
Beta-interferon was administered by intravenous infusion to 16 patients affected with fulminant hepatitis B virus infection in third or fourth-grade coma. Ten patients presented a superinfection or a co-infection due to the delta (delta)-agent. None had detectable interferon (IFN) activity before therapy was begun. Besides fever, no significant side-effects were observed during treatment. Both the IFN-treated group as well as the "historical" control group, made up of 70 cases of fulminant virus hepatitis, not treated with IFN and observed during a previous ten year-period, received supportive therapy; survival rates were similar in both groups. Furthermore, the presence or absence of the delta-agent did not appear to affect survival rates significantly.
Adult, Hepatitis delta Antigens, Male, Clinical Trials as Topic, Adolescent, Hepatitis B Antigens; Humans; Adult; Interferon Type I; Hepatitis B; Clinical Trials as Topic; Hepatitis delta Antigens; Adolescent; Infusions, Parenteral; Male; Female, Hepatitis B, Hepatitis B Antigens, Interferon Type I, Humans, Female, Infusions, Parenteral
Adult, Hepatitis delta Antigens, Male, Clinical Trials as Topic, Adolescent, Hepatitis B Antigens; Humans; Adult; Interferon Type I; Hepatitis B; Clinical Trials as Topic; Hepatitis delta Antigens; Adolescent; Infusions, Parenteral; Male; Female, Hepatitis B, Hepatitis B Antigens, Interferon Type I, Humans, Female, Infusions, Parenteral
| citations The total number of citations received by all articles of the researcher of interest. | 16 | |
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