Bridging Hepatitis C Care Gaps: A Modeling Approach for Achieving the WHO’s Targets in Ontario, Canada

Author:

Sahakyan Yeva1ORCID,Erman Aysegul12ORCID,Wong William W. L.123,Greenaway Christina4,Janjua Naveed5ORCID,Kwong Jeffrey C.267ORCID,Sander Beate1278

Affiliation:

1. Toronto Health Economics and Technology Assessment Collaborative (THETA), University Health Network, Toronto, ON M5G 2C4, Canada

2. ICES, Toronto, ON M4N 3M5, Canada

3. School of Pharmacy, University of Waterloo, Kitchener, ON N2G 1C5, Canada

4. Division of Infectious Diseases, Jewish General Hospital, McGill University, Montreal, QC H3A 0G4, Canada

5. British Columbia Centre for Disease Control (BCDC), Vancouver, BC V5Z 4R4, Canada

6. Department of Family and Community Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada

7. Public Health Ontario, Toronto, ON M5G 1M1, Canada

8. Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, ON M5T 3M6, Canada

Abstract

Background: The World Health Organization (WHO) has set hepatitis C (HCV) elimination targets for 2030. Understanding existing gaps in the “HCV care-cascade” is essential for meeting these targets. We aimed to identify the level of service scale-up needed along the “HCV care-cascade” to achieve the WHO’s HCV elimination targets in Ontario, Canada. Methods: By employing a decision analytic model, we projected the quality-adjusted life years (QALYs) and healthcare costs for individuals with HCV in Ontario. We increased RNA testing and treatment rates to 98%, followed by increasing antibody testing uptake until we achieved the WHO’s mortality target (i.e., a 65% reduction in liver-related mortality by 2030 vs. 2015). Results: Without scaling up by 2030, the expected QALYs and costs per person were 9.156 and CAD 48,996, respectively. Improved RNA testing and treatment rates reduced liver-related deaths to 3.3/100,000, a 57% reduction from 2015. Further doubling the antibody testing rates can achieve the WHO’s mortality target in 2035, but not in 2030. Compared to the status quo, such program would be cost-effective considering a 50,000 CAD/QALY gained threshold if annual implementation costs stayed under 2.3 M CAD/100,000 people. Conclusions: Doubling the antibody testing rates, along with increased RNA testing and treatment rates, showed promise in meeting the WHO’s goals by 2035.

Funder

Canadian Institute of Health Research

Canada Research Chair in the Economics of Infectious Diseases held by Beate Sander

CIHR

Publisher

MDPI AG

Reference40 articles.

1. World Health Organization (2023, April 09). Hepatitis C Fact Sheet. Available online: https://www.who.int/news-room/fact-sheets/detail/hepatitis-c.

2. Direct-acting antivirals for chronic hepatitis C;Jakobsen;Cochrane Database Syst. Rev.,2017

3. Effectiveness and Safety of Sofosbuvir/Velpatasvir/Voxilaprevir as a Hepatitis C Virus Infection Salvage Therapy in the Real World: A Systematic Review and Meta-analysis;Xie;Infect. Dis. Ther.,2022

4. Pangenotypic direct acting antivirals for the treatment of chronic hepatitis C virus infection: A systematic literature review and meta-analysis;Zoratti;EClinicalMedicine,2020

5. World Health Organization (2023, February 17). Combating Hepatitis B and C to Reach Elimination by 2030. World Health Organization. Available online: https://www.who.int/hepatitis/publications/hep-elimination-by-2030-brief/en/.

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