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Updated: Jun 22, 2026

Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
A 19-year-old male with palpitations
Shailendra Upadhyay1, Shweta Upadhyay
1Department of Pediatric Cardiology, Long Island Jewish Medical Center, Schneider Children's Hospital, 269-01, 76 Avenue, New Hyde Park, NY 11040, USA.
Early recognition of arrhythmogenic right ventricular dysplasia (ARVD) in young adults is crucial. Prompt diagnosis in the emergency department can prevent life-threatening cardiac events associated with this genetic heart condition.
Area of Science:
- Cardiology
- Genetics
- Emergency Medicine
Background:
- Arrhythmogenic right ventricular dysplasia (ARVD) is a primary genetic cardiomyopathy.
- It predisposes individuals to potentially fatal ventricular arrhythmias.
- Early identification is key to managing ARVD risk.
Observation:
- A 19-year-old male presented with intermittent palpitations.
- Electrocardiogram revealed characteristic epsilon waves.
- These findings suggested ARVD.
Findings:
- Diagnostic workup including cardiac MRI and stress testing confirmed ARVD.
- The patient's condition was identified and managed promptly.
- This aggressive approach was vital in preventing adverse outcomes.
Implications:
- Emergency department physicians must be vigilant for ARVD signs.
- Timely diagnosis and intervention can significantly reduce ARVD-related mortality.
- This case highlights the importance of recognizing subtle cardiac indicators in young patients.
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