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Heart Transplant Using Hepatitis C-Seropositive and Viremic Organs in Seronegative Recipients
Yuanjia Zhu1, Yasuhiro Shudo1, Roy Lee2,3
1Department of Cardiothoracic Surgery, Stanford University, Stanford, CA, USA.
Insights
HCV-positive donor hearts can be safely transplanted into HCV-negative patients. Direct-acting antiviral (DAA) treatment effectively cures hepatitis C, leading to excellent short-term survival after heart transplantation.
Area of Science:
- Cardiology
- Hepatology
- Transplantation
Background:
- Hepatitis C virus (HCV)-seropositive donor hearts are underutilized for orthotopic heart transplantation (OHT).
- Direct-acting antiviral (DAA) agents offer a new possibility for using these organs in HCV-seronegative recipients.
Purpose of the Study:
- To evaluate the outcomes of HCV-seronegative recipients who received HCV-seropositive donor hearts.
- To assess the efficacy of DAA treatment in managing post-transplant hepatitis C viremia.
Main Methods:
- Retrospective review of adult OHT patients from 1997-2019.
- Analysis of 10 HCV-seronegative recipients who received HCV-seropositive donor hearts.
- Survival analysis using Kaplan-Meier curves.
Main Results:
- Eighty percent 30-day and 1-year survival rates were observed.
- Four recipients developed post-transplant viremia, with 3 successfully treated with DAA.
- One donor was HCV-cured pre-transplant via DAA.
Conclusions:
- HCV-seronegative recipients can achieve excellent short-term outcomes with HCV-seropositive donor hearts.
- DAA treatment is effective for managing hepatitis C viremia before and after OHT.
- Further large-scale studies are needed to assess long-term outcomes.
Abstract:
BACKGROUND Hepatitis C virus (HCV)-seropositive donor hearts are underutilized for orthotopic heart transplantation (OHT). The advancement of direct-acting antiviral agent (DAA) treatment for HCV makes utilizing HCV-seropositive and viremic donor organs in HCV-seronegative recipients a possibility. MATERIAL AND METHODS From 1997 to 2019, adult patients who underwent OHT at our institution were retrospectively reviewed. Ten HCV-seronegative patients received HCV-seropositive donor hearts, 3 of which tested nucleic acid-positive. Kaplan-Meier curves were performed for survival analyses. This study was approved by the Institutional Review Board. RESULTS Recipient median age was 57.5 years old, and 2 (20%) were female. Donor median age was 42 years old, and 3 (30%) were female. One donor was cured from HCV with DAA prior to OHT. Four recipients developed hepatitis C viremia immediately after OHT. DAA treatment was completed in 3 recipients who demonstrated cure. Thirty-day and 1-year survival rates were both 80%. CONCLUSIONS We describe 10 HCV-seronegative patients who received HCV-seropositive donor hearts at our institution, with excellent short-term outcomes, even in those who received nucleic acid testing positive organs. DAA can be effective in treating hepatitis C viremia before and after OHT, with excellent recipient survival. Large clinical studies are needed to further evaluate the long-term outcomes of DAA therapy in patients after heart transplantation.
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