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      Prevalence of HBV and HCV infections, Bhutan, 2017: Progress and next steps

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          Abstract

          Background

          Bhutan is committed to eliminating hepatitis B and hepatitis C, though recent baseline estimates of disease burden in the general population are unknown. In 2017, we carried out a biomarker survey in the general population to estimate the prevalence of hepatitis B virus (HBV) and hepatitis C virus (HCV) biomarkers to evaluate the impact of immunization and guide further efforts.

          Methods

          In 2017, a cross-sectional, population-based, three-stage cluster survey was undertaken of the general population (1–17 and 20+ years of age). We visited households, collected blood specimens and administered a standard questionnaire. Specimens were collected for hepatitis B surface antigen (HBsAg) and hepatitis C virus antibody (anti-HCV) testing. We calculated prevalence of infection and selected characteristics, along with confidence intervals (CIs).

          Results

          Of 1372 individuals approached, 1358 (99%) participated. Of those, 1321 (97%) had a specimen tested for HBsAg, and among 1173 enrolled individuals 5 years of age or older, 1150 (98%) individuals were tested for anti-HCV. The prevalence of HBsAg was 2.0% in 775 persons 20 years of age or older (95% CI: 1.0–4.0) and 0.5% in 546 persons 1–17 years of age (95% CI: 0.1–1.8). The prevalence of anti-HCV was 0.3% (95% CI: 0.1–0.8) among persons ≥5 years.

          Conclusions

          Universal hepatitis B immunization of infants has resulted in a low prevalence of chronic HBV infection in persons 1–17 years of age and the prevalence of anti-HCV is low among persons aged ≥5 years. Efforts should continue to reach high coverage of the timely birth dose along with completion of the hepatitis B vaccine series. To reduce the chronic liver disease burden among adults, HBV and HCV testing and treatment as indicated might be restricted to pregnant women, blood donors, individuals with chronic liver diseases, and other groups with history of high-risk exposures.

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          Most cited references8

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          Hepatitis B vaccines: WHO position paper – July 2017.

          (2017)
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            Laboratory diagnostics for hepatitis C virus infection.

            Identification of prevalent infection by hepatitis C virus (HCV) is based serologically on detecting anti-HCV immunoglobulin G, using immunoassays, immunoblot assays, and, more recently, immunochromatography-based rapid tests. None discriminate between active and resolved HCV infection. Tests for detecting HCV RNA identify active HCV infection but are costly. Serologic assays for HCV antigens have been developed and show potential for diagnosis of active HCV infection, and their performance characteristics are undergoing evaluation. The diagnosis of acute HCV infection without the demonstration of seroconversion remains elusive.
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              HCV transmission in industrialized countries and resource-constrained areas.

              HCV is a blood-borne virus transmitted by percutaneous exposure to infected blood or blood-derived body fluids. The main routes of transmission are blood transfusions, medical procedures and injection drug use. In industrialized countries, HCV transmission through blood transfusions has been virtually eliminated and iatrogenic transmission occurs only sporadically during local breaches of infection control procedures. As most new cases originate from injection drug use, harm-reduction programmes (including opiate substitution, needle exchange and health education) can greatly reduce HCV transmission. Currently, the main approach to reduce the HCV disease burden is by increasing awareness of both the public and health-care providers to hepatitis C, enhancing screening opportunities and treatment of the infected population. In resource-limited countries, the priority is reducing transmission through blood transfusions and invasive medical procedures. This approach requires training of health-care providers and also structural changes and financial investments in countries where antibody screening, disposable materials and effective sterilization procedures are not routinely available. In these countries, reducing the HCV burden has been hampered by limited access to treatment, largely owing to the cost of drugs. Access to treatment is moving up on the agenda of international and non-governmental organizations in conjunction with the future availability of highly efficacious oral drug regimens.
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                Author and article information

                Contributors
                hutiny@who.int
                Journal
                BMC Infect Dis
                BMC Infect. Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                8 July 2020
                8 July 2020
                2020
                : 20
                : 485
                Affiliations
                [1 ]GRID grid.490687.4, Department of Public Health, , Ministry of Health, ; Thimphu, Bhutan
                [2 ]Department of Medicine, Jigme Dorji Wangchuk National Referral Hospital, Thimphu, Bhutan
                [3 ]WHO Country Office, Thimphu, Bhutan
                [4 ]GRID grid.490687.4, Royal Centre for Disease Control, Department of Public Health, , Ministry of Health, ; Thimphu, Bhutan
                [5 ]GRID grid.3575.4, ISNI 0000000121633745, WHO Headquarters, ; 20 Avenue Appia, 1211 Geneva, Switzerland
                [6 ]GRID grid.483405.e, ISNI 0000 0001 1942 4602, WHO Regional Office for the Eastern Mediterranean Region, ; Monazamet El Seha El Alamia Street, Nasr City, Po Box 7608, Cairo, 11371 Egypt
                [7 ]GRID grid.416738.f, ISNI 0000 0001 2163 0069, United States Centers for Disease Control and Prevention, ; Atlanta, GA USA
                [8 ]GRID grid.483403.8, ISNI 0000 0001 0685 5219, WHO Regional Office for the South East Asia Region, ; New Delhi, India
                Author information
                http://orcid.org/0000-0003-1110-6794
                Article
                5176
                10.1186/s12879-020-05176-3
                7346496
                32641006
                9159f194-4688-4c3f-8ab5-60ee3327b64a
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 18 March 2019
                : 17 June 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000030, Centers for Disease Control and Prevention;
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2020

                Infectious disease & Microbiology
                hepatitis b,epidemiology,immunization,prevention of mother to child transmission,perinatal infections,evaluation,survey hbsag

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