Predictors of augmented renal clearance based on iohexol plasma clearance in critically ill children.


Journal

Pediatric nephrology (Berlin, Germany)
ISSN: 1432-198X
Titre abrégé: Pediatr Nephrol
Pays: Germany
ID NLM: 8708728

Informations de publication

Date de publication:
May 2024
Historique:
received: 19 06 2023
accepted: 26 10 2023
revised: 26 10 2023
medline: 18 3 2024
pubmed: 23 11 2023
entrez: 23 11 2023
Statut: ppublish

Résumé

Augmented renal clearance (ARC) holds a risk of subtherapeutic drug concentrations. Knowledge of patient-, disease-, and therapy-related factors associated with ARC would allow predicting which patients would benefit from intensified dosing regimens. This study aimed to identify ARC predictors and to describe ARC time-course in critically ill children, using iohexol plasma clearance (CL This is a retrospective analysis of data from the "IOHEXOL" study which validated GFR estimating formulas (eGFR) against CL Eighty-five patients were included; 57% were postoperative patients. Median CL Our findings raise PICU clinician awareness about increased risk for ARC after major surgery and in patients with eGFR above age-specific thresholds. This knowledge enables identification of patients with an ARC risk profile who would potentially benefit from a dose increase at initiation of treatment to avoid underexposure. ClinicalTrials.gov NCT05179564, registered retrospectively on January 5, 2022.

Sections du résumé

BACKGROUND BACKGROUND
Augmented renal clearance (ARC) holds a risk of subtherapeutic drug concentrations. Knowledge of patient-, disease-, and therapy-related factors associated with ARC would allow predicting which patients would benefit from intensified dosing regimens. This study aimed to identify ARC predictors and to describe ARC time-course in critically ill children, using iohexol plasma clearance (CL
METHODS METHODS
This is a retrospective analysis of data from the "IOHEXOL" study which validated GFR estimating formulas (eGFR) against CL
RESULTS RESULTS
Eighty-five patients were included; 57% were postoperative patients. Median CL
CONCLUSIONS CONCLUSIONS
Our findings raise PICU clinician awareness about increased risk for ARC after major surgery and in patients with eGFR above age-specific thresholds. This knowledge enables identification of patients with an ARC risk profile who would potentially benefit from a dose increase at initiation of treatment to avoid underexposure.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov NCT05179564, registered retrospectively on January 5, 2022.

Identifiants

pubmed: 37994980
doi: 10.1007/s00467-023-06221-4
pii: 10.1007/s00467-023-06221-4
doi:

Substances chimiques

Iohexol 4419T9MX03
Creatinine AYI8EX34EU

Banques de données

ClinicalTrials.gov
['NCT05179564']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1607-1616

Subventions

Organisme : Trasher Research Fund
ID : 15174
Organisme : Research Foundation Flanders
ID : 1881020N

Informations de copyright

© 2023. The Author(s), under exclusive licence to International Pediatric Nephrology Association.

Références

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Auteurs

Evelyn Dhont (E)

Pediatric Intensive Care Unit, Department of Intensive Care Medicine, Ghent University Hospital, C. Heymanslaan 10, 9000, Ghent, Belgium. evelyn.dhont@uzgent.be.
Department of Basic and Applied Medical Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium. evelyn.dhont@uzgent.be.
Department of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium. evelyn.dhont@uzgent.be.

Tatjana Van Der Heggen (T)

Department of Basic and Applied Medical Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Evelien Snauwaert (E)

Department of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Department of Pediatric Nephrology, ERKNet Center, Ghent University Hospital, Ghent, Belgium.

Jef Willems (J)

Pediatric Intensive Care Unit, Department of Intensive Care Medicine, Ghent University Hospital, C. Heymanslaan 10, 9000, Ghent, Belgium.
Department of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Siska Croubels (S)

Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

Joris Delanghe (J)

Department of Diagnostic Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Jan J De Waele (JJ)

Department of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.

Roos Colman (R)

Biostatistics Unit, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Johan Vande Walle (J)

Department of Internal Medicine and Pediatrics, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Department of Pediatric Nephrology, ERKNet Center, Ghent University Hospital, Ghent, Belgium.

Peter De Paepe (P)

Department of Basic and Applied Medical Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Pieter A De Cock (PA)

Pediatric Intensive Care Unit, Department of Intensive Care Medicine, Ghent University Hospital, C. Heymanslaan 10, 9000, Ghent, Belgium.
Department of Basic and Applied Medical Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Department of Pharmacy, Ghent University Hospital, Ghent, Belgium.

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