Circulation, Vol 86, 1147-1155, Copyright © 1992 by American Heart Association
JC Pressley, JM Wharton, AS Tang, JE Lowe, JJ Gallagher and EN Prystowsky
BACKGROUND. Ebstein's anomaly is the most commonly occurring congenital
abnormality associated with the Wolff-Parkinson-White (WPW) syndrome.
However, the effects of Ebstein's anomaly on the risks and benefits of
surgical ablation of accessory pathways in patients with WPW syndrome are
unknown. METHODS AND RESULTS. This study compared the long-term outcome of
38 WPW patients with Ebstein's anomaly undergoing accessory pathway
ablation to a reference population of 384 similarly treated patients
without the anomaly. Ebstein's anomaly was mild in 21 patients (55%) and
moderate-to-severe in 17 patients (45%). Sixteen patients (42%) required
tricuspid valve surgery, and 23 (61%) had an atrial septal defect or patent
foramen ovale repaired. Baseline clinical characteristics and preoperative
clinical arrhythmias were similar in both groups. Ten-year survival was
92.4% and 91.2% for patients with and without Ebstein's anomaly,
respectively (p = NS). During a mean follow-up of 6.2 +/- 3.8 and 5.3 +/-
3.6 years, 82% of patients with and 90% without Ebstein's anomaly had
either clinically insignificant or no arrhythmias, and 18% versus 10%
reported symptoms suggesting arrhythmias lasting longer than 1 minute,
respectively. Atrial fibrillation was reduced postoperatively to 9% (p less
than 0.001) in patients with and to 4% (p less than 0.001) in those without
the anomaly. Fewer hospitalizations were reported postoperatively by 90%
versus 96% of patients with and without Ebstein's anomaly; 9.4% versus 6.0%
of patients were disabled at follow-up, respectively (p = NS). CONCLUSIONS.
Patients with Ebstein's anomaly are improved significantly after accessory
pathway ablation. The presence of this anomaly should not preclude
accessory pathway ablation in these patients.
ARTICLES
Effect of Ebstein's anomaly on short- and long-term outcome of surgically treated patients with Wolff-Parkinson-White syndrome
Department of Medicine, Duke University Medical Center, Durham, NC 27710.
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