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Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients
The desired target steady-state average colistin concentration (C(ss,avg)) to balance between therapeutic effectiveness and nephrotoxicity is largely unclear. The objective of this study was to evaluate the effect of the desired target colistin C(ss,avg) on the effectiveness and safety of IV colisti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584744/ https://www.ncbi.nlm.nih.gov/pubmed/31217523 http://dx.doi.org/10.1038/s41598-019-44965-y |
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author | Jung, Sunmi Chung, Eun Kyoung Jun, Min Sun Son, Eun Sun Rhie, Sandy Jeong |
author_facet | Jung, Sunmi Chung, Eun Kyoung Jun, Min Sun Son, Eun Sun Rhie, Sandy Jeong |
author_sort | Jung, Sunmi |
collection | PubMed |
description | The desired target steady-state average colistin concentration (C(ss,avg)) to balance between therapeutic effectiveness and nephrotoxicity is largely unclear. The objective of this study was to evaluate the effect of the desired target colistin C(ss,avg) on the effectiveness and safety of IV colistin therapy in critically ill patients. Overall, 153 critically ill patients (71% males) receiving IV colistin were retrospectively analyzed. The desired target colistin C(ss,avg) was estimated based on the daily colistin dose and creatinine clearance of each patient. No significant predictor for clinical cure was identified. However, microbiological outcome was significantly associated with pneumonia compared to bacteremia (odds ratio [OR] 0.092, 95% confidence interval [CI] [0.033–0.251], P < 0.001) and the use of IV colistin loading dose (OR 2.783, 95% CI [1.126–6.880], P = 0.027). Colistin-associated nephrotoxicity was significantly less likely to occur in patients who received inhaled colistin close to the time of IV colistin therapy (OR 0.331, CI [0.119–0.925], P = 0.035). The desired target C(ss,avg) of colistin was not associated with treatment outcomes or the risk of nephrotoxicity. Loading dose and inhaled colistin use near the time of IV colistin therapy may be considered to maximize therapeutic effectiveness and minimize the risk of colistin-associated nephrotoxicity, respectively. |
format | Online Article Text |
id | pubmed-6584744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65847442019-06-26 Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients Jung, Sunmi Chung, Eun Kyoung Jun, Min Sun Son, Eun Sun Rhie, Sandy Jeong Sci Rep Article The desired target steady-state average colistin concentration (C(ss,avg)) to balance between therapeutic effectiveness and nephrotoxicity is largely unclear. The objective of this study was to evaluate the effect of the desired target colistin C(ss,avg) on the effectiveness and safety of IV colistin therapy in critically ill patients. Overall, 153 critically ill patients (71% males) receiving IV colistin were retrospectively analyzed. The desired target colistin C(ss,avg) was estimated based on the daily colistin dose and creatinine clearance of each patient. No significant predictor for clinical cure was identified. However, microbiological outcome was significantly associated with pneumonia compared to bacteremia (odds ratio [OR] 0.092, 95% confidence interval [CI] [0.033–0.251], P < 0.001) and the use of IV colistin loading dose (OR 2.783, 95% CI [1.126–6.880], P = 0.027). Colistin-associated nephrotoxicity was significantly less likely to occur in patients who received inhaled colistin close to the time of IV colistin therapy (OR 0.331, CI [0.119–0.925], P = 0.035). The desired target C(ss,avg) of colistin was not associated with treatment outcomes or the risk of nephrotoxicity. Loading dose and inhaled colistin use near the time of IV colistin therapy may be considered to maximize therapeutic effectiveness and minimize the risk of colistin-associated nephrotoxicity, respectively. Nature Publishing Group UK 2019-06-19 /pmc/articles/PMC6584744/ /pubmed/31217523 http://dx.doi.org/10.1038/s41598-019-44965-y Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jung, Sunmi Chung, Eun Kyoung Jun, Min Sun Son, Eun Sun Rhie, Sandy Jeong Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients |
title | Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients |
title_full | Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients |
title_fullStr | Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients |
title_full_unstemmed | Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients |
title_short | Differences in Colistin Administration and Bacterial and Treatment Outcomes in Critically Ill Patients |
title_sort | differences in colistin administration and bacterial and treatment outcomes in critically ill patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584744/ https://www.ncbi.nlm.nih.gov/pubmed/31217523 http://dx.doi.org/10.1038/s41598-019-44965-y |
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