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Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model
Augmented renal clearance (ARC) observed in the critically ill pediatric population has received an increased attention over the last years due to its major impact on the disposition and pharmacokinetics of mainly renally excreted drugs. Apart from an important inflammatory trigger, fluid administra...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870502/ https://www.ncbi.nlm.nih.gov/pubmed/33574754 http://dx.doi.org/10.3389/fphar.2020.607101 |
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author | Dhondt, Laura Croubels, Siska De Paepe, Peter Goethals, Klara De Cock, Pieter Devreese, Mathias |
author_facet | Dhondt, Laura Croubels, Siska De Paepe, Peter Goethals, Klara De Cock, Pieter Devreese, Mathias |
author_sort | Dhondt, Laura |
collection | PubMed |
description | Augmented renal clearance (ARC) observed in the critically ill pediatric population has received an increased attention over the last years due to its major impact on the disposition and pharmacokinetics of mainly renally excreted drugs. Apart from an important inflammatory trigger, fluid administration has been suggested to contribute to the development of ARC. Therefore, the primary objective of this study was to evaluate the effect of continuous intravenous fluid administration on renal function using a conventional piglet animal model and to quantify the impact of fluid administration on the pharmacokinetics of renally excreted drugs. At baseline, twenty-four piglets (12 treatment/12 control; 7 weeks old, all ♂) received the marker drugs iohexol (64.7 mg/kg body weight (BW)) and para-aminohippuric acid (10 mg/kg BW) to quantify glomerular filtration rate and effective renal plasma flow, respectively. In addition, the hydrophilic antibiotic amikacin (7.5 mg/kg BW) was administered. Following this baseline measurement, the treatment group received fluid therapy as a constant rate infusion of 0.9% saline at 6 mL/kg/h over 36 h. After 24 h of fluid administration, the marker drugs and amikacin were administered again. When comparing both groups, a significant effect of fluid administration on the total body clearances of iohexol (p = 0.032) and amikacin (p = 0.0014) was observed. Clearances of iohexol and amikacin increased with on average 15 and 14%, although large interindividual variability was observed. This led to decreased systemic exposure to amikacin, which was manifested as decrease in area under the plasma concentration-time curve from time 0 h to infinity from 34,807 to 30,804 ng.h/mL. These results suggest that fluid therapy is a key factor involved in the development of ARC and should be taken into account when administering mainly renally excreted drugs. However, further research is necessary to confirm these results in children. |
format | Online Article Text |
id | pubmed-7870502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78705022021-02-10 Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model Dhondt, Laura Croubels, Siska De Paepe, Peter Goethals, Klara De Cock, Pieter Devreese, Mathias Front Pharmacol Pharmacology Augmented renal clearance (ARC) observed in the critically ill pediatric population has received an increased attention over the last years due to its major impact on the disposition and pharmacokinetics of mainly renally excreted drugs. Apart from an important inflammatory trigger, fluid administration has been suggested to contribute to the development of ARC. Therefore, the primary objective of this study was to evaluate the effect of continuous intravenous fluid administration on renal function using a conventional piglet animal model and to quantify the impact of fluid administration on the pharmacokinetics of renally excreted drugs. At baseline, twenty-four piglets (12 treatment/12 control; 7 weeks old, all ♂) received the marker drugs iohexol (64.7 mg/kg body weight (BW)) and para-aminohippuric acid (10 mg/kg BW) to quantify glomerular filtration rate and effective renal plasma flow, respectively. In addition, the hydrophilic antibiotic amikacin (7.5 mg/kg BW) was administered. Following this baseline measurement, the treatment group received fluid therapy as a constant rate infusion of 0.9% saline at 6 mL/kg/h over 36 h. After 24 h of fluid administration, the marker drugs and amikacin were administered again. When comparing both groups, a significant effect of fluid administration on the total body clearances of iohexol (p = 0.032) and amikacin (p = 0.0014) was observed. Clearances of iohexol and amikacin increased with on average 15 and 14%, although large interindividual variability was observed. This led to decreased systemic exposure to amikacin, which was manifested as decrease in area under the plasma concentration-time curve from time 0 h to infinity from 34,807 to 30,804 ng.h/mL. These results suggest that fluid therapy is a key factor involved in the development of ARC and should be taken into account when administering mainly renally excreted drugs. However, further research is necessary to confirm these results in children. Frontiers Media S.A. 2021-01-26 /pmc/articles/PMC7870502/ /pubmed/33574754 http://dx.doi.org/10.3389/fphar.2020.607101 Text en Copyright © 2021 Dhondt, Croubels, De Paepe, Goethals, De Cock and Devreese. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (http://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Dhondt, Laura Croubels, Siska De Paepe, Peter Goethals, Klara De Cock, Pieter Devreese, Mathias Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model |
title | Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model |
title_full | Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model |
title_fullStr | Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model |
title_full_unstemmed | Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model |
title_short | Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model |
title_sort | unraveling the contribution of fluid therapy to the development of augmented renal clearance in a piglet model |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870502/ https://www.ncbi.nlm.nih.gov/pubmed/33574754 http://dx.doi.org/10.3389/fphar.2020.607101 |
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