CSF penetration of vancomycin in critical care patients with proven or suspected ventriculitis: a prospective observational study. (27th January 2019)

• Record Type: Journal Article
• Authors: Blassmann, Ute; Hope, William; Roehr, Anka C; Frey, Otto R; Vetter-Kerkhoff, Cornelia; Thon, Niklas; Briegel, Josef; Huge, Volker
• Is Part Of: Journal of antimicrobial chemotherapy. Volume 74:Number 4(2019)
• Page Start: 991
• Page End: 996
• Publication Date: 2019-01-27
• Subjects: Anti-infective agents -- Periodicals; Chemotherapy -- Periodicals; 615.58
• DOI: 10.1093/jac/dky543
• Languages: English
• ISSNs: 0305-7453

Abstract

Abstract: Background: Vancomycin is recommended for ventriculitis. However, penetration into the CNS is relatively poor. Objectives: To investigate the population pharmacokinetics of vancomycin in serum and CSF in critical care patients with proven or suspected CNS infections from neurosurgical procedures. Patients and methods: This was an observational pharmacokinetic study in critical care patients with proven or suspected CNS infections receiving intravenous vancomycin. Multiple blood and intraventricular CSF samples were collected. Population pharmacokinetic analysis and simulation were undertaken with ADAPT5 and Pmetrics. Results: A total of 187 blood and CSF samples were collected from 21 patients. The median (range) C max and C min concentrations in serum were 25.67 (10.60–50.78) and 9.60 (4.46–23.56) mg/L, respectively, with a median daily dose of 2500 (500–4000) mg. The corresponding median concentrations in CSF were 0.65 (<0.24–3.83) mg/L and 0.58 (<0.24–3.95) mg/L, respectively. The median AUC0–24 in serum and CSF was 455.09 and 14.10 mg·h/L, respectively. A three-compartment linear population pharmacokinetic model best fitted the observed data. Vancomycin demonstrated poor penetration into CSF, with a median CSF/serum ratio of 3% and high intersubject pharmacokinetic variability of its penetration. Conclusions: Therapeutic drug monitoring in both serum and CSF and higher daily doses may be an option to ensure adequate trough levels and to optimize patient therapy. Novel dosing strategies designed to reduce renal toxicity, such as administration by continuous infusion, should be investigated in further clinical studies to avoid antibiotic underexposure in CSF.