Experience with Continuous Infusion Vancomycin Dosing in a Large Pediatric Hospital

Amanda L Hurst1, Christine Baumgartner1, Christine E MacBrayne1

  • 1Department of Pharmacy, Children's Hospital Colorado, Aurora.

Insights

Continuous infusion vancomycin (CIV) is effective in pediatric patients. Younger children (<8 years) require higher CIV doses than older children to achieve therapeutic serum vancomycin concentrations (SVCs).

Area of Science:

  • Pediatric Pharmacology
  • Infectious Diseases
  • Pharmacokinetics

Background:

  • Limited data exists on continuous infusion vancomycin (CIV) dosing in pediatric patients.
  • CIV offers an alternative to intermittent vancomycin infusions, potentially avoiding dose escalation.
  • Establishing optimal CIV dosing is crucial for therapeutic efficacy in children.

Purpose of the Study:

  • To determine the total daily dose of CIV needed for therapeutic serum vancomycin concentrations (SVCs) in pediatric patients.
  • To analyze CIV dosing requirements across different pediatric age groups (≥31 days to <2 years, 2 to <8 years, and 8 to <18 years).

Main Methods:

  • Retrospective evaluation of pediatric patients transitioned from intermittent to continuous infusion vancomycin.
  • Data collected included patient demographics, vancomycin dosing, steady-state SVCs, and adverse events.
  • Analysis focused on identifying CIV doses required to achieve target SVCs (10-15 µg/mL and 15-20 µg/mL).

Main Results:

  • Younger pediatric patients (<2 years and 2 to <8 years) required higher daily CIV doses (48.4 mg/kg/day and 50.2-50.6 mg/kg/day, respectively) to reach target SVCs compared to older children (≥8 years).
  • Specifically, for SVCs of 10-15 µg/mL, doses were 48.4 mg/kg/day (youngest) vs. 45.6 and 39.4 mg/kg/day (older).
  • For SVCs of 15-20 µg/mL, doses were 50.2-50.6 mg/kg/day (younger) vs. 44.7 mg/kg/day (older).

Conclusions:

  • Continuous infusion vancomycin (CIV) is an effective strategy for achieving therapeutic serum vancomycin concentrations in pediatric patients.
  • Pediatric patients under 8 years of age necessitate higher CIV doses to attain target SVCs compared to older pediatric patients.
  • These findings support age-specific dosing adjustments for CIV in pediatric populations.
Abstract

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