Analysis of surgical outcome in complex double-outlet right ventricle with heterotaxy syndrome or complete atrioventricular canal defect

被引:36
作者
Takeuchi, K
McGowan, FX
Bacha, EA
Mayer, JE
Zurakowski, D
Otaki, M
del Nido, PJ
机构
[1] Harvard Univ, Sch Med, Childrens Hosp, Dept Cardiac Surg, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Childrens Hosp, Dept Biostat, Boston, MA 02115 USA
[4] Saiseikai Kyotofu Hosp, Dept Cardiovasc Surg, Tokyo, Japan
关键词
D O I
10.1016/j.athoracsur.2006.02.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Double-outlet right ventricle encompasses a broad spectrum of anomalies. Heterotaxy syndrome, which is often associated with total anomalous pulmonary venous connection and complete atrioventricular canal defect, has been considered a risk factor for surgical repair of double-outlet right ventricle. Methods. From January 1992 to May 1999, medical records of 96 patients (50 males, 46 females) who had complex double-outlet right ventricle with heterotaxy and/or complete atrioventricular canal defect were reviewed (median age at initial surgery 3 months). Seventeen patients were neonates requiring surgery. Follow-up ranged from 1 day to 7.4 years (median, 16 months). Results. Sixty-eight patients had heterotaxy syndrome (27 with total anomalous pulmonary venous connection). Eighty-three had complete atrioventricular canal defect, 22 with moderate to severe atrioventricular valve regurgitation at the time of surgical repair. Eight patients had two-ventricle repair, and 88 patients were considered for single-ventricle management ( bidirectional Glenn, 37; Fontan, 44). One patient had heart transplantation after bidirectional Glenn. There were 16 deaths including 10 early (< 30 days postoperatively). Overall survival (95% confidence interval) estimated by the Kaplan-Meier method was 89% (83% to 96%) at 1 month, 84% (76% to 91%) at 1 year, and 81% (73% to 89%) at 5 years. Multivariate analysis revealed that neonatal presentation requiring surgery (p < 0.0001), moderate to severe atrioventricular valve regurgitation (p = 0.03), and pulmonary venous obstruction (p = 0.02) were risk factors for death. Conclusions. Atrioventricular valve regurgitation, pulmonary venous obstruction, and neonatal presentation are risk factors for mortality in patients with complex double-outlet right ventricle. Early surgical intervention in symptomatic neonates and infants, including those with pulmonary venous obstruction, may reduce mortality and improve outcome after staged operation.
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页码:146 / 152
页数:7
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