Impact of Donor Hepatitis C Virus on Kidney Transplant Outcomes for Hepatitis C-positive Recipients in the Direct-acting Antiviral Era: Time to Revise the Kidney Donor Risk Index?

Impact of Donor Hepatitis C Virus on Kidney Transplant Outcomes for Hepatitis C-positive Recipients in the Direct-acting Antiviral Era: Time to Revise the Kidney Donor Risk Index?
复制标题

DOI:
10.1097/tp.0000000000002949
复制
发表时间:
2020-06-01
期刊:
影响因子:
6.2
通讯作者:
Jones, Christopher M.
Jones, Christopher M.
中科院分区:
医学2区
文献类型:
--
作者:
Cannon, Robert M.;Locke, Jayme E.;Jones, Christopher M.

文献摘要

被引文献

相似文献

背景:传统上认为来自丙型肝炎病毒(HCV)感染供体的肾脏存在较差生存结局的风险,这反映在肾脏供体特征指数(KDPI)中。现代直接作用的抗病毒药物可能会改变这种风险。方法:使用器官共享联合网络数据,对2014年至2017年HCV感染的成人首次肾移植受者进行了检查。移植物和患者存活率在HCV抗体(Ab)(+)肾与Ab(-)肾的倾向匹配队列中进行比较。随后的分析在HCV病毒血症(RNA阳性)和HCV未感染肾的受者的倾向匹配队列中进行。结果:HCV抗体(+)和HCV抗体(-)肾的受者的匹配队列中各有379名受者。尽管KDPI较高(HCV Ab[+]组为58.2%,HCV Ab[-]组为38.8%),但HCV(+)和HCV(-)组的1年患者和移植物存活率相似(分别为95.4%和94.9%与97.9%和96.0%,P = 0.543和P = 0.834)。HCV-病毒血症组与HCV-初治肾组接受者各有200名接受者,HCV-病毒血症组的KDPI再次较高(56.8%对35.2%)。在病毒血症组中,移植肾衰竭(HR,4.69; P = 0.009)和死亡(HR,7.60; P = 0.003)的基线风险比(HR)显著升高,但在21和24个月时分别超过1。供体病毒血症传递了一种早期风险,随着时间的推移似乎会消退。这些结果表明,可能是时候修改肾脏供体风险指数了。
Background.Kidneys from donors with hepatitis C virus (HCV) infection are traditionally considered to be at risk for poorer survival outcomes, as reflected in the kidney donor profile index (KDPI). Modern direct-acting antivirals may modify this risk.Methods.Using United Network for Organ Sharing data, HCV-infected adult first-time kidney transplant recipients from 2014 to 2017 were examined. Graft and patient survival were compared in a propensity-matched cohort of recipients of HCV antibody (Ab)(+) kidneys versus Ab(-) kidneys. Subsequent analysis was performed in a propensity-matched cohort of recipients of HCV-viremic (RNA positive) versus HCV-naive kidneys.Results.There were 379 recipients each in the matched cohort of recipients of HCV Ab(+) versus HCV Ab(-) kidneys. Despite a higher KDPI (58.2% for HCV Ab[+] versus 38.8% for HCV Ab[-]), 1-year patient and graft survival were similar in the HCV(+) and HCV(-) groups (95.4% and 94.9% versus 97.9% and 96.0%, P = 0.543 and P = 0.834, respectively). There were 200 recipients each in the cohort of recipients of HCV-viremic versus HCV-naive kidneys, with the KDPI again higher in the HCV-viremic group (56.8% versus 35.2%). Baseline hazard ratios (HRs) for graft failure (HR, 4.69; P = 0.009) and death (HR, 7.60; P = 0.003) were significantly elevated in the viremic group, but crossed 1 at 21 and 24 months, respectively.Conclusions.In the modern direct-acting antiviral era, calculated likely KDPI overestimates risk kidneys from HCV (+) donors. Donor viremia conveys an early risk which appears to subside over time. These results suggest that it may be time to revise the kidney donor risk index.