Key result
Amiodarone successfully terminates sustained VT due to acute myocarditis in a pediatric arterial switch patient.
Why the study?
VT in children after arterial switch operation raises concern for coronary compromise, but alternative causes like acute myocarditis present similarly, creating a diagnostic challenge.
Case Report (n=1)
Acute myocarditis can mimic coronary ischemia in children with prior arterial switch operation presenting with wide-complex tachycardia and ventricular dysfunction.
Consider myocarditis in post-arterial switch VT with dysfunction; single case leaves open generalizability of amiodarone-IVIG response.
Background Ventricular tachycardia (VT) in children following arterial switch operation (ASO) for dextro-transposition of the great arteries (D-TGA) is uncommon and typically raises concern for coronary artery compromise. However, alternative causes such as acute myocarditis may present with similar clinical and biomarker features, creating a diagnostic challenge in the acute setting. Case Report A 7-year-old boy with a history of D-TGA repaired with neonatal ASO presented with vomiting, palpitations, and lethargy. Electrocardiogram demonstrated sustained monomorphic VT at 220 beats/min. He remained hemodynamically stable. The arrhythmia did not respond to adenosine or lidocaine but terminated with amiodarone. Post-conversion evaluation revealed depressed left ventricular systolic function (ejection fraction 35%) and elevated troponin and NT-proBNP levels. Coronary computed tomography angiography demonstrated unobstructed coronary arteries. Cardiac magnetic resonance imaging showed elevated T1 and T2 values with subepicardial late gadolinium enhancement, consistent with acute myocarditis. The patient was managed with antiarrhythmic therapy, including amiodarone acutely followed by beta-blockade and mexiletine, along with intravenous immunoglobulin. Ventricular function improved rapidly, and no recurrence of VT was observed during hospitalization or early follow-up. Why Should an Emergency Physician Be Aware of This? In patients with prior ASO presenting with wide-complex tachycardia and ventricular dysfunction, coronary insufficiency is often the leading concern. This case highlights that acute myocarditis may mimic ischemia in this population. In the emergency setting, prompt recognition and appropriate antiarrhythmic selection, including escalation to amiodarone for refractory VT, are critical. Early use of advanced imaging can clarify the diagnosis, guide management, and avoid unnecessary invasive evaluation. Timely arrhythmia control may result in rapid recovery of ventricular function.
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Upadhyay et al. (2026) conducted a case report in Monomorphic ventricular tachycardia and acute myocarditis (n=1). Antiarrhythmic therapy (amiodarone, beta-blockade, mexiletine) and intravenous immunoglobulin was evaluated on Arrhythmia termination and ventricular function recovery. In a 7-year-old boy with prior arterial switch operation, sustained monomorphic ventricular tachycardia (220 beats/min) due to acute myocarditis was successfully terminated with amiodarone.
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