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?

被引:22
作者
Cannon, Robert M. [1 ]
Locke, Jayme E. [1 ]
Orandi, Babak J. [1 ]
Anderson, Douglas J. [1 ]
Davis, Eric G. [2 ]
Mackelaite, Lina [3 ]
Dave, Hitarth [3 ]
Eng, Mary [2 ]
Jones, Christopher M. [2 ]
机构
[1] Univ Alabama Birmingham, Dept Surg, Div Transplantat, 701 19th St South,LHRB 748, Birmingham, AL 35294 USA
[2] Univ Louisville, Div Transplantat, Hiram C Polk Jr MD Dept Surg, Louisville, KY 40292 USA
[3] Univ Louisville, Dept Med, Div Nephrol & Hypertens, Louisville, KY 40292 USA
关键词
PROPENSITY SCORE; HCV; INFECTION; SOFOSBUVIR; RIBAVIRIN; SURVIVAL;
D O I
10.1097/TP.0000000000002949
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1215 / 1228
页数:14
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