1998•Current Opinion in Infectious DiseasesRequires access

Pharmacokinetic and pharmacodynamic modelling of antibiotic therapy

Pamela A. Moise, Jerome J. Schentag

Open publisher page 8 citations

Abstract

Despite the advances in pharmacokinetic and pharmacodynamic modelling, there is still much more to gain from this concept. The use of pharmacokinetic and pharmacodynamic modelling in vitro, in animal and in human models has confirmed that an index, such as peak concentration divided by the minimum inhibitory concentration (Cmax/MIC), the area under the curve divided by the minimum inhibitory concentration (AUC/MIC) and time above the minimum inhibitory concentration (T>MIC), may be used as an aid to understanding better the variability between patients who receive similar antibiotic dosage regimens but have dissimilar outcomes. Efforts to find the optimal pharmacokinetic or pharmacodynamic index predictive of response is crucial to identify targets that will ensure efficacy and for the prediction of failure.

About this research paper

What this paper is about

Despite the advances in pharmacokinetic and pharmacodynamic modelling, there is still much more to gain from this concept. The use of pharmacokinetic and pharmacodynamic modelling in vitro, in animal and in human models has confirmed that an index, such as peak concentration divided by the minimum inhibitory concentration (Cmax/MIC), the area under the curve divided by the minimum inhibitory concentration (AUC/MIC) and time above the minimum inhibitory concentration (T>MIC), may be used as an aid to understanding better the variability between patients who receive similar antibiotic dosage regimens but have dissimilar outcomes. Efforts to find the optimal pharmacokinetic or pharmacodynamic index predictive of response is crucial to identify targets that will ensure efficacy and for the prediction of failure.

Why it matters

OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Despite the advances in pharmacokinetic and pharmacodynamic modelling, there is still much more to gain from this concept. The use of pharmacokinetic and pharmacodynamic modelling in vitro, in animal and in human models has confirmed that an index, such as peak concentration divided by the minimum inhibitory concentration (Cmax/MIC), the area under the curve divided by the minimum inhibitory concentration (AUC/MIC) and time above the minimum inhibitory concentration (T>MIC), may be used as an aid to understanding better the variability between patients who receive similar antibiotic dosage regimens but have dissimilar outcomes. Efforts to find the optimal pharmacokinetic or pharmacodynamic index predictive of response is crucial to identify targets that will ensure efficacy and for the prediction of failure.

Key concepts: Pharmacokinetics, Pharmacodynamics, Medicine, Minimum inhibitory concentration, Cmax, Pharmacology, Area under the curve, Plasma concentration

Related papers

Back to paper searchBrowse research topicsOriginal source
Pharmacokinetic and pharmacodynamic modelling of antibiotic therapy — Research Paper | ScholarLens