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Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit

INTRODUCTION: Nephrotoxicity is the most important adverse effect of colistin therapy. We investigated the frequency of nephrotoxicity, risk factors related to nephrotoxicity, and its relationship with mortality in patients who received intravenous colistin in intensive care units (ICUs). MATERIALS...

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Autores principales: Gunay, Emrah, Kaya, Safak, Baysal, Birol, Yuksel, Enver, Arac, Esref
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470093/
https://www.ncbi.nlm.nih.gov/pubmed/32703065
http://dx.doi.org/10.1080/0886022X.2020.1795878
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author Gunay, Emrah
Kaya, Safak
Baysal, Birol
Yuksel, Enver
Arac, Esref
author_facet Gunay, Emrah
Kaya, Safak
Baysal, Birol
Yuksel, Enver
Arac, Esref
author_sort Gunay, Emrah
collection PubMed
description INTRODUCTION: Nephrotoxicity is the most important adverse effect of colistin therapy. We investigated the frequency of nephrotoxicity, risk factors related to nephrotoxicity, and its relationship with mortality in patients who received intravenous colistin in intensive care units (ICUs). MATERIALS AND METHODS: We retrospectively reviewed the data of patients who received intravenous colistin in ICUs between 2011 and 2017. Acute kidney injury (AKI) diagnosis and staging were made based on the Kidney Disease Improving Global Outcome criteria. RESULTS: There were 149 patients included in the study with 61% being male. The mean age was 58.7 ± 20.3 years. AKI was detected in 96 (64.4%) patients. There were 25 patients with AKI stage 1 (16.8%) and 71 patients with AKI stage 2 or 3 (47.7%). Advanced age (65.0 vs. 47.4 years; p < .001), diabetes mellitus (p < .001), heart failure (p = .01), high APACHE II score (31.7 vs. 28.08, p = .019), and inotrope usage (p = .01) were found as risk factors for AKI. The 14-day mortality rate was higher in the AKI group (p = .027). DISCUSSION: Higher AKI and mortality rates are observed in patients with diabetes, heart failure, advanced age and the hemodynamically impaired. However, it is a fact that there are no alternative therapies other than colistin in the treatment of multidrug-resistant Gram-negative bacterial infections. Therefore, the development of AKI in this patient group should not be considered a sufficient reason for discontinuing colistin treatment. Understanding the risk factors in this potential nephrotoxic treatment can provide a more careful patient follow-up.
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spelling pubmed-74700932020-09-15 Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit Gunay, Emrah Kaya, Safak Baysal, Birol Yuksel, Enver Arac, Esref Ren Fail Clinical Study INTRODUCTION: Nephrotoxicity is the most important adverse effect of colistin therapy. We investigated the frequency of nephrotoxicity, risk factors related to nephrotoxicity, and its relationship with mortality in patients who received intravenous colistin in intensive care units (ICUs). MATERIALS AND METHODS: We retrospectively reviewed the data of patients who received intravenous colistin in ICUs between 2011 and 2017. Acute kidney injury (AKI) diagnosis and staging were made based on the Kidney Disease Improving Global Outcome criteria. RESULTS: There were 149 patients included in the study with 61% being male. The mean age was 58.7 ± 20.3 years. AKI was detected in 96 (64.4%) patients. There were 25 patients with AKI stage 1 (16.8%) and 71 patients with AKI stage 2 or 3 (47.7%). Advanced age (65.0 vs. 47.4 years; p < .001), diabetes mellitus (p < .001), heart failure (p = .01), high APACHE II score (31.7 vs. 28.08, p = .019), and inotrope usage (p = .01) were found as risk factors for AKI. The 14-day mortality rate was higher in the AKI group (p = .027). DISCUSSION: Higher AKI and mortality rates are observed in patients with diabetes, heart failure, advanced age and the hemodynamically impaired. However, it is a fact that there are no alternative therapies other than colistin in the treatment of multidrug-resistant Gram-negative bacterial infections. Therefore, the development of AKI in this patient group should not be considered a sufficient reason for discontinuing colistin treatment. Understanding the risk factors in this potential nephrotoxic treatment can provide a more careful patient follow-up. Taylor & Francis 2020-07-24 /pmc/articles/PMC7470093/ /pubmed/32703065 http://dx.doi.org/10.1080/0886022X.2020.1795878 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Gunay, Emrah
Kaya, Safak
Baysal, Birol
Yuksel, Enver
Arac, Esref
Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
title Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
title_full Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
title_fullStr Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
title_full_unstemmed Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
title_short Evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
title_sort evaluation of prognosis and nephrotoxicity in patients treated with colistin in intensive care unit
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470093/
https://www.ncbi.nlm.nih.gov/pubmed/32703065
http://dx.doi.org/10.1080/0886022X.2020.1795878
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