Effects of alpha interferon induction plus ribavirin with or without amantadine in the treatment of interferon non-responsive chronic hepatitis C: a randomised trial

التفاصيل البيبلوغرافية
العنوان: Effects of alpha interferon induction plus ribavirin with or without amantadine in the treatment of interferon non-responsive chronic hepatitis C: a randomised trial
المؤلفون: Le Adinolfi, G Ruggiero, A Tonziello, Riccardo Utili
المساهمون: Adinolfi, Luigi Elio, Utili, Riccardo, Tonziello, A, Ruggiero, G.
بيانات النشر: Copyright 2003 by Gut, 2003.
سنة النشر: 2003
مصطلحات موضوعية: Adult, Liver Cirrhosis, Male, medicine.medical_specialty, Letter, Genotype, Amantadine Hydrochloride, Alpha interferon, Gastroenterology, Antiviral Agents, Drug Administration Schedule, chemistry.chemical_compound, Interferon, Internal medicine, Ribavirin, medicine, Amantadine, Humans, Prospective Studies, Interferon alfa, business.industry, Interferon-alpha, Alanine Transaminase, Hepatitis C, Hepatitis C, Chronic, Middle Aged, medicine.disease, Surgery, Regimen, Treatment Outcome, chemistry, Liver, RNA, Viral, Drug Therapy, Combination, Female, business, medicine.drug
الوصف: Background: Fifty per cent of chronic hepatitis C patients are non-responders to interferon. At present, there are no recommended therapeutic options for non-responders. Aims: The safety and long term effect of alpha interferon induction plus ribavirin with or without amantadine in the treatment of interferon non-responsive chronic hepatitis C was evaluated. Patients and methods: A total of 114 consecutive patients were randomly divided into three groups with a final 2:2:1 ratio: group A (44 patients) received interferon alfa 2b, 3 million units (MU), three times a week, and oral ribavirin (1000 mg/day); group B (46 patients) received interferon 3 MU daily for the first four weeks and subsequently 3 MU three times a week, and ribavirin as in regimen A; and group C (24 patients) received interferon and ribavirin as in regimen B, plus oral amantadine hydrochloride (200 mg/day). The duration of treatment was 12 months. Results: The end of treatment response for groups A and B was 25% and 29%, respectively, and for group C, 68% (p
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78cc8623490424b984873773707cec06Test
https://europepmc.org/articles/PMC1773644Test/
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....78cc8623490424b984873773707cec06
قاعدة البيانات: OpenAIRE