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  • S. Karger AG  (1)
  • Kim, Ji Hoon  (1)
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  • S. Karger AG  (1)
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  • 1
    In: Intervirology, S. Karger AG, Vol. 58, No. 1 ( 2015), p. 14-21
    Kurzfassung: 〈 b 〉 〈 i 〉 Objectives: 〈 /i 〉 〈 /b 〉 Interferon (IFN)-based therapy for chronic hepatitis C (CHC) is cost-effective and is associated with reduced risk of disease progression. We aimed to assess the incidence of cirrhosis and hepatocellular carcinoma (HCC) and to identify risk factors associated with disease progression. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 We retrospectively reviewed 280 CHC patients who were registered at our hospital between 2001 and 2010. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 About 80% of patients received antiviral treatment. The 10-year cumulative incidence of cirrhosis was significantly lower among patients who received antiviral therapy than among those who did not (8.3 vs. 44.0%; p = 0.001). Among them, patients with sustained virological response (SVR) had a significantly lower incidence of cirrhosis than those without SVR (0.6 vs. 33.9%; p 〈 0.001). Cox proportional hazards regression showed that SVR was the significant independent factor for reducing the risk of cirrhosis (hazard ratio, HR = 0.03; p = 0.034). The 10-year cumulative incidence of HCC was higher among patients who did not receive antiviral therapy than among those who did (43.9 vs. 6.1%; p 〈 0.001). Multivariate analysis showed that underlying cirrhosis was the only independent risk factor associated with HCC development (HR = 7.70; p = 0.010). 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 SVR secondary to IFN-based therapy could reduce cirrhosis development in CHC patients. Underlying cirrhosis was the strongest predictor of HCC development.
    Materialart: Online-Ressource
    ISSN: 0300-5526 , 1423-0100
    RVK:
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 2015
    ZDB Id: 1482863-7
    SSG: 12
    Standort Signatur Einschränkungen Verfügbarkeit
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