Systemic fluoroquinolone prescriptions for hospitalized children in Belgium, results of a multicenter retrospective

Kevin Meesters1,2, Reiner Mauel3,4, Evelyn Dhont5

  • 1Department of Pediatrics, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, 1090, Brussels, Belgium. kevin.meesters@ugent.be.

BMC Infectious Diseases
|February 24, 2018
PubMed

Insights

Fluoroquinolone (FQ) use in children is often off-label, with nearly 30% of prescriptions having inappropriate doses. Infants and preschoolers are at higher risk for dosing errors, highlighting the need for better pediatric antimicrobial stewardship.

Area of Science:

  • Pediatric Pharmacology
  • Antimicrobial Stewardship
  • Drug Utilization Studies

Background:

  • Fluoroquinolones (FQ) are increasingly prescribed for pediatric patients, often for indications not approved by regulatory agencies.
  • Limited data exists on the appropriateness of systemic FQ use and dosing in hospitalized children.
  • This study addresses the gap in understanding FQ prescribing patterns and dosing accuracy in a pediatric population.

Purpose of the Study:

  • To analyze the indications for systemic fluoroquinolone (FQ) prescriptions in hospitalized children.
  • To evaluate the appropriateness of prescribed FQ doses in pediatric patients.
  • To identify risk factors associated with inadequate FQ dosing in children.

Main Methods:

  • Retrospective drug utilization study conducted in two Belgian university children's hospitals (2010-2013).
  • Inclusion of all hospitalized children receiving systemic FQ prescriptions.
  • Analysis of prescription data, indications, and prescribed daily doses; logistic regression used to identify dosing error risk factors.

Main Results:

  • 262 FQ prescriptions analyzed; 16.8% for labeled indications, 35.1% guided by bacteriological findings.
  • 30.2% of FQ prescriptions had inappropriate doses, with underdosing being the most common error (56.9% of errors).
  • Infants and preschool children showed significantly higher risk for dosing errors (adjusted ORs < 0.6).

Conclusions:

  • Systemic fluoroquinolone (FQ) prescriptions in children are frequently off-label and not guided by microbiological data.
  • Dosing errors, particularly underdosing, are common in pediatric FQ use, especially in younger children.
  • Improved pediatric antimicrobial stewardship and further pharmacokinetic research are crucial for optimizing FQ dosing in children.
Abstract

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