Population pharmacokinetics of vancomycin in patients with external ventricular drain‐associated ventriculitis

Background To determine the distribution of vancomycin into the cerebrospinal fluid (CSF) in patients with external ventricular drain (EVD)‐associated ventriculitis, the pharmacokinetics of vancomycin were evaluated and covariate relationships explored. Methods For the population pharmacokinetic mod...

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Bibliographic Details
Published in:	British journal of clinical pharmacology Vol. 87; no. 6; pp. 2502 - 2510
Main Authors:	Jalusic, Kris Oliver, Hempel, Georg, Arnemann, Philip‐Helge, Spiekermann, Christina, Kampmeier, Tim‐Gerald, Ertmer, Christian, Gastine, Silke, Hessler, Michael
Format:	Journal Article
Language:	English
Published:	England 01-06-2021
Subjects:	NONMEM nosocomial ventriculitis population pharmacokinetics vancomycin vancomycin nosocomial ventriculitis NONMEM population pharmacokinetics
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Summary:	Background To determine the distribution of vancomycin into the cerebrospinal fluid (CSF) in patients with external ventricular drain (EVD)‐associated ventriculitis, the pharmacokinetics of vancomycin were evaluated and covariate relationships explored. Methods For the population pharmacokinetic model patients were recruited in a neurocritical care unit at the University Hospital of Muenster in the period between January 2014 and June 2015. All patients had a clinical evidence of EVD‐associated ventriculitis. Population pharmacokinetic analysis of vancomycin was performed using NONMEM. Results A total of 184 blood and 133 CSF samples were collected from 29 patients. The final population pharmacokinetic model is a three‐compartment model with linear elimination. Creatinine clearance (ClCr) and CSF‐lactate were detected as significant covariates, showing that the total vancomycin plasma clearance (Cl) depends on ClCr and furthermore the clearance (Cldif) between the central and CSF compartment correlates with CSF lactate concentration. Based on the final model, the following values were estimated by NONMEM: Cl = 5.15 L/h, Q (intercompartmental clearance) = 3.31 L/h, Cldif = 0.0031 L/h, Vcentral = 42.1 L, VCSF = 0.32 L and the value of Vperipheral was fixed to 86.2 L. With the developed pharmacokinetic model, area under the curve (AUC) values as well as CSF trough levels were simulated. Conclusion Based on our analysis, the dosing of vancomycin should be referred to the degree of inflammation (derived from the CSF lactate concentration) and renal function (derived from ClCr).
ISSN:	0306-5251 1365-2125
DOI:	10.1111/bcp.14657