Cost-effectiveness analysis of 21-valent pneumococcal conjugated vaccine among adults in Canada

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2025-03-06 DOI:10.1016/j.vaccine.2025.126985
Raphael Ximenes , Alison E. Simmons , Gebremedhin B. Gebretekle , Austin Nam , Eva Wong , Marina I. Salvadori , Alyssa R. Golden , Beate Sander , Kyla J. Hildebrand , Matthew Tunis , Ashleigh R. Tuite
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Abstract

Background

A 21-valent pneumococcal conjugate vaccine (PCV21) was recently authorized in Canada to protect adults against invasive pneumococcal disease (IPD).

Objective

To assess the cost-effectiveness of PCV21 compared to current Canadian vaccination recommendations for adults of different age and risk groups.

Methods

We used a static cohort model to estimate lifetime incremental cost-effectiveness ratios (ICERs), in 2023 Canadian dollars per quality-adjusted life year (QALY), discounted at 1.5 %, in population cohorts aged 33 (midpoint of the 18–49 year age group), 50, and 65 years from the health system and societal perspectives. The primary analysis used 2022 serotype distributions for IPD cases. Additional analyses incorporated indirect effects from pediatric vaccination and used IPD serotype distributions from 2015 to 2019, to explore the impact of changes over time observed in some age groups.

Results

For population groups currently recommended to receive PCV20 in Canada (65 years and older, 50–64 years with additional risk factors for IPD, or 18–49 years with immunocompromising conditions), PCV21 was cost-effective at a $50,000 per QALY threshold and dominated PCV20 in most scenarios when PCV21 serotypes were more prevalent. When PCV20 serotypes were equally or more prevalent than PCV21 serotypes, results were more sensitive to assumptions about indirect effects and serotype replacement. For groups not currently recommended a conjugate vaccine (50–64 years without additional IPD risk factors and 18–49 years with chronic medical conditions or unhoused populations), use of a higher-valency conjugate vaccine was a cost-effective intervention compared to no vaccination, with the optimal vaccine dependent on the proportion of IPD attributable to PCV20 and PCV21 serotypes in the population of interest. Results were sensitive to vaccine price in most scenarios.

Interpretation

The use of PCV21 may be cost-effective in some populations, depending on the prevalence of IPD serotypes covered by PCV20 and PCV21.
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加拿大成人21价肺炎球菌结合疫苗的成本-效果分析
加拿大最近批准了一种21价肺炎球菌结合疫苗(PCV21),以保护成人免受侵袭性肺炎球菌疾病(IPD)的侵害。目的评估PCV21与目前加拿大不同年龄和危险人群成人疫苗接种建议的成本-效果。方法:我们使用静态队列模型,从卫生系统和社会角度估计33岁(18-49岁年龄组的中点)、50岁和65岁人口队列的终身增量成本-效果比(ICERs),每个质量调整生命年(QALY)为2023加元,折扣率为1.5%。主要分析使用2022年IPD病例的血清型分布。其他分析纳入了儿童疫苗接种的间接影响,并使用了2015年至2019年的IPD血清型分布,以探索在一些年龄组中观察到的随时间变化的影响。结果对于加拿大目前推荐接受PCV20的人群(65岁及以上,50-64岁有额外IPD危险因素,或18-49岁有免疫功能低下的人群),PCV21在每个QALY阈值为50,000美元时具有成本效益,并且在PCV21血清型更普遍的大多数情况下占主导地位。当PCV20血清型与PCV21血清型相同或更普遍时,结果对间接效应和血清型替代的假设更为敏感。对于目前未推荐使用结合疫苗的人群(50-64岁无额外IPD危险因素,18-49岁有慢性疾病或无住房人群),与不接种相比,使用高价结合疫苗是一种具有成本效益的干预措施,最佳疫苗取决于所研究人群中PCV20和PCV21血清型引起IPD的比例。结果在大多数情况下对疫苗价格敏感。根据PCV20和PCV21覆盖的IPD血清型的患病率,在某些人群中使用PCV21可能具有成本效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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