对成人15价和20价肺炎球菌疫苗成本-效果分析的系统文献综述。

Vaccine Pub Date : 2025-02-06 Epub Date: 2024-12-27 DOI:10.1016/j.vaccine.2024.126656
Jeong-Yeon Cho, Haeseon Lee, Warisa Wannaadisai, Jeffrey Vietri, Nathorn Chaiyakunapruk
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引用次数: 0

摘要

背景:由于不同的流行病学和成本,成人肺炎球菌疫苗的经济和公共卫生效益因国家而异。我们系统地回顾和总结了最近在成人中引入的15价和20价肺炎球菌结合疫苗(PCV15和PCV20)的成本效益分析(CEA)的发现和假设。方法:我们通过PubMed、EMBASE、CEA Registry、EconLit、HTA数据库和NITAG资源中心对PCV15和/或PCV20与现有策略的CEA研究进行了系统检索,截止到2024年4月23日。研究特征、方法、假设和发现由两位审稿人独立提取;使用ECOBIAS评估质量。对结果进行定性综合,总结关键属性和结论。结果:在137份确定的记录中,包括26项研究;大多数(24/26)涉及高收入国家。所有研究均采用静态马尔可夫型模型,比较单独使用或与23价肺炎球菌多糖疫苗(PPSV23)联合使用的高价pcv与目前推荐的(单独使用PPSV23、单独使用PCV13、PCV13 + PPSV23、不接种)。大多数研究(22/26)得出结论,与其他成人肺炎球菌策略(单独使用PPSV23、PCV13±PPSV23、PCV15±PPSV23或不接种)相比,单独使用PCV20节省成本(占主导地位)或具有成本效益。在关键试验中,pcv通常被认为具有与PCV13相同的血清型特异性有效性,尽管有四项研究使用了德尔菲小组的估计;保护作用被认为可以持续10到20年。PPSV23被认为对非菌源性肺炎的有效性较低,保护时间较短。一半(13/26)的研究中包括了儿童时期高价pcv(12/26)、血清型替代(2/26)或两者(1/26)的群体效应,这些研究减弱了成人疫苗的影响。大多数研究被评估为低偏倚风险;5个摘要没有为评估提供足够的信息。结论:目前的证据表明,单独使用20价PCV可能具有成本效益或主导其他成人肺炎球菌策略。未来的研究需要解决假设中剩余的不确定性,并支持基于证据的政策制定。
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Systematic literature review of cost-effectiveness analyses of adult 15- and 20-valent pneumococcal vaccines.

Background: The economic and public health benefits of adult pneumococcal vaccines vary across countries due to different epidemiology and costs. We systematically reviewed and summarized findings and assumptions of cost-effectiveness analyses (CEA) of the recently introduced 15- and 20-valent pneumococcal conjugate vaccines (PCV15 and PCV20) in adults.

Methods: We performed a systematic search for CEA studies of PCV15 and/or PCV20 versus existing strategies via PubMed, EMBASE, CEA Registry, EconLit, HTA Database, and NITAG resource center through April 23, 2024. Study characteristics, methods, assumptions, and findings were extracted independently by two reviewers; quality was assessed using ECOBIAS. Results were synthesized qualitatively to summarize key attributes and conclusions.

Results: Of 137 identified records, 26 studies were included; the majority (24/26) concerned high-income countries. All employed static Markov-type models comparing higher-valent PCVs used alone or in combination with 23-valent pneumococcal polysaccharide vaccine (PPSV23) to current recommendations (PPSV23 alone, PCV13 alone, PCV13 + PPSV23, no vaccination). Most studies (22/26) concluded PCV20 used alone was cost-saving (dominant) or cost-effective compared to other adult pneumococcal strategies (PPSV23 alone, PCV13 ± PPSV23, PCV15 ± PPSV23, or no vaccination). PCVs were generally assumed to have serotype-specific effectiveness equal to PCV13 efficacy in the pivotal trial, though four studies used estimates from a Delphi panel; protection was assumed to last between 10 and 20 years. PPSV23 was assumed to have lower effectiveness against non-bacteremic pneumonia and shorter duration of protection. Herd effects from higher-valent PCVs in childhood (12/26), serotype replacement (2/26), or both (1/26) were included in half (13/26) of studies, which attenuated adult vaccine impact. Most studies were assessed as low risk of bias; five abstracts did not provide sufficient information for assessment.

Conclusion: Current evidence indicates that 20-valent PCV used alone is likely to be cost-effective or dominate other adult pneumococcal strategies. Future research is needed to address remaining uncertainties in assumptions and to support evidence-based policymaking.

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