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      Chronic hepatitis B in pregnant women: Current trends and approaches

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          Abstract

          Chronic hepatitis B (CHB) is a significant public health problem worldwide. The aim of the present review is to summarize the actual trends in the management of CHB in pregnant women. The prevalence of hepatitis B virus (HBV) infection in pregnant women is usually comparable to that in the general population in the corresponding geographic area. All women have to be screened for hepatitis B surface antigen (HBsAg) during pregnancy. Additional examinations of pregnant women with CHB may include maternal hepatitis B e antigen, HBV viral load, alanine aminotransferase level, and HBsAg level. The management of pregnancy depends on the phase of the HBV infection, which has to be determined before pregnancy. In women of childbearing age with CHB, antiviral therapy can pursue two main goals: Treatment of active CHB, and vertical transmission prevention. During pregnancy, tenofovir is the drug of choice in both cases. A combination of hepatitis B immunoglobulin and vaccine against hepatitis B should be administered within the first 12 h to all infants born to mothers with CHB. In such cases, there are no contraindications to breastfeeding.

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          Most cited references66

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          EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection.

          Hepatitis B virus (HBV) infection remains a global public health problem with changing epidemiology due to several factors including vaccination policies and migration. This Clinical Practice Guideline presents updated recommendations for the optimal management of HBV infection. Chronic HBV infection can be classified into five phases: (I) HBeAg-positive chronic infection, (II) HBeAg-positive chronic hepatitis, (III) HBeAg-negative chronic infection, (IV) HBeAg-negative chronic hepatitis and (V) HBsAg-negative phase. All patients with chronic HBV infection are at increased risk of progression to cirrhosis and hepatocellular carcinoma (HCC), depending on host and viral factors. The main goal of therapy is to improve survival and quality of life by preventing disease progression, and consequently HCC development. The induction of long-term suppression of HBV replication represents the main endpoint of current treatment strategies, while HBsAg loss is an optimal endpoint. The typical indication for treatment requires HBV DNA >2,000IU/ml, elevated ALT and/or at least moderate histological lesions, while all cirrhotic patients with detectable HBV DNA should be treated. Additional indications include the prevention of mother to child transmission in pregnant women with high viremia and prevention of HBV reactivation in patients requiring immunosuppression or chemotherapy. The long-term administration of a potent nucleos(t)ide analogue with high barrier to resistance, i.e., entecavir, tenofovir disoproxil or tenofovir alafenamide, represents the treatment of choice. Pegylated interferon-alfa treatment can also be considered in mild to moderate chronic hepatitis B patients. Combination therapies are not generally recommended. All treated and untreated patients should be monitored for treatment response and adherence, and the risk of progression and development of complications. HCC remains the major concern for treated chronic hepatitis B patients. Several subgroups of patients with HBV infection require specific focus. Future treatment strategies to achieve 'cure' of disease and new biomarkers are discussed.
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            Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance.

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              Asian-Pacific clinical practice guidelines on the management of hepatitis B: a 2015 update

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                Author and article information

                Contributors
                Journal
                World J Gastroenterol
                World J Gastroenterol
                WJG
                World Journal of Gastroenterology
                Baishideng Publishing Group Inc
                1007-9327
                2219-2840
                21 June 2021
                21 June 2021
                : 27
                : 23
                : 3279-3289
                Affiliations
                Polyclinical Department, Botkin's Infectious Disease Hospital, St-Petersburg 195067, Russia
                Chronic Viral Infectious Disease Lab, Institute of Experimental Medicine, St-Petersburg 197376, Russia. belopolskaya.maria@ 123456yahoo.com
                Institute for Systems Theory, University of Stuttgart, Stuttgart 70569, Baden-Wurttemberg, Germany
                Faculty of Biomedical Sciences, Almazov National Medical Research Centre, St-Petersburg 197341, Russia
                Department of Molecular Microbiology, Institute of Experimental Medicine, St-Petersburg 197376, Russia
                Botkin's Infectious Disease Hospital, St-Petersburg 195067, Russia
                Author notes

                Author contributions: Belopolskaya M: Conceptualization, Methodology, Investigation, Formal Analysis, Writing - original draft, Writing - review & editing. Avrutin V: Conceptualization, Formal Analysis, Writing - review & editing, Validation. Kalinina O: Methodology, Writing - review & editing. Dmitriev A and Gusev D: Writing - review & editing, Supervision.

                Corresponding author: Maria Belopolskaya, MD, PhD, Doctor, Senior Scientist, Polyclinical Department, Botkin's Infectious Disease Hospital, Piskarevsky 49, St-Petersburg 195067, Russia. belopolskaya.maria@ 123456yahoo.com

                Article
                jWJG.v27.i23.pg3279
                10.3748/wjg.v27.i23.3279
                8218362
                34163111
                4d18d7cb-3394-40a3-8b4e-c1d65bded2ac
                ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.

                This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/

                History
                : 28 January 2021
                : 10 March 2021
                : 21 April 2021
                Categories
                Minireviews

                chronic hepatitis b,hepatitis b viral load,pregnancy,antiviral treatment,newborns,mother-to-child transmission

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