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Sample size calculations based on a difference in medians for positively skewed outcomes in health care studies

机译:根据医疗保健研究中出现正偏结果的中位数差异计算样本量

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In healthcare research, outcomes with skewed probability distributions are common. Sample size calculations for such outcomes are typically based on estimates on a transformed scale (e.g. log) which may sometimes be difficult to obtain. In contrast, estimates of median and variance on the untransformed scale are generally easier to pre-specify. The aim of this paper is to describe how to calculate a sample size for a two group comparison of interest based on median and untransformed variance estimates for log-normal outcome data. A log-normal distribution for outcome data is assumed and a sample size calculation approach for a two-sample t-test that compares log-transformed outcome data is demonstrated where the change of interest is specified as difference in median values on the untransformed scale. A simulation study is used to compare the method with a non-parametric alternative (Mann-Whitney U test) in a variety of scenarios and the method is applied to a real example in neurosurgery. The method attained a nominal power value in simulation studies and was favourable in comparison to a Mann-Whitney U test and a two-sample t-test of untransformed outcomes. In addition, the method can be adjusted and used in some situations where the outcome distribution is not strictly log-normal. We recommend the use of this sample size calculation approach for outcome data that are expected to be positively skewed and where a two group comparison on a log-transformed scale is planned. An advantage of this method over usual calculations based on estimates on the log-transformed scale is that it allows clinical efficacy to be specified as a difference in medians and requires a variance estimate on the untransformed scale. Such estimates are often easier to obtain and more interpretable than those for log-transformed outcomes.
机译:在医疗保健研究中,偏态概率分布的结果很常见。对于此类结果的样本量计算通常基于有时可能难以获得的转换规模(例如,对数)的估计。相比之下,未转换规模的中位数和方差的估计值通常更容易预先指定。本文的目的是描述如何基于对数正态结果数据的中值和未转换方差估计来计算两组感兴趣的比较的样本量。假定结果数据为对数正态分布,并且证明了对两样本t检验的样本量计算方法,该方法比较了对数转换后的结果数据,其中将感兴趣的变化指定为未转换标度上的中值差异。仿真研究用于在各种情况下将该方法与非参数替代方法(Mann-Whitney U检验)进行比较,并将该方法应用于神经外科的实际案例。该方法在模拟研究中达到了标称功效值,与Mann-Whitney U检验和未转换结果的两样本t检验相比是有利的。此外,该方法可以调整,并在某些情况下,结果的分布不是严格的对数正态分布。我们建议将这种样本量计算方法用于预期正偏斜的结果数据,并计划对数转换后的规模进行两组比较。该方法相对于基于对数转换后的标度的估计值进行常规计算的优势在于,它可以将临床功效指定为中位数的差异,并且需要对未转换后的标度进行方差估计。与对数转换后的结果相比,这种估计通常更容易获得和更易解释。

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