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Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients

The effect of heart transplantation (HTx) on the pharmacokinetics (PK) of caspofungin is not well-characterized. The aim of this study was to investigate the population PK of caspofungin in HTx and non-HTx patients and to identify covariates that may affect the PK of caspofungin. Seven successive bl...

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Autores principales: Wu, Zheng, Lan, Jinhua, Wang, Xipei, Wu, Yijin, Yao, Fen, Wang, Yifan, Zhao, Bo-xin, Wang, Yirong, Chen, Jingchun, Chen, Chunbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116478/
https://www.ncbi.nlm.nih.gov/pubmed/35389237
http://dx.doi.org/10.1128/aac.02249-21
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author Wu, Zheng
Lan, Jinhua
Wang, Xipei
Wu, Yijin
Yao, Fen
Wang, Yifan
Zhao, Bo-xin
Wang, Yirong
Chen, Jingchun
Chen, Chunbo
author_facet Wu, Zheng
Lan, Jinhua
Wang, Xipei
Wu, Yijin
Yao, Fen
Wang, Yifan
Zhao, Bo-xin
Wang, Yirong
Chen, Jingchun
Chen, Chunbo
author_sort Wu, Zheng
collection PubMed
description The effect of heart transplantation (HTx) on the pharmacokinetics (PK) of caspofungin is not well-characterized. The aim of this study was to investigate the population PK of caspofungin in HTx and non-HTx patients and to identify covariates that may affect the PK of caspofungin. Seven successive blood samples were collected before administration and at 1, 2, 6, 10, 16, and 24 h after the administration of caspofungin for at least 3 days. This study recruited 27 HTx recipients and 31 non-HTx patients with 414 plasma concentrations in total. A nonlinear mixed-effects model was used to describe the population PK of caspofungin. The PK of caspofungin was best described by a two-compartment model. The clearance (CL) and volume of the central compartment (V(c)) of caspofungin were 0.385 liter/h and 4.27 liters, respectively. The intercompartmental clearance (Q) and the volume of the peripheral compartment (V(p)) were 2.85 liters/h and 6.01 liters, respectively. In the final model, we found that albumin (ALB) affected the CL of caspofungin with an adjustment factor of −1.01, and no other covariates were identified. In this study, HTx was not found to affect the PK of caspofungin. Based on the simulations, the dose of caspofungin should be proportionately increased in patients with decreased ALB levels.
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spelling pubmed-91164782022-05-19 Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients Wu, Zheng Lan, Jinhua Wang, Xipei Wu, Yijin Yao, Fen Wang, Yifan Zhao, Bo-xin Wang, Yirong Chen, Jingchun Chen, Chunbo Antimicrob Agents Chemother Pharmacology The effect of heart transplantation (HTx) on the pharmacokinetics (PK) of caspofungin is not well-characterized. The aim of this study was to investigate the population PK of caspofungin in HTx and non-HTx patients and to identify covariates that may affect the PK of caspofungin. Seven successive blood samples were collected before administration and at 1, 2, 6, 10, 16, and 24 h after the administration of caspofungin for at least 3 days. This study recruited 27 HTx recipients and 31 non-HTx patients with 414 plasma concentrations in total. A nonlinear mixed-effects model was used to describe the population PK of caspofungin. The PK of caspofungin was best described by a two-compartment model. The clearance (CL) and volume of the central compartment (V(c)) of caspofungin were 0.385 liter/h and 4.27 liters, respectively. The intercompartmental clearance (Q) and the volume of the peripheral compartment (V(p)) were 2.85 liters/h and 6.01 liters, respectively. In the final model, we found that albumin (ALB) affected the CL of caspofungin with an adjustment factor of −1.01, and no other covariates were identified. In this study, HTx was not found to affect the PK of caspofungin. Based on the simulations, the dose of caspofungin should be proportionately increased in patients with decreased ALB levels. American Society for Microbiology 2022-04-07 /pmc/articles/PMC9116478/ /pubmed/35389237 http://dx.doi.org/10.1128/aac.02249-21 Text en Copyright © 2022 Wu et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Pharmacology
Wu, Zheng
Lan, Jinhua
Wang, Xipei
Wu, Yijin
Yao, Fen
Wang, Yifan
Zhao, Bo-xin
Wang, Yirong
Chen, Jingchun
Chen, Chunbo
Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients
title Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients
title_full Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients
title_fullStr Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients
title_full_unstemmed Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients
title_short Population Pharmacokinetics of Caspofungin and Dose Simulations in Heart Transplant Recipients
title_sort population pharmacokinetics of caspofungin and dose simulations in heart transplant recipients
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116478/
https://www.ncbi.nlm.nih.gov/pubmed/35389237
http://dx.doi.org/10.1128/aac.02249-21
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