Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2004 Dec;38(12):2136-44.
doi: 10.1345/aph.1E260. Epub 2004 Oct 26.

Population pharmacokinetics III: design, analysis, and application of population pharmacokinetic Studies

Affiliations
Review

Population pharmacokinetics III: design, analysis, and application of population pharmacokinetic Studies

Ene I Ette et al. Ann Pharmacother. 2004 Dec.

Abstract

Objective: To present a framework within which population pharmacokinetic (PPK) studies should be designed and analyzed and discuss the application of developed PPK models.

Methods: Information on PPK was retrieved from a MEDLINE search (1979-December 2003) of the literature and a bibliographic evaluation of review articles and books. This information is used in conjunction with experience to explain the design and analysis of PPK studies. Also, examples are included to demonstrate the usefulness of PPK.

Synthesis: A great deal of thought must be given to the design and analysis of PPK studies (ie, development of PPK models). Models are of 2 primary types--descriptive and predictive--and the process applied to these models is necessarily different. An approach that ensures model applicability is presented.

Conclusions: PPK models have great utility, and the applications are many. They are very different from single-subject pharmacokinetic models and therefore require different approaches to model estimation.

PubMed Disclaimer

MeSH terms

Substances

LinkOut - more resources