Shaffer K M, Denfield S W, Schowengerdt K O, Towbin J A, Radovancević B, Frazier O H, Price J K, Gajarski R J
Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
Tex Heart Inst J. 1998;25(1):57-63.
Recent studies have reported the expanding use of transplantation as the definitive option for pediatric patients with inoperable congenital heart disease. This study compares perioperative risk factors and outcomes in pediatric patients who received heart transplants for congenital heart disease with those in pediatric patients who received heart transplants for cardiomyopathy. Retrospective data collected on 40 consecutive pediatric patients undergoing cardiac transplantation from 1 January 1990 through 31 January 1995 provided the following results: 26 patients with cardiomyopathy (mean age, 7.6 years) and 14 patients with congenital heart disease (mean age, 7.2 years) underwent heart transplantation. Between groups, no significant difference was detected in waiting time for a donor heart (cardiomyopathy = 85 days, range = 2 to 409; congenital heart disease = 126 days, range = 9 to 396; P = NS); in donor/recipient weight ratio (1.27 +/- 0.34 vs 1.27 +/- 0.28, P = NS); or in ischemic times (209 +/- 92 minutes vs 248 +/- 70 minutes, P = NS). Cardiopulmonary bypass times accounted for the only significant difference (73 +/- 21 minutes vs 102 +/- 29 minutes, P = 0.003). No significant difference was found in the number of infection episodes, total days hospitalized, rejection episodes, or incidence of transplant coronary artery disease. Forty-month actuarial survival was 88% +/- 6% and 92% +/- 7% for cardiomyopathy and congenital heart disease transplant recipients, respectively (P = NS). We conclude that post-transplantation morbidity and mortality in patients with previous congenital heart disease are not significantly different from morbidity and mortality in patients with cardiomyopathy. Transplantation should be considered an acceptable therapeutic option for patients with congenital heart disease when surgical repair of the native heart is not possible.
近期研究报告称,对于患有无法手术的先天性心脏病的儿科患者,移植作为最终治疗选择的应用正在不断增加。本研究比较了因先天性心脏病接受心脏移植的儿科患者与因心肌病接受心脏移植的儿科患者的围手术期风险因素和结局。收集了1990年1月1日至1995年1月31日期间连续40例接受心脏移植的儿科患者的回顾性数据,结果如下:26例患有心肌病的患者(平均年龄7.6岁)和14例患有先天性心脏病的患者(平均年龄7.2岁)接受了心脏移植。两组之间,在等待供体心脏的时间(心肌病组 = 85天,范围 = 2至409天;先天性心脏病组 = 126天,范围 = 9至396天;P = 无显著差异)、供体/受体体重比(1.27 ± 0.34对1.27 ± 0.28,P = 无显著差异)或缺血时间(209 ± 92分钟对248 ± 70分钟,P = 无显著差异)方面未检测到显著差异。体外循环时间是唯一的显著差异(73 ± 21分钟对102 ± 29分钟,P = 0.003)。在感染发作次数、总住院天数、排斥发作次数或移植冠状动脉疾病发生率方面未发现显著差异。心肌病和先天性心脏病移植受者的40个月精算生存率分别为88% ± 6%和92% ± 7%(P = 无显著差异)。我们得出结论,既往患有先天性心脏病的患者移植后的发病率和死亡率与心肌病患者的发病率和死亡率无显著差异。当无法对自身心脏进行手术修复时,移植应被视为先天性心脏病患者可接受的治疗选择。