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Published on: November 7, 2020
Recurrent hepatitis C after retransplantation: factors affecting graft and patient outcome
Michal Carmiel-Haggai1, M Isabel Fiel, Himabindu C Gaddipati
1Recanati/Miller Transplantation Institute, Mount Sinai Hospital, The Mount Sinai School of Medicine, PO Box 1504, New York, NY 10029-6574, USA.
Insights
Liver retransplantation for recurrent hepatitis C virus (HCV) leads to high mortality. Avoiding older donor organs and understanding recurrence patterns are crucial for improving outcomes in liver transplant (LT) patients.
Area of Science:
- Hepatology
- Transplantation Immunology
- Virology
Background:
- Recurrent hepatitis C virus (HCV) infection is a major cause of liver allograft failure.
- Liver retransplantation (re-LT) for HCV recurrence faces challenges with significant patient morbidity and mortality.
- The scarcity of donor organs necessitates careful consideration of re-LT candidates.
Purpose of the Study:
- To investigate patient and allograft outcomes following re-LT for recurrent HCV.
- To identify risk factors associated with mortality and recurrence after re-LT.
- To evaluate the predictability of recurrence timing after re-LT based on prior LT history.
Main Methods:
- Retrospective analysis of 47 patients undergoing re-LT for HCV-related graft failure between 1989 and 2002.
- Clinical HCV recurrence defined by elevated liver enzymes and histological confirmation.
- Cox regression and Chi-squared tests used to analyze survival and recurrence variables.
Main Results:
- High mortality rate: 66% of patients died post-re-LT (median 2.2 months).
- Significant mortality risk factors: Donor age >60, clinical HCV recurrence, and cirrhosis-related graft failure.
- Early recurrence (within 3 months) observed in 50% of biopsied patients, correlated with high-dose solumedrol.
Conclusions:
- Patients with cirrhosis due to recurrent HCV have a very high mortality risk after re-LT.
- Older donor allografts should be avoided in re-LT for recurrent HCV.
- Recurrence timing after initial LT does not predict recurrence timing after re-LT; re-LT should not be withheld based on prior accelerated HCV disease.
Abstract:
Retransplantation (re-LT) of patients with recurrent hepatitis C virus (HCV) carries significant morbidity and mortality, negatively impacting on an already scarce donor allograft pool. In this study, we investigated the outcome of allografts and patients after re-LT due to recurrent HCV. Between 1989 and 2002, 47 patients were retransplanted at our institution due to HCV-related graft failure. Clinical HCV recurrence after re-LT was diagnosed when patients had acute liver enzyme elevation correlated with histological recurrence. The independent influence of these variables on survival was tested using Cox regression model. Chi-squared tests were used to examine the influence of individual demographic and pre/perioperative variables on recurrence. Thirty-one (66%) patients died after re-LT (median 2.2 months). Donor age >60, clinical HCV recurrence, and graft failure due to cirrhosis were significant risk factors for mortality (risk ratios of 3.6, 3.3, and 2.4, respectively). Pre-LT MELD score was lower among survivors (22+/- 5 vs. 27+/- 8). Following re-LT, 38 patients had at least one biopsy due to acute liver dysfunction; 19 of them (50%) had recurrence within the first 3 months. High-dose solumedrol was correlated with early recurrence. No association was found between time of recurrence after the first LT and time of recurrence after re-LT. In conclusion, patients with cirrhosis due to recurrent HCV undergoing re-LT have an extremely high mortality rate; older allografts should be avoided in retransplanting these patients. The timing of clinical recurrence after initial liver transplantation is not predictive of the timing of recurrence after re-LT. Patients experiencing early graft failure due to accelerated forms of HCV should not be denied re-LT with the expectation that a similar disease course will occur after re-LT.
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