Key result
Catheter ablation successfully terminates dual macro-reentrant right atrial tachycardias in a ccTGA patient without recurrence.
Why the study?
Adults with congenital heart disease are at risk for unique arrhythmias due to variant anatomy and complex surgical repairs, requiring detailed anatomical and procedural knowledge for ablation.
Case Report (n=1)
No
Catheter ablation guided by high-density electroanatomic and entrainment mapping can successfully treat complex macro-reentrant atrial tachycardias in patients with congenitally corrected transposition of the great arteries.
Extends sparse case experience with ablation in ccTGA; leaves open need for prospective data before wider adoption.
Adults with congenital heart disease represent a complex and growing patient population. By virtue of their variant anatomy and the complex surgical repair often required in infancy, these patients are at risk of developing unique atrial and ventricular arrhythmias throughout their lifetimes. Electrophysiologists involved in the care of these patients should have a detailed understanding of their underlying anatomy and any prior surgical procedures to guide procedural planning and should have knowledge of the range of possible arrhythmia mechanisms that may differ from patients without structural heart disease. Despite this complexity, standard mapping techniques and electrophysiologic maneuvers may still be used to elucidate arrhythmia mechanisms, map tachycardia circuits, and guide catheter ablation. We report a case of two different macroreentrant right atrial tachycardias that were successfully ablated in a patient with congenitally-corrected transposition of the great arteries.
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Pennoyer et al. (2020) conducted a case report in Congenitally corrected transposition of the great arteries (cc-TGA) with supraventricular tachycardia (n=1). Catheter ablation was evaluated on Termination of tachycardia and freedom from recurrence. Catheter ablation successfully terminated two different macro-reentrant right atrial tachycardias in a 15-year-old female with congenitally corrected transposition of the great arteries, with no recurrence at six months.
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