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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...

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Autores principales: Xu, Ying, Liang, Pei, Liu, Ning, Dong, Danjiang, Gu, Qin, Wang, Xinying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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