Development of Population and Bayesian Models for Applied Use in Patients Receiving Cefepime.


Journal

Clinical pharmacokinetics
ISSN: 1179-1926
Titre abrégé: Clin Pharmacokinet
Pays: Switzerland
ID NLM: 7606849

Informations de publication

Date de publication:
08 2020
Historique:
pubmed: 7 3 2020
medline: 21 9 2021
entrez: 7 3 2020
Statut: ppublish

Résumé

Understanding pharmacokinetic disposition of cefepime, a β-lactam antibiotic, is crucial for developing regimens to achieve optimal exposure and improved clinical outcomes. This study sought to develop and evaluate a unified population pharmacokinetic model in both pediatric and adult patients receiving cefepime treatment. Multiple physiologically relevant models were fit to pediatric and adult subject data. To evaluate the final model performance, a withheld group of 12 pediatric patients and two separate adult populations were assessed. Seventy subjects with a total of 604 cefepime concentrations were included in this study. All adults (n = 34) on average weighed 82.7 kg and displayed a mean creatinine clearance of 106.7 mL/min. All pediatric subjects (n = 36) had mean weight and creatinine clearance of 16.0 kg and 195.6 mL/min, respectively. A covariate-adjusted two-compartment model described the observed concentrations well (population model R The identified model serves well for population dosing and as a Bayesian prior for precision dosing.

Sections du résumé

BACKGROUND AND OBJECTIVE
Understanding pharmacokinetic disposition of cefepime, a β-lactam antibiotic, is crucial for developing regimens to achieve optimal exposure and improved clinical outcomes. This study sought to develop and evaluate a unified population pharmacokinetic model in both pediatric and adult patients receiving cefepime treatment.
METHODS
Multiple physiologically relevant models were fit to pediatric and adult subject data. To evaluate the final model performance, a withheld group of 12 pediatric patients and two separate adult populations were assessed.
RESULTS
Seventy subjects with a total of 604 cefepime concentrations were included in this study. All adults (n = 34) on average weighed 82.7 kg and displayed a mean creatinine clearance of 106.7 mL/min. All pediatric subjects (n = 36) had mean weight and creatinine clearance of 16.0 kg and 195.6 mL/min, respectively. A covariate-adjusted two-compartment model described the observed concentrations well (population model R
CONCLUSION
The identified model serves well for population dosing and as a Bayesian prior for precision dosing.

Identifiants

pubmed: 32140940
doi: 10.1007/s40262-020-00873-3
pii: 10.1007/s40262-020-00873-3
pmc: PMC7222999
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cefepime 807PW4VQE3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1027-1036

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Auteurs

Jiajun Liu (J)

Midwestern University Chicago College of Pharmacy, 555 31st Street, Downers Grove, IL, 60515, USA.
Northwestern Memorial Hospital, Chicago, IL, USA.
Pharmacometrics Center of Excellence, Midwestern University Chicago College of Pharmacy, Downers Grove, IL, USA.

Michael Neely (M)

Children's Hospital Los Angeles and University of Southern California, Los Angeles, CA, USA.

Jeffrey Lipman (J)

UQ Centre for Clinical Research, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.
Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Division of Anaesthesiology Critical Care Emergency and Pain Medicine, Nîmes University Hospital, University of Montpellier, Nîmes, France.

Fekade Sime (F)

UQ Centre for Clinical Research, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.
Centre for Translational Anti-Infective Pharmacodynamics, School of Pharmacy, University of Queensland, Brisbane, QLD, Australia.

Jason A Roberts (JA)

UQ Centre for Clinical Research, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.
Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Centre for Translational Anti-Infective Pharmacodynamics, School of Pharmacy, University of Queensland, Brisbane, QLD, Australia.
Division of Anaesthesiology Critical Care Emergency and Pain Medicine, Nîmes University Hospital, University of Montpellier, Nîmes, France.

Patrick J Kiel (PJ)

Indiana University Health, Indianapolis, IN, USA.

Sean N Avedissian (SN)

Antiviral Pharmacology Laboratory, University of Nebraska, Medical Center (UNMC) Center for Drug Discovery, Omaha, NE, USA.
College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, USA.

Nathaniel J Rhodes (NJ)

Midwestern University Chicago College of Pharmacy, 555 31st Street, Downers Grove, IL, 60515, USA.
Northwestern Memorial Hospital, Chicago, IL, USA.
Pharmacometrics Center of Excellence, Midwestern University Chicago College of Pharmacy, Downers Grove, IL, USA.

Marc H Scheetz (MH)

Midwestern University Chicago College of Pharmacy, 555 31st Street, Downers Grove, IL, 60515, USA. mschee@midwestern.edu.
Northwestern Memorial Hospital, Chicago, IL, USA. mschee@midwestern.edu.
Pharmacometrics Center of Excellence, Midwestern University Chicago College of Pharmacy, Downers Grove, IL, USA. mschee@midwestern.edu.

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