Long-term outcomes of single-ventricle palliation for unbalanced atrioventricular septal defects: Fontan survivors do better than previously thought

被引:44
作者
Buratto, Edward [1 ,3 ,4 ]
BBiomed, Xin Tao Ye [1 ,3 ,4 ]
BBiomed, Gregory King [1 ,3 ,4 ]
Shi, William Y. [1 ,3 ,4 ]
Weintraub, Robert G. [2 ,3 ,4 ]
d'Udekem, Yves [1 ,3 ,4 ]
Brizard, Christian P. [1 ,3 ,4 ]
Konstantinov, Igor E. [1 ,3 ,4 ]
机构
[1] Dept Cardiac Surg, Melbourne, Australia
[2] Royal Childrens Hosp, Dept Cardiol, Melbourne, Australia
[3] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[4] Murdoch Childrens Res Inst, Melbourne, Australia
关键词
Fontan; single-ventricle palliation; unbalanced atrioventricular septal defect; LEFT-HEART SYNDROME; HETEROTAXY SYNDROME; FOLLOW-UP; OPERATION; VALVE; REPAIR; CIRCULATION; EXPERIENCE; 2ND-STAGE;
D O I
10.1016/j.jtcvs.2016.09.051
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Single-ventricle palliation (SVP) for children with unbalanced atrioventricular septal defect (uAVSD) is thought to carry a poor prognosis, but limited data have been reported. Methods: We performed a retrospective review of children with uAVSD who underwent SVP at a single institution. Data were obtained from medical records and correspondence with general practitioners and cardiologists. Results: Between 1976 and 2016, a total of 139 patients underwent SVP for uAVSD. A neonatal palliative procedure was performed in 83.5% of these patients (116 of 139), and early mortality occurred in 11.2% (13 of 116). Ninety-four patients underwent stage II palliation, with an early mortality of 6.4% (6 of 94). Eighty patients (57.6%) underwent Fontan completion, with an early mortality of 3.8% (3 of 80). Interstage mortality was 11.7% (12 of 103) between stages I and II and 17.0% (15 of 88) between stage II and Fontan. Long-term survival was 66.5%(95% confidence interval [CI], 57.9%-73.9%) at 5 years, 64.4% (95% CI, 55.5%-72.0%) at 15 years, and 57.8% (95% CI, 47.5%-66.8%) at 25 years. Survival post-Fontan was 94.9% (95% CI, 86.9%-98.0%) at 5 years, 92.0% (95% CI, 80.6%-96.8%) at 15 years, and 82.4% (95% CI, 61.5%-92.6%) at 25 years. Risk factors associated with death or transplantation were aortic atresia (hazard ratio [HR], 5.3; P =.03) and hypoplastic aortic arch (HR, 2.5; P =.02). Atrioventricular valve operations were required in 31.7% of the patients (44 of 139), with 31.8% of them (14 of 44) requiring a further operation. Conclusions: Children undergoing SVP for uAVSD have substantial mortality, with< 60% survival at 25 years. However, survival of children who achieve Fontan completion is better than has been reported previously.
引用
收藏
页码:430 / 438
页数:9
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