Literature DB >> 19404206

Treatment of chronic hepatitis C in sickle cell disease and thalassaemic patients with interferon and ribavirin.

David Ancel1, Xavier Amiot, Dominique Chaslin-Ferbus, Isabelle Hagege, Armand Garioud, Robert Girot, Stanislas Pol, Jean-Didier Grange.   

Abstract

BACKGROUND/AIM: Hepatic complications are a major cause of death in patients with congenital anaemia and chronic hepatitis C. Ribavirin is usually contraindicated in patients with haemolytic anaemia. This pilot study evaluated the efficacy and safety of antiviral treatment in patients with sickle cell disease (SCD) or beta-thalassaemia major (TM).
METHODS: Eleven consecutive SCD and TM patients were included. Interferon monotherapy was administrated in the two first thalassaemic patients. Other patients received combination therapy with full dose of pegylated interferon 2b and increasing doses of ribavirin, starting with a low dose of ribavirin (400 mg/day).
RESULTS: Hepatitis C virus genotypes were 1 or 4 in nine cases. A sustained virological response achieved in five of 11 patients despite unfavourable factors to response (genotypes, nonresponders to an earlier treatment). Haemoglobin level at the end of treatment was higher than baseline levels in five of six SCD patients. No SCD patient needed a transfusion during and after treatment period, neither presented vasoocclusive crisis. The mean increase in transfusion requirements was 32.5% in the thalassaemic group.
CONCLUSION: A sustained virological response can be obtained in SCD and TM patients. No earlier study of excellent haematological tolerance among SCD patients under ribavirin has been reported to date. The results of this study suggest that full dose ribavirin could be used from the start of treatment in SCD patients.

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Year:  2009        PMID: 19404206     DOI: 10.1097/MEG.0b013e3283097699

Source DB:  PubMed          Journal:  Eur J Gastroenterol Hepatol        ISSN: 0954-691X            Impact factor:   2.566


  8 in total

1.  Safety of pegylated interferon and ribavirin therapy for chronic hepatitis C in patients with sickle cell anemia.

Authors:  Hussain Issa
Journal:  World J Hepatol       Date:  2010-05-27

Review 2.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

3.  Efficacy of interferon alpha-2b with or without ribavirin in thalassemia major patients with chronic hepatitis C virus infection: A randomized, double blind, controlled, parallel group trial.

Authors:  Hamid Kalantari; Neda Rad
Journal:  J Res Med Sci       Date:  2010-11       Impact factor: 1.852

4.  Peg-interfon alpha-2a and low-dose ribavirin for treatment of hepatitis C virus infection in patients with sickle-cell anemia in Saudi Arabia.

Authors:  Adnan Agha; Rafaat Chakik; Mamdouh M Abdulhadi Ali; Dib Alsaudi; Giorgio Sammito; Edoardo Giovanni Giannini
Journal:  Ann Saudi Med       Date:  2013 Nov-Dec       Impact factor: 1.526

5.  Hepatitis C virus (HCV) infection among patients with sickle cell disease at the Korle-Bu teaching hospital.

Authors:  Gifty Mawuli; Bartholomew Dzudzor; Kenneth Tachi; Amma Anima Benneh-Akwasi Kuma; James Odame-Aboagye; Billal Musah Obeng; Anthony Twumasi Boateng; Elijah Paa Edu-Quansah; Keren Okyerebea Attiku; Esinam Agbosu; Augustina Arjarquah; Joseph Humphrey Kofi Bonney
Journal:  Virol J       Date:  2022-04-22       Impact factor: 5.913

6.  [Evaluation of tolerance and efficacy of the treatment of chronic viral hepatitis C in homozygous sickle cell patients].

Authors:  Mohamed Ould Mohamed El Agheb; Jean-Didier Grange
Journal:  Pan Afr Med J       Date:  2015-02-04

Review 7.  Safety and Efficacy of Adding Ribavirin to Interferon or Peginterferon in Treatment of Hepatitis C Infection in Patients With Thalassemia: A Systematic Review on Randomized Controlled Trials.

Authors:  Ehsan Aminizadeh; Seyed Moayyed Alavian; Ali Akbari Sari; Nasser Ebrahimi Daryani; Bita Behnava
Journal:  Hepat Mon       Date:  2016-03-06       Impact factor: 0.660

Review 8.  Hepatobiliary Manifestations of Sickle Cell Anemia.

Authors:  Hussain Issa; Ahmed H Al-Salem
Journal:  Gastroenterology Res       Date:  2010-01-20
  8 in total

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