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Population pharmacokinetic model of cefazolin in total hip arthroplasty

Cefazolin is an antibiotic recommended for infection prevention in total hip arthroplasty (THA). However, the dosing regimen necessary to achieve therapeutic concentrations in obese patients remains unclear. The aim of this study was to conduct a population analysis of cefazolin pharmacokinetics (PK...

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Autores principales: Lanoiselée, J., Chaux, R., Hodin, S., Bourayou, S., Gibert, A., Philippot, R., Molliex, S., Zufferey, P. J., Delavenne, X., Ollier, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492877/
https://www.ncbi.nlm.nih.gov/pubmed/34611213
http://dx.doi.org/10.1038/s41598-021-99162-7
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author Lanoiselée, J.
Chaux, R.
Hodin, S.
Bourayou, S.
Gibert, A.
Philippot, R.
Molliex, S.
Zufferey, P. J.
Delavenne, X.
Ollier, E.
author_facet Lanoiselée, J.
Chaux, R.
Hodin, S.
Bourayou, S.
Gibert, A.
Philippot, R.
Molliex, S.
Zufferey, P. J.
Delavenne, X.
Ollier, E.
author_sort Lanoiselée, J.
collection PubMed
description Cefazolin is an antibiotic recommended for infection prevention in total hip arthroplasty (THA). However, the dosing regimen necessary to achieve therapeutic concentrations in obese patients remains unclear. The aim of this study was to conduct a population analysis of cefazolin pharmacokinetics (PK) and assess whether cefazolin administration should be weight adapted in THA. Adult patients undergoing THA surgery received an injection of 2000 mg of cefazolin, doubled in the case of BMI > 35 kg/m(2) and total body weight > 100 kg. A population PK study was conducted to quantify cefazolin exposure over time compared to the therapeutic concentration threshold. A total of 484 cefazolin measurements were acquired in 100 patients, of whom 29% were obese. A 2-compartment model best fitted the data, and creatinine clearance determined interpatient variability in elimination clearance. Our PK simulations using a 2000 mg cefazolin bolus showed that cefazolin concentrations remained above the threshold throughout surgery, regardless of weight or renal function. A 2000 mg cefazolin single injection without adaptation to weight or renal function and without intraoperative reinjection was efficient in maintaining therapeutic concentrations throughout surgery. The optimal target concentration and necessary duration of its maintenance remain unclear.
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spelling pubmed-84928772021-10-07 Population pharmacokinetic model of cefazolin in total hip arthroplasty Lanoiselée, J. Chaux, R. Hodin, S. Bourayou, S. Gibert, A. Philippot, R. Molliex, S. Zufferey, P. J. Delavenne, X. Ollier, E. Sci Rep Article Cefazolin is an antibiotic recommended for infection prevention in total hip arthroplasty (THA). However, the dosing regimen necessary to achieve therapeutic concentrations in obese patients remains unclear. The aim of this study was to conduct a population analysis of cefazolin pharmacokinetics (PK) and assess whether cefazolin administration should be weight adapted in THA. Adult patients undergoing THA surgery received an injection of 2000 mg of cefazolin, doubled in the case of BMI > 35 kg/m(2) and total body weight > 100 kg. A population PK study was conducted to quantify cefazolin exposure over time compared to the therapeutic concentration threshold. A total of 484 cefazolin measurements were acquired in 100 patients, of whom 29% were obese. A 2-compartment model best fitted the data, and creatinine clearance determined interpatient variability in elimination clearance. Our PK simulations using a 2000 mg cefazolin bolus showed that cefazolin concentrations remained above the threshold throughout surgery, regardless of weight or renal function. A 2000 mg cefazolin single injection without adaptation to weight or renal function and without intraoperative reinjection was efficient in maintaining therapeutic concentrations throughout surgery. The optimal target concentration and necessary duration of its maintenance remain unclear. Nature Publishing Group UK 2021-10-05 /pmc/articles/PMC8492877/ /pubmed/34611213 http://dx.doi.org/10.1038/s41598-021-99162-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lanoiselée, J.
Chaux, R.
Hodin, S.
Bourayou, S.
Gibert, A.
Philippot, R.
Molliex, S.
Zufferey, P. J.
Delavenne, X.
Ollier, E.
Population pharmacokinetic model of cefazolin in total hip arthroplasty
title Population pharmacokinetic model of cefazolin in total hip arthroplasty
title_full Population pharmacokinetic model of cefazolin in total hip arthroplasty
title_fullStr Population pharmacokinetic model of cefazolin in total hip arthroplasty
title_full_unstemmed Population pharmacokinetic model of cefazolin in total hip arthroplasty
title_short Population pharmacokinetic model of cefazolin in total hip arthroplasty
title_sort population pharmacokinetic model of cefazolin in total hip arthroplasty
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492877/
https://www.ncbi.nlm.nih.gov/pubmed/34611213
http://dx.doi.org/10.1038/s41598-021-99162-7
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