Daly Kevin P
1Department of Cardiology,Transplant Research Program,Boston Children's Hospital,Boston,Massachusetts,United States of America.
Cardiol Young. 2015 Aug;25 Suppl 2(Suppl 2):117-23. doi: 10.1017/S1047951115000918.
Heart transplantation offers excellent survival benefit to children with end-stage heart failure. With its success, the number of potential recipients continues to exceed the number of available donors. Developing strategies to safely increase donor utilisation is crucial to decreasing wait-list mortality. A new paediatric heart allocation policy is set to be implemented with the goal of prioritising the most urgent listed candidates. Owing to excellent outcomes of ABO-incompatible heart transplantation, the sickest infants will soon receive priority for heart offers irrespective of blood group. Allosensitisation poses unique challenges within the paediatric population; ongoing multi-centre studies are poised to refine our understanding of key risk factors and optimal treatment strategies. Biomarkers for acute cellular rejection, such as donor-specific cell-free DNA, and cardiac allograft vasculopathy, such as VEGF-A, may lead to a decreased need for invasive screening. Ultimately, well-designed and executed randomised control trials of post-transplant immunosuppression are required to improve long-term outcomes after paediatric heart transplantation.
心脏移植为终末期心力衰竭患儿带来了极佳的生存益处。随着其成功开展,潜在受者的数量持续超过可用供体的数量。制定安全提高供体利用率的策略对于降低等待名单上的死亡率至关重要。一项新的儿童心脏分配政策即将实施,目标是优先考虑最紧急的在册候选人。由于ABO血型不相容心脏移植取得了出色的效果,病情最严重的婴儿很快将不论血型而优先获得心脏供体。同种致敏在儿科人群中带来了独特的挑战;正在进行的多中心研究有望深化我们对关键风险因素和最佳治疗策略的理解。急性细胞排斥反应的生物标志物,如供体特异性游离DNA,以及心脏移植血管病变的生物标志物,如VEGF-A,可能会减少侵入性筛查的需求。最终,需要精心设计和实施的儿童心脏移植后免疫抑制随机对照试验来改善长期预后。