非金属
样本量测定
瓦尔德试验
协变量
人口
统计
数学
采样(信号处理)
线性模型
非线性系统
计量经济学
统计假设检验
计算机科学
应用数学
医学
环境卫生
滤波器(信号处理)
量子力学
物理
计算机视觉
作者
Kayode Ogungbenro,Leon J Aarons
摘要
This paper describes an approach for calculating sample size for population pharmacokinetic experiments that involve hypothesis testing based on multi-group comparison detecting the difference in parameters between groups under mixed-effects modelling. This approach extends what has been described for generalized linear models and nonlinear population pharmacokinetic models that involve only binary covariates to more complex nonlinear population pharmacokinetic models. The structural nonlinear model is linearized around the random effects to obtain the marginal model and the hypothesis testing involving model parameters is based on Wald's test. This approach provides an efficient and fast method for calculating sample size for hypothesis testing in population pharmacokinetic models. The approach can also handle different design problems such as unequal allocation of subjects to groups and unbalanced sampling times between and within groups. The results obtained following application to a one compartment intravenous bolus dose model that involved three different hypotheses under different scenarios showed good agreement between the power obtained from NONMEM simulations and nominal power.
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