Schindler Ehrenfried, Müller Matthias, Akintürk Hakan, Valeske Klaus, Bauer Juergen, Zickmann Bernfried, Hempelmann Gunter
Department of Anesthesiology and Intensive Care Medicine, Asklepios Klinik Sankt Augustin, German Pediatric Heart Center, Sankt Augustin, Germany.
Pediatr Transplant. 2004 Jun;8(3):237-42. doi: 10.1111/j.1399-3046.2004.00155.x.
Pediatric cardiac transplantation is currently an accepted option for end-stage heart disease and congenital cardiac malformations. This report focuses on the anesthetic perioperative management in 12 yr. From 1988 to 2001 we performed 90 heart transplantations in 88 children, infants and neonates. The pediatric heart transplant program of the children's heart center at our university hospital started in June 1988 with the transplantation of a 2-yr-old boy who was suffering from congenital heart disease. Since then, 88 transplants have been performed. We divided our patients into two groups. Group 1 ranged from 1988 to 1996 and Group 2 from 1997 to 2001. The patient characteristics have not significantly changed over the years in our institution. At the time of transplantation, mean age of the patients was 2.6 +/- 4.3 yr from the period of 1988-1996 and 2.5 +/- 4.1 yr from 1997 to 2001. Since 1988, 90 transplants (Tx) in 88 patients have been performed. Two patients needed re-Tx within 2 days after the initial operation because of primary graft failure. Indications for Tx were congenital heart disease (n = 67) and cardiomyopathy (n = 21). In the subgroup of the patients suffering from congenital heart disease there were 46 with the diagnosis of HLHS, followed by endocardial fibroelastosis (n = 7); the remaining 14 patients had other complex cardiac malformations and some underwent corrective palliative cardiac surgery before Tx. Sixty-three patients were younger than 1 yr of age and only five children were older than 10 yr. Twenty-three percent of the patients on the waiting list died before Tx was possible. The overall survival rate was 79% at 1 yr and 73% at 5 and 10 yr. Infants with HLHS had a lower probability of survival after 5 yr compared with other diagnosis (69% vs. 84%). Until now 21 patients have died after Tx. The duration of anesthesia, time of CPB and the age at the time of surgery decreased over the years. It is always a challenge for the anesthesiologist to treat these patients with pulmonary hypertension as one of the most critical risks in this group of patients. The preventive therapy with vasodilators as well as the availability of mechanical assist devices before and after heart transplantation reduces the effects of transitional pulmonary hypertension and prevents the development of post-operative right heart failure.
小儿心脏移植目前是终末期心脏病和先天性心脏畸形的一种可接受的治疗选择。本报告重点关注12年中的麻醉围手术期管理。1988年至2001年,我们在88名儿童、婴儿和新生儿中进行了90例心脏移植手术。我们大学医院儿童心脏中心的小儿心脏移植项目始于1988年6月,当时为一名患有先天性心脏病的2岁男孩进行了移植手术。从那时起,共进行了88例移植手术。我们将患者分为两组。第1组为1988年至1996年,第2组为1997年至2001年。多年来,我们机构的患者特征没有显著变化。移植时,1988 - 1996年患者的平均年龄为2.6±4.3岁,1997年至2001年为2.5±4.1岁。自1988年以来,已对88例患者进行了90例移植手术。两名患者因原发性移植物功能衰竭在初次手术后2天内需要再次移植。移植的适应证为先天性心脏病(n = 67)和心肌病(n = 21)。在患有先天性心脏病的患者亚组中,有46例诊断为左心发育不全综合征(HLHS),其次是心内膜弹力纤维增生症(n = 7);其余14例患者有其他复杂心脏畸形,部分患者在移植前接受了矫正性姑息性心脏手术。63例患者年龄小于1岁,只有5名儿童年龄大于10岁。23%的等待名单上的患者在可能进行移植之前死亡。1年时的总体生存率为79%,5年和10年时为73%。与其他诊断相比,HLHS婴儿5年后的生存概率较低(69%对84%)。到目前为止,已有21例患者在移植后死亡。多年来,麻醉持续时间、体外循环时间和手术时的年龄有所下降。对于麻醉医生来说,治疗这些患有肺动脉高压的患者始终是一项挑战,肺动脉高压是这组患者中最关键的风险之一。使用血管扩张剂的预防性治疗以及心脏移植前后机械辅助装置的可用性降低了过渡性肺动脉高压的影响,并预防了术后右心衰竭的发生。