| Literature DB >> 26239933 |
Xingang Li1, Yuanxing Wu2, Shusen Sun3, Shenghui Mei1, Jiaqing Wang1, Qiang Wang4, Zhigang Zhao5.
Abstract
Neurosurgical procedures may damage the blood-brain barrier to allow more vancomycin distribution into the cerebrospinal fluid (CSF) from blood after intravenous administration. However, a large intersubject variability in CSF vancomycin concentration was observed. We aimed to develop a population pharmacokinetic model to guide vancomycin dosing in patients after neurosurgical operation. Blood and CSF samples were collected and determined from postoperative neurosurgical patients after vancomycin administration. A three-compartment (central, peripheral, and CSF) model was proposed to characterize the pharmacokinetics of vancomycin. A nonlinear mixed-effects modeling approach was applied to fit the blood and CSF data simultaneously. The covariate analysis found that the CSF albumin level was strongly associated with the clearance between central and CSF compartment. Visual predictive check indicated that the proposed population pharmacokinetic model agrees well with the observed vancomycin concentrations. Individualized vancomycin dosage regimens could be developed for postoperative neurosurgical patients with different CSF albumin levels through model simulations. The CSF albumin level is a determinant of CSF vancomycin concentration.Entities:
Keywords: CSF albumin; HPLC; blood-CSF barrier; distribution; individualized therapy; population pharmacokinetics; postoperative neurosurgical patient; simulation; vancomycin
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Year: 2015 PMID: 26239933 DOI: 10.1002/jps.24604
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534