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Bootstrap approach for constructing confidence intervals for population pharmacokinetic parameters. I: A use of bootstrap standard error.

机译:Bootstrap方法用于构建总体药代动力学参数的置信区间。 I:使用引导程序标准错误。

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In population pharmacokinetic studies, one of the main objectives is to estimate population pharmacokinetic parameters specifying the population distributions of pharmacokinetic parameters. Confidence intervals for population pharmacokinetic parameters are generally estimated by assuming the asymptotic normality, which is a large-sample property, that is, a property which holds for the cases where sample sizes are large enough. In actual clinical trials, however, sample sizes are limited and not so large in general. Likelihood functions in population pharmacokinetic modelling include a multiple integral and are quite complicated. We hence suspect that the sample sizes of actual trials are often not large enough for assuming the asymptotic normality and that the asymptotic confidence intervals underestimate the uncertainties of the estimates of population pharmacokinetic parameters. As an alternative to the asymptotic normality approach, we can employ a bootstrap approach. This paper proposes a bootstrap standard error approach for constructing confidence intervals for population pharmacokinetic parameters. Comparisons between the asymptotic and bootstrap confidence intervals are made through applications to a simulated data set and an actual phase I trial.
机译:在人群药代动力学研究中,主要目标之一是估计人群药代动力学参数,以指定药代动力学参数的人群分布。通常,通过假设渐进正态性来估计总体药代动力学参数的置信区间,渐进正态性是一个大样本属性,即对于样本量足够大的情况适用的属性。但是,在实际的临床试验中,样本数量有限,通常不会太大。群体药代动力学模型中的似然函数包括多个积分,并且非常复杂。因此,我们怀疑实际试验的样本量通常不足以假定渐近正态性,并且渐近置信区间低估了群体药代动力学参数估计值的不确定性。作为渐近正态性方法的替代方法,我们可以采用自举方法。本文提出了一种bootstrap标准误差方法,用于构建总体药代动力学参数的置信区间。渐近和自举置信区间之间的比较是通过应用到模拟数据集和实际的I期试验进行的。

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