Abstract

Effective antibiotic therapy of cerebral infections such as meningitis or ventriculitis is hindered by low penetration into the cerebrospinal fluid (CSF). Because continuous infusion of meropenem and vancomycin and routine therapeutic drug monitoring (TDM) have been proposed to optimize antimicrobial exposure in ventriculitis patients, an individualized dosing strategy was implemented in our department. We present a retrospective analysis of meropenem and vancomycin concentrations in serum and CSF in the first nine ventriculitis patients treated with continuous infusion and TDM-guided dose optimization aiming at 20–30 mg/L. Median initial dosing was 8.8 g/24 h meropenem and 4.25 g/24 h vancomycin, respectively, resulting in median serum concentrations of 21.3 mg/L for meropenem and 24.5 mg/L for vancomycin and CSF concentrations of 3.4 mg/L for meropenem and 1.7 mg/L for vancomycin. Median CSF penetration was 15% for meropenem and 7% for vancomycin. With initial dosing, all but one patient achieved CSF concentrations above 1 mg/L. Dose adjustment according to TDM ensured sufficient CSF concentrations in all patients within 48 h of treatment. Given the limited penetration, continuous infusion of meropenem and vancomycin based on renal function and TDM-guided dose optimization appears a reasonable approach to attain sufficient CSF concentrations in ventriculitis patients.

Highlights

  • Acute subarachnoid hemorrhage, intraventricular bleeding, tumors of the brain stem, and other acute intracranial pathologies may require insertion of external ventricular drains to manage hydrocephalus and monitor intracranial pressure

  • Infection parameters C-reactive protein (CRP) and cerebrospinal fluid (CSF) leukocyte count decreased within 7 days after initiation of antibiotic therapy in all patients (Supplementary Materials: Figure S1)

  • We retrospectively evaluated vancomycin and meropenem concentrations in serum and CSF of ventriculitis patients receiving continuous infusion and routine therapeutic drug monitoring (TDM)

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Summary

Introduction

Intraventricular bleeding, tumors of the brain stem, and other acute intracranial pathologies may require insertion of external ventricular drains to manage hydrocephalus and monitor intracranial pressure. Ventriculitis is the most frequent complication in these patients with significant morbidity, prolonged ICU and hospital length of stay, and higher costs [1]. The Infectious Diseases Society of America recommends vancomycin in combination with meropenem (or ceftazidime) for the initial treatment of infections after neurosurgery or infections related to external ventricular drains [3]. Achieving and maintaining appropriate concentrations at the target site of infection is a significant challenge for critical care physicians. Pathophysiological changes in volume of distribution and augmented renal clearance alter pharmacokinetics in critically ill patients compared to what is observed in other patient groups [5–7]

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