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Risk stratification of allograft failure secondary to hepatitis C recurrence after liver transplantation.
Shiba, Hiroaki; Hashimoto, Koji; Kelly, Dympna; Fujiki, Masato; Quintini, Cristiano; Aucejo, Federico; Uso, Teresa Diago; Yerian, Lisa; Yanaga, Katsuhiko; Matsushima, Masato; Eghtesad, Bijan; Fung, John; Miller, Charles.
Afiliação
  • Shiba H; Department of General Surgery, Digestive Disease Institute.
  • Hashimoto K; Department of Hepatobiliary Surgery.
  • Kelly D; Department of General Surgery, Digestive Disease Institute. hashimk@ccf.org.
  • Fujiki M; Department of General Surgery, Digestive Disease Institute.
  • Quintini C; Department of General Surgery, Digestive Disease Institute.
  • Aucejo F; Department of General Surgery, Digestive Disease Institute.
  • Uso TD; Department of General Surgery, Digestive Disease Institute.
  • Yerian L; Department of General Surgery, Digestive Disease Institute.
  • Yanaga K; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Matsushima M; Department of Hepatobiliary Surgery.
  • Eghtesad B; Division of Clinical Research and Development, Jikei University School of Medicine, Tokyo, Japan.
  • Fung J; Department of General Surgery, Digestive Disease Institute.
  • Miller C; Department of General Surgery, Digestive Disease Institute.
Hepatol Res ; 46(11): 1099-1106, 2016 Oct.
Article em En | MEDLINE | ID: mdl-26833562
ABSTRACT

AIM:

Hepatitis C virus (HCV) recurrence after liver transplantation decreases survival rates. Improved understanding of the multiple factors influencing HCV recurrence could aid decision-making for donor-recipient pairing and maximize transplant outcomes. The aim of this study was to create a model based on pretransplant variables to stratify patients at risk of HCV-related allograft failure.

METHODS:

This retrospective study enrolled 154 liver transplant recipients with HCV at Cleveland Clinic.

RESULTS:

Among the study population, 54 recipients (35.1%) experienced HCV recurrence, histologically defined as moderate to severe hepatitis and/or bridging fibrosis to cirrhosis. The multivariate analysis found donor age (≥60 years, P < 0.002), donor body mass index (≥30 kg/m2 , P < 0.05), African American recipient (P < 0.01) and genotype 1 (P < 0.02) as risk factors for HCV-related allograft failure. When these four factors were scored as a combined index (no factor [n = 15], one factor [n = 76], two factors [n = 43] and three or more factors [n = 20]), the HCV recurrence-free survival showed good stratification according to the scores 93.3% with no factor, 79.3% with one factor, 52.0% with two factors and 24.4% with three or more factors at 3 years after transplant (P < 0.0001). Moreover, this risk index also identified the patient group at high risk of HCV recurrence after acute rejection.

CONCLUSION:

While the introduction of direct-acting antiviral agents has been changing the paradigm of HCV treatment, the natural history of recipients with HCV as shown in this study would help estimate the risk of HCV-related allograft failure in those who do not tolerate such new treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Hepatol Res Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Hepatol Res Ano de publicação: 2016 Tipo de documento: Article