Objective: Hepatitis C (HCV) is now the most common indication for orthotopic liver transplantation (OLT). While graft reinfection remains universal, progression to graft cirrhosis is highly variable. This study examined donor, recipient, and operative variables to identify factors that affect recurrence of HCV post-OLT to facilitate graft-recipient matching. Methods: Retrospective review of 307 patients who underwent OLT for HCV over a 10-year period at our center. Recurrence of HCV was identified by the presence of biochemical graft dysfunction and concurrent liver biopsy showing diagnostic pathologic features. Time to recurrence was the endpoint for statistical analysis. Five donor, 6 recipient, and 2 operative variables that may affect recurrence were analyzed by univariate comparison and Cox proportional hazard regression models. Results: Recurrence-free survival in the 307 study patients was 69% and 34% at 1 and 5 years, respectively. Four predictive variables related to either donor or recipient characteristics were identified. Advanced donor age, prolonged donor hospitalization, increasing recipient age, and elevated recipient MELD scores were found to increase the relative risk of HCV recurrence. Examination of HLA disparity between donors and recipients demonstrated no correlation between class I or class II mismatches and recurrence-free survival. Conclusions: We have identified donor and recipient characteristics that significantly predict hepatitis C recurrence following liver transplantation. These factors are identifiable before transplant and, if considered when matching donors to HCV recipients, may decrease the incidence of HCV recurrence after OLT. A change in the current national liver allocation system would be needed to realize the full value of this benefit.
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Liver Unit,Queen Elizabeth Hospital,Birmingham,B15 2TH,United Kingdom
Hepatology Unit,Department of Internal Medicine,University of "Tor Vergata",00133 Rome,ItalyLiver Unit,Queen Elizabeth Hospital,Birmingham,B15 2TH,United Kingdom
Marco Carbone
Ilaria Lenci
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Hepatology Unit,Department of Internal Medicine,University of "Tor Vergata",00133 Rome,ItalyLiver Unit,Queen Elizabeth Hospital,Birmingham,B15 2TH,United Kingdom
Ilaria Lenci
Leonardo Baiocchi
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Hepatology Unit,Department of Internal Medicine,University of "Tor Vergata",00133 Rome,ItalyLiver Unit,Queen Elizabeth Hospital,Birmingham,B15 2TH,United Kingdom
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Univ Paris 11, Assistance Publ Hop Paris, Hop Paul Brousse, INSERM,Contrat Rech 98 04,Ctr Hepatobiliaire, F-94800 Villejuif, FranceUniv Paris 11, Assistance Publ Hop Paris, Hop Paul Brousse, INSERM,Contrat Rech 98 04,Ctr Hepatobiliaire, F-94800 Villejuif, France
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Univ Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, CanadaUniv Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, Canada
Asthana, Sonal
Toso, Christian
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Univ Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, CanadaUniv Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, Canada
Toso, Christian
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Meeberg, Glenda
Bigam, David L.
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Univ Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, CanadaUniv Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, Canada
Bigam, David L.
Shapiro, Andrew J.
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Univ Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, CanadaUniv Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, Canada
Shapiro, Andrew J.
Mason, Andrew
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Univ Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, CanadaUniv Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, Canada
Mason, Andrew
Kneteman, Norman M.
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Univ Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, CanadaUniv Alberta Hosp, Div Multiorgan Transplantat, Edmonton, AB T6G 2B7, Canada