Groetzner J, Reichart B, Roemer U, Tiete A, Sachweh J, Kozlik-Feldmann R, Netz H, Daebritz S
Department of Cardiac Surgery, Ludwig-Maximilians University Hospital Munich-Grosshadern, Munich, Germany.
Thorac Cardiovasc Surg. 2005 Feb;53 Suppl 2:S149-54. doi: 10.1055/s-2004-830456.
Heart transplantation (HTx) has increasingly become a therapeutic option for end-stage heart failure of any origin in children. Short- and mid-term results are promising. However, long-term outcome has been a matter of concern because of acute or chronic rejection and side effects of immunosuppression. We performed a retrospective study of up to 15-years of follow-up on this patient entity.
Between 1988 and 2004, 58 HTx were performed in 55 children (cardiomyopathy (DCM) 32, congenital heart disease (CHD) 23, Re-HTx 3). Mean age was 9.1 +/- 7.2 years (4 days - 17.9 years). Twenty-nine patients had a total of 51 previous operations.
Operative mortality was 4/58 (6.8 %) due to primary graft failure. Late mortality was 7/54 (12.1 %) due to acute rejection (2), pneumonia (2), intracranial hemorrhage (1), suicide (1) and lymphoma (1). Mean follow-up was 5.2 +/- 4.2 years. One-, 5-, and 10-year survival was 86 %, 80 % and 80 %, respectively, and improved significantly after 1995 (92 % and 92 %; p = 0.04). Survival was comparable for DCM and CHD patients (1-year: 88 % vs. 82 %; p = 0.19; 5-years: 84 % vs. 77 %; p = 0.12). Three patients with therapy resistant rejection and assisted circulation required retransplantation and are alive. Freedom from acute rejection was 46 % with primary cyclosporine immunosuppression and 63 % with tacrolimus. Ninety-eight percent of the survivors are at home and in excellent cardiac condition.
Pediatric heart transplantation is a curative treatment for DCM and CHD with excellent clinical mid-term results. However, further follow-up is necessary to evaluate long-term side effects of immunosuppressants. Donor shortage remains a problem.
心脏移植(HTx)越来越成为治疗儿童各种原因所致终末期心力衰竭的一种治疗选择。短期和中期结果令人鼓舞。然而,由于急性或慢性排斥反应以及免疫抑制的副作用,长期预后一直是人们关注的问题。我们对这一患者群体进行了长达15年的随访回顾性研究。
1988年至2004年间,对55名儿童进行了58例心脏移植手术(扩张型心肌病(DCM)32例,先天性心脏病(CHD)23例,再次心脏移植3例)。平均年龄为9.1±7.2岁(4天至17.9岁)。29例患者此前共接受过51次手术。
手术死亡率为4/58(6.8%),原因是原发性移植物功能衰竭。晚期死亡率为7/54(12.1%),原因是急性排斥反应(2例)、肺炎(2例)、颅内出血(1例)、自杀(1例)和淋巴瘤(1例)。平均随访时间为5.2±4.2年。1年、5年和10年生存率分别为86%、80%和80%,1995年后显著提高(92%和92%;p=0.04)。DCM和CHD患者的生存率相当(1年:88%对82%;p=0.19;5年:84%对77%;p=0.12)。3例发生治疗抵抗性排斥反应且需要辅助循环的患者接受了再次移植,目前存活。采用环孢素进行初始免疫抑制时,无急性排斥反应的比例为46%,采用他克莫司时为63%。98%的幸存者在家中,心脏状况良好。
小儿心脏移植是治疗DCM和CHD的一种治愈性疗法,中期临床效果良好。然而,需要进一步随访以评估免疫抑制剂的长期副作用。供体短缺仍然是一个问题。