Greutmann M, Prêtre R, Furrer L, Bauersfeld U, Turina M, Noll G, Luescher T F, Trindade P T
Department of Cardiology and Cardiovascular Surgery, University Hospital, Zurich and Children's Hospital, Zurich, Switzerland.
Transplant Proc. 2009 Nov;41(9):3821-6. doi: 10.1016/j.transproceed.2009.06.198.
The number of adolescent and adult patients with congenital heart disease undergoing heart transplantation is increasing. We aimed to better define the characteristics of these patients and their survival after transplantation.
We describe a group of patients with end-stage heart failure owing to congenital heart disease undergoing heart transplantation at a single tertiary center and compare their short- and long-term survival with a group of matched controls with dilated cardiomyopathy and the entire cohort of transplanted patients at our center.
Between 1985 and 2006, a total of 322 orthotopic heart transplantations were performed at our center. Thirteen patients (mean age, 27.5 years) had a diagnosis of congenital heart disease with a wide spectrum of lesions. The survival of these 13 patients was 85% at 30 days, 1, 5, and 10 years and 77% at 20 years, which did not differ significantly to the short- and long-term survival of the entire cohort of patients with heart transplantation and to the survival of age-matched controls with dilated cardiomyopathy.
In our single-center experience, short- and long-term survival after heart transplantation in a selected, small group of patients with end-stage heart failure owing to congenital heart disease did not differ significantly compared with a group of age-matched controls and the entire cohort.
接受心脏移植的先天性心脏病青少年及成年患者数量正在增加。我们旨在更好地明确这些患者的特征及其移植后的生存率。
我们描述了一组因先天性心脏病导致终末期心力衰竭并在单一三级中心接受心脏移植的患者,并将他们的短期和长期生存率与一组匹配的扩张型心肌病对照患者以及我们中心的所有移植患者队列进行比较。
1985年至2006年间,我们中心共进行了322例原位心脏移植。13例患者(平均年龄27.5岁)被诊断为先天性心脏病,病变范围广泛。这13例患者在30天、1年、5年和10年时的生存率为85%,20年时为77%,与心脏移植患者全队列的短期和长期生存率以及年龄匹配的扩张型心肌病对照患者的生存率相比,差异无统计学意义。
根据我们单中心的经验,在一小部分因先天性心脏病导致终末期心力衰竭的选定患者中,心脏移植后的短期和长期生存率与年龄匹配的对照组及全队列相比,差异无统计学意义。