Dapper F, Bauer J, Kroll J, Zickmann B, Bohle R M, Hagel K J, Schranz D
Department of Cardiovascular Surgery, Justus-Liebig-University, Giessen, Germany.
Eur J Cardiothorac Surg. 1998 Jul;14(1):1-5; discussion 5-6. doi: 10.1016/s1010-7940(98)00136-5.
Orthotopic heart transplantation has become an accepted therapeutic concept for adult patients with endstage heart disease. In newborns and infants this procedure is still a matter of discussion because of unknown long-term results and the lack of donor organs.
Since March 1988 we have performed 40 orthotopic heart transplantation in 39 infants who were from 1 to 280 days of age. Indications for transplantation included hypoplastic left-heart syndrome (n = 28), dilative cardiomyopathy (n = 4), endocardial fibroelastosis (n = 4) and other complex structural anomalies (n = 3). The mean waiting period for transplantation was 53 days. A donor-recipient weight ratio up to 4.0 was accepted. Profound hypothermic circulatory arrest was used for graft implantation in all those patients who required extensive aortic arch reconstruction (71%). The initial immunomodulation was based on Cyclosporine, Azathioprine and Prednisolone. Patients who underwent transplantation during the first 6 weeks of life received a chronic single-drug therapy with Cyclosporine after 1 year.
There were six peri-operative deaths caused by drug-resistant right-heart failure in three cases, humoral rejection (n = 1), CMV infection (n = 1) and multi organ failure (n = 1). One infant died late, due to rejection. The actuarial survival rate for the entire group is now 82%. There is a remarkable influence of increasing experience. Whereas six of 15 infants who had heart transplantation between 1988 and 1993 died early post-operatively (survival rate: 60%), only one late death occurred among 24 recipients in the period from 1994 to April 1997 (survival rate: 96%). Episodes of rejection occurred once or several times in about half of the patients in this series (48%). All surviving children are living at home in excellent condition.
Heart transplantation during early infancy is a rational and durable therapy for heart diseases with irreversible myocardial failure or severe structural anomalies. The intermediate-term results have been encouraging in many centers, but more data must be accumulated to determine the sequelae of chronic immunosuppression. The lack of donor organs remains one of the major problems in pediatric heart transplantation.
原位心脏移植已成为终末期心脏病成年患者公认的治疗方法。对于新生儿和婴儿,由于长期结果未知且供体器官短缺,该手术仍存在争议。
自1988年3月以来,我们对39例年龄在1至280天的婴儿进行了40例原位心脏移植。移植指征包括左心发育不全综合征(n = 28)、扩张型心肌病(n = 4)、心内膜弹力纤维增生症(n = 4)和其他复杂结构异常(n = 3)。移植的平均等待期为53天。供体与受体体重比高达4.0是可以接受的。所有需要广泛主动脉弓重建的患者(71%)在植入移植物时采用了深低温停循环。初始免疫调节基于环孢素、硫唑嘌呤和泼尼松龙。出生后6周内接受移植的患者在1年后接受环孢素单一药物长期治疗。
围手术期死亡6例,其中3例死于耐药性右心衰竭,1例死于体液排斥,1例死于巨细胞病毒感染,1例死于多器官功能衰竭。1例婴儿后期死于排斥反应。整个组的实际生存率目前为82%。经验的增加有显著影响。1988年至1993年期间接受心脏移植的15例婴儿中有6例术后早期死亡(生存率:60%),而在1994年至1997年4月期间的24例接受者中仅发生1例后期死亡(生存率:96%)。在该系列中约一半的患者(48%)发生过一次或多次排斥反应。所有存活儿童均在家中,状况良好。
婴儿早期心脏移植是治疗不可逆心肌衰竭或严重结构异常心脏病的合理且持久的治疗方法。许多中心的中期结果令人鼓舞,但必须积累更多数据以确定慢性免疫抑制的后遗症。供体器官短缺仍然是小儿心脏移植的主要问题之一。