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The risk of vancomycin toxicity in patients with liver impairment

BACKGROUND: The influence of liver disease on the pharmacokinetic profile, the risk of acute kidney injury, and excessive drug exposure in patients treated with vancomycin was examined. METHODS: A retrospective cohort study was performed with patients discharged from a medical center between January...

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Autores principales: Brunetti, Luigi, Song, Jong Hwa, Suh, David, Kim, Heui Jae, Seong, Yeon Hee, Lee, Dae Song, Lee, Seung-Mi, Suh, Dong-Churl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110653/
https://www.ncbi.nlm.nih.gov/pubmed/32234065
http://dx.doi.org/10.1186/s12941-020-00354-2
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author Brunetti, Luigi
Song, Jong Hwa
Suh, David
Kim, Heui Jae
Seong, Yeon Hee
Lee, Dae Song
Lee, Seung-Mi
Suh, Dong-Churl
author_facet Brunetti, Luigi
Song, Jong Hwa
Suh, David
Kim, Heui Jae
Seong, Yeon Hee
Lee, Dae Song
Lee, Seung-Mi
Suh, Dong-Churl
author_sort Brunetti, Luigi
collection PubMed
description BACKGROUND: The influence of liver disease on the pharmacokinetic profile, the risk of acute kidney injury, and excessive drug exposure in patients treated with vancomycin was examined. METHODS: A retrospective cohort study was performed with patients discharged from a medical center between January 2011 and June 2018 who received vancomycin therapy. Patients were stratified according to liver dysfunction (no to mild liver dysfunction (NMLD) and moderate to severe liver dysfunction (MSLD) based on the Child–Pugh score. The risk of acute kidney injury was compared between patients who were stratified by the attainment of a target serum trough concentration (10 mg/dL to 20 mg/dL) and the vancomycin ratio formed between the area under the curve and minimum inhibitory concentration. The impact of liver dysfunction and a daily dose of vancomycin on the risk of acute kidney injury and vancomycin AUC:MIC > 600 were tested using logistic regression with and without adjusting for the study variables. RESULTS: A total of 408 patients empirically treated with vancomycin were included in this study (237 with NMLD and 171 with MSLD). Mean vancomycin trough concentrations (17.5 ± 8.4 mg/dL versus 15.3 ± 5.2 mg/dL, p = 0.0049) and AUC:MIC ratios (549.4 ± 217.2 versus 497.5 ± 117.3, 0.0065) were significantly higher in the MSLD group when compared to the NMLD group, respectively. Vancomycin clearance was also lower in the MSLD group and corresponded to a longer half-life. The proportion of patients who developed acute kidney injury was greater in patients with MSLD when compared to NMLD (7.6% versus 3.8%, respectively; p = 0.0932); however, the difference was statistically insignificant. Furthermore, supratherapeutic serum trough concentrations and AUC:MIC ratios were more common in the MSLD group versus the NMLD group (27.5% versus 13.9%, p = 0.0007 and 28.7% versus 17.3%, respectively; p = 0.0063). CONCLUSIONS: MSLD correlates with an increased risk of supratherapeutic vancomycin exposure. Although patients with MSLD had a higher risk of acute kidney injury, the difference was not significant.
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spelling pubmed-71106532020-04-07 The risk of vancomycin toxicity in patients with liver impairment Brunetti, Luigi Song, Jong Hwa Suh, David Kim, Heui Jae Seong, Yeon Hee Lee, Dae Song Lee, Seung-Mi Suh, Dong-Churl Ann Clin Microbiol Antimicrob Research BACKGROUND: The influence of liver disease on the pharmacokinetic profile, the risk of acute kidney injury, and excessive drug exposure in patients treated with vancomycin was examined. METHODS: A retrospective cohort study was performed with patients discharged from a medical center between January 2011 and June 2018 who received vancomycin therapy. Patients were stratified according to liver dysfunction (no to mild liver dysfunction (NMLD) and moderate to severe liver dysfunction (MSLD) based on the Child–Pugh score. The risk of acute kidney injury was compared between patients who were stratified by the attainment of a target serum trough concentration (10 mg/dL to 20 mg/dL) and the vancomycin ratio formed between the area under the curve and minimum inhibitory concentration. The impact of liver dysfunction and a daily dose of vancomycin on the risk of acute kidney injury and vancomycin AUC:MIC > 600 were tested using logistic regression with and without adjusting for the study variables. RESULTS: A total of 408 patients empirically treated with vancomycin were included in this study (237 with NMLD and 171 with MSLD). Mean vancomycin trough concentrations (17.5 ± 8.4 mg/dL versus 15.3 ± 5.2 mg/dL, p = 0.0049) and AUC:MIC ratios (549.4 ± 217.2 versus 497.5 ± 117.3, 0.0065) were significantly higher in the MSLD group when compared to the NMLD group, respectively. Vancomycin clearance was also lower in the MSLD group and corresponded to a longer half-life. The proportion of patients who developed acute kidney injury was greater in patients with MSLD when compared to NMLD (7.6% versus 3.8%, respectively; p = 0.0932); however, the difference was statistically insignificant. Furthermore, supratherapeutic serum trough concentrations and AUC:MIC ratios were more common in the MSLD group versus the NMLD group (27.5% versus 13.9%, p = 0.0007 and 28.7% versus 17.3%, respectively; p = 0.0063). CONCLUSIONS: MSLD correlates with an increased risk of supratherapeutic vancomycin exposure. Although patients with MSLD had a higher risk of acute kidney injury, the difference was not significant. BioMed Central 2020-03-31 /pmc/articles/PMC7110653/ /pubmed/32234065 http://dx.doi.org/10.1186/s12941-020-00354-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Brunetti, Luigi
Song, Jong Hwa
Suh, David
Kim, Heui Jae
Seong, Yeon Hee
Lee, Dae Song
Lee, Seung-Mi
Suh, Dong-Churl
The risk of vancomycin toxicity in patients with liver impairment
title The risk of vancomycin toxicity in patients with liver impairment
title_full The risk of vancomycin toxicity in patients with liver impairment
title_fullStr The risk of vancomycin toxicity in patients with liver impairment
title_full_unstemmed The risk of vancomycin toxicity in patients with liver impairment
title_short The risk of vancomycin toxicity in patients with liver impairment
title_sort risk of vancomycin toxicity in patients with liver impairment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110653/
https://www.ncbi.nlm.nih.gov/pubmed/32234065
http://dx.doi.org/10.1186/s12941-020-00354-2
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