Evolution of Pneumococcal Vaccine Recommendations and Criteria for Decision Making in 5 Western European Countries and the United States.

IF 1.9 Q3 HEALTH CARE SCIENCES & SERVICES MDM Policy and Practice Pub Date : 2023-01-01 DOI:10.1177/23814683231174432
Roxane Noharet-Koenig, Katarzyna Lasota, Pascaline Faivre, Edith Langevin
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引用次数: 1

Abstract

Objectives: Pneumococcal vaccine recommendations have become increasingly complex. This study aims to understand how national immunization technical advisory groups (NITAGs) and health technology assessment (HTA) agencies of 5 European countries and the United States formed their pneumococcal vaccine recommendations, by providing reviewed evidence and key drivers for new recommendations.

Methods: Centers for Disease Control and Prevention, European Centre for Disease Prevention and Control, and National Health Authorities Web sites were screened to capture the evolution of pneumococcal recommendations. A narrative review was conducted on NITAGs and HTA bodies' Web sites. Assessments of pneumococcal vaccines published from 2009 to 2022 were included.

Results: Thirty-four records were identified including 21 assessments for risk groups, 17 for elderly, and 12 for children. Burden of disease and vaccine characteristics were almost systematically reviewed during assessments. All 6 countries recommended the use of higher-valent pneumococcal vaccine (PCV; i.e., PCV10 and PCV13) in childhood vaccination programs, given their broader serotype coverage and their comparable profile to PCV7. PCV13 was progressively added to the vaccine schedule (in addition to polysaccharide vaccine) in at least the high-risk group, given the high burden in this population and expected additional benefits of PCV13. For the elderly, unlike the United States, European countries issued negative recommendation for PCV13 routine use because of substantial herd effects from childhood vaccination program making PCV13 likely not cost-effective.

Conclusions: This research provides an overview of decision-making processes for higher-valent PCVs recommendations and could be of interest to anticipate the place of next generation of PCVs in the vaccination landscape.

Highlights: By describing evidence-based criteria for decision making, this study emphasizes the framework analysis of NITAGs and HTA bodies when assessing pneumococcal vaccines and demonstrates that variation exists between countries and also according to population evaluated.While the burden of disease and immunogenicity/efficacy data were almost systematically reviewed by national stakeholders, economic assessments were reported to a lesser extent but played a major role in the limited use of PCV13 in the adult population.

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5个西欧国家和美国肺炎球菌疫苗建议和决策标准的演变
目的:肺炎球菌疫苗的建议已变得越来越复杂。本研究旨在了解5个欧洲国家和美国的国家免疫技术咨询小组(NITAGs)和卫生技术评估机构(HTA)如何形成其肺炎球菌疫苗建议,通过提供审查证据和新建议的关键驱动因素。方法:筛选疾病控制和预防中心、欧洲疾病预防和控制中心以及国家卫生当局的网站,以获取肺炎球菌建议的演变。对NITAGs和HTA机构的网站进行了叙述性审查。包括2009年至2022年发表的肺炎球菌疫苗评估。结果:共确定34条记录,其中21条为危险人群评估,17条为老年人评估,12条为儿童评估。在评估期间几乎系统地审查了疾病负担和疫苗特性。所有6个国家都建议使用高价肺炎球菌疫苗(PCV;鉴于其更广泛的血清型覆盖率以及与PCV7相似的特征,将PCV10和PCV13纳入儿童疫苗接种规划。至少在高危人群中,PCV13被逐步添加到疫苗计划中(除了多糖疫苗之外),考虑到该人群的高负担和PCV13的预期额外益处。对于老年人,与美国不同,欧洲国家对常规使用PCV13提出了负面建议,因为儿童疫苗接种计划的大量群体效应使PCV13可能不具有成本效益。结论:本研究概述了高价pcv推荐的决策过程,并可能对预测下一代pcv在疫苗接种领域的地位感兴趣。重点:通过描述基于证据的决策标准,本研究强调在评估肺炎球菌疫苗时对NITAGs和HTA机构进行框架分析,并表明在国家之间以及根据所评估的人群存在差异。虽然国家利益攸关方几乎系统地审查了疾病负担和免疫原性/有效性数据,但报告的经济评估程度较低,但在成人人群中有限使用PCV13方面发挥了主要作用。
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来源期刊
MDM Policy and Practice
MDM Policy and Practice Medicine-Health Policy
CiteScore
2.50
自引率
0.00%
发文量
28
审稿时长
15 weeks
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