98%
921
2 minutes
20
Long-term outcomes of using HCV-positive donors in HCV-negative recipients in liver transplantation (LT) are not well established. Data from the United Network for Organ Sharing (UNOS) database between July 1, 2015, and December 31, 2023, were analyzed. The cohort included 44,447 HCV antibody-negative (Ab-) candidates who underwent deceased donor LT. Changes in case numbers and utilization rates of HCV-positive donors, divided into HCV-viremic (NAT+) or Ab+ nonviremic (Ab+/NAT-), were assessed. Kaplan-Meier analysis and propensity score matching were used to evaluate 5-year graft survival. The number of HCV-viremic donation after brain death (DBD) donors and their use in LT for HCV Ab- recipients peaked at 640 donors in 2019 and 289 LTs in 2022. In contrast, Ab+ nonviremic DBD donations are rising, with 536 donors and 284 LTs in 2023. The utilization rate of viremic DBD grafts has continuously decreased despite increased willingness by waitlist candidates to accept them. HCV-positive donation after circulatory death donors were seldom utilized in the study period. The 5-year graft survival rates for HCV-viremic, Ab+ nonviremic, and naïve donors were not significantly different in either DBD ( p = 0.56) or donation after circulatory death ( p = 0.52). Furthermore, Ishak stage 2 or 3 fibrotic DBD grafts had similar 5-year graft survival to nonfibrotic grafts. The findings suggest that the long-term outcome of using HCV-viremic DBD or donation after circulatory death grafts for HCV-negative recipients is comparable to that of other graft types and that fibrotic grafts have the potential to expand the DBD donor pool.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1097/LVT.0000000000000557 | DOI Listing |
Transplantation
July 2025
Department of Surgery, Westchester Medical Center and New York Medical College, Valhalla, NY.
Background: Starting in March 2021, the Organ Procurement and Transplantation Network (OPTN) mandated testing and reporting of hepatitis C virus (HCV), hepatitis B virus, and HIV at 4-8 wk posttransplantation. The aim of this study was to assess the rates of detectable HCV viremia in HCV nucleic acid test (NAT) negative recipients of liver allografts from HCV antibody-positive/NAT-negative (Ab+/NAT-) donors in a nationwide cohort after the institution of the reporting mandate.
Methods: Post-liver transplant (LT) HCV viremia and patient/graft outcomes were compared between 2 groups using the OPTN database: HCV negative LT recipients of donors with HCV Ab+/NAT- and HCV Ab-/NAT- between March 2021 and March 2023.
Liver Transpl
September 2025
Division of Abdominal Transplant, Department of Surgery, Stanford University, Stanford, California, USA.
Long-term outcomes of using HCV-positive donors in HCV-negative recipients in liver transplantation (LT) are not well established. Data from the United Network for Organ Sharing (UNOS) database between July 1, 2015, and December 31, 2023, were analyzed. The cohort included 44,447 HCV antibody-negative (Ab-) candidates who underwent deceased donor LT.
View Article and Find Full Text PDFJ Heart Lung Transplant
November 2021
Division of Cardiology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, New York.
The trends and outcomes of multiorgan heart-transplantation (HT) using hepatitis C virus (HCV) donors in the contemporary era are sparsely known. Using UNOS registry, 1322 adult multiorgan-HTs (n = 986 heart-kidney, n = 155 heart-lung, n = 181 heart-liver) between August-2015 and August-2020 were identified, of which 109 were performed using HCV-donors (n = 77 HCV nucleic-acid-amplification testing [NAT] positive irrespective of antibody status [HCV-viremic]; and n = 32 HCV Ab+/NAT-[HCV antibody + nonviremic]). The percentage of HCV-donors used for multiorgan-HT increased from 0% in 2015 to 14% in 2020 (p < 0.
View Article and Find Full Text PDFAfr Health Sci
June 2019
Department of Infection Disease and Clinical Microbiology, Mustafa Kemal University School of Medicine, Hatay, Turkey.
Background: Previous trials have investigated the effect of hepatitis C on lung functions; however, the role of viral load levels is unclear. The aim of this study was to investigate the effect of HCV viremia status on lung functions.
Methods: This study was in 60 patients with chronic hepatitis C (CHC).
J Heart Lung Transplant
September 2019
Division of Cardiology. Electronic address:
Background: Hepatitis C virus (HCV) donors should be categorized as HCV-viremic (antibody [Ab] negative or positive/Nucleic Acid testing [NAT] positive) or HCV Abnonviremic (Ab/NAT). Whereas recipients of hearts from HCV-viremic donors will develop viremia but can be cured of HCV shortly after transplant with direct-acting antivirals (DAAs), recipients of hearts from HCV Ab nonviremic donors are highly unlikely to become viremic or require DAAs. Given this important difference in risk, we assessed the utilization trends and post-heart-transplantation outcomes of HCV-naive (Ab/NAT), HCV-viremic, and HCV Ab nonviremic donor hearts.
View Article and Find Full Text PDF