;14(4):459-66. doi: 10.1097/01.ede.0000072106.65262.ae.
Optimal use of epidemiologic findings in decision making requires more information than standard analyses provide. It requires calculating and reporting the total uncertainty in the results, which in turn requires methods for quantifying the uncertainty introduced by systematic error. Quantified uncertainty can improve policy and clinical decisions, better direct further research, and aid public understanding, and thus enhance the contributions of epidemiology. The error quantification approach proposed here is based on estimating a probability distribution for a bias-corrected effect measure based on externally-derived distributions of bias levels. Using Monte Carlo simulation, corrections for multiple biases are combined by identifying the steps through which true causal effects become data, and (in reverse order) correcting for the errors introduced by each step. The bias-correction calculations are the same as those used in sensitivity analysis, but the resulting distribution of possible true values is more than a sensitivity analysis; it is a more complete reporting of the actual study results. The approach is illustrated with an application to a recent study that resulted in the drug, phenylpropanolamine, being removed from the market.
在决策过程中优化利用流行病学研究结果需要比标准分析提供更多的信息。这需要计算和报告结果中的总不确定性,而这反过来又需要量化系统误差所引入的不确定性的方法。量化的不确定性可以改善政策和临床决策,更好地指导进一步的研究,并有助于公众理解,从而提高流行病学的贡献。这里提出的误差量化方法基于根据外部得出的偏倚水平分布来估计偏差校正效应量的概率分布。使用蒙特卡洛模拟,通过确定真实因果效应转化为数据的步骤,并(按相反顺序)校正每个步骤引入的误差,来合并对多种偏倚的校正。偏差校正计算与敏感性分析中使用的计算相同,但得到的可能真实值分布不仅仅是敏感性分析;它是对实际研究结果更完整的报告。通过应用于最近一项导致药物苯丙醇胺退市的研究来说明该方法。