Biventricular Repair of Critically Ill Neonate with Ebstein's Anomaly: Report of 1 case.
- Author:
Joon Hyuk KONG
1
;
Woong Han KIM
;
Jae Wook RYU
;
Seog Ki LEE
;
Man Jong BAEK
;
Cheong LIM
;
Soo Cheol KIM
;
Sam Se OH
;
Chan Young NA
;
Soo Jin KIM
;
Young Kwan PARK
;
Chong Whan KIM
Author Information
1. Department of Thoracic and Cardiovascular Surgery, Sejong General Hospital, Sejong Heart Institute, Puchon, Korea. woonghan@korea.com
- Publication Type:Case Report
- Keywords:
Ebstein's anomaly;
Neonate;
Surgery method
- MeSH:
Angioplasty;
Critical Illness*;
Diagnosis;
Ebstein Anomaly*;
Echocardiography;
Fontan Procedure;
Heart Septal Defects, Atrial;
Heart Ventricles;
Humans;
Infant;
Infant, Newborn*;
Male;
Physiology;
Pulmonary Atresia;
Pulmonary Circulation;
Tricuspid Valve Insufficiency
- From:The Korean Journal of Thoracic and Cardiovascular Surgery
2002;35(4):303-306
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Patients with severe Ebstein's anomaly showing in the neonatal period, represent progressive cardiac enlargement with pulmonary hypoplasia and functional pulmonary atresia with patent ductus arteriosus-dependent pulmonary circulation. Biventricular repair in these patients had been mostly unsuccessful except for Starnes' procedure that converts the anatomy to single ventricle physiology for Fontan procedure. A 4-days old male was admitted with the diagnosis of severe Ebstein's anomaly with anatomic pulmonary atresia and severe cardiac enlargement. He successfully underwent biventricular repair with vertical plication method of atrialized right ventricle, tricupid annuloplasty, transannular right ventricular outflow tract reconstruction, atrial septal defect patch closure with fenestration, and right atrial reduction angioplasty. Postoperatively, cardiothoracic ratio was significantly reduced and mild tricuspid regurgitation was remnant in echocardiography. The patient is currently 10 months old and is fully active without restrictions.
