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Published on: February 26, 2013
Time Course of Atrial Fibrillation in Patients With Congenital Heart Defects
Christophe P Teuwen1, Tanwier T T K Ramdjan1, Marco Götte1
1From the Department of Cardiology (C.P.T., T.T.T.K.R., C.H., A.Y., L.J.J., M.W., J.W.R.-H., N.M.S.d.G.) and Department of Cardio-Thoracic Surgery (A.J.J.C.B.), Erasmus University Medical Center, Rotterdam, The Netherlands; Department of Cardiology, Haga Hospital, The Hague, The Netherlands (M.G., J.W.J.V.); Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, Groningen, The Netherlands (B.J.J.M.B.); Department of Cardiology, VU University Medical Center, Amsterdam, The Netherlands (B.J.J.M.B., T.C.K.); Department of Cardiology, Radboud University Medical Center, Nijmegen; The Netherlands (R.E.); Department of Cardiology, Amphia Hospital, Breda, The Netherlands (S.G.M.); Department of Cardiology; Medisch Spectrum Twente, Enschede, The Netherlands (H.G.R.D., J.M.v.O.); Department of Cardiology, Catharina Hospital, Eindhoven, The Netherlands (P.v.d.V.); Cardiology, Inselspital, University of Bern, Bern, Switzerland (E.D.); Department of Cardiology, Boston Children's Hospital, MA (J.K.T.); and Department of Pediatrics, Harvard Medical School, Boston, MA (J.K.T.).
Insights
Congenital heart defect patients develop atrial fibrillation (AF) and atrial tachycardia (AT) at a younger age. Early, aggressive treatment is crucial due to rapid progression from paroxysmal to persistent AF.
Area of Science:
- Cardiology
- Electrophysiology
- Congenital Heart Disease
Background:
- Rising incidence of atrial fibrillation (AF) in aging patients with congenital heart defects (CHD).
- Limited research on AF prevalence and characteristics in CHD populations.
- Need for comprehensive data on AF onset, progression, and associated arrhythmias in CHD.
Purpose of the Study:
- To investigate the age of onset and initial management of AF in a large, diverse CHD cohort.
- To assess the coexistence and presentation of atrial tachyarrhythmia (AT) with AF.
- To evaluate the progression of paroxysmal AF to persistent or permanent forms during long-term follow-up.
Main Methods:
- Multicenter study of 199 patients with 15 different types of CHD and documented AF.
- Analysis of AF onset age, initial treatment, and coexisting AT.
- Long-term follow-up to assess AF progression and cerebrovascular events.
Main Results:
- AF onset occurred at a mean age of 49±17 years.
- Atrial tachycardia (AT) coexisted with AF in 33% of patients, with 65% initially presenting with AT.
- AF progressed from paroxysmal to persistent/permanent forms in 26% of patients within 3 years.
- Cerebrovascular accidents/transient ischemic attacks occurred in 13% of patients.
Conclusions:
- AF develops at a relatively young age in CHD patients compared to the general population.
- A significant proportion of CHD patients experience both AF and AT, often with AT presenting first.
- The rapid progression necessitates vigilant monitoring and prompt, assertive treatment for both AT and AF in this population.
Background:
The incidence of atrial fibrillation (AF) is rising in the aging patients with congenital heart defects (CHD). However, studies reporting on AF in patients with CHD are scarce. The aim of this multicenter study was to examine in a large cohort of patients with a variety of CHD: (1) the age of onset and initial treatment of AF, coexistence of atrial tachyarrhythmia and (2) progression of paroxysmal to (long-standing) persistent/permanent AF during long-term follow-up.
Methods And Results:
Patients (n=199) with 15 different CHD and documented AF episodes were studied. AF developed at 49±17 years. Regular atrial tachycardia (AT) coexisting with AF occurred in 65 (33%) patients; 65% initially presented with regular AT. At the end of a follow-up period of 5 (0-24) years, the ECG showed AF in 81 patients (41%). In a subgroup of 114 patients, deterioration from paroxysm of AF to (long-standing) persistent/permanent AF was observed in 29 patients (26%) after only 3 (0-18) years of the first AF episode. Cerebrovascular accidents/transient ischemic attacks occurred in 26 patients (13%), although a substantial number (n=16) occurred before the first documented AF episode.
Conclusions:
Age at development of AF in patients with CHD is relatively young compared with the patients without CHD. Coexistence of episodes of AF and regular AT occurred in a considerable number of patients; most of them initially presented with regular AT. The fast and frequent progression from paroxysmal to (long-standing) persistent or permanent AF episodes justifies close follow-up and early, aggressive therapy of both AT and AF.
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