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Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study
In recent years, polymyxin B‐associated acute kidney injury (PB‐AKI) in critically ill patients has been reported frequently, but polymyxin B (PB) is mainly cleared through non‐renal pathways, and the reasons of PB‐AKI remain unclear. The aim of this study was to investigate the relationship between...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542723/ https://www.ncbi.nlm.nih.gov/pubmed/36206131 http://dx.doi.org/10.1002/prp2.1010 |
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author | Xu, Ying Liang, Pei Liu, Ning Dong, Danjiang Gu, Qin Wang, Xinying |
author_facet | Xu, Ying Liang, Pei Liu, Ning Dong, Danjiang Gu, Qin Wang, Xinying |
author_sort | Xu, Ying |
collection | PubMed |
description | In recent years, polymyxin B‐associated acute kidney injury (PB‐AKI) in critically ill patients has been reported frequently, but polymyxin B (PB) is mainly cleared through non‐renal pathways, and the reasons of PB‐AKI remain unclear. The aim of this study was to investigate the relationship between the serum concentration of PB and PB‐AKI. We conducted a prospective cohort study in an intensive care unit between May 2019 and July 2021. Over the study period, 52 patients were included and divided into an AKI group (n = 26) and a non‐AKI group (n = 26). The loading dose of PB in the AKI group was significantly higher than that in the non‐AKI group. The C (1/2), C (min), and estimated area under the concentration–time curve (AUC)(0–24) of PB in the AKI group were dramatically increased compared with those in the non‐AKI group, but the C (max) between the two groups showed no differences. Upon obtaining the ROC curve, the areas for the C (1/2), C (min), and estimated AUC(0–24) were 0.742, 0.710, and 0.710, respectively. The sensitivity was ascertained to be 61.54%, and the specificity was 76.92% when the cutoff value for the estimated AUC(0–24) of 97.72 mg·h/L was used preferentially. The incidence of PB‐AKI is high and related to the loading dose of PB. PB‐AKI could be predicted when the estimated AUC(0–24) of PB was greater than 97.72 mg·h/L. |
format | Online Article Text |
id | pubmed-9542723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95427232022-10-14 Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study Xu, Ying Liang, Pei Liu, Ning Dong, Danjiang Gu, Qin Wang, Xinying Pharmacol Res Perspect Original Articles In recent years, polymyxin B‐associated acute kidney injury (PB‐AKI) in critically ill patients has been reported frequently, but polymyxin B (PB) is mainly cleared through non‐renal pathways, and the reasons of PB‐AKI remain unclear. The aim of this study was to investigate the relationship between the serum concentration of PB and PB‐AKI. We conducted a prospective cohort study in an intensive care unit between May 2019 and July 2021. Over the study period, 52 patients were included and divided into an AKI group (n = 26) and a non‐AKI group (n = 26). The loading dose of PB in the AKI group was significantly higher than that in the non‐AKI group. The C (1/2), C (min), and estimated area under the concentration–time curve (AUC)(0–24) of PB in the AKI group were dramatically increased compared with those in the non‐AKI group, but the C (max) between the two groups showed no differences. Upon obtaining the ROC curve, the areas for the C (1/2), C (min), and estimated AUC(0–24) were 0.742, 0.710, and 0.710, respectively. The sensitivity was ascertained to be 61.54%, and the specificity was 76.92% when the cutoff value for the estimated AUC(0–24) of 97.72 mg·h/L was used preferentially. The incidence of PB‐AKI is high and related to the loading dose of PB. PB‐AKI could be predicted when the estimated AUC(0–24) of PB was greater than 97.72 mg·h/L. John Wiley and Sons Inc. 2022-10-07 /pmc/articles/PMC9542723/ /pubmed/36206131 http://dx.doi.org/10.1002/prp2.1010 Text en © 2022 The Authors. Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Xu, Ying Liang, Pei Liu, Ning Dong, Danjiang Gu, Qin Wang, Xinying Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study |
title | Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study |
title_full | Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study |
title_fullStr | Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study |
title_full_unstemmed | Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study |
title_short | Correlation between the drug concentration of polymyxin B and polymyxin B‐associated acute kidney injury in critically ill patients: A prospective study |
title_sort | correlation between the drug concentration of polymyxin b and polymyxin b‐associated acute kidney injury in critically ill patients: a prospective study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542723/ https://www.ncbi.nlm.nih.gov/pubmed/36206131 http://dx.doi.org/10.1002/prp2.1010 |
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