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Factors predicting outcomes of hepatitis B-related cirrhosis patients

                                      with long-term antiviral therapy


                                        1,
                         1
                                                                                            1
                                                                                                           3
                                                           2
                                                                             1
             Yi-Lin Chen , Chih-Lin Lin , Kuo-Chih Tseng,  Kuan-Yang Chen,  Li-Ying Liao,  Jia-Horng Kao
                   1 Department of Gastroenterology, Taipei City Hospital, Ren-Ai branch, Taipei, Taiwan.
             2 Department of Internal Medicine, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation,
                             Chia-Yi; School of Medicine, Tzuchi University, Hualien, Taiwan


             3 Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan

                                           University Hospital, Taipei, Taiwan.





               Key words: decompensated cirrhosis, hepatitis B virus, hepatocellular carcinoma, nucleos(t)ide

                                                        analogue


            Abstract

            Background and aims:


            Long-term nucleos(t)ide analogues (NA) therapy has been shown to improve the survival in patients

            with HBV-related cirrhosis. The aim of this study was to evaluate the clinical outcomes and factors


            associated  with  survival  in  HBV-related  cirrhotic  patients  receiving  long-term  NA  treatment.  In

            addition,  the  impact  of  HCC  development  on  the  survival  of  HBV-related  cirrhotic  patients  with


            antiviral therapy was also examined.

            Methods:

            A total of 126 HBV-related cirrhosis, treatment naive patients with serum levels of HBV DNA more


            than  2000  IU,  including  67  compensated  cirrhosis  and  59  decompensated  cirrhosis,  were

            retrospectively enrolled. Patients who had hepatitis C or D virus, or human immunodeficiency virus


            co-infection, had a history of heavy alcohol use, had hepatocellular carcinoma and other causes of

            liver disease were also excluded from this study. The effectiveness of treatment, survival and risk


            factors of mortality were determined. Baseline data of biochemical tests were collected before the
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