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Antimicrobial Original Research Papers

Evaluation of association between parameters related to penetration into cerebrospinal fluid and the microbiological efficacy of vancomycin in patients with bacterial meningitis

, , , , , , & show all
Pages 157-165 | Received 19 Aug 2021, Accepted 25 Nov 2021, Published online: 16 Dec 2021
 

Abstract

Vancomycin (VM) is used as empirical therapy for bacterial meningitis (BM). We investigated the relationship of the microbiological efficacy of VM for BM with VM minimum inhibitory concentration (MICVM), serum VM trough concentration (VMser) and cerebrospinal fluid (CSF) protein (P)/serum albumin (SA) ratio, which may reflect the extent of blood–brain barrier (BBB) disruption. Twelve BM patients were enrolled and VM was microbiologically effective in seven (58.3%). VMser, MICVM, and CSF-P/SA ratio were not associated with the microbiological efficacy of VM. The microbiological efficacy of VM was significantly associated with CSF-P/SA ratio multiplied by VMser relative to the MICVM (η = 0.61, p = 0.04). These results indicate that the parameter combining VMser, MICVM, and the extent of BBB disruption could be associated with the microbiological efficacy of VM in BM patients.

Acknowledgement

The authors thank the neurology and neurosurgery staff of Chiba University Hospital for their assistance in this work.

Statement ethics

Ethical approval was obtained from the medical research ethics committee at Chiba University (No. 2743). The information disclosure document is available on the Chiba University Hospital website. Patients were notified about their participation in the study and informed that they were free to opt out.

Disclosure statement

No potential conflict of interest was reported by the authors.

Author contributions

All authors meet the ICMJE authorship criteria. MI and MU contributed to the implementation of the research and the analysis of the results. YS and YK checked the statistical analysis and provided statistical advice. SY, TS, YI, and II interpreted the data. All authors contributed to writing the final manuscript.

Additional information

Funding

This work was supported by JSPS KAKENHI Grant Number 19K16406.

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