成人先天性心脏病的多器官移植:不同患者群体的独特挑战。

Q2 Medicine
Methodist DeBakey cardiovascular journal Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.14797/mdcvj.1576
Valeria E Duarte, Marcus A Urey, Eric D Adler, Brenda Merkelz, Mark J Hobeika, Erik E Suarez, Andrea G Quarti, Rayan Yousefzai
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引用次数: 0

摘要

成人先天性心脏病(ACHD)的患病率正在上升,心力衰竭是导致死亡的主要原因。对于许多ACHD患者来说,心脏移植是晚期心力衰竭的唯一治疗选择,尽管严重的心外受累可能需要多器官移植。尽管ACHD移植数量不断增加,但这一人群的多器官移植仍然具有挑战性,有需要的人与接受移植的人之间仍然存在巨大差距。虽然ACHD患者的短期预后可能更差,但长期预后与其他心肌病患者相当,甚至优于其他心肌病患者。心外器官功能障碍在ACHD患者中很常见,这通常阻碍了单心移植。fontan相关性肝病、肺血管性和限制性肺疾病以及肾功能不全往往需要多器官移植。ACHD患者具有独特的免疫和致敏特征,增加了他们感染、排斥和恶性肿瘤的风险,需要专门的移植前脱敏和移植后免疫抑制策略。ACHD移植带来了独特的手术挑战,包括胸腔再入、血管通路问题、出血风险、广泛的解剖重建、需要更长的供体血管段和延长的缺血时间。决定单独心脏移植还是心脏-肝脏、心肺或心脏-肾脏移植需要仔细评估。这些复杂的手术计划需要广泛的多模式成像,并与ACHD心脏成像专家和腹部移植团队合作。在整个移植过程中,全面的协调和社会心理支持对ACHD患者至关重要。一个专门的多学科团队,建立一个独立的途径,在中心进行ACHD的术前、围手术期和术后护理,以及多器官移植的专业知识是必不可少的。有必要修订器官分配制度,以确保ACHD患者及时获得移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-Organ Transplantation in Adult Congenital Heart Disease: Navigating the Unique Challenges of a Distinct Patient Population.

The prevalence of adult congenital heart disease (ACHD) is increasing, with heart failure being the leading cause of death. For many ACHD patients, heart transplantation is the only treatment option for advanced heart failure, though significant extracardiac involvement may require multi-organ transplantation. Despite the rising number of ACHD transplants, multi-organ transplants in this population remain challenging, and a substantial gap remains between those in need and those who receive a transplant. While short-term outcomes may be worse for ACHD patients, long-term outcomes are comparable and even superior to other cardiomyopathies. Extracardiac organ dysfunction is common in ACHD patients, often precluding heart-alone transplantation. Fontan-associated liver disease, pulmonary vascular and restrictive lung disease, and renal dysfunction frequently necessitate multi-organ transplantation. ACHD patients have a unique immunological and sensitization profile, increasing their risk for infection, rejection, and malignancies, requiring specialized pretransplant desensitization and post-transplant immunosuppression strategies. ACHD transplantation presents unique surgical challenges, including chest reentry, vascular access issues, bleeding risks, extensive anatomical reconstruction, the need for longer vascular segments from donors, and prolonged ischemic times. Decisions regarding heart-alone versus heart-liver, heart-lung, or heart-kidney transplantation demand careful evaluation. These complex surgical plans require extensive multimodal imaging and collaboration with ACHD cardiac imaging specialists and abdominal transplant teams. Comprehensive coordination and psychosocial support are crucial for ACHD patients throughout the transplant process. A dedicated multidisciplinary team and an established and separate pathway for pre-, peri-, and postoperative care in centers with ACHD and multi-organ transplant expertise are essential. There is need for a revised organ allocation system to ensure timely access to transplantation for ACHD patients.

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