Zhang Jingwen, Vietri Jeffrey, Averin Ahuva, Hariharan Dhwani, Atwood Mark, Huang Liping
Pfizer Pvt Ltd, Singapore.
Pfizer Inc, Collegeville, PA, USA.
Value Health Reg Issues. 2025 Sep;49:101136. doi: 10.1016/j.vhri.2025.101136. Epub 2025 May 23.
The Singapore Ministry of Health recommends vaccination with 23-valent pneumococcal polysaccharide vaccine (PPSV23) in adults aged 18 to 64 years with chronic medical conditions ("at risk"), 13-valent pneumococcal conjugate vaccine (PCV13) followed by PPSV23 (PCV13 → PPSV23) with PPSV23 revaccination in adults aged 18 to 64 years with immunocompromising conditions ("high risk"), and PCV13 → PPSV23 in all adults aged ≥65 years. We conducted a cost-effectiveness analysis of the newly licensed 20-valent PCV (PCV20) versus current recommendations.
Risks and costs of invasive pneumococcal disease, all-cause nonbacteremic pneumonia, and the expected impact of vaccination were projected over a lifetime modeling horizon using a probabilistic cohort model. Model inputs were based on local data, as available. Cost per quality-adjusted life year (QALY) gained with PCV20 (vs current recommendations) was assessed overall and among subgroups of the target population from a healthcare system perspective (discounting, 3%/year). Sensitivity analyses were also conducted.
PCV20 was estimated to reduce invasive pneumococcal disease cases by 41, nonbacteremic pneumonia cases by 4335, and deaths by 196 among the model population (N = 1.6M). Net costs (vaccination + medical) and QALYs increased by S$0.3 million and 2693, respectively, yielding a cost/QALY of S$105 for PCV20. PCV20 was dominant among high-risk adults aged 18 to 64 years and all adults 65 to 99 years; among at-risk adults aged 18 to 64 years, cost/QALY for PCV20 was S$2081. PCV20 remained cost saving or highly cost-effective in sensitivity analyses.
Cost-effectiveness analysis suggests use of PCV20-in lieu of current Singapore Ministry of Health recommendations for adult pneumococcal vaccination-would represent a cost-effective use of scarce healthcare resources.
新加坡卫生部建议,18至64岁患有慢性疾病(“有风险”)的成年人接种23价肺炎球菌多糖疫苗(PPSV23);18至64岁有免疫功能低下状况(“高风险”)的成年人先接种13价肺炎球菌结合疫苗(PCV13),随后接种PPSV23(PCV13→PPSV23),并对PPSV23进行再接种;所有65岁及以上的成年人接种PCV13→PPSV23。我们对新获批的20价肺炎球菌结合疫苗(PCV20)与当前建议进行了成本效益分析。
使用概率队列模型,在终生建模期内预测侵袭性肺炎球菌疾病、全因非菌血症性肺炎的风险和成本,以及疫苗接种的预期影响。模型输入基于可得的本地数据。从医疗保健系统角度(贴现率为每年3%)评估使用PCV20(与当前建议相比)每获得一个质量调整生命年(QALY)的成本。还进行了敏感性分析。
据估计,PCV20可使模型人群(N = 160万)中的侵袭性肺炎球菌疾病病例减少41例,非菌血症性肺炎病例减少4335例,死亡减少196例。净成本(疫苗接种+医疗)和QALY分别增加了30万新元及2693个,PCV20的成本/QALY为105新元。PCV20在18至64岁的高风险成年人以及所有65至99岁的成年人中占主导地位;在18至64岁的有风险成年人中,PCV20的成本/QALY为2081新元。在敏感性分析中,PCV20仍具有成本节约或高成本效益。
成本效益分析表明,使用PCV20(代替新加坡卫生部目前针对成人肺炎球菌疫苗接种的建议)将是对稀缺医疗资源的一种具有成本效益的利用方式。