Cost-effectiveness of Hepatitis B Virus Infection Screening and Treatment or Vaccination in 6 High-risk Populations in the United States

Author:

Chahal Harinder S12ORCID,Peters Marion G13,Harris Aaron M4,McCabe Devon15,Volberding Paul13,Kahn James G15

Affiliation:

1. Consortium to Assess Prevention Economics, San Francisco, San Francisco, California

2. Department of Clinical Pharmacy, San Francisco, San Francisco, California

3. Department of Medicine, University of California, San Francisco, San Francisco, California

4. Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia

5. Institute for Health Policy Studies, University of California, San Francisco, San Francisco, California

Abstract

Abstract Background Two million individuals with chronic hepatitis B (CHB) in the United States are at risk for premature death due to liver cancer and cirrhosis. CHB can be prevented by vaccination and controlled with treatment. Methods We created a lifetime Markov model to estimate the cost-effectiveness of strategies to prevent or treat CHB in 6 high-risk populations: foreign-born Asian/Pacific Islanders (API), Africa-born blacks (AbB), incarcerated, refugees, persons who inject drugs (PWID), and men who have sex with men (MSM). We studied 3 strategies: (a) screen for HBV infection and treat infected (“treatment only”), (b) screen for HBV susceptibility and vaccinate susceptible (“vaccination only”), and (c) screen for both and follow-up appropriately (“inclusive”). Outcomes were expressed in incremental cost-effectiveness ratios (ICERs), clinical outcomes, and new infections. Results Vaccination-only and treatment-only strategies had ICERs of $6000–$21 000 per quality-adjusted life-year (QALY) gained, respectively. The inclusive strategy added minimal cost with substantial clinical benefit, with the following costs per QALY gained vs no intervention: incarcerated $3203, PWID $8514, MSM $10 954, AbB $17 089, refugees $17 432, and API $18 009. Clinical complications dropped in the short/intermediate (1%–25%) and long (0.4%–16%) term. Findings were sensitive to age, discount rate, health state utility in immune or susceptible stages, progression rate to cirrhosis or inactive disease, and tenofovir cost. The probability of an inclusive program costing <$50 000 per QALY gained varied between 61% and 97% by population. Conclusions An inclusive strategy to screen and treat or vaccinate is cost-effective in reducing the burden of hepatitis B virus among all 6 high-risk, high-prevalence populations.

Funder

Centers for Disease Control and Prevention

National Center for HIV, Viral Hepatitis, STD, and TB Prevention Epidemiologic

Economic Modeling Agreement

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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5. Chronic hepatitis B: current epidemiology in the Americas and implications for management;Gish;J Viral Hepat,2006

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