BACKGROUND, Acute hepatitis C becomes chronic in 50% of cases. Early treatment seems to be effective in eradicating HCV infection, although no clear recommendations are available in terms of time of initiation, regimen and duration of therapy. We report a retrospective review of 48 patients with acute HCV infection between January 2006 and December 2007. PATIENTS AND METHODS, This multicenter retrospective study involved three Infectious Disease Units in Sicily and was carried out in three stages: (1) Collection of patients data; (2) Selection of patients according to: elevated ALT (at least 5 times above normal values), seroconversion from negative to positive anti-HCV status; (3) Final selection of patients with a minimum of 12 months follow-up. RESULTS; Out of 60 patients with a diagnosis of acute HCV infection, 48 were eligible for the study. In 13 subjects (52%) of the 25 who were not treated, the disease resolved spontaneously. 23 patients received pegylated interferon in monotherapy or in combination with ribavirin. 95% achieved a sustained virological response (SVR). Of the 22 sustained responders, 17 (70%) negativized HCV RNA within 8 weeks. No difference appeared between patients receiving monotherapy and those treated with combination therapy. Also, no difference was observed, in terms of SVR, between the two different pegylated interferons given for treatment. CONCLUSIONS, The rate of viral clearance was higher in the treated group versus the untreated one (95% versus 52%). The SVR found in our study population (95%) was comparable to that reported in other studies. The combination with ribavirin did not appear to impact our sustained response rate, although ribavirin appeared to induce a faster normalization of ALT levels.
机构:Vancouver Gen Hosp, Div Gastroenterol, Dept Med, Vancouver, BC V5Z 3P1, Canada
Wong, Victor K.
Cheong-Lee, Cindy
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Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
British Columbia Hepatitis Program, Vancouver, BC, CanadaVancouver Gen Hosp, Div Gastroenterol, Dept Med, Vancouver, BC V5Z 3P1, Canada
Cheong-Lee, Cindy
Ford, Jo-Ann E.
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Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
British Columbia Hepatitis Program, Vancouver, BC, CanadaVancouver Gen Hosp, Div Gastroenterol, Dept Med, Vancouver, BC V5Z 3P1, Canada
Ford, Jo-Ann E.
Yoshida, Eric M.
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Vancouver Gen Hosp, Div Gastroenterol, Dept Med, Vancouver, BC V5Z 3P1, Canada
Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
British Columbia Hepatitis Program, Vancouver, BC, CanadaVancouver Gen Hosp, Div Gastroenterol, Dept Med, Vancouver, BC V5Z 3P1, Canada
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Department of Gastroenterology and Hepatology,Institute of NutritionDepartment of Gastroenterology and Hepatology,Institute of Nutrition
Vasily Isakov
Igor Nikitin
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Department of Gastroenterology and Hematology,Russian Academy of SciencesDepartment of Gastroenterology and Hepatology,Institute of Nutrition
Igor Nikitin
Vladimir Chulanov
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Clinical Diagnostics and Research Center,Central Research Institute of EpidemiologyDepartment of Gastroenterology and Hepatology,Institute of Nutrition
Vladimir Chulanov
Pavel Ogurtsov
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Hospital Medicine, Peoples’ Friendship Univer-sity of RussiaDepartment of Gastroenterology and Hepatology,Institute of Nutrition
Pavel Ogurtsov
Ekaterina Lukyanova
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Medical Affairs, MSD Pharmaceuticals LLCDepartment of Gastroenterology and Hepatology,Institute of Nutrition
Ekaterina Lukyanova
Jianmin Long
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Clinical Research, Merck & Co., Inc.Department of Gastroenterology and Hepatology,Institute of Nutrition
Jianmin Long
Janice Wahl
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Clinical Research, Merck & Co., Inc.Department of Gastroenterology and Hepatology,Institute of Nutrition
Janice Wahl
Frans A Helmond
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Clinical Research, Merck & Co., Inc.Department of Gastroenterology and Hepatology,Institute of Nutrition
Frans A Helmond
the P08160 trial Investigators
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机构:Department of Gastroenterology and Hepatology,Institute of Nutrition