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Berge et al. Hepatoma Res 2017;3:209-14                              Hepatoma Research
           DOI: 10.20517/2394-5079.2017.28
                                                                                                  www.hrjournal.net
            Original Article                                                                    Open Access

           Clinical outcomes of direct-acting antiviral

           therapy in patients with compensated

           hepatitis C virus-related cirrhosis



           Estefania Berge, Ana Arencibia, Elena Otón, Luis Cejas, Silvia Acosta, Francisco Pérez

           Liver Unit, Hospital Universitario Nuestra Señora de la Candelaria, 38010 Santa Cruz de Tenerife, Spain.

           Correspondence to: Dr. Estefanía Berge, Liver Unit, Hospital Universitario Nuestra Señora de la Candelaria, Carretera General del Rosario, 145, 38010
           Santa Cruz de Tenerife, Spain. E-mail: estefania.berge@gmail.com
           How to cite this article: Berge E, Arencibia A, Otón E, Cejas L, Acosta S, Pérez F. Clinical outcomes of direct acting antiviral therapy in patients
           with compensated hepatitis C virus-related cirrhosis. Hepatoma Res 2017;3:209-14.
                                         ABSTRACT

            Article history:              Aim:  The aim was to assess the clinical impact  of direct-acting antiviral treatment in
            Received: 25 Jun 2017         patients with compensated hepatitis C virus-related cirrhosis after one year of follow-up.
            Accepted: 12 Sep 2017         Methods: An observational retrospective study was conducted on 129 consecutive patients
                                          with compensated cirrhosis treated in 2015, analyzing the evolution of liver function and
            Published: 27 Sep 2017
                                          the development of hepatocellular carcinoma and clinical decompensations. Results: The
            Key words:                    median follow-up time was 16 months. Most patients were males (73%), the mean age was
            Direct-acting antiviral therapy,   58.1 years and the most frequent genotype was 1b (52.2%). All participants were Child-Pugh
            compensated cirrhosis,        A class at the start of the treatment and the median model for end-stage liver disease (MELD)
                                          score was 7. Four patients (4.4%) suffered a decompensation: three episodes of ascites and one
            hepatocellular carcinoma,     acute on chronic liver failure. The incidence of de novo hepatocellular carcinoma during the
            clinical decompensation
                                          follow-up was 3.6%. Seven patients (7.8%) improved MELD score more than one point and
                                          in 11 patients (12.2%) it worsened more than one point. There was a significant improvement
                                          in the mean platelets count [P < 0.001, 95% confidence interval (CI): -26,360, -12,096] and
                                          in the mean albumin levels (P < 0.001, 95% CI: -322, -130) after treatment. Conclusion:
                                          Direct-acting antiviral treatment is not associated in the short term with a decrease in the
                                          development of hepatic decompensation or hepatocellular carcinoma compared to what it
                                          was reported for untreated compensated cirrhotic patients. There is an improvement in pre
                                          and post-treatment platelet counts and albumin levels showing a probable improvement of
                                          the hepatic function.


           INTRODUCTION                                       to several factors such as age, alcohol consumption
                                                              or hepatitis B or human immunodeficiency virus (HIV)
           Chronic hepatitis C virus (HCV) infection affects   co-infection .  Once  cirrhosis  is  established,  a  yearly
                                                                        [3]
           around 160 million people worldwide . Around 16%   incidence of hepatocellular carcinoma of 1.4-3.4% [4-6] ,
                                             [1]
           of  patients  will develop  cirrhosis  after  20  years  of   and a yearly incidence of hepatic decompensation
           infection , although fibrosis progression can vary due   (including episodes of ascites, jaundice, hepatic
                   [2]
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