Pharmacological resynchronisation with flecainide in an infant with Ebstein anomaly and Wolff-Parkinson-White

Gajon Uthayakumaran1, Hiroko Asakai1, Ganesh Gnanappa1

  • 1The Heart Centre for Children, The Children's Hospital at Westmead, Corner Hawkesbury Road and Hainsworth St, Westmead, NSW 2145, Australia.

PubMed

Insights

Flecainide safely treated left ventricular dysfunction in an infant with Ebstein anomaly and Wolff-Parkinson-White pattern. This approach improved heart function by blocking accessory pathway conduction.

Area of Science:

  • Pediatric Cardiology
  • Electrophysiology
  • Congenital Heart Disease

Background:

  • Ebstein anomaly is associated with conduction abnormalities, including accessory pathways.
  • Accessory pathways can lead to ventricular dysfunction, particularly in infants.

Observation:

  • An infant with Ebstein anomaly presented with progressive left ventricular dilatation and dysfunction.
  • Electrocardiogram revealed a Wolff-Parkinson-White pattern indicative of a right-sided septal accessory pathway.

Findings:

  • Accessory pathway-mediated dyssynchrony was suspected as the cause of left ventricular dysfunction.
  • Flecainide effectively blocked antegrade conduction via the accessory pathway.
  • This resulted in reduced left ventricular volume and improved systolic function.

Implications:

  • Flecainide is a safe and effective treatment for accessory-pathway mediated cardiomyopathy in infants with Ebstein anomaly.
  • This strategy offers an alternative when accessory pathway ablation is not feasible.
  • Early intervention can lead to sustained asymptomatic status in affected infants.
Abstract

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