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Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study
INTRODUCTION: Severe infections in intensive care patients show high morbidity and mortality rates. Linezolid is an antimicrobial drug frequently used in critically ill patients. Recent data indicates that there might be high variability of linezolid serum concentrations in intensive care patients r...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227093/ https://www.ncbi.nlm.nih.gov/pubmed/25011656 http://dx.doi.org/10.1186/cc13984 |
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author | Zoller, Michael Maier, Barbara Hornuss, Cyrill Neugebauer, Christina Döbbeler, Gundula Nagel, Dorothea Holdt, Lesca Miriam Bruegel, Mathias Weig, Thomas Grabein, Béatrice Frey, Lorenz Teupser, Daniel Vogeser, Michael Zander, Johannes |
author_facet | Zoller, Michael Maier, Barbara Hornuss, Cyrill Neugebauer, Christina Döbbeler, Gundula Nagel, Dorothea Holdt, Lesca Miriam Bruegel, Mathias Weig, Thomas Grabein, Béatrice Frey, Lorenz Teupser, Daniel Vogeser, Michael Zander, Johannes |
author_sort | Zoller, Michael |
collection | PubMed |
description | INTRODUCTION: Severe infections in intensive care patients show high morbidity and mortality rates. Linezolid is an antimicrobial drug frequently used in critically ill patients. Recent data indicates that there might be high variability of linezolid serum concentrations in intensive care patients receiving standard doses. This study was aimed to evaluate whether standard dosing of linezolid leads to therapeutic serum concentrations in critically ill patients. METHODS: In this prospective observational study, 30 critically ill adult patients with suspected infections received standard dosing of 600 mg linezolid intravenously twice a day. Over 4 days, multiple serum samples were obtained from each patient, in order to determine the linezolid concentrations by liquid chromatography tandem mass spectrometry. RESULTS: A high variability of serum linezolid concentrations was observed (range of area under the linezolid concentration time curve over 24 hours (AUC(24)) 50.1 to 453.9 mg/L, median 143.3 mg*h/L; range of trough concentrations (C(min)) < 0.13 to 14.49 mg/L, median 2.06 mg/L). Furthermore, potentially subtherapeutic linezolid concentrations over 24 hours and at single time points (defined according to the literature as AUC(24) < 200 mg*h/L and C(min) < 2 mg/L) were observed for 63% and 50% of the patients, respectively. Finally, potentially toxic levels (defined as AUC(24) > 400 mg*h/L and C(min) > 10 mg/L) were observed for 7 of the patients. CONCLUSIONS: A high variability of linezolid serum concentrations with a substantial percentage of potentially subtherapeutic levels was observed in intensive care patients. The findings suggest that therapeutic drug monitoring of linezolid might be helpful for adequate dosing of linezolid in critically ill patients. TRIAL REGISTRATION: Clinicaltrials.gov NCT01793012. Registered 24 January 2013. |
format | Online Article Text |
id | pubmed-4227093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42270932014-11-12 Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study Zoller, Michael Maier, Barbara Hornuss, Cyrill Neugebauer, Christina Döbbeler, Gundula Nagel, Dorothea Holdt, Lesca Miriam Bruegel, Mathias Weig, Thomas Grabein, Béatrice Frey, Lorenz Teupser, Daniel Vogeser, Michael Zander, Johannes Crit Care Research INTRODUCTION: Severe infections in intensive care patients show high morbidity and mortality rates. Linezolid is an antimicrobial drug frequently used in critically ill patients. Recent data indicates that there might be high variability of linezolid serum concentrations in intensive care patients receiving standard doses. This study was aimed to evaluate whether standard dosing of linezolid leads to therapeutic serum concentrations in critically ill patients. METHODS: In this prospective observational study, 30 critically ill adult patients with suspected infections received standard dosing of 600 mg linezolid intravenously twice a day. Over 4 days, multiple serum samples were obtained from each patient, in order to determine the linezolid concentrations by liquid chromatography tandem mass spectrometry. RESULTS: A high variability of serum linezolid concentrations was observed (range of area under the linezolid concentration time curve over 24 hours (AUC(24)) 50.1 to 453.9 mg/L, median 143.3 mg*h/L; range of trough concentrations (C(min)) < 0.13 to 14.49 mg/L, median 2.06 mg/L). Furthermore, potentially subtherapeutic linezolid concentrations over 24 hours and at single time points (defined according to the literature as AUC(24) < 200 mg*h/L and C(min) < 2 mg/L) were observed for 63% and 50% of the patients, respectively. Finally, potentially toxic levels (defined as AUC(24) > 400 mg*h/L and C(min) > 10 mg/L) were observed for 7 of the patients. CONCLUSIONS: A high variability of linezolid serum concentrations with a substantial percentage of potentially subtherapeutic levels was observed in intensive care patients. The findings suggest that therapeutic drug monitoring of linezolid might be helpful for adequate dosing of linezolid in critically ill patients. TRIAL REGISTRATION: Clinicaltrials.gov NCT01793012. Registered 24 January 2013. BioMed Central 2014 2014-07-10 /pmc/articles/PMC4227093/ /pubmed/25011656 http://dx.doi.org/10.1186/cc13984 Text en Copyright © 2014 Zoller et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Zoller, Michael Maier, Barbara Hornuss, Cyrill Neugebauer, Christina Döbbeler, Gundula Nagel, Dorothea Holdt, Lesca Miriam Bruegel, Mathias Weig, Thomas Grabein, Béatrice Frey, Lorenz Teupser, Daniel Vogeser, Michael Zander, Johannes Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
title | Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
title_full | Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
title_fullStr | Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
title_full_unstemmed | Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
title_short | Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
title_sort | variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227093/ https://www.ncbi.nlm.nih.gov/pubmed/25011656 http://dx.doi.org/10.1186/cc13984 |
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