𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Anemia is not predictive of sustained virological response in liver transplant recipients with hepatitis C virus who are treated with pegylated interferon and ribavirin

✍ Scribed by Michela Giusto; Maria Rodriguez; Laia Navarro; Angel Rubin; Victoria Aguilera; Fernando San-Juan; Cecilia Ortiz; Rafael López-Andujar; Martín Prieto; Marina Berenguer


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
148 KB
Volume
17
Category
Article
ISSN
1527-6465

No coin nor oath required. For personal study only.

✦ Synopsis


In the immunocompetent setting, antiviral therapy-related anemia has recently been shown to be associated with a sustained virological response (SVR). Our goal was to assess whether this is also true for liver transplantation (LT). We included 160 LT patients with recurrent hepatitis C virus (HCV) who were treated with pegylated interferon and ribavirin (RBV) between 2002 and 2010; 76% of the patients were men, the median age of the patients was 56 years (range ¼ 33-75 years), 63% had advanced fibrosis, and 86% were infected with HCV genotype 1a or 1b. The baseline immunosuppression was tacrolimus in 56% of the patients. Mycophenolate mofetil (MMF) was used in 15%. Anemia was defined as a hemoglobin (Hb) level < 10 g/dL. Significant anemia was present when the Hb decline was >5 g/dL. Anemia and significant anemia developed in 67% and 41% of the patients, respectively. Erythropoietin was used in 60%. Factors independently associated with significant anemia included low estimated creatinine clearance [relative risk (RR) ¼ 0.951, 95% confidence interval (CI) ¼ 0.925-0.978, P ¼ 0.0001], a longer time from LT to therapy (RR ¼ 1.001, 95% CI ¼ 1.000-1.001, P ¼ 0.002), high baseline viremia (RR ¼ 3.2, 95% CI ¼ 1.3-8.1, P ¼ 0.01), cyclosporine A (CSA)-based immunosuppression (RR: 3.472, 95% CI: 1.386-8.695; P ¼ 0.008), and the use of MMF (RR: 5.346, 95% CI: 1.398-20.447; P ¼ 0.014). An SVR occurred in 43% of the patients; the factors associated with an SVR included baseline variables (younger recipient age, younger donor age, infections with non-1 HCV genotypes, body mass index, and mild fibrosis) and on-treatment factors related to adherence or viral kinetics. Anemia resulted in RBV dose reductions but was not associated with the virological response at any time. In conclusion, anemia is a very frequent complication in LT patients during antiviral therapy and is associated with increased RBV dose reduction but not with an SVR. Predictors of anemia include MMF or CSA immunosuppression, high viremia, and renal insufficiency.


📜 SIMILAR VOLUMES


Prediction of sustained virological resp
✍ Guy W. Neff; Christopher B. O'Brien; Robert Cirocco; Marzia Montalbano; Maria de 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 69 KB 👁 2 views

The optimal duration of therapy for pegylated interferon combined with ribavirin in recurrent Hepatitis C virus (HCV) following liver transplantation is not known. We wanted to determine if testing for HCV in liver tissue by reverse transcriptase polymerase chain reaction (RT-PCR) was superior in pr

Virological response is associated with
✍ William Sievert; Gregory J. Dore; Geoffrey W. McCaughan; Motoko Yoshihara; Darre 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 336 KB 👁 1 views

Anemia may increase the likelihood of achieving a sustained virological response (SVR) during pegylated interferon and ribavirin treatment of hepatitis C virus (HCV) infection. To determine whether hemoglobin decline is associated with SVR, we retrospectively evaluated the CHARIOT study of 871 treat

Twelve weeks posttreatment follow-up is
✍ Michelle Martinot-Peignoux; Christiane Stern; Sarah Maylin; Marie-Pierre Ripault 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 167 KB 👁 1 views

A sustained virologic response (SVR) in patients with chronic hepatitis C receiving pegylated interferon (PEG-IFN) plus ribavirin is defined as undetectable serum HCV-RNA at 24 weeks (W+24) posttreatment follow-up. Viral load outcome in patients with virological relapse (VR) has not been explored. T