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Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke
BACKGROUND: The majority of patients with hemorrhagic stroke experience enhanced renal clearance or augmented renal clearance (ARC). The purpose of this study was to determine the impact of enhanced renal clearance or ARC on vancomycin pharmacokinetic (PK) parameters. METHODS: This was a post hoc an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868795/ https://www.ncbi.nlm.nih.gov/pubmed/31832200 http://dx.doi.org/10.1186/s40560-019-0408-y |
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author | Morbitzer, Kathryn A. Rhoney, Denise H. Dehne, Kelly A. Jordan, J. Dedrick |
author_facet | Morbitzer, Kathryn A. Rhoney, Denise H. Dehne, Kelly A. Jordan, J. Dedrick |
author_sort | Morbitzer, Kathryn A. |
collection | PubMed |
description | BACKGROUND: The majority of patients with hemorrhagic stroke experience enhanced renal clearance or augmented renal clearance (ARC). The purpose of this study was to determine the impact of enhanced renal clearance or ARC on vancomycin pharmacokinetic (PK) parameters. METHODS: This was a post hoc analysis of a prospective study of adult patients with aneurysmal subarachnoid hemorrhage (aSAH) or intracerebral hemorrhage (ICH) admitted to the neurosciences intensive care unit who received vancomycin. Creatinine clearance (CrCl) was measured and also estimated using the Cockcroft-Gault equation. Predicted PK parameters were compared with calculated PK parameters using serum peak and trough concentrations. RESULTS: Seventeen hemorrhagic stroke patients met inclusion criteria. All patients experienced enhanced renal clearance on the day that the vancomycin concentrations were obtained, and 12 patients (71%) experienced ARC. The mean calculated elimination rate constant was significantly higher than the predicted value (0.141 ± 0.02 vs. 0.087 ± 0.01 h(−1); p = 0.004) and the mean calculated half-life was significantly lower than the predicted half-life (6.5 ± 0.9 vs. 8.7 ± 0.6 h; p = 0.03). CONCLUSIONS: Patients with hemorrhagic stroke and enhanced renal clearance displayed PK alterations favoring an increased elimination of vancomycin than expected. This may result in underexposure to vancomycin, leading to treatment failure. |
format | Online Article Text |
id | pubmed-6868795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68687952019-12-12 Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke Morbitzer, Kathryn A. Rhoney, Denise H. Dehne, Kelly A. Jordan, J. Dedrick J Intensive Care Research BACKGROUND: The majority of patients with hemorrhagic stroke experience enhanced renal clearance or augmented renal clearance (ARC). The purpose of this study was to determine the impact of enhanced renal clearance or ARC on vancomycin pharmacokinetic (PK) parameters. METHODS: This was a post hoc analysis of a prospective study of adult patients with aneurysmal subarachnoid hemorrhage (aSAH) or intracerebral hemorrhage (ICH) admitted to the neurosciences intensive care unit who received vancomycin. Creatinine clearance (CrCl) was measured and also estimated using the Cockcroft-Gault equation. Predicted PK parameters were compared with calculated PK parameters using serum peak and trough concentrations. RESULTS: Seventeen hemorrhagic stroke patients met inclusion criteria. All patients experienced enhanced renal clearance on the day that the vancomycin concentrations were obtained, and 12 patients (71%) experienced ARC. The mean calculated elimination rate constant was significantly higher than the predicted value (0.141 ± 0.02 vs. 0.087 ± 0.01 h(−1); p = 0.004) and the mean calculated half-life was significantly lower than the predicted half-life (6.5 ± 0.9 vs. 8.7 ± 0.6 h; p = 0.03). CONCLUSIONS: Patients with hemorrhagic stroke and enhanced renal clearance displayed PK alterations favoring an increased elimination of vancomycin than expected. This may result in underexposure to vancomycin, leading to treatment failure. BioMed Central 2019-11-21 /pmc/articles/PMC6868795/ /pubmed/31832200 http://dx.doi.org/10.1186/s40560-019-0408-y Text en © The Author(s). 2019 Open Access This 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 | Research Morbitzer, Kathryn A. Rhoney, Denise H. Dehne, Kelly A. Jordan, J. Dedrick Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
title | Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
title_full | Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
title_fullStr | Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
title_full_unstemmed | Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
title_short | Enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
title_sort | enhanced renal clearance and impact on vancomycin pharmacokinetic parameters in patients with hemorrhagic stroke |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868795/ https://www.ncbi.nlm.nih.gov/pubmed/31832200 http://dx.doi.org/10.1186/s40560-019-0408-y |
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