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Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure

BACKGROUND: Continuous venovenous hemodiafiltration (CVVHDF) is one of the treatments of critically ill children presenting severe acute liver failure. This affliction might be induced by HSV infection requiring a treatment by acyclovir. Continuous kidney replacement therapy (CKRT) can alter its pha...

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Autores principales: Collignon, Charlotte, de Marcellus, Charles, Oualha, Mehdi, Neuranter, Valentin, Heilbronner, Claire, Hirt, Déborah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880359/
https://www.ncbi.nlm.nih.gov/pubmed/36702934
http://dx.doi.org/10.1007/s00467-023-05881-6
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author Collignon, Charlotte
de Marcellus, Charles
Oualha, Mehdi
Neuranter, Valentin
Heilbronner, Claire
Hirt, Déborah
author_facet Collignon, Charlotte
de Marcellus, Charles
Oualha, Mehdi
Neuranter, Valentin
Heilbronner, Claire
Hirt, Déborah
author_sort Collignon, Charlotte
collection PubMed
description BACKGROUND: Continuous venovenous hemodiafiltration (CVVHDF) is one of the treatments of critically ill children presenting severe acute liver failure. This affliction might be induced by HSV infection requiring a treatment by acyclovir. Continuous kidney replacement therapy (CKRT) can alter its pharmacokinetics, according to its physicochemical properties and CVVHDF settings. CASE–DIAGNOSIS/TREATMENT: The patient was a 21-month-old female presenting liver failure with hyperammonemia treated by acyclovir with presumed HSV infection. CKRT was initiated on day 1 with substantial replacement and dialysate flow rates (respectively 75 and 220 mL/kg/h). Acyclovir was intravenously administered every 8 h with a 1-h infusion of 500 mg/m(2). Plasma and effluent concentrations were measured by liquid chromatography-tandem mass spectrometry assay to estimate the area under a curve (AUC) and CKRT clearance by 2 methods (one based on pre- and post-filter concentrations and the other one on dialysate flow rates). Clearance was estimated between 19.2 and 26.3 mL/min with the first method and between 27.6 and 44.3 mL/min with the second one. Concentrations were highly above the therapeutic index (peak concentration was measured at 28 mg/L), but AUC was appropriate. CONCLUSIONS: This case describes acyclovir pharmacokinetics during CKRT in a pediatric patient treated by acyclovir. The patient was treated with adapted exposure with the usual dosing, but lower dosing should be investigated with complementary studies. TRIAL REGISTRATION: ClinicalTrials.gov NCT02539407.
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spelling pubmed-98803592023-01-27 Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure Collignon, Charlotte de Marcellus, Charles Oualha, Mehdi Neuranter, Valentin Heilbronner, Claire Hirt, Déborah Pediatr Nephrol Brief Report BACKGROUND: Continuous venovenous hemodiafiltration (CVVHDF) is one of the treatments of critically ill children presenting severe acute liver failure. This affliction might be induced by HSV infection requiring a treatment by acyclovir. Continuous kidney replacement therapy (CKRT) can alter its pharmacokinetics, according to its physicochemical properties and CVVHDF settings. CASE–DIAGNOSIS/TREATMENT: The patient was a 21-month-old female presenting liver failure with hyperammonemia treated by acyclovir with presumed HSV infection. CKRT was initiated on day 1 with substantial replacement and dialysate flow rates (respectively 75 and 220 mL/kg/h). Acyclovir was intravenously administered every 8 h with a 1-h infusion of 500 mg/m(2). Plasma and effluent concentrations were measured by liquid chromatography-tandem mass spectrometry assay to estimate the area under a curve (AUC) and CKRT clearance by 2 methods (one based on pre- and post-filter concentrations and the other one on dialysate flow rates). Clearance was estimated between 19.2 and 26.3 mL/min with the first method and between 27.6 and 44.3 mL/min with the second one. Concentrations were highly above the therapeutic index (peak concentration was measured at 28 mg/L), but AUC was appropriate. CONCLUSIONS: This case describes acyclovir pharmacokinetics during CKRT in a pediatric patient treated by acyclovir. The patient was treated with adapted exposure with the usual dosing, but lower dosing should be investigated with complementary studies. TRIAL REGISTRATION: ClinicalTrials.gov NCT02539407. Springer Berlin Heidelberg 2023-01-27 /pmc/articles/PMC9880359/ /pubmed/36702934 http://dx.doi.org/10.1007/s00467-023-05881-6 Text en © The Author(s), under exclusive licence to International Pediatric Nephrology Association 2023 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Brief Report
Collignon, Charlotte
de Marcellus, Charles
Oualha, Mehdi
Neuranter, Valentin
Heilbronner, Claire
Hirt, Déborah
Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
title Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
title_full Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
title_fullStr Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
title_full_unstemmed Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
title_short Pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
title_sort pharmacokinetic profile of acyclovir in a child receiving continuous kidney replacement therapy for acute liver failure
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880359/
https://www.ncbi.nlm.nih.gov/pubmed/36702934
http://dx.doi.org/10.1007/s00467-023-05881-6
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