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Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients

Objective: Vancomycin is commonly used in postoperative neurosurgical patients for empirical anti-infective treatment due to the low success rate of bacterial culture in cerebrospinal fluid (about 20%) and the high mortality of intracranial infection. At conventional doses, the rate of target achiev...

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Autores principales: Wei, Shifeng, Zhang, Dongjie, Zhao, Zhigang, Mei, Shenghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548544/
https://www.ncbi.nlm.nih.gov/pubmed/36225566
http://dx.doi.org/10.3389/fphar.2022.1005791
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author Wei, Shifeng
Zhang, Dongjie
Zhao, Zhigang
Mei, Shenghui
author_facet Wei, Shifeng
Zhang, Dongjie
Zhao, Zhigang
Mei, Shenghui
author_sort Wei, Shifeng
collection PubMed
description Objective: Vancomycin is commonly used in postoperative neurosurgical patients for empirical anti-infective treatment due to the low success rate of bacterial culture in cerebrospinal fluid (about 20%) and the high mortality of intracranial infection. At conventional doses, the rate of target achievement for vancomycin trough concentration is low and the pharmacokinetics of vancomycin varies greatly in these patients, which often leads to treatment failure. The objective of this study was to establish a population pharmacokinetic (PPK) model of vancomycin in postoperative neurosurgical patients for precision medicine. Method: A total of 895 vancomycin plasma concentrations from 560 patients (497 postoperative neurosurgical patients) were retrospectively collected. The model was analyzed by nonlinear mixed effects modeling method. One-compartment model and mixed residual model was employed. The influence of covariates on model parameters was tested by forward addition and backward elimination. Goodness-of-fit, bootstrap and visual predictive check were used for model evaluation. Monte Carlo simulations were employed for dosing strategies with AUC(24) targets 400–600. Result: Estimated glomerular filtration rate (eGFR), body weight (BW) and mannitol had significant influence on vancomycin clearance (CL). [Formula: see text] , for female, a = 0.7, Scr [Formula: see text] 0.7 mg/dl, b = −0.329, Scr [Formula: see text] 0.7 mg/dl, b = −1.209; for male, a = 0.9, Scr [Formula: see text] 0.9 mg/dl, b = −0.411, Scr [Formula: see text] 0.9 mg/dl, b = −1.210. Vancomycin clearance was accelerated when co-medicated with mannitol and increased with eGFR and BW. In the final model, the population typical value is 7.98 L/h for CL and 60.2 L for apparent distribution volume, [Formula: see text] , where A = 0.13 when co-medicated with mannitol, otherwise A = 0. The model is stable and effective, with good predictability. Conclusion: In postoperative neurosurgical patients, a higher dose of vancomycin may be required due to the augmented renal function and the commonly used mannitol, especially in those with high body weight. Our vancomycin PPK model could be used for individualized treatment in postoperative neurosurgical patients.
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spelling pubmed-95485442022-10-11 Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients Wei, Shifeng Zhang, Dongjie Zhao, Zhigang Mei, Shenghui Front Pharmacol Pharmacology Objective: Vancomycin is commonly used in postoperative neurosurgical patients for empirical anti-infective treatment due to the low success rate of bacterial culture in cerebrospinal fluid (about 20%) and the high mortality of intracranial infection. At conventional doses, the rate of target achievement for vancomycin trough concentration is low and the pharmacokinetics of vancomycin varies greatly in these patients, which often leads to treatment failure. The objective of this study was to establish a population pharmacokinetic (PPK) model of vancomycin in postoperative neurosurgical patients for precision medicine. Method: A total of 895 vancomycin plasma concentrations from 560 patients (497 postoperative neurosurgical patients) were retrospectively collected. The model was analyzed by nonlinear mixed effects modeling method. One-compartment model and mixed residual model was employed. The influence of covariates on model parameters was tested by forward addition and backward elimination. Goodness-of-fit, bootstrap and visual predictive check were used for model evaluation. Monte Carlo simulations were employed for dosing strategies with AUC(24) targets 400–600. Result: Estimated glomerular filtration rate (eGFR), body weight (BW) and mannitol had significant influence on vancomycin clearance (CL). [Formula: see text] , for female, a = 0.7, Scr [Formula: see text] 0.7 mg/dl, b = −0.329, Scr [Formula: see text] 0.7 mg/dl, b = −1.209; for male, a = 0.9, Scr [Formula: see text] 0.9 mg/dl, b = −0.411, Scr [Formula: see text] 0.9 mg/dl, b = −1.210. Vancomycin clearance was accelerated when co-medicated with mannitol and increased with eGFR and BW. In the final model, the population typical value is 7.98 L/h for CL and 60.2 L for apparent distribution volume, [Formula: see text] , where A = 0.13 when co-medicated with mannitol, otherwise A = 0. The model is stable and effective, with good predictability. Conclusion: In postoperative neurosurgical patients, a higher dose of vancomycin may be required due to the augmented renal function and the commonly used mannitol, especially in those with high body weight. Our vancomycin PPK model could be used for individualized treatment in postoperative neurosurgical patients. Frontiers Media S.A. 2022-09-26 /pmc/articles/PMC9548544/ /pubmed/36225566 http://dx.doi.org/10.3389/fphar.2022.1005791 Text en Copyright © 2022 Wei, Zhang, Zhao and Mei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wei, Shifeng
Zhang, Dongjie
Zhao, Zhigang
Mei, Shenghui
Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
title Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
title_full Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
title_fullStr Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
title_full_unstemmed Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
title_short Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
title_sort population pharmacokinetic model of vancomycin in postoperative neurosurgical patients
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548544/
https://www.ncbi.nlm.nih.gov/pubmed/36225566
http://dx.doi.org/10.3389/fphar.2022.1005791
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