a Departments of Medicine and Family Medicine , University of Pittsburgh School of Medicine , Pittsburgh , PA , USA.
b Department of Health Policy , Vanderbilt University School of Medicine , Nashville , TN , USA.
Hum Vaccin Immunother. 2019;15(4):863-872. doi: 10.1080/21645515.2018.1564439. Epub 2019 Feb 20.
In the U.S., pneumococcal polysaccharide vaccine (PPSV23) uptake among high-risk adults aged <65 years is consistently low and improvement is needed. One barrier to improved vaccine coverage is the complexity of the adult vaccination schedule. This exploratory analysis compared the cost-effectiveness of strategies to increase pneumococcal vaccine uptake in high-risk adults aged 50-64 years. We used a Markov model to compare strategies for non-immunocompromised 50-64 year olds: 1) current pneumococcal polysaccharide vaccine (PPSV23) recommendations; 2) current recommendations enhanced by an intervention; 3) PPSV23 plus pneumococcal conjugate vaccine (PCV13) for high-risk patients with no intervention; or 4) both vaccines for all 50-year-olds with no intervention. Parameters included CDC data and other US data, varied extensively in sensitivity analyses. In the analysis, vaccinating high-risk individuals with PPSV23/PCV13 was the least costly strategy, with total costs of $424/person. Vaccinating all 50 year olds with PPSV23/PCV13 cost $40 more and gained 0.00068 quality-adjusted life years (QALY), or $57,786/QALY gained. Current recommendations with or without an intervention program were more expensive and less effective than other strategies. In multi-way sensitivity analyses, the current recommendations/intervention program strategy was favored at a $100,000/QALY threshold only if non-bacteremic pneumococcal pneumonia rate or PCV13 serotype coverage were substantially lower than base case values. Thus, an intervention program to improve pneumococcal vaccine uptake among high-risk 50-64 year-olds was not cost-effective in most scenarios. High-risk individuals receiving both PCV13 and PPSV23 could be economically favorable, and vaccinating all 50-year-olds with both vaccines could be considered.
在美国,<65 岁的高危成年人中肺炎球菌多糖疫苗(PPSV23)的接种率一直很低,需要有所提高。提高疫苗接种率的一个障碍是成人疫苗接种计划的复杂性。本探索性分析比较了提高 50-64 岁高危成年人肺炎球菌疫苗接种率的策略的成本效益。我们使用马尔可夫模型比较了非免疫功能低下的 50-64 岁人群的策略:1)当前肺炎球菌多糖疫苗(PPSV23)建议;2)通过干预措施增强当前建议;3)对无干预措施的高危患者使用 PPSV23 和肺炎球菌结合疫苗(PCV13);4)对所有 50 岁的人进行两疫苗接种,无干预措施。参数包括美国疾病控制与预防中心的数据和其他数据,在敏感性分析中广泛变化。在分析中,为高危人群接种 PPSV23/PCV13 的策略成本最低,每人总成本为 424 美元。为所有 50 岁的人接种 PPSV23/PCV13 的费用增加 40 美元,增加 0.00068 个质量调整生命年(QALY),即每获得 1 个 QALY 的成本为 57786 美元。与干预计划一起使用或不使用当前建议的策略比其他策略更昂贵且效果更差。在多方敏感性分析中,只有在非菌血症性肺炎球菌肺炎率或 PCV13 血清型覆盖率明显低于基础值的情况下,当前建议/干预计划策略在 10 万美元/QALY 的阈值内才具有成本效益。因此,在大多数情况下,提高高危 50-64 岁人群肺炎球菌疫苗接种率的干预计划不具有成本效益。为高危人群同时接种 PCV13 和 PPSV23 可能具有经济优势,并且可以考虑为所有 50 岁的人同时接种两种疫苗。