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首页> 外文期刊>Journal of pharmacokinetics and pharmacodynamics >A Bayesian hierarchical nonlinear mixture model in the presence of artifactual outliers in a population pharmacokinetic study.
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A Bayesian hierarchical nonlinear mixture model in the presence of artifactual outliers in a population pharmacokinetic study.

机译:在群体药代动力学研究中存在人为异常值的贝叶斯分层非线性混合模型。

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摘要

The purpose of this study is to develop a statistical methodology to handle a large proportion of artifactual outliers in a population pharmacokinetic (PK) modeling. The motivating PK data were obtained from a population PK study to examine associations between PK parameters such as clearance of dexmedetomidine (DEX) and cytochrome P450 2A6 phenotypes. The blood samples were sparsely sampled from patients in intensive care units (ICUs) while different doses of DEX were continuously infused. Conventional population PK analysis of these data revealed several challenges and intricacies. Especially, there was strong evidence that some plasma drug concentrations were artifactually high and likely contaminated with the infused drug due to blood sampling processes that are sometimes unavoidable in an ICU setting. If not addressed, or if arbitrarily excluded, these outlying values could lead to biased estimates of PK parameters and miss important relationships between PK parameters and covariates due to increased variability. We propose a novel population PK model, a Bayesian hierarchical nonlinear mixture model, to accommodate the artifactual outliers using a finite mixture as the residual error model. Our results showed that the proposed model handles the outliers well. We also conducted simulation studies with a varying proportion of the outliers. These simulation results showed that the proposed model can accommodate the outliers well so that the estimated PK parameters are less biased.
机译:本研究的目的是开发一种统计方法,以处理群体药代动力学(PK)建模中的大部分人为异常值。激励性PK数据是从一项人口PK研究获得的,该研究旨在检查PK参数(如右美托咪定(DEX)的清除率)与细胞色素P450 2A6表型之间的关联。从重症监护病房(ICU)的患者中稀疏采集血样,同时连续输注不同剂量的DEX。这些数据的常规人群PK分析显示了一些挑战和复杂性。尤其是,有强有力的证据表明,某些血浆药物的浓度过高,由于血液采样过程(有时在ICU中不可避免),其人为浓度过高,并可能被注入的药物污染。如果未解决或任意排除,则这些偏远值可能导致PK参数的估计偏差,并由于可变性增加而错过PK参数与协变量之间的重要关系。我们提出了一种新颖的种群PK模型,即贝叶斯分层非线性混合模型,以使用有限混合作为残差模型来适应人为异常值。我们的结果表明,提出的模型能够很好地处理离群值。我们还对不同比例的异常值进行了模拟研究。这些仿真结果表明,所提出的模型可以很好地适应离群值,因此估计的PK参数的偏差较小。

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