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Published on: May 31, 2024
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.
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.
Background:
Conduction abnormalities are frequently encountered in patients with Ebstein anomaly. The following case describes the safe use of flecainide in an infant with accessory-pathway mediated left ventricular dysfunction in the setting of Ebstein anomaly.
Case Summary:
An infant with an antenatal diagnosis of Ebstein anomaly developed progressive left ventricular dilatation and dysfunction over the first 2 months of life. ECG demonstrated persistent Wolff-Parkinson-White pattern with delta-wave polarity suggesting a right-sided septal accessory pathway. In the absence of SVT, accessory-pathway mediated dyssynchrony was suspected as the cause for left ventricular dilatation and dysfunction. He was commenced on flecainide which successfully blocked antegrade conduction via the accessory pathway resulting in a reduction in left ventricular volume and improvement in left ventricular systolic function. He remains asymptomatic at 12 months of age.
Discussion:
There is a known association between Ebstein anomaly and Wolff-Parkinson-White pattern. Right-sided septal accessory pathways can cause cardiomyopathy secondary to dyssynchronous left ventricular contraction. In patients who are unsuitable for accessory pathway ablation, flecainide can be used to block antegrade conduction via the accessory pathway resulting in improved left ventricular function, which was successful on this occasion.
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