>From the Veterans Affairs Pittsburgh Healthcare System, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Exp Clin Transplant. 2020 Oct;18(5):605-611. doi: 10.6002/ect.2019.0065. Epub 2019 Jul 19.
The opioid epidemic and the associated deaths have increased the availability of increased-risk donor organs. Here, we assessed factors associated with increased-risk donor liver transplant and determined their impact on survival and response to direct-acting antivirals.
We analyzed anti-hepatitis C virus-positive deceased-donor liver transplant recipients from August 2013 through December 2017. We compared recipient and donor clinical and virologic features, response to direct-acting antivirals, and graft and patient survival rates in increased-risk versus tradi-tional or non-increased risk donor organ transplants.
Of 153 transplant recipients, 89 (58%) were anti-hepatitis C virus positive, with 42/89 receiving increased-risk donor livers (mean age 62 years, 1 female, 80% white, and 60% with hepatoma). On univariable analysis, receipt of increased-risk donor liver was associated with simultaneous liver-kidney transplant, lower Model for End-Stage Liver Disease score, hepatitis C virus RNA positivity, pretransplant direct-acting antiviral nonresponse, and younger donor age. On multivariable analysis, only donor age and Model for End-Stage Liver Disease score were associated with increased-risk donor transplant. Among increased-risk donors, 12 (29%) were hepatitis C virus RNA positive, including one who was anti-hepatitis C virus antibody negative. Among recipients, 62 were hepatitis C virus RNA positive (35 with increased-risk livers), with 50 recipients (81%) having genotype 1. Posttransplant, recipient genotype changed in 6 and was mixed in 4 recipients. Of 55 recipients treated with direct-acting antivirals, 54 (98%) achieved viral clearance. Overall 1-year graft and patient survival was 93%.
Increased-risk donor organs provided high levels of utility in liver transplant recipients who were anti-HCV positive, showing optimal graft and patient survival. Increased-risk donors were younger and preferably transplanted in hepatitis C virus RNA-positive recipients with lower Model for End-Stage Liver Disease score. Posttransplant direct-acting antiviral therapy was highly efficacious irrespective of pretransplant recipient and donor virologic status.
阿片类药物流行及其导致的死亡事件增加了高风险供体器官的可获得性。在此,我们评估了与高风险供体肝移植相关的因素,并确定了这些因素对生存和直接作用抗病毒药物反应的影响。
我们分析了 2013 年 8 月至 2017 年 12 月期间接受抗丙型肝炎病毒阳性的已故供体肝移植的患者。我们比较了高风险与传统或非高风险供体器官移植中受者和供者的临床和病毒学特征、对直接作用抗病毒药物的反应以及移植物和患者的生存率。
在 153 例接受肝移植的患者中,89 例(58%)抗丙型肝炎病毒阳性,其中 42 例(平均年龄 62 岁,1 例女性,80%为白人,60%患有肝癌)接受高风险供体肝脏。单变量分析显示,接受高风险供体肝移植与同时进行肝-肾移植、较低的终末期肝病模型评分、丙型肝炎病毒 RNA 阳性、移植前直接作用抗病毒药物无反应以及供体年龄较小有关。多变量分析显示,只有供体年龄和终末期肝病模型评分与高风险供体移植相关。在高风险供体中,12 例(29%)丙型肝炎病毒 RNA 阳性,其中 1 例抗丙型肝炎病毒抗体阴性。在受者中,62 例丙型肝炎病毒 RNA 阳性(50 例为高风险供体肝脏),其中 50 例(81%)为基因型 1。移植后,6 例受者的基因型发生改变,4 例受者的基因型混合。55 例接受直接作用抗病毒药物治疗的患者中,54 例(98%)病毒清除。总的 1 年移植物和患者生存率为 93%。
高风险供体器官在抗 HCV 阳性的肝移植受者中提供了高水平的效用,显示出最佳的移植物和患者生存率。高风险供体年龄较小,优选在丙型肝炎病毒 RNA 阳性、终末期肝病模型评分较低的受者中移植。移植后直接作用抗病毒治疗无论受者和供者的病毒学状态如何都具有高度疗效。