TY - JOUR
T1 - The association of donor hepatitis C virus infection with 3-year kidney transplant outcomes in the era of direct-acting antiviral medications
AU - Sutcliffe, Siobhan
AU - Ji, Mengmeng
AU - Chang, Su Hsin
AU - Stewart, Darren
AU - Axelrod, David A.
AU - Lentine, Krista L.
AU - Wellen, Jason
AU - Alrata, Louai
AU - Gupta, Gaurav
AU - Alhamad, Tarek
N1 - Publisher Copyright:
© 2022 American Society of Transplantation & American Society of Transplant Surgeons
PY - 2023/5
Y1 - 2023/5
N2 - To determine the effect of donor hepatitis C virus (HCV) infection on kidney transplant (KT) outcomes in the era of direct-acting antiviral (DAA) medications, we examined 68,087 HCV-negative KT recipients from a deceased donor between March 2015 and May 2021. A Cox regression analysis was used to estimate adjusted hazard ratios (aHRs) of KT failure, incorporating inverse probability of treatment weighting to control for patient selection to receive an HCV-positive kidney (either nucleic acid amplification test positive [NAT+, n = 2331] or antibody positive (Ab+)/NAT− [n = 1826]) based on recipient characteristics. Compared with kidney from HCV-negative donors, those from Ab+/NAT− (aHR = 0.91; 95% confidence interval [CI], 0.75-1.10) and HCV NAT+ (aHR = 0.89; 95% CI, 0.73-1.08) donors were not associated with an increased risk of KT failure over 3 years after transplant. Moreover, HCV NAT+ kidneys were associated with a higher 1-year estimated glomerular filtration (63.0 vs 61.0 mL/min/1.73 m2, P = .007) and lower risk of delayed graft function (aOR = 0.76; 95% CI, 0.68-0.84) compared with HCV-negative kidneys. Our findings suggest that donor HCV positivity is not associated with an elevated risk of graft failure. The inclusion of donor HCV status in the Kidney Donor Risk Index may no longer be appropriate in contemporary practice.
AB - To determine the effect of donor hepatitis C virus (HCV) infection on kidney transplant (KT) outcomes in the era of direct-acting antiviral (DAA) medications, we examined 68,087 HCV-negative KT recipients from a deceased donor between March 2015 and May 2021. A Cox regression analysis was used to estimate adjusted hazard ratios (aHRs) of KT failure, incorporating inverse probability of treatment weighting to control for patient selection to receive an HCV-positive kidney (either nucleic acid amplification test positive [NAT+, n = 2331] or antibody positive (Ab+)/NAT− [n = 1826]) based on recipient characteristics. Compared with kidney from HCV-negative donors, those from Ab+/NAT− (aHR = 0.91; 95% confidence interval [CI], 0.75-1.10) and HCV NAT+ (aHR = 0.89; 95% CI, 0.73-1.08) donors were not associated with an increased risk of KT failure over 3 years after transplant. Moreover, HCV NAT+ kidneys were associated with a higher 1-year estimated glomerular filtration (63.0 vs 61.0 mL/min/1.73 m2, P = .007) and lower risk of delayed graft function (aOR = 0.76; 95% CI, 0.68-0.84) compared with HCV-negative kidneys. Our findings suggest that donor HCV positivity is not associated with an elevated risk of graft failure. The inclusion of donor HCV status in the Kidney Donor Risk Index may no longer be appropriate in contemporary practice.
KW - Organ Procurement and Transplantation Network (OPTN)
KW - deceased
KW - donors and donation
KW - glomerular filtration rate (GFR)
KW - graft survival
KW - kidney (allograft) function/dysfunction
UR - http://www.scopus.com/inward/record.url?scp=85153179419&partnerID=8YFLogxK
U2 - 10.1016/j.ajt.2022.11.005
DO - 10.1016/j.ajt.2022.11.005
M3 - Article
C2 - 37130619
AN - SCOPUS:85153179419
SN - 1600-6135
VL - 23
SP - 629
EP - 635
JO - American Journal of Transplantation
JF - American Journal of Transplantation
IS - 5
ER -