DR. TAORAN LIU
Author(s)
Taoran Liu, PhD, YANGYANG GAO, PhD, Wai-kit Ming, MD, PhD, MPH, MMSc;
City University of Hong Kong, Department of Infectious Diseases and Public Health, Hong Kong, Hong Kong
City University of Hong Kong, Department of Infectious Diseases and Public Health, Hong Kong, Hong Kong
OBJECTIVES: To model the province-level cost-effectiveness and value-based price (VBP) thresholds of maternal vaccination (MV) during pregnancy, and infant monoclonal antibody prophylaxis (nirsevimab, NIR) compared with the status quo (no intervention) in mainland China.
METHODS: We conducted a decision-analytic Markov model based on monthly cycles spanning the initial 6 months of infants' lives, evaluated by monthly birth cohorts, from a governmental perspective. We aggregated to province-specific target months dependent on RSV seasonality. Our analyses were stratified by 32 provinces/municipalities in China. We also assessed the cost-effectiveness in a high-risk subgroup scenario (higher disease incidence, mortality rate, and disease-related costs). We compare the incremental cost-effectiveness ratio to the province-level one-time three-times GDP per capita. Probabilistic sensitivity analysis (PSA) were also conducted.
RESULTS: The median MV value-based price (VBP) threshold at one time GDP per capita was approximately CNY 298 (range: CNY 140-909) for a province's local GDP per capita, and the median NIR VBP threshold versus no intervention was approximately CNY 404 (range: CNY 215-1215). In the subgroup scenario analysis of the high-risk group, NIR became more cost-effective at one time GDP per capita in 7 high-income provinces or municipalities (i.e., Beijing, Shanghai, Tianjin, Jiangsu, Zhejiang, Shenzhen, Guangzhou). One-way sensitivity analyses indicated that MV early hospitalization efficacy and incidence scaling were key drivers of MV VBP thresholds. PSA results were consistent with deterministic findings.
CONCLUSIONS: At a current price of over USD 400 or USD 500, universal MV or NIR programs are less likely to be cost-effective. To be cost-effective, policymakers and governments should set the price of universal MV and NIR at around CNY 298, or only target the high-risk infants in high-income jurisdictions.
METHODS: We conducted a decision-analytic Markov model based on monthly cycles spanning the initial 6 months of infants' lives, evaluated by monthly birth cohorts, from a governmental perspective. We aggregated to province-specific target months dependent on RSV seasonality. Our analyses were stratified by 32 provinces/municipalities in China. We also assessed the cost-effectiveness in a high-risk subgroup scenario (higher disease incidence, mortality rate, and disease-related costs). We compare the incremental cost-effectiveness ratio to the province-level one-time three-times GDP per capita. Probabilistic sensitivity analysis (PSA) were also conducted.
RESULTS: The median MV value-based price (VBP) threshold at one time GDP per capita was approximately CNY 298 (range: CNY 140-909) for a province's local GDP per capita, and the median NIR VBP threshold versus no intervention was approximately CNY 404 (range: CNY 215-1215). In the subgroup scenario analysis of the high-risk group, NIR became more cost-effective at one time GDP per capita in 7 high-income provinces or municipalities (i.e., Beijing, Shanghai, Tianjin, Jiangsu, Zhejiang, Shenzhen, Guangzhou). One-way sensitivity analyses indicated that MV early hospitalization efficacy and incidence scaling were key drivers of MV VBP thresholds. PSA results were consistent with deterministic findings.
CONCLUSIONS: At a current price of over USD 400 or USD 500, universal MV or NIR programs are less likely to be cost-effective. To be cost-effective, policymakers and governments should set the price of universal MV and NIR at around CNY 298, or only target the high-risk infants in high-income jurisdictions.
Conference/Value in Health Info
2026-05, ISPOR 2026, Philadelphia, PA, USA
Value in Health, Volume 29, Issue S6
Code
EE337
Topic
Economic Evaluation
Disease
SDC: Infectious Disease (non-vaccine), SDC: Pediatrics