Hughes M D
Department of Biostatistics, Harvard School of Public Health, Boston, MA 02115.
Stat Med. 1993 Sep 30;12(18):1651-63. doi: 10.1002/sim.4780121802.
Many clinicians wrongly interpret p-values as probabilities that treatment has an adverse effect and confidence intervals as probability intervals. Such inferences can be validly drawn from Bayesian analyses of trial results. These analyses use the data to update the prior (or pre-trial) beliefs to give posterior (or post-trial) beliefs about the magnitude of a treatment effect. However, for these methods to gain acceptance in the medical literature, understanding between statisticians and clinicians of the issues involved in choosing appropriate prior distributions for trial reporting needs to be reached. I focus on two types of prior that deserve consideration. The first is the non-informative prior giving standardized likelihood distributions as post-trial probability distributions. Their use is unlikely to be controversial among statisticians whilst being intuitively appealing to clinicians. The second type of prior has a spike of probability mass at the point of no treatment effect. Varying the magnitude of the spike illustrates the sensitivity of the conclusions drawn to the degree of prior scepticism in a treatment effect. With both, graphical displays provide clinical readers with the opportunity to explore the results more fully. An example of how a clinical trial might be reported in the medical literature using these methods is given.
许多临床医生错误地将P值解释为治疗有不良影响的概率,将置信区间解释为概率区间。从试验结果的贝叶斯分析中可以有效地得出这样的推断。这些分析利用数据更新先验(或试验前)信念,以得出关于治疗效果大小的后验(或试验后)信念。然而,要使这些方法在医学文献中被接受,统计学家和临床医生需要就为试验报告选择合适的先验分布所涉及的问题达成共识。我重点关注两类值得考虑的先验。第一类是无信息先验,它给出标准化的似然分布作为试验后的概率分布。它们的使用在统计学家中不太可能有争议,同时对临床医生来说直观上很有吸引力。第二类先验在无治疗效果点有一个概率质量峰值。改变峰值的大小说明了得出的结论对治疗效果先验怀疑程度的敏感性。对于这两类先验,图形展示为临床读者提供了更全面探索结果的机会。给出了一个如何使用这些方法在医学文献中报告临床试验的例子。