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As part of efforts to improve Hepatitis C care for underserved groups, OUCRU hosted a dialogue bringing together community members, social scientists and insurance representatives. Participants, including people who inject drugs, LGBT+ individuals and low-income groups, discussed barriers to accessing health insurance despite policy improvements. Challenges include complex hospital systems, documentation issues, limited awareness, financial constraints and privacy concerns. The session highlighted the importance of continued community-based participatory research to address health inequities and strengthen support networks.

Group photo of a Community discussion in Vietnam

As part of the project to Improve Hepatitis C Access and Treatment for Underserved Communities, OUCRU’s Public and Community Engagement Group together with Social Science, Ethics, and Implementation Research Group organised a dialogue session between community members, social insurance representatives, and social scientists.  

The session brought together representatives from underserved communities who had contributed to the project through community-based participatory research (CBPR), including people who inject drugs (PWID), people with limited financial resources, and LGBT+ individuals. They shared their challenges in accessing health insurance for hepatitis C treatment and care.  

Vietnam has the fifth highest liver cancer incidence and death rate in the world and approximately 8 million people have hepatitis B, C or both. Even though Hepatitis C treatment is available in Vietnam, several barriers affect hepatitis C testing, diagnosis, and treatment. These barriers include that testing and diagnosis can only be performed at provincial and central hospitals, people may be asymptomatic or unaware they need testing, and test results often take a long time. High treatment costs before they are covered by insurance are also a big challenge.   

In 2018, Vietnam changed the insurance regulations related to Hepatitis C treatment. Specifically, Hepatitis C patients can receive financial support from health insurance for testing costs, treatment costs using approved medications listed in the insurance catalog, and necessary medical procedures and treatments during treatment (which may be partially or fully covered). Typically, health insurance in Vietnam supports 30% – 50% of the costs for those defined medical services, depending on insurance registration conditions and insurance types.  

Community members face both systematic and objective challenges.  

The event opened an open discussion for community members to highlight several challenges they face despite recent improvements in social insurance policies.  

Systematic challenges:  

  • Complex healthcare system. Vietnam’s multi-tiered hospital system has specific scopes and facilities at each level. For Hepatitis C, lower-tier hospitals may lack diagnostic and treatment capabilities, requiring patient transfers to higher tiers. Insurance coverage varies between tiers with different terms and paperwork, creating additional administrative complexity.  
  • Information gaps. Despite the government’s efforts in simplifying the registration and renewal process through the People’s Committees’ ward offices and post offices, many community members remain unaware of these options as well as their HepC treatment benefits under health insurance.  

Objective challenges:  

  • Documentation barriers. One outstanding challenge for marginalised populations is insufficient personal documentation (such as government ID) needed to obtain health insurance. While the government has appointed some certain social enterprises as community representatives to help, it’s a long way to go.  
  • Financial constraints. Though social health insurance in Vietnam is designed to be affordable, it remains challenging for many, especially those without stable employment or those facing personal financial burdens such as debts or medical expenses for family members.  
  • Medical privacy concerns. The hospital referral process may require patients to disclose HIV status or other chronic conditions in order to access HepC treatment at higher-tier hospitals, compromising their right to privacy.  

“We need to keep the conversation going.”  

Acknowledging the power of listening to community voices, Associate Professor Jennifer Van Nuil, Head of Social Science, Ethics, and Implementation Research Group, emphasised the importance of how CBPR (community-based participatory research method) can help to set up strong support networks within and for the community.  

The full story is available on the OUCRU website