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Cerebrospinal fluid penetration of very high-dose meropenem: a case report
BACKGROUND: Standard dosing of meropenem (2 g t.i.d.) produces CSF concentrations of only 1–2 mg/L which is inferior to the clinical breakpoint for most Gram-negative bacteria. There is therefore concern that dosing must be increased in order to achieve therapeutic CSF concentrations for bacteria wi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310956/ https://www.ncbi.nlm.nih.gov/pubmed/30594199 http://dx.doi.org/10.1186/s12941-018-0299-0 |
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author | Kerz, Thomas von Loewenich, Friederike D. Roberts, Jason Neulen, Axel Ringel, Florian |
author_facet | Kerz, Thomas von Loewenich, Friederike D. Roberts, Jason Neulen, Axel Ringel, Florian |
author_sort | Kerz, Thomas |
collection | PubMed |
description | BACKGROUND: Standard dosing of meropenem (2 g t.i.d.) produces CSF concentrations of only 1–2 mg/L which is inferior to the clinical breakpoint for most Gram-negative bacteria. There is therefore concern that dosing must be increased in order to achieve therapeutic CSF concentrations for bacteria with susceptibility close to clinical breakpoints. Yet, the effects of high-dose meropenem on CSF concentrations are not well described in literature. We therefore determined meropenem CSF-levels in a patient who was treated with 15 g/day of meropenem. CASE PRESENTATION: Our patient suffered from a brain trauma and an external ventricular drainage was implanted. Later, a carbapenemase-producing Acinetobacter baumannii (OXA-23, NDM-1) was isolated from blood cultures and CSF. The MIC for meropenem was > 32 mg/L (R), and we opted for a combination therapy of meropenem, colistin and fosfomycin. Meropenem was given at an unusual high-dose (15 g/day) with the aim of achieving high CSF concentrations. CSF concentrations peaked at 64 mg/L. Yet, the patient succumbed to an intracranial bleed into a preexisting cerebral contusion. CONCLUSIONS: High-dose meropenem can achieve CSF levels largely superior to those achieved with commonly recommended dosing regimens. Though our patient succumbed to an intracranial bleed which could be regarded as a severe adverse event, we suggest that meropenem dosing can be increased when pathogens with increased MICs are found in the CSF. More in vivo data are however needed to determine the safety of high-dose meropenem. |
format | Online Article Text |
id | pubmed-6310956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63109562019-01-07 Cerebrospinal fluid penetration of very high-dose meropenem: a case report Kerz, Thomas von Loewenich, Friederike D. Roberts, Jason Neulen, Axel Ringel, Florian Ann Clin Microbiol Antimicrob Case Report BACKGROUND: Standard dosing of meropenem (2 g t.i.d.) produces CSF concentrations of only 1–2 mg/L which is inferior to the clinical breakpoint for most Gram-negative bacteria. There is therefore concern that dosing must be increased in order to achieve therapeutic CSF concentrations for bacteria with susceptibility close to clinical breakpoints. Yet, the effects of high-dose meropenem on CSF concentrations are not well described in literature. We therefore determined meropenem CSF-levels in a patient who was treated with 15 g/day of meropenem. CASE PRESENTATION: Our patient suffered from a brain trauma and an external ventricular drainage was implanted. Later, a carbapenemase-producing Acinetobacter baumannii (OXA-23, NDM-1) was isolated from blood cultures and CSF. The MIC for meropenem was > 32 mg/L (R), and we opted for a combination therapy of meropenem, colistin and fosfomycin. Meropenem was given at an unusual high-dose (15 g/day) with the aim of achieving high CSF concentrations. CSF concentrations peaked at 64 mg/L. Yet, the patient succumbed to an intracranial bleed into a preexisting cerebral contusion. CONCLUSIONS: High-dose meropenem can achieve CSF levels largely superior to those achieved with commonly recommended dosing regimens. Though our patient succumbed to an intracranial bleed which could be regarded as a severe adverse event, we suggest that meropenem dosing can be increased when pathogens with increased MICs are found in the CSF. More in vivo data are however needed to determine the safety of high-dose meropenem. BioMed Central 2018-12-29 /pmc/articles/PMC6310956/ /pubmed/30594199 http://dx.doi.org/10.1186/s12941-018-0299-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Kerz, Thomas von Loewenich, Friederike D. Roberts, Jason Neulen, Axel Ringel, Florian Cerebrospinal fluid penetration of very high-dose meropenem: a case report |
title | Cerebrospinal fluid penetration of very high-dose meropenem: a case report |
title_full | Cerebrospinal fluid penetration of very high-dose meropenem: a case report |
title_fullStr | Cerebrospinal fluid penetration of very high-dose meropenem: a case report |
title_full_unstemmed | Cerebrospinal fluid penetration of very high-dose meropenem: a case report |
title_short | Cerebrospinal fluid penetration of very high-dose meropenem: a case report |
title_sort | cerebrospinal fluid penetration of very high-dose meropenem: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310956/ https://www.ncbi.nlm.nih.gov/pubmed/30594199 http://dx.doi.org/10.1186/s12941-018-0299-0 |
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