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Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study

This prospective observational study aimed to clinically describe voriconazole administrations and trough concentrations in patients with Child–Pugh class C and to investigate the variability of trough concentration. A total of 144 voriconazole trough concentrations from 43 Child–Pugh class C patien...

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Autores principales: Zhao, Yichang, Hou, Jingjing, Xiao, Yiwen, Wang, Feng, Zhang, Bikui, Zhang, Min, Jiang, Yongfang, Li, Jiakai, Gong, Guozhong, Xiang, Daxiong, Yan, Miao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8470058/
https://www.ncbi.nlm.nih.gov/pubmed/34572712
http://dx.doi.org/10.3390/antibiotics10091130
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author Zhao, Yichang
Hou, Jingjing
Xiao, Yiwen
Wang, Feng
Zhang, Bikui
Zhang, Min
Jiang, Yongfang
Li, Jiakai
Gong, Guozhong
Xiang, Daxiong
Yan, Miao
author_facet Zhao, Yichang
Hou, Jingjing
Xiao, Yiwen
Wang, Feng
Zhang, Bikui
Zhang, Min
Jiang, Yongfang
Li, Jiakai
Gong, Guozhong
Xiang, Daxiong
Yan, Miao
author_sort Zhao, Yichang
collection PubMed
description This prospective observational study aimed to clinically describe voriconazole administrations and trough concentrations in patients with Child–Pugh class C and to investigate the variability of trough concentration. A total of 144 voriconazole trough concentrations from 43 Child–Pugh class C patients were analyzed. The majority of patients (62.8%) received adjustments. The repeated measured trough concentration was higher than the first and final ones generally (median, 4.33 vs. 2.99, 3.90 mg/L). Eight patients with ideal initial concentrations later got supratherapeutic with no adjusted daily dose, implying accumulation. There was a significant difference in concentrations among the six groups by daily dose (p = 0.006). The bivariate correlation analysis showed that sex, CYP2C19 genotyping, daily dose, prothrombin time activity, international normalized ratio, platelet, and Model for end-stage liver disease score were significant factors for concentration. Subsequently, the first four factors mentioned above entered into a stepwise multiple linear regression model (variance inflation factor <5), implying that CYP2C19 testing makes sense for precision medicine of Child–Pugh class C cirrhosis patients. The equation fits well and explains the 34.8% variety of concentrations (R(2) = 0.348). In conclusion, it needs more cautious administration clinically due to no recommendation for Child–Pugh class C patients in the medication label. The adjustment of the administration regimen should be mainly based on the results of repeated therapeutic drug monitoring.
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spelling pubmed-84700582021-09-27 Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study Zhao, Yichang Hou, Jingjing Xiao, Yiwen Wang, Feng Zhang, Bikui Zhang, Min Jiang, Yongfang Li, Jiakai Gong, Guozhong Xiang, Daxiong Yan, Miao Antibiotics (Basel) Article This prospective observational study aimed to clinically describe voriconazole administrations and trough concentrations in patients with Child–Pugh class C and to investigate the variability of trough concentration. A total of 144 voriconazole trough concentrations from 43 Child–Pugh class C patients were analyzed. The majority of patients (62.8%) received adjustments. The repeated measured trough concentration was higher than the first and final ones generally (median, 4.33 vs. 2.99, 3.90 mg/L). Eight patients with ideal initial concentrations later got supratherapeutic with no adjusted daily dose, implying accumulation. There was a significant difference in concentrations among the six groups by daily dose (p = 0.006). The bivariate correlation analysis showed that sex, CYP2C19 genotyping, daily dose, prothrombin time activity, international normalized ratio, platelet, and Model for end-stage liver disease score were significant factors for concentration. Subsequently, the first four factors mentioned above entered into a stepwise multiple linear regression model (variance inflation factor <5), implying that CYP2C19 testing makes sense for precision medicine of Child–Pugh class C cirrhosis patients. The equation fits well and explains the 34.8% variety of concentrations (R(2) = 0.348). In conclusion, it needs more cautious administration clinically due to no recommendation for Child–Pugh class C patients in the medication label. The adjustment of the administration regimen should be mainly based on the results of repeated therapeutic drug monitoring. MDPI 2021-09-20 /pmc/articles/PMC8470058/ /pubmed/34572712 http://dx.doi.org/10.3390/antibiotics10091130 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhao, Yichang
Hou, Jingjing
Xiao, Yiwen
Wang, Feng
Zhang, Bikui
Zhang, Min
Jiang, Yongfang
Li, Jiakai
Gong, Guozhong
Xiang, Daxiong
Yan, Miao
Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study
title Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study
title_full Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study
title_fullStr Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study
title_full_unstemmed Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study
title_short Predictors of Voriconazole Trough Concentrations in Patients with Child–Pugh Class C Cirrhosis: A Prospective Study
title_sort predictors of voriconazole trough concentrations in patients with child–pugh class c cirrhosis: a prospective study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8470058/
https://www.ncbi.nlm.nih.gov/pubmed/34572712
http://dx.doi.org/10.3390/antibiotics10091130
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