Clinical Study on the Efficacy and Safety of Lamivudine in the Treatment of Chronic Severe Hepatitis B
Peng Hong
Abstract
Peng Hong
Abstract
Objective:To evaluate the efficacy and safety of Lamivudine in the treatment of chronic severe hepatitis due to hepatitis B virus (HBV). Methods:Eighty-six patients with chronic severe hepatitis caused by HBV were randomly allocated into two groups. Control group (n=38) was given conventional therapy;Lamivudine group(n=48) was treated with Lamivudine, 100mg daily on the basis of routine management. The mortality rate and hospital stay duration of two groups were analyzed. Results:The mortality rate of Lamivudine group was 41.7%. The mortality rate of control group was 68.4%. There was significant difference in mortality between the two groups( P 0.05). The mean hospital stay duration of control group was greatly longer than that of Lamivudine group[(114.3±26.2) days vs.(74.6±22.7) days, P 0.05].No remarkable adverse effects of Lamivudine were observed.Conclusions:Lamivudine may be effective and safe in the treatment of chronic severe hepatitis due to exacerbation of chronic hepatitis B.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To evaluate the efficacy and safety of Lamivudine in the treatment of chronic severe hepatitis due to hepatitis B virus (HBV). Methods:Eighty-six patients with chronic severe hepatitis caused by HBV were randomly allocated into two groups. Control group (n=38) was given conventional therapy;Lamivudine group(n=48) was treated with Lamivudine, 100mg daily on the basis of routine management. The mortality rate and hospital stay duration of two groups were analyzed. Results:The mortality rate of Lamivudine group was 41.7%. The mortality rate of control group was 68.4%. There was significant difference in mortality between the two groups( P 0.05). The mean hospital stay duration of control group was greatly longer than that of Lamivudine group[(114.3±26.2) days vs.(74.6±22.7) days, P 0.05].No remarkable adverse effects of Lamivudine were observed.Conclusions:Lamivudine may be effective and safe in the treatment of chronic severe hepatitis due to exacerbation of chronic hepatitis B.
Key concepts: Lamivudine, Medicine, Exacerbation, Internal medicine, Chronic hepatitis, Gastroenterology, Hepatitis B, Mortality rate