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Updated: Aug 9, 2026

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
[Isolated congenital complete atrio-ventricular block]
Insights
Congenital complete atrio-ventricular block (CAVB) generally has a good prognosis, though some patients may develop dilated cardiomyopathy. Most patients with CAVB require a pacemaker, often implanted later in life.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Electrophysiology
Context:
- Congenital complete atrio-ventricular block (CAVB) is a rare condition.
- Long-term outcomes and surveillance methods for isolated CAVB are not well-defined.
Purpose:
- To investigate the long-term evolution of isolated CAVB in a retrospective series of 54 patients.
- To evaluate the effectiveness of different surveillance methods for CAVB.
Summary:
- This study followed 54 patients with isolated CAVB for an average of 14.5 years.
- Pacemakers were implanted in 76% of patients, with implantation age varying based on diagnosis age.
- While prognosis is generally good, rare cases of dilated cardiomyopathy occurred despite pacemaker use.
Impact:
- This research highlights the generally favorable long-term outlook for isolated CAVB.
- It underscores the need for continued monitoring due to the potential for rare but severe complications like dilated cardiomyopathy.
- Findings inform clinical surveillance strategies and pacemaker implantation decisions in CAVB patients.
Abstract:
The objective of this work was to study the long term evolution of a retrospective series of 54 patients affected with congenital isolated complete atrio-ventricular block (CAVB) and to analyse the value of the different methods used for surveillance. Our series included 54 patients affected with isolated CAVB, without associated cardiopathy, diagnosed at an average age of 5.3 +/- 5.5 years, of which 9 were in utero. The average duration of follow up was 14.5 +/- 9.6 years. During the evolution, a cardiac stimulator was placed in 41 patients (76%) at a relatively late average age of 13.3 +/- 9 years, significantly lower for CAVB diagnosed before the age of 1 year (9.6 +/- 7.4 years) than for those diagnosed after the age of 1 year (16.2 +/- 9.2 years) (p < 0.02). The approach was endocavitary in 39 cases and epicardial in 2 cases. The only 2 deaths in our series (4%) concerned 2 patients of 18 and 26 years already fitted with a stimulator. Three patients progressed to severe dilated cardiomyopathy despite implantation of a stimulator. The decisive arguments for implantation of a PM were clinical (11 patients), Holter ECG (25 patients), stress test (17 patients), electrophysiological investigation (5 patients), echocardiography (3 patients) and surgical intervention (2 patients). In conclusion, our study confirms the good prognosis of isolated congenital complete atrio-ventricular block, but underlines the possible progression in rare cases in spite of stimulation towards dilated cardiomyopathy for which the aetiology remains uncertain. Three quarters of the patients required a stimulator at a somewhat late age.
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