Management of warfarin in children with heart disease

William T Mahle1, Scott A Simpson, Paulette Fye

  • 1Children's Healthcare of Atlanta, Emory University School of Medicine, 1405 Clifton Rd. NE, Atlanta, GA 30322, USA. mahlew@kidsheart.com

Pediatric Cardiology
|April 19, 2011
PubMed

Insights

Computerized warfarin dosing software improved INR control in pediatric cardiac patients, increasing time within the target range. Further strategies are needed to address sex and racial disparities in warfarin management.

Area of Science:

  • Pediatric Cardiology
  • Pharmacogenomics and Drug Dosing
  • Medical Informatics

Background:

  • Warfarin is crucial for pediatric cardiac patients, but achieving therapeutic International Normalized Ratio (INR) ranges can be challenging.
  • Current warfarin management relies on physician judgment and established guidelines, with variable success in maintaining optimal INR levels.
  • Patient-related factors, including sex and race, have been associated with difficulties in achieving target INR control.

Purpose of the Study:

  • To evaluate the impact of a computerized warfarin-dosing software on INR control in pediatric cardiac patients.
  • To compare the percentage of time within the target INR range before and after the implementation of dosing software.
  • To identify patient-related factors associated with suboptimal INR control.

Main Methods:

  • A historical case-control study design was employed, analyzing data from pediatric patients (infant to 20 years) with cardiac disease on warfarin.
  • INR values and warfarin dosing adjustments were compared between a period before and after the introduction of computerized dosing software.
  • Statistical analyses were performed to assess the change in time within the target INR range and identify associated patient factors.

Main Results:

  • The study included 86 pediatric patients, with prosthetic valve being the most common indication for warfarin.
  • Overall incidence of adverse bleeding events was 1.3% per patient-year.
  • Implementation of the computerized dosing software significantly increased the percentage of time within the target INR range from 41.4% to 53.1% (P < 0.001).
  • Female sex and nonwhite race were significantly associated with less time within the target INR range (P = 0.048 and P = 0.037, respectively).

Conclusions:

  • Computerized warfarin-dosing software can significantly improve INR control in pediatric cardiac patients.
  • Despite software improvements, disparities in warfarin management based on sex and race persist.
  • Further research and targeted strategies are necessary to optimize warfarin therapy and reduce inequities in this vulnerable population.

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