Literature DB >> 32605935

Combating hepatitis B and C by 2030: achievements, gaps, and options for actions in China.

Shu Chen1, Wenhui Mao2, Lei Guo2, Jiahui Zhang3, Shenglan Tang4.   

Abstract

China has the highest number of hepatitis B and C cases globally. Despite remarkable achievements, China faces daunting challenges in achieving international targets for hepatitis elimination. As part of a large-scale project assessing China's progress in achieving health-related Sustainable Development Goals using quantitative, qualitative data and mathematical modelling, this paper summarises the achievements, gaps and challenges, and proposes options for actions for hepatitis B and C control. China has made substantial progress in controlling chronic viral hepatitis. The four most successful strategies have been: (1) hepatitis B virus childhood immunisation; (2) prevention of mother-to-child transmission; (3) full coverage of nucleic acid amplification testing in blood stations and (4) effective financing strategies to support treatment. However, the total number of deaths due to hepatitis B and C is estimated to increase from 434 724 in 2017 to 527 829 in 2030 if there is no implementation of tailored interventions. Many health system barriers, including a fragmented governance system, insufficient funding, inadequate service coverage, unstandardised treatment and flawed information systems, have compromised the effective control of hepatitis B and C in China. We suggest five strategic priority actions to help eliminate hepatitis B and C in China: (1) restructure the viral hepatitis control governance system; (2) optimise health resource allocation and improve funding efficiency; (3) improve access to and the quality of the health benefits package, especially for high-risk groups; (4) strengthen information systems to obtain high-quality hepatitis epidemiological data; (5) increase investment in viral hepatitis research and development. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Entities:  

Keywords:  health systems; viral hepatitis

Mesh:

Year:  2020        PMID: 32605935      PMCID: PMC7328743          DOI: 10.1136/bmjgh-2020-002306

Source DB:  PubMed          Journal:  BMJ Glob Health        ISSN: 2059-7908


China has made considerable achievements in controlling hepatitis B and C through multiple strategies with efforts focused on prevention and increased treatment financing. Formidable challenges remain in combating hepatitis by 2030. Key health system barriers, including a fragmented governance system, insufficient funding, inadequate service coverage and unstandardised treatment, and flawed information systems, have compromised the effective control of viral hepatitis. To tackle these challenges, China must take five immediate actions: restructuring the governance system of viral hepatitis, optimising resource allocation and increasing the efficiency of funding, improving access to and the quality of the health benefits package, strengthening information systems and boosting investment on hepatitis research and development.

Introduction

Infection with chronic viral hepatitis can be caused by exposure to five different types of viruses (hepatitis A, B, C, D, E). Hepatitis B virus (HBV) and hepatitis C virus (HCV) account for 96% of all deaths related to viral hepatitis.1 China is the country experiencing the highest burden of these infections,2 3 with the WHO estimating that in 2016, 90 million people were living with chronic HBV infection and 10 million with chronic HCV infection in China, accounting for one-third and 7% of the global infections, respectively.4 Chronic HBV and HCV infection can progress to cirrhosis, hepatocellular carcinoma and premature death without proper treatment.5 Chronic HBV infections are associated with increased risk of other cancers including stomach cancer, colorectal cancer, oral cancer, pancreatic cancer and lymphoma.6 Among people living with chronic HBV and HCV, around 7 million and 2.5 million needed urgent treatment in China due to advanced liver diseases or the high risk of developing into cancer, respectively, in 2016.4 In 2017, there were an estimated 310 079 and 124 645 deaths due to chronic HBV and HCV infections, respectively, in China, according to the Global Burden of Diseases (GBD) 2017 Study.7 Viral hepatitis control in China is governed by the Bureau of Disease Prevention and Control, National Health Commission (NHC) and overseen by health commissions at the provincial, prefecture and county levels across the country. Under the regulatory supervision of NHC, the Chinese Center for Disease Control and Prevention (China CDC) is responsible for disease prevention and management, while hospitals provide clinical diagnosis and treatment. The Division of Immunization Planning Management and Division of HIV/AIDS Prevention and Control within NHC is responsible for hepatitis B and C control, respectively. The same governance structure for hepatitis B and C control has been put in place at the China CDC system nationwide. Viral hepatitis is increasingly garnering global attention and is included in the United Nations’ 2030 Agenda for Sustainable Development Goals (SDGs) where SDG 3.3 calls for ‘combat viral hepatitis’.8 At the same time, in 2016, WHO published its first Global Health Sector Strategy on Viral Hepatitis 2016–2021, which established nine quantitative global targets, such as ‘reducing new cases of chronic viral hepatitis B and C infections by 90% and deaths by 65% by 2030’.9 The first Action Plan for the Prevention and Treatment of Viral Hepatitis in China (2017–2020) was jointly published by 11 ministries in 2017, which set out 6 targets, 4 of which corresponded with WHO’s targets (table 1).10 Despite the priorities and action recommendations put forward by the international community to eliminate hepatitis globally and analysis of eliminating hepatitis B in China,11 12 we present key achievements, identify gaps and challenges, and proposes next steps to specifically help China end hepatitis B and C as a major public health threat by 2030.
Table 1

The hepatitis targets set by WHO and China

Target areaWHO 2020 targets(base year: 2015)WHO 2030 targets(base year: 2015)China 2020 targets
Impact targets
Incidence: new cases of chronic viral hepatitis B and C infections30% reduction(equivalent to 1% prevalence of HBsAg among children)90% reduction(equivalent to 0.1% prevalence of HBsAg among children)Keeping <1% prevalence of HBsAg among children under 5
Mortality: viral hepatitis B and C deaths10% reduction65% reductionNo quantitative target
Service coverage targets
HBV vaccination: childhood third dose vaccination coverage90%90%Keeping >95%
Prevention of HBV mother-to-child transmission: HBV birth-dose vaccination coverage or other approaches to prevent mother-to-child transmission50%90%Keeping >90%
Blood safety95% of donations screened in a quality-assured manner100% of donations screened in a quality-assured manner100% of donations screened in a quality-assured manner
Safe injections: percentage of injections administered with safety-engineered devices in and out of health facilities50%90%No quantitative target
Harm reduction: number of sterile needles and syringes provided per person who injects drugs per year200300No quantitative target
Viral hepatitis B and C diagnosis30%90%No quantitative target
Viral hepatitis B and C treatmentGlobally 5 million people receiving HBV treatment and 3 million people receiving HCV treatment80%No quantitative target
China-specific service coverage targets
Public awareness of viral hepatitis prevention and control knowledge>50%
Drug dependence treatment coverage to opioid users>70%

Sources: Global health sector strategy on viral hepatitis 2016–2021: towards ending viral hepatitis & Action plan for the prevention and treatment of viral hepatitis in China (2017–2020).

HBsAg, HBV surface antigen; HBV, Hepatitis B virus; HCV, hepatitis C virus.

The hepatitis targets set by WHO and China Sources: Global health sector strategy on viral hepatitis 2016–2021: towards ending viral hepatitis & Action plan for the prevention and treatment of viral hepatitis in China (2017–2020). HBsAg, HBV surface antigen; HBV, Hepatitis B virus; HCV, hepatitis C virus.

Approach

This article collected quantitative and qualitative data for analysis. Quantitative data were collected from published literature in Chinese and English, GBD 2017 Study estimates,3 the infectious diseases surveillance reporting system (IDSRS) and reports published by related governmental agencies. The health outcome projection results are estimated using the adjusted model developed by the GBD SDG team.13 Also, this paper includes qualitative findings from nine interviews purposively conducted among key stakeholders, including policy-makers, hepatitis control professionals and clinicians at national and provincial levels from Jiangsu, Hubei and Yunnan provinces representing eastern, central and western China, respectively, in 2017. The current study is part of a large-scale project assessing the progress of China in achieving health-related SDGs, and which has published detailed methods on the qualitative data collection and analysis and the projection model.14

Achievements in hepatitis B and C control in China

China has made substantial progress in controlling HBV and HCV infections over the past few decades. Based on the national seroepidemiology surveys conducted by China CDC since the 1990s, the seroprevalence of HBV surface antigen (HBsAg) among children <15 years old has declined from 10.5% in 1992 to 0.8% in 2014, and reached 0.3% among children under age 5 in 2014.15 The overall seroprevalence of anti-HCV antibody fell from 3.2% in 1996 to 0.43% in 2006.16 17 These achievements in China may, to a large extent, be attributed to the four national programmes or policies as outlined below. First, China’s HBV childhood immunisation programme has been recognised by WHO for its remarkable success.18 China was among the first developing countries to establish an HBV immunisation programme in 1992, recommending timing the first dose vaccination within 24 hours of birth and the second and third doses at 1 month and 6 months of birth, respectively.19 In 2002, with financial support from both the GAVI Alliance and the Chinese Government, the HBV vaccine was included in the National Immunization Program and made available free of charge to all newborns by 2005.20 An estimated total of ¥20.3 billion (¥1≈ US$0.14) was allocated by the central government to support the programme between 1992 and 2005.21 In 2009, the programme was further expanded to vaccinate children aged ≤15 years, with 68 million children successfully vaccinated.22 Thanks to the effective implementation of this policy, the three-dose vaccine coverage tripled from 30.0% in 1992 to 99.6% in 2015 with the timely first dose rate increasing from 22.2% to 95.6% during the same period.23 Second, comprehensive programmes to prevent mother-to-child transmission boosted HBV transmission control. Mother-to-child transmission is estimated to be responsible for 40%–50% of new HBV infections in China.24 Beginning in 2011, China initiated a national programme for integrated prevention of mother-to-child transmission (PMTCT) of HIV, syphilis and HBV. The programme includes free HBV screening services during pregnancy and administration of hepatitis B immunoglobulin within 12 hours of birth for babies born to HBV-infected mothers. It was expanded nationwide in 2015, and around ¥1.4 billion has been invested annually to cover the HBV-related services, which reached 95.6% coverage in 2015.25 26 Third, full coverage of nucleic acid amplification testing (NAT) in all blood stations substantially improved blood safety and prevented transfusion-transmitted infections, including HBV and HCV. The probability of transmitting via blood is especially high for HCV, and NAT can detect low levels of virus during a window period. NAT was included in routine donor screenings and piloted in 14 selected blood stations of 11 provinces since 2010.27 This practice was expanded nationwide in 2014 and received 1 billion RMB from the central budget to fund implementation in all blood stations.28 Lastly, China has made remarkable progress in implementing effective financing policies to make HBV and HCV drugs affordable over the past few years. Entecavir and tenofovir, two WHO-recommended first-line HBV drugs, were included in the updated National List of Reimbursable Medicines (NLRM) in February 2017.29 The two drugs were further selected into the ‘4+7 Cities Centralized Drug Procurement Document’, published in November 2018, a novel procurement pilot scheme aiming to dramatically cut the price paid for generic drugs through centralised joint procurement.30 Due to these efforts, the prices of entecavir and tenofovir have been substantially reduced, especially in the ‘4+7 Cities’ where it only takes around ¥18 (less than US$3) to complete 1 month entecavir or tenofovir treatment. By 2017, all the antiviral drugs recommended by the Chinese guidelines to treat HBV, including interferon-alfa, pegylated interferon-alfa and five nucleoside analogues, had been included in the NLRM.28 Remarkably, in recent years, treatment for HCV has vastly improved, and the sustained virological response rate of pan-genotypic Direct-Acting Antivirals (DAAs) has reached over 95%.31 Elbasvir–grazoprevir, ledipasvir–sofosbuvir and sofosbuvir–velpatasvir tablets can cure two, four and six main genotypes of HCV, respectively, though these medications are very expensive. They received expedited approval from the National Medical Products Administration to be marketed in China in 2018.32 The recent NLRM updated on 28 November 2019 has included the three HCV drugs, and the prices are expected to drop by 85% on average.33 34

Gaps and challenges

China has almost reached WHO’s targets for HBsAg prevalence (0.3% in 2014 among children under 5), HBV vaccination (99.6% in 2015), PMTCT (95.6% in 2015) and blood safety (100% blood screening since 2014; See table 1 for specific target definition).15 23 28 However, progress has been much slower in reaching the remaining five targets surrounding deaths, diagnosis and treatment of hepatitis B and C, and safe injections and harm reduction. China’s Hepatitis Action Plan has not established any quantitative goals to close this gap. Based on data available, we were only able to project the number of expected deaths. It is estimated that the total number of deaths due to hepatitis B and C would increase from 434 724 in 2017 to 527 829 in 2030. Particularly, mortality will be predominately driven by liver cancer caused by hepatitis B and C (figure 1). Based on our interviews, reversing this trend cannot be done without addressing the following challenges.
Figure 1

The historical change of deaths due to hepatitis B and C from 1990 to 2017 and projected changes from 2017 to 2030 in China. Data source: GBD 2017 Study.

The historical change of deaths due to hepatitis B and C from 1990 to 2017 and projected changes from 2017 to 2030 in China. Data source: GBD 2017 Study. The governance system of viral hepatitis control is fragmented in China. There is no specific single department or unit within the NHC or CDC to plan and lead hepatitis control work centrally. Currently, viral hepatitis is managed by different departments at the NHC or CDC based on similar transmission patterns or control strategies with other diseases. The Division of Immunization Planning Management leads HBV prevention through the vaccination programme, while the Division of HIV/AIDS Prevention and Control leads hepatitis C prevention given similar transmission patterns between HIV and HCV. The fragmented governance system has resulted in a lack of central strategic planning and leadership, which has further led to inadequate financial and personnel support. For example, we found through our interviews that hepatitis C control is highly dependent on the work plan, budget, skills and personnel of HIV/AIDS. Health financing is insufficient to fund the elimination of hepatitis B and C in China. Prevention and control strategies rely on domestic governmental funding that currently covers vaccination and PMTCT services of hepatitis B. However, a minimal amount of funding is explicitly allocated to hepatitis C, except for that bundled within HIV/AIDS control. Consequently, there is a massive gap in funding for crucial routine work such as disease surveillance (eg, the HBV seroepidemiology surveys have been funded by the Ministry of Science and Technology through research project applications), and the gap is even more massive for hepatitis C control with little support to implement effective prevention strategies. Although recommended HBV drugs have been included in the NLRM for over 3 years, the actual reimbursement rates vary greatly across China due to the decentralised management and risk pooling across Chinese health insurance schemes. This policy poses formidable challenges in achieving universal hepatitis treatment. It will be the same case for the HCV drugs recently added into the NLRM if no effective actions are taken. The delivery of comprehensive health services for hepatitis B and C, including prevention, testing, diagnosis and treatment, has not achieved its ideal coverage and standardisation. Hospital-acquired infections have not been prevented in low-tiered hospitals or hospitals in remote areas, which may follow less strict sterilisation procedures and skip testing HCV before surgical operations. The coverage of harm reduction practices to prevent HCV infection among drug users is low given stigma, discrimination and legality of using drugs.11 HBV testing was removed from routine health check-ups for new employees and students in 2010 to avoid discrimination against people infected with HBV.35 The diagnosis and treatment rate of hepatitis B and C remains extremely low according to our interviews, though there is no public data available to confirm this. For people who are diagnosed and treated, overtreatment is common with hospitals in China incentivised to prescribe drugs, particularly auxiliary medications to generate income. The information system of viral hepatitis is unable to provide adequate data on the hepatitis epidemic for strategic planning. The current information system, IDSRS, primarily captures HBV and HCV new infections and deaths while providing little information on critical indicators such as service coverage, diagnosis and treatment. Duplication of data undermines its quality and accuracy.

Options for actions towards eliminating viral hepatitis B and C in China

In light of the above challenges and taking into account recommendations from literature and key stakeholder interviews, we propose five strategic priority actions to help achieve the international and domestic targets and eliminate viral hepatitis in China. First, restructure the governance system for viral hepatitis control within NHC and the China CDC to change the current fragmented management situation. It is suggested that the NHC establish a separate and independent division for viral hepatitis under the Disease Control Bureau to lead the national viral hepatitis control effort, with the Health Commission and CDC at different administrative levels making similar structural changes. The department should have its own team, budget and work plan with performance indicators to ensure successful operation. Second, optimise resource allocation and increase the efficiency of funding to ensure sufficient and sustainable health financing for hepatitis elimination. It is essential that the NHC identify the funding required to achieve targets, and develop a comprehensive and feasible hepatitis control budget to cover the continuum of health services. The NHC worked with WHO to develop an investment plan for hepatitis in 2016, though it remains unclear if and how this plan will be used for strategic planning. Meanwhile, the NHC can work with the Ministry of Finance and the National Healthcare Security Administration on funding resource mobilisation and reallocation for sustained viral hepatitis health financing, ideally under the designated leadership of the State Council. It is essential to standardise treatment and reduce drug prices to increase funding efficiency. Regional disparities in health insurance coverage need to be assessed and addressed through central budgeting compensations. Third, improve access to and quality of the health benefits package for patients with viral hepatitis, especially for high-risk groups. The five core interventions proposed by WHO (box 1) to be included in benefits packages are available in China, while extra efforts need to be invested in strengthening surgical safety and other sources of hospital-acquired infections and harm reduction services.9 It is critical to increase the identification of the number of infected individuals with an effective disease surveillance system using better testing and diagnosis accuracy, coverage and reporting. It is vital to increase the treatment rate by developing a standard treatment package with sufficient financial coverage, particularly for low-income populations, and an individualised patient management system, especially for HBV lifelong treatment (box 2). High-risk populations, including healthcare workers, people born to mothers with hepatitis B, injection drug users, indigenous peoples and ethnic minorities, prisoners, migrants, men who have sex with men, persons coinfected with HIV and hepatitis, and blood donors need to be identified and prioritised for specific prevention, testing, diagnosis, care and treatment.9 Tailored interventions for these high-risk populations can be implemented to microeliminate hepatitis within the discrete group.36 It is important to address HBV and HCV-related stigma and discrimination, through identifying the drivers of this discrimination, alongside population-wide health education programmes. HBV vaccination; Injection, blood and surgical safety and universal precautions; Prevention of mother-to-child transmission of hepatitis B virus; Harm reduction services for people who inject drugs; Treatment of chronic hepatitis B virus and hepatitis C virus infection. Source: Global Health Sector Strategy on Viral Hepatitis, 2016–2021, WHO Effective prevention interventions have reduced new hepatitis B virus (HBV) infections and put new hepatitis C virus (HCV) infections under control in China. Treating the large number of people with HBV and HCV needs to be prioritised to meet viral hepatitis elimination targets. Addressing low hepatitis B and C treatment rates largely due to inadequate case identification and high patient financial burden face formidable challenges with respect to service coverage, service quality and financial protection. The treatment success rate is an issue for people infected with hepatitis B, who have to receive lifelong treatment despite the asymptotic nature and side effects. The quality of service provided varies by hospital, and there are no standardised treatment packages. Overprescription of medicines is prevalent, especially auxiliary medicines, as a way to generate revenues. Effective financing strategies have improved the financial protections for patients with hepatitis, especially for patients with hepatitis B in the ‘4+7 Cities’. Looking ahead, China must take urgent actions to improve the treatment service coverage, quality and affordability for people infected with HBV and HCV. Key recommendations are: Increase identification of infected individuals through a better surveillance system and improved testing and diagnosis accuracy. Resource-rich provinces and cities can implement active patient identification strategies, while working on removing stigma and discrimination through population-wide health education programs. Develop a standardised treatment package and ensure it is well implemented at different levels of clinical institutions. Considering the root cause of overprescription, strategies to rationalise physicians’ salary and apply the diagnosis-related groups or capitation payment need to be in place. Capacity training for physicians and carefully designed performance evaluation indicators are also essential to ensure the successful implementation. Strengthen patient management to improve medication adherence. This is especially important for patients with hepatitis B. Hospitals should apply individual patient management to them, similar to the treatment and management of patients with HIV/AIDs. Decrease patient financial burden due to treatment, especially for low-income groups. Economic analysis has demonstrated high cost effectiveness of investing HBV and HCV treatment drugs in many countries. Despite the huge progress, continuing investment needs to be made on reducing drug price and increasing reimbursement rate especially for the low-income patients to increase equity. Fourth, strengthen information systems to obtain high-quality hepatitis epidemiological data. A well-designed quality control system needs to be established and implemented to avoid inaccurate and duplicate cases of hepatitis infection and hepatitis-related death. The system should also integrate process indicators for service coverage to capture data throughout the continuum of care, making it possible to assess the national hepatitis burden and monitor access to, uptake of and quality of services delivered. Lastly, boost investment for hepatitis research and development (R&D) innovations. It is unlikely for either the world or China to eliminate the viral hepatitis burden unless significant progress is made to develop new medicines, technologies and innovative service delivery approaches. Continuing and increasing investment is necessary to improve the prevention, testing, diagnostics, treatment and patient management of chronic viral hepatitis. Particularly, priority should be placed on R&D in effective HCV vaccination and short-course HBV curative treatments.

Conclusion

This article highlights recent improvements in the control of hepatitis B and C in China and how they can be furthered. Given projections for increased deaths due to hepatitis B and C in China and the large numbers of individuals infected with hepatitis B and C, it is critical to urgently develop and implement a set of concerted actions, as proposed above, with adequate resources put in place to support the effective implementation of these actions. Inaction, or delay in taking these actions, would have to make a negative impact on a large number of Chinese households and society.
  16 in total

Review 1.  Global prevalence and genotype distribution of hepatitis C virus infection in 2015: a modelling study.

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Journal:  Lancet Gastroenterol Hepatol       Date:  2016-12-16

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Authors:  Shun-xiang Zhang; Ru-bo Dang; Wei-dong Zhang; Xiao-feng Liang; Fu-qiang Cui
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Review 3.  The inception, achievements, and implications of the China GAVI Alliance Project on Hepatitis B Immunization.

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Journal:  Vaccine       Date:  2013-12-27       Impact factor: 3.641

Review 4.  Oral Direct-Acting Agent Therapy for Hepatitis C Virus Infection: A Systematic Review.

Authors:  Oluwaseun Falade-Nwulia; Catalina Suarez-Cuervo; David R Nelson; Michael W Fried; Jodi B Segal; Mark S Sulkowski
Journal:  Ann Intern Med       Date:  2017-03-21       Impact factor: 25.391

5.  Requirements for global elimination of hepatitis B: a modelling study.

Authors:  Shevanthi Nayagam; Mark Thursz; Elisa Sicuri; Lesong Conteh; Stefan Wiktor; Daniel Low-Beer; Timothy B Hallett
Journal:  Lancet Infect Dis       Date:  2016-09-13       Impact factor: 71.421

6.  Prevention of Chronic Hepatitis B after 3 Decades of Escalating Vaccination Policy, China.

Authors:  Fuqiang Cui; Lipin Shen; Li Li; Huaqing Wang; Fuzhen Wang; Shengli Bi; Jianhua Liu; Guomin Zhang; Feng Wang; Hui Zheng; Xiaojin Sun; Ning Miao; Zundong Yin; Zijian Feng; Xiaofeng Liang; Yu Wang
Journal:  Emerg Infect Dis       Date:  2017-05       Impact factor: 6.883

7.  Associations Between Hepatitis B Virus Infection and Risk of All Cancer Types.

Authors:  Ci Song; Jun Lv; Yao Liu; Jian Guo Chen; Zijun Ge; Jian Zhu; Juncheng Dai; Ling-Bin Du; Canqing Yu; Yu Guo; Zheng Bian; Ling Yang; Yiping Chen; Zhengming Chen; Jibin Liu; Jie Jiang; Liguo Zhu; Xiangjun Zhai; Yue Jiang; Hongxia Ma; Guangfu Jin; Hongbing Shen; Liming Li; Zhibin Hu
Journal:  JAMA Netw Open       Date:  2019-06-05

8.  Countdown to 2030: eliminating hepatitis B disease, China.

Authors:  Jue Liu; Wannian Liang; Wenzhan Jing; Min Liu
Journal:  Bull World Health Organ       Date:  2019-01-28       Impact factor: 9.408

9.  Global, Regional, and National Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life-Years for 29 Cancer Groups, 1990 to 2017: A Systematic Analysis for the Global Burden of Disease Study.

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Morteza Arab-Zozani; Jalal Arabloo; Zohreh Arefi; Olatunde Aremu; Habtamu Abera Areri; Al Artaman; Hamid Asayesh; Ephrem Tsegay Asfaw; Alebachew Fasil Ashagre; Reza Assadi; Bahar Ataeinia; Hagos Tasew Atalay; Zerihun Ataro; Suleman Atique; Marcel Ausloos; Leticia Avila-Burgos; Euripide F G A Avokpaho; Ashish Awasthi; Nefsu Awoke; Beatriz Paulina Ayala Quintanilla; Martin Amogre Ayanore; Henok Tadesse Ayele; Ebrahim Babaee; Umar Bacha; Alaa Badawi; Mojtaba Bagherzadeh; Eleni Bagli; Senthilkumar Balakrishnan; Abbas Balouchi; Till Winfried Bärnighausen; Robert J Battista; Masoud Behzadifar; Meysam Behzadifar; Bayu Begashaw Bekele; Yared Belete Belay; Yaschilal Muche Belayneh; Kathleen Kim Sachiko Berfield; Adugnaw Berhane; Eduardo Bernabe; Mircea Beuran; Nickhill Bhakta; Krittika Bhattacharyya; Belete Biadgo; Ali Bijani; Muhammad Shahdaat Bin Sayeed; Charles Birungi; Catherine Bisignano; Helen Bitew; Tone Bjørge; Archie Bleyer; Kassawmar Angaw Bogale; Hunduma Amensisa Bojia; Antonio M Borzì; Cristina Bosetti; Ibrahim R Bou-Orm; Hermann Brenner; Jerry D Brewer; Andrey Nikolaevich Briko; Nikolay Ivanovich Briko; Maria Teresa Bustamante-Teixeira; Zahid A Butt; Giulia Carreras; Juan J Carrero; Félix Carvalho; Clara Castro; Franz Castro; Ferrán Catalá-López; Ester Cerin; Yazan Chaiah; Wagaye Fentahun Chanie; Vijay Kumar Chattu; Pankaj Chaturvedi; Neelima Singh Chauhan; Mohammad Chehrazi; Peggy Pei-Chia Chiang; Tesfaye Yitna Chichiabellu; Onyema Greg Chido-Amajuoyi; Odgerel Chimed-Ochir; Jee-Young J Choi; Devasahayam J Christopher; Dinh-Toi Chu; Maria-Magdalena Constantin; Vera M Costa; Emanuele Crocetti; Christopher Stephen Crowe; Maria Paula Curado; Saad M A Dahlawi; Giovanni Damiani; Amira Hamed Darwish; Ahmad Daryani; José das Neves; Feleke Mekonnen Demeke; Asmamaw Bizuneh Demis; Birhanu Wondimeneh Demissie; Gebre Teklemariam Demoz; Edgar Denova-Gutiérrez; Afshin Derakhshani; Kalkidan Solomon Deribe; Rupak Desai; Beruk Berhanu Desalegn; Melaku Desta; Subhojit Dey; Samath Dhamminda Dharmaratne; Meghnath Dhimal; Daniel Diaz; Mesfin Tadese Tadese Dinberu; Shirin Djalalinia; David Teye Doku; Thomas M Drake; Manisha Dubey; Eleonora Dubljanin; Eyasu Ejeta Duken; Hedyeh Ebrahimi; Andem Effiong; Aziz Eftekhari; Iman El Sayed; Maysaa El Sayed Zaki; Shaimaa I El-Jaafary; Ziad El-Khatib; Demelash Abewa Elemineh; Hajer Elkout; Richard G Ellenbogen; Aisha Elsharkawy; Mohammad Hassan Emamian; Daniel Adane Endalew; Aman Yesuf Endries; Babak Eshrati; Ibtihal Fadhil; Vahid Fallah Omrani; Mahbobeh Faramarzi; Mahdieh Abbasalizad Farhangi; Andrea Farioli; Farshad Farzadfar; Netsanet Fentahun; Eduarda Fernandes; Garumma Tolu Feyissa; Irina Filip; Florian Fischer; James L Fisher; Lisa M Force; Masoud Foroutan; Marisa Freitas; Takeshi Fukumoto; Neal D Futran; Silvano Gallus; Fortune Gbetoho Gankpe; Reta Tsegaye Gayesa; Tsegaye Tewelde Gebrehiwot; Gebreamlak Gebremedhn Gebremeskel; Getnet Azeze Gedefaw; Belayneh K Gelaw; Birhanu Geta; Sefonias Getachew; Kebede Embaye Gezae; Mansour Ghafourifard; Alireza Ghajar; Ahmad Ghashghaee; Asadollah Gholamian; Paramjit Singh Gill; Themba T G Ginindza; Alem Girmay; Muluken Gizaw; Ricardo Santiago Gomez; Sameer Vali Gopalani; Giuseppe Gorini; Bárbara Niegia Garcia Goulart; Ayman Grada; Maximiliano Ribeiro Guerra; Andre Luiz Sena Guimaraes; Prakash C Gupta; Rahul Gupta; Kishor Hadkhale; Arvin Haj-Mirzaian; Arya Haj-Mirzaian; Randah R Hamadeh; Samer Hamidi; Lolemo Kelbiso Hanfore; Josep Maria Haro; Milad Hasankhani; Amir Hasanzadeh; Hamid Yimam Hassen; Roderick J Hay; Simon I Hay; Andualem Henok; Nathaniel J Henry; Claudiu Herteliu; Hagos D Hidru; Chi Linh Hoang; Michael K Hole; Praveen Hoogar; Nobuyuki Horita; H Dean Hosgood; Mostafa Hosseini; Mehdi Hosseinzadeh; Mihaela Hostiuc; Sorin Hostiuc; Mowafa Househ; Mohammedaman Mama Hussen; Bogdan Ileanu; Milena D Ilic; Kaire Innos; Seyed Sina Naghibi Irvani; Kufre Robert Iseh; Sheikh Mohammed Shariful Islam; Farhad Islami; Nader Jafari Balalami; Morteza Jafarinia; Leila Jahangiry; Mohammad Ali Jahani; Nader Jahanmehr; Mihajlo Jakovljevic; Spencer L James; Mehdi Javanbakht; Sudha Jayaraman; Sun Ha Jee; Ensiyeh Jenabi; Ravi Prakash Jha; Jost B Jonas; Jitendra Jonnagaddala; Tamas Joo; Suresh Banayya Jungari; Mikk Jürisson; Ali Kabir; Farin Kamangar; André Karch; Narges Karimi; Ansar Karimian; Amir Kasaeian; Gebremicheal Gebreslassie Kasahun; Belete Kassa; Tesfaye Dessale Kassa; Mesfin Wudu Kassaw; Anil Kaul; Peter Njenga Keiyoro; Abraham Getachew Kelbore; Amene Abebe Kerbo; Yousef Saleh Khader; Maryam Khalilarjmandi; Ejaz Ahmad Khan; Gulfaraz Khan; Young-Ho Khang; Khaled Khatab; Amir Khater; Maryam Khayamzadeh; Maryam Khazaee-Pool; Salman Khazaei; Abdullah T Khoja; Mohammad Hossein Khosravi; Jagdish Khubchandani; Neda Kianipour; Daniel Kim; Yun Jin Kim; Adnan Kisa; Sezer Kisa; Katarzyna Kissimova-Skarbek; Hamidreza Komaki; Ai Koyanagi; Kristopher J Krohn; Burcu Kucuk Bicer; Nuworza Kugbey; Vivek Kumar; Desmond Kuupiel; Carlo La Vecchia; Deepesh P Lad; Eyasu Alem Lake; Ayenew Molla Lakew; Dharmesh Kumar Lal; Faris Hasan Lami; Qing Lan; Savita Lasrado; Paolo Lauriola; Jeffrey V Lazarus; James Leigh; Cheru Tesema Leshargie; Yu Liao; Miteku Andualem Limenih; Stefan Listl; Alan D Lopez; Platon D Lopukhov; Raimundas Lunevicius; Mohammed Madadin; Sameh Magdeldin; Hassan Magdy Abd El Razek; Azeem Majeed; Afshin Maleki; Reza Malekzadeh; Ali Manafi; Navid Manafi; Wondimu Ayele Manamo; Morteza Mansourian; Mohammad Ali Mansournia; Lorenzo Giovanni Mantovani; Saman Maroufizadeh; Santi Martini S Martini; Tivani Phosa Mashamba-Thompson; Benjamin Ballard Massenburg; Motswadi Titus Maswabi; Manu Raj Mathur; Colm McAlinden; Martin McKee; Hailemariam Abiy Alemu Meheretu; Ravi Mehrotra; Varshil Mehta; Toni Meier; Yohannes A Melaku; Gebrekiros Gebremichael Meles; Hagazi Gebre Meles; Addisu Melese; Mulugeta Melku; Peter T N Memiah; Walter Mendoza; Ritesh G Menezes; Shahin Merat; Tuomo J Meretoja; Tomislav Mestrovic; Bartosz Miazgowski; Tomasz Miazgowski; Kebadnew Mulatu M Mihretie; Ted R Miller; Edward J Mills; Seyed Mostafa Mir; Hamed Mirzaei; Hamid Reza Mirzaei; Rashmi Mishra; Babak Moazen; Dara K Mohammad; Karzan Abdulmuhsin Mohammad; Yousef Mohammad; Aso Mohammad Darwesh; Abolfazl Mohammadbeigi; Hiwa Mohammadi; Moslem Mohammadi; Mahdi Mohammadian; Abdollah Mohammadian-Hafshejani; Milad Mohammadoo-Khorasani; Reza Mohammadpourhodki; Ammas Siraj Mohammed; Jemal Abdu Mohammed; Shafiu Mohammed; Farnam Mohebi; Ali H Mokdad; Lorenzo Monasta; Yoshan Moodley; Mahmood Moosazadeh; Maryam Moossavi; Ghobad Moradi; Mohammad Moradi-Joo; Maziar Moradi-Lakeh; Farhad Moradpour; Lidia Morawska; Joana Morgado-da-Costa; Naho Morisaki; Shane Douglas Morrison; Abbas Mosapour; Seyyed Meysam Mousavi; Achenef Asmamaw Muche; Oumer Sada S Muhammed; Jonah Musa; Ashraf F Nabhan; Mehdi Naderi; Ahamarshan Jayaraman Nagarajan; Gabriele Nagel; Azin Nahvijou; Gurudatta Naik; Farid Najafi; Luigi Naldi; Hae Sung Nam; Naser Nasiri; Javad Nazari; Ionut Negoi; Subas Neupane; Polly A Newcomb; Haruna Asura Nggada; Josephine W Ngunjiri; Cuong Tat Nguyen; Leila Nikniaz; Dina Nur Anggraini Ningrum; Yirga Legesse Nirayo; Molly R Nixon; Chukwudi A Nnaji; Marzieh Nojomi; Shirin Nosratnejad; Malihe Nourollahpour Shiadeh; Mohammed Suleiman Obsa; Richard Ofori-Asenso; Felix Akpojene Ogbo; In-Hwan Oh; Andrew T Olagunju; Tinuke O Olagunju; Mojisola Morenike Oluwasanu; Abidemi E Omonisi; Obinna E Onwujekwe; Anu Mary Oommen; Eyal Oren; Doris D V Ortega-Altamirano; Erika Ota; Stanislav S Otstavnov; Mayowa Ojo Owolabi; Mahesh P A; Jagadish Rao Padubidri; Smita Pakhale; Amir H Pakpour; Adrian Pana; Eun-Kee Park; Hadi Parsian; Tahereh Pashaei; Shanti Patel; Snehal T Patil; Alyssa Pennini; David M Pereira; Cristiano Piccinelli; Julian David Pillay; Majid Pirestani; Farhad Pishgar; Maarten J Postma; Hadi Pourjafar; Farshad Pourmalek; Akram Pourshams; Swayam Prakash; Narayan Prasad; Mostafa Qorbani; Mohammad Rabiee; Navid Rabiee; Amir Radfar; Alireza Rafiei; Fakher Rahim; Mahdi Rahimi; Muhammad Aziz Rahman; Fatemeh Rajati; Saleem M Rana; Samira Raoofi; Goura Kishor Rath; David Laith Rawaf; Salman Rawaf; Robert C Reiner; Andre M N Renzaho; Nima Rezaei; Aziz Rezapour; Ana Isabel Ribeiro; Daniela Ribeiro; Luca Ronfani; Elias Merdassa Roro; Gholamreza Roshandel; Ali Rostami; Ragy Safwat Saad; Parisa Sabbagh; Siamak Sabour; Basema Saddik; Saeid Safiri; Amirhossein Sahebkar; Mohammad Reza Salahshoor; Farkhonde Salehi; Hosni Salem; Marwa Rashad Salem; Hamideh Salimzadeh; Joshua A Salomon; Abdallah M Samy; Juan Sanabria; Milena M Santric Milicevic; Benn Sartorius; Arash Sarveazad; Brijesh Sathian; Maheswar Satpathy; Miloje Savic; Monika Sawhney; Mehdi Sayyah; Ione J C Schneider; Ben Schöttker; Mario Sekerija; Sadaf G Sepanlou; Masood Sepehrimanesh; Seyedmojtaba Seyedmousavi; Faramarz Shaahmadi; Hosein Shabaninejad; Mohammad Shahbaz; Masood Ali Shaikh; Amir Shamshirian; Morteza Shamsizadeh; Heidar Sharafi; Zeinab Sharafi; Mehdi Sharif; Ali Sharifi; Hamid Sharifi; Rajesh Sharma; Aziz Sheikh; Reza Shirkoohi; Sharvari Rahul Shukla; Si Si; Soraya Siabani; Diego Augusto Santos Silva; Dayane Gabriele Alves Silveira; Ambrish Singh; Jasvinder A Singh; Solomon Sisay; Freddy Sitas; Eugène Sobngwi; Moslem Soofi; Joan B Soriano; Vasiliki Stathopoulou; Mu'awiyyah Babale Sufiyan; Rafael Tabarés-Seisdedos; Takahiro Tabuchi; Ken Takahashi; Omid Reza Tamtaji; Mohammed Rasoul Tarawneh; Segen Gebremeskel Tassew; Parvaneh Taymoori; Arash Tehrani-Banihashemi; Mohamad-Hani Temsah; Omar Temsah; Berhe Etsay Tesfay; Fisaha Haile Tesfay; Manaye Yihune Teshale; Gizachew Assefa Tessema; Subash Thapa; Kenean Getaneh Tlaye; Roman Topor-Madry; Marcos Roberto Tovani-Palone; Eugenio Traini; Bach Xuan Tran; Khanh Bao Tran; Afewerki Gebremeskel Tsadik; Irfan Ullah; Olalekan A Uthman; Marco Vacante; Maryam Vaezi; Patricia Varona Pérez; Yousef Veisani; Simone Vidale; Francesco S Violante; Vasily Vlassov; Stein Emil Vollset; Theo Vos; Kia Vosoughi; Giang Thu Vu; Isidora S Vujcic; Henry Wabinga; Tesfahun Mulatu Wachamo; Fasil Shiferaw Wagnew; Yasir Waheed; Fitsum Weldegebreal; Girmay Teklay Weldesamuel; Tissa Wijeratne; Dawit Zewdu Wondafrash; Tewodros Eshete Wonde; Adam Belay Wondmieneh; Hailemariam Mekonnen Workie; Rajaram Yadav; Abbas Yadegar; Ali Yadollahpour; Mehdi Yaseri; Vahid Yazdi-Feyzabadi; Alex Yeshaneh; Mohammed Ahmed Yimam; Ebrahim M Yimer; Engida Yisma; Naohiro Yonemoto; Mustafa Z Younis; Bahman Yousefi; Mahmoud Yousefifard; Chuanhua Yu; Erfan Zabeh; Vesna Zadnik; Telma Zahirian Moghadam; Zoubida Zaidi; Mohammad Zamani; Hamed Zandian; Alireza Zangeneh; Leila Zaki; Kazem Zendehdel; Zerihun Menlkalew Zenebe; Taye Abuhay Zewale; Arash Ziapour; Sanjay Zodpey; Christopher J L Murray
Journal:  JAMA Oncol       Date:  2019-12-01       Impact factor: 31.777

10.  Current situation and progress toward the 2030 health-related Sustainable Development Goals in China: A systematic analysis.

Authors:  Shu Chen; Lei Guo; Zhan Wang; Wenhui Mao; Yanfeng Ge; Xiaohua Ying; Jing Fang; Qian Long; Qin Liu; Hao Xiang; Chenkai Wu; Chaowei Fu; Di Dong; Jiahui Zhang; Ju Sun; Lichun Tian; Limin Wang; Maigeng Zhou; Mei Zhang; Mengcen Qian; Wei Liu; Weixi Jiang; Wenmeng Feng; Xinying Zeng; Xiyu Ding; Xun Lei; Rachel Tolhurst; Ling Xu; Haidong Wang; Faye Ziegeweid; Scott Glenn; John S Ji; Mary Story; Gavin Yamey; Shenglan Tang
Journal:  PLoS Med       Date:  2019-11-19       Impact factor: 11.069

View more
  8 in total

1.  Costs and health impact of delayed implementation of a national hepatitis B treatment program in China.

Authors:  Mehlika Toy; David Hutton; Jidong Jia; Samuel So
Journal:  J Glob Health       Date:  2022-07-08       Impact factor: 7.664

2.  Conventional and genetic risk factors for chronic Hepatitis B virus infection in a community-based study of 0.5 million Chinese adults.

Authors:  Elizabeth Hamilton; Ling Yang; Alexander J Mentzer; Yu Guo; Yiping Chen; Jun Lv; Robert Fletcher; Neil Wright; Kuang Lin; Robin Walters; Christiana Kartsonaki; Yingcai Yang; Sushila Burgess; Sam Sansome; Liming Li; Iona Y Millwood; Zhengming Chen
Journal:  Sci Rep       Date:  2022-07-15       Impact factor: 4.996

3.  Diagnosis experiences from 50 hepatitis B patients in Chongqing, China: a qualitative study.

Authors:  Xiangxi Zhou; Fan Zhang; Yongping Ao; Chunli Lu; Tingting Li; Xianglong Xu; Huan Zeng
Journal:  BMC Public Health       Date:  2021-12-01       Impact factor: 3.295

4.  Trend in the incidence of hepatitis A in mainland China from 2004 to 2017: a joinpoint regression analysis.

Authors:  Yuan-Sheng Li; Bei-Bei Zhang; Xi Zhang; Ya-Mei Luo; Jun-Hui Zhang; Song Fan; Li-Ping Fei; Chao Yang; Ning-Jun Ren; Xiang Li
Journal:  BMC Infect Dis       Date:  2022-08-01       Impact factor: 3.667

5.  The research of SARIMA model for prediction of hepatitis B in mainland China.

Authors:  Daren Zhao; Huiwu Zhang; Qing Cao; Zhiyi Wang; Ruihua Zhang
Journal:  Medicine (Baltimore)       Date:  2022-06-10       Impact factor: 1.817

6.  Association between hepatitis B virus infection and colorectal liver metastasis: a meta-analysis.

Authors:  Rongqiang Liu; Weihao Kong; Mingbin Deng; Guozhen Lin; Tianxing Dai; Linsen Ye
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

7.  Effect of a Community-Based Hepatitis B Virus Infection Detection Combined with Vaccination Program in China.

Authors:  Xinyao Liu; Wuqi Qiu; Yan Liang; Wei Zhang; Qian Qiu; Xinxin Bai; Guolin Dai; Hao Ma; Hongpu Hu; Wei Zhao; Guangyu Hu
Journal:  Vaccines (Basel)       Date:  2021-12-24

8.  Cost-Effectiveness Analysis of Pan-Genotypic Sofosbuvir-Based Regimens for Treatment of Chronic Hepatitis C Genotype 1 Infection in China.

Authors:  Hui Jun Zhou; Jing Cao; Hui Shi; Nasheen Naidoo; Sherehe Semba; Pei Wang; Yi Fan Fan; Shui Cheng Zhu
Journal:  Front Public Health       Date:  2021-12-09
  8 in total

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