Your browser doesn't support javascript.
loading
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.
Affiliation
  • Collignon C; Pediatric Intensive Care Unit, APHP University Hospital Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France. charlotte.collignon@aphp.fr.
  • de Marcellus C; Pediatric Intensive Care Unit, APHP University Hospital Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.
  • Oualha M; Pediatric Intensive Care Unit, APHP University Hospital Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.
  • Neuranter V; Université de Paris, Paris, France.
  • Heilbronner C; Pharmacology and Drug Evaluation in Children and Pregnant Women EA7323, Paris Descartes University, Paris, France.
  • Hirt D; Department of Clinical Pharmacology, Cochin Hospital, Paris, France.
Pediatr Nephrol ; 38(10): 3493-3497, 2023 10.
Article in En | MEDLINE | ID: mdl-36702934
ABSTRACT

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/m2. 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liver Failure, Acute / Hemodiafiltration / Acute Kidney Injury / Continuous Renal Replacement Therapy Limits: Child / Female / Humans / Infant Language: En Journal: Pediatr Nephrol Journal subject: NEFROLOGIA / PEDIATRIA Year: 2023 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liver Failure, Acute / Hemodiafiltration / Acute Kidney Injury / Continuous Renal Replacement Therapy Limits: Child / Female / Humans / Infant Language: En Journal: Pediatr Nephrol Journal subject: NEFROLOGIA / PEDIATRIA Year: 2023 Document type: Article Affiliation country: France