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Nonparametric Methods in Population Pharmacokinetics.
Goutelle, Sylvain; Woillard, Jean-Baptiste; Neely, Michael; Yamada, Walter; Bourguignon, Laurent.
Affiliation
  • Goutelle S; Hospices Civils de Lyon, Groupement Hospitalier Nord, Service de Pharmacie, Lyon, France.
  • Woillard JB; CNRS, UMR 5558, Laboratoire de Biométrie et Biologie Évolutive, Villeurbanne, France.
  • Neely M; Univ Lyon, Université Claude Bernard Lyon 1, Lyon, France.
  • Yamada W; Univ. Limoges, Limoges, France.
  • Bourguignon L; INSERM, IPPRITT, Limoges, France.
J Clin Pharmacol ; 62(2): 142-157, 2022 02.
Article in En | MEDLINE | ID: mdl-33103785
ABSTRACT
Population pharmacokinetic (PK) modeling is a widely used approach to analyze PK data obtained from groups of individuals, in both industry and academic research. The approach can also be used to analyze pharmacodynamic (PD) data and pooled PK/PD data. There are 2 main families of population PK

methods:

parametric and nonparametric. The objectives of this article are to present an overview of nonparametric methods used in population pharmacokinetic modeling and to explain their specific characteristics to inform scientists and clinicians about their potential value for data analysis, simulation, dosage design, and therapeutic drug monitoring (TDM). Nonparametric methods have several interesting characteristics for population PK analysis, including computation of exact likelihoods, the ability to accommodate parameter probability distributions of any shape (eg, non-Gaussian), and to detect subpopulations and outliers. Nonparametric population methods are also highly relevant for model-based TDM and design of individualized drug dosage regimens. Several algorithms have been developed to estimate model parameter values within an individual and compute that individual's dosage to achieve target drug exposure with maximum precision and accuracy. Nonparametric modeling methods for both population and individual PK analysis are available under user-friendly packages.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Algorithms / Software Design / Pharmacokinetics / Models, Statistical / Models, Biological Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Clin Pharmacol Year: 2022 Document type: Article Affiliation country: Francia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Algorithms / Software Design / Pharmacokinetics / Models, Statistical / Models, Biological Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Clin Pharmacol Year: 2022 Document type: Article Affiliation country: Francia