4.4 Article

Daptomycin Plasma and CSF Levels in Patients with Healthcare-Associated Meningitis

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NEUROCRITICAL CARE
卷 31, 期 1, 页码 116-124

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HUMANA PRESS INC
DOI: 10.1007/s12028-018-0657-y

关键词

Daptomycin; Ventriculitis; Meningitis; Pharmacokinetics; Healthcare-associated meningitis; Ventriculitis

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BackgroundThere are currently few data concerning the cerebrospinal fluid (CSF) penetration of daptomycin in patients with healthcare-associated meningitis. This study aims (1) to better characterize the pharmacokinetics of daptomycin in humans during a 7-day intravenous (IV) therapy course, and (2) to study the penetration of daptomycin in the CSF after IV infusion at the dose of 10mg/kg.ResultsIn this prospective observational study, we enrolled nine patients with an implanted external ventricular drainage and a diagnosis of a healthcare-associated meningitis. Daptomycin was administered at 10mg/kg for a maximum of 7days. The pharmacokinetic of daptomycin was studied using a two-compartment population/pharmacokinetic (POP/PK) model and by means of a nonlinear mixed effects modeling approach. A large inter-individual variability in plasma area under the curve (Range: 574.7-1366.3hmg/L), paralleled by high-peak plasma concentration (C-max) (all values>60mg/L), was noted. The inter-individual variability of CSF-AUC although significant (range: 1.17-6.81hmg/L) was narrower than previously reported and with a late occurrence of CSF-C-max (range: 6.04-9.54h). The terminal half-life between plasma and CSF was similar. t(max) values in CSF did not show a high inter-individual variability, and the fluctuations of predicted CSF concentrations were minimal. The mean value for daptomycin penetration obtained from our model was 0.45%.ConclusionsOur POP/PK model was able to describe the pharmacokinetics of daptomycin in both plasma and CSF, showing that daptomycin (up to 7days at 10mg/kg) has minimal penetration into central nervous system. Furthermore, the observed variability of AUC, t(max) and predicted concentration in CSF was lower than what previously reported in the literature. Based on the present findings, it is unlikely that daptomycin could reach CSF concentrations high enough to have clinical efficacy; this should be tested in future studies.

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