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Impact of vancomycin administration modality on target attainment in acutely ill children-a propensity score matching

Dominik Armatys1, Anaïs Briant2, Pascal Thibon2,3

  • 1Department of Pharmacy, University Hospital of Caen Normandie, Caen, France.

Insights

Continuous vancomycin infusions (CI) in children significantly improve achieving therapeutic targets compared to intermittent infusions (II). This method is safe and effective for pediatric patients requiring vancomycin therapy.

Area of Science:

  • Pediatric Pharmacology
  • Infectious Diseases
  • Clinical Pharmacy

Background:

  • Achieving therapeutic vancomycin exposure in children is challenging due to pharmacokinetic variability, with intermittent infusions often failing to meet AUC targets.
  • Continuous infusion (CI) shows promise in neonates and adults, but pediatric data, especially as a first-line strategy, are limited.

Purpose of the Study:

  • To compare the efficacy and safety of vancomycin continuous infusion (CI) versus intermittent infusion (II) as a first-line strategy in acutely ill hospitalized children.
  • To evaluate target attainment (TA) and time to TA with both administration methods.

Main Methods:

  • Retrospective single-center study of pediatric inpatients (0-17 years) receiving intravenous vancomycin.
  • Used propensity score matching (PSM) and inverse probability of treatment weighting (IPWT) to compare CI and II groups.
  • Included patients with at least one plasma vancomycin level measurement.

Main Results:

  • Continuous infusion (CI) achieved significantly higher target attainment (TA) at first measurement (50% vs. 23%) and overall (77.3% vs. 45.8%) compared to intermittent infusion (II).
  • Propensity score-adjusted analyses confirmed CI's superiority in TA.
  • Time to TA was shorter with CI (median 2 days vs. 3 days), and adverse events were comparable between groups.

Conclusions:

  • Vancomycin CI as a first-line strategy in acutely ill children appears more efficient for achieving therapeutic targets than intermittent infusion (II).
  • CI did not increase adverse events and may allow for lower daily doses.
  • Further prospective multicenter studies are needed to confirm optimal CI dosing regimens.

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