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Dofetilide for atrial arrhythmias in congenital heart disease: a multicenter study
Ronald Wells1, Paul Khairy, Louise Harris
1Division of Pediatric Cardiology, Department of Pediatrics, Oregon Health & Science University, Portland, Oregon, USA.
Insights
Dofetilide, a class III antiarrhythmic, shows promise for treating refractory atrial arrhythmias in adults with congenital heart disease (CHD). While initial adverse effects occurred, many patients achieved sustained arrhythmia control, suggesting dofetilide is a viable treatment option.
Area of Science:
- Cardiology
- Electrophysiology
- Pharmacology
Background:
- Limited data exists on dofetilide use in congenital heart disease (CHD) patients.
- Atrial arrhythmias are common complications in adults with CHD.
Purpose of the Study:
- To evaluate the safety and efficacy of dofetilide in adult patients with CHD and refractory atrial arrhythmias.
Main Methods:
- Multicenter retrospective review of 20 adult CHD patients treated with dofetilide.
- Analysis of adverse events, arrhythmia control, and long-term outcomes.
Main Results:
- 15% of patients experienced adverse effects during in-hospital initiation (torsade de pointes, QTc prolongation).
- 55% remained on dofetilide at follow-up, with 35% achieving complete arrhythmia resolution.
- No torsade de pointes occurred after the initial in-hospital period.
Conclusions:
- Dofetilide is a potentially effective treatment for atrial arrhythmias in adult CHD patients.
- It can be a valuable adjunct to ablation and other pharmacological therapies.
Background:
Very little is known about use of the class III antiarrhythmic dofetilide in patients with congenital heart disease (CHD).
Methods:
A multicenter retrospective review of experience with dofetilide in CHD patients was undertaken.
Results:
Twenty adults with CHD and refractory atrial arrhythmias were treated with dofetilide at four institutions over a 7-year period. Three (15%) experienced adverse effects during in-hospital initiation of dofetilide (two with torsade de pointes, one with excessive QTc prolongation) and were not continued on this therapy. The remaining 17 were discharged taking dofetilide, with either resolved or improved arrhythmia. One was lost to follow-up. Five subsequently discontinued dofetilide due to waning effectiveness, manifest by recurrence of their arrhythmias. Eleven (55%) remained on dofetilide at most recent visit, with a median follow-up of nearly 1 year. Seven of these 11, or 35% of the CHD patients originally started on dofetilide, experienced a complete resolution of their arrhythmia. The remaining four had breakthrough episodes of atrial arrhythmia, but remained on dofetilide. No patient experienced torsade de pointes after the in-hospital initiation period.
Conclusions:
Used appropriately, dofetilide appears to be a viable adjunct to catheter-based ablation and alternative pharmacological approaches for the treatment of atrial arrhythmias in adult patients with congenital heart disease.
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