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20价肺炎球菌结合疫苗在新加坡≥18岁成年人中的成本效益分析

Cost-Effectiveness of 20-Valent Pneumococcal Conjugate Vaccine in Adults Aged ≥18 Years in Singapore.

作者信息

Zhang Jingwen, Vietri Jeffrey, Averin Ahuva, Hariharan Dhwani, Atwood Mark, Huang Liping

机构信息

Pfizer Pvt Ltd, Singapore.

Pfizer Inc, Collegeville, PA, USA.

出版信息

Value Health Reg Issues. 2025 Sep;49:101136. doi: 10.1016/j.vhri.2025.101136. Epub 2025 May 23.

Abstract

OBJECTIVES

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目标

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。

方法

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。

结果

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。

结论

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。

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