Lamour Jacqueline M, Kanter Kirk R, Naftel David C, Chrisant Maryanne R, Morrow William R, Clemson Barry S, Kirklin James K
Department of Pediatric Cardiology, Columbia University, New York, NY, USA.
J Am Coll Cardiol. 2009 Jul 7;54(2):160-5. doi: 10.1016/j.jacc.2009.04.020.
We sought to evaluate the outcomes and identify risk factors for mortality after heart transplantation (HT) for congenital heart disease (CHD) in infants, children, and adults.
CHD is considered a risk factor for mortality after HT, yet this unique group of patients represents a spectrum of complexity.
There were 488 patients transplanted for CHD from the combined Pediatric Heart Transplant Study (1993 to 2002, n = 367) and the Cardiac Transplant Registry Database (1990 to 2002, n = 121) who were analyzed.
The median age at HT was 12.4 years. Primary diagnosis included single ventricle (36%), d-transposition of the great arteries (12%), right ventricular outflow tract lesions (10%), l-transposition of the great arteries (8%), ventricular/atrial septal defects (8%), left ventricular outflow obstruction (8%), and other (18%). Ninety-three percent of patients had at least 1 operation before HT. Survival at 3 months post-HT was significantly worse in CHD patients versus children with cardiomyopathy, but not adults with cardiomyopathy (86%, 94%, and 91%, respectively). There was no difference in conditional 3-month survival among the 3 groups. Five-year survival was 80%. Risk factors for early mortality were older recipient age, older donors with longer ischemic times, and pre-HT Fontan operations. Predicted survival in Fontan patients was lower (77% and 70% at 1 and 5 years) versus non-Fontan patients (88% and 81% at 1 and 5 years). Risk factors for constant phase mortality included younger recipient age, higher transpulmonary gradient, cytomegalovirus mismatch at HT, and earlier classical Glenn operation.
Patients undergoing transplantation for CHD have a good late survival if they survive the early post-operative period. Risk factors for reduced survival are older age at transplant and a previous Fontan operation.
我们试图评估先天性心脏病(CHD)婴儿、儿童和成人心脏移植(HT)后的结局,并确定死亡风险因素。
CHD被认为是HT后死亡的一个风险因素,但这一独特的患者群体具有一系列复杂性。
对来自儿科心脏移植联合研究(1993年至2002年,n = 367)和心脏移植登记数据库(1990年至2002年,n = 121)的488例因CHD接受移植的患者进行了分析。
HT时的中位年龄为12.4岁。主要诊断包括单心室(36%)、大动脉d转位(12%)、右心室流出道病变(10%)、大动脉l转位(8%)、心室/房间隔缺损(8%)、左心室流出道梗阻(8%)和其他(18%)。93%的患者在HT前至少接受过1次手术。与患有心肌病的儿童相比,CHD患者HT后3个月的生存率显著更低,但与患有心肌病的成人相比则无差异(分别为86%、94%和91%)。3组患者的3个月条件生存率无差异。5年生存率为80%。早期死亡的风险因素包括受者年龄较大、供者年龄较大且缺血时间较长以及HT前的Fontan手术。Fontan患者的预测生存率低于非Fontan患者(1年和5年时分别为77%和70%与88%和81%)。持续期死亡的风险因素包括受者年龄较小、跨肺梯度较高、HT时巨细胞病毒不匹配以及较早进行经典Glenn手术。
因CHD接受移植的患者如果能在术后早期存活,则后期生存率良好。生存率降低的风险因素是移植时年龄较大以及既往接受过Fontan手术。