Back to Search Start Over

Surgical outcome in pediatric patients with Ebstein's anomaly: A multicenter, long-term study.

Authors :
Geerdink LM
du Marchie Sarvaas GJ
Kuipers IM
Helbing WA
Delhaas T
Ter Heide H
Rozendaal L
de Korte CL
Singh SK
Ebels T
Hazekamp MG
Haas F
Bogers AJ
Kapusta L
Source :
Congenital heart disease [Congenit Heart Dis] 2017 Jan; Vol. 12 (1), pp. 32-39. Date of Electronic Publication: 2016 Aug 25.
Publication Year :
2017

Abstract

Objective: Surgical outcomes of pediatric patients with Ebstein's anomaly are often described as part of all-age-inclusive series. Our objective is to focus on patients treated surgically in childhood (0-18 y). We study the intended treatment (biventricular or 1.5 ventricle repair or univentricular palliation), freedom from unplanned reoperation and survival of this specific age group, in a nationwide study.<br />Design: Records of all Ebstein's anomaly patients born between 1980 and 2013 were reviewed. Demographic variables, intraoperative procedures and postoperative outcomes were analyzed.<br />Results: Sixty-three patients underwent 109 operations. Median follow-up after diagnosis was 121 months (range 0-216 months). Twenty-nine (46%) patients required surgery in the first year of life, including 21 who required neonatal surgery. The intended treatment was biventricular (n = 37, 59%) and 1.5 ventricle (n = 5, 8%) repair or univentricular (n = 21, 33%) palliation. The one-, five-, and 10-year freedom from unplanned reoperation was 89%, 79%, and 75% respectively. There were nine (14%) in hospital deaths (within 30 d after surgery). Causes of death were low cardiac output syndrome, cardiac failure, hypoxemia, pulmonary hypertension or an unknown cause. There were no late deaths.<br />Conclusions: Surgery in childhood represents the worse spectrum of disease, biventricular repair is often not applied. Patients often face revision surgery. Mortality is limited to the immediate postsurgical period.<br /> (© 2016 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1747-0803
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Congenital heart disease
Publication Type :
Academic Journal
Accession number :
27558473
Full Text :
https://doi.org/10.1111/chd.12404