Clinical spectrum and long-term outcome of ebstein's anomaly based on a 26-year experience in an asian cohort
Journal
European Journal of Pediatrics
Journal Volume
168
Journal Issue
6
Pages
685-690
Date Issued
2009
Abstract
Ebstein's anomaly is a rare, congenital cardiac anomaly that may result in cyanosis, right heart failure, and tachyarrhythmia during the newborn stage or after adolescence. This study investigated the data of 77 patients diagnosed between 1980 and 2006 at a tertiary care center in Taiwan. Patients were grouped into either an early group or a late group. Survival declined rapidly within the newborn stage in the early group, but declined only during the third decade in the late group. Surgical results were poor (20% success rate) for neonatal systemic-to-pulmonary shunts in those cases with associated pulmonary atresia, but were satisfactory for other surgical modes. Supraventricular tachyarrhythmia occurred in 31 (41%) patients at a median age of 10 years and could be eliminated by radiofrequency ablation (81% success rate), though the recurrence rate was high (41%). In conclusion, other than those cases requiring shunts at the newborn stage, the long-term outcome was favorable. ? 2008 Springer-Verlag.
SDGs
Other Subjects
article; disease association; disease course; Ebstein anomaly; heart rhythm; human; priority journal; pulmonary valve atresia; radiofrequency ablation; supraventricular tachycardia; survival rate; systemic pulmonary shunt; Adolescent; Adult; Catheter Ablation; Child; Child, Preschool; Ebstein Anomaly; Female; Humans; Infant; Infant, Newborn; Kaplan-Meiers Estimate; Male; Retrospective Studies; Tachycardia, Supraventricular; Taiwan; Treatment Outcome; Young Adult
Type
journal article