Delayed Transition to 20-Valent Pneumococcal Conjugate Vaccine in Pediatric National Immunization Programs: Forgone Public Health and Economic Benefit.

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2025-03-01 Epub Date: 2025-02-03 DOI:10.1007/s40121-025-01108-3
Johnna Perdrizet, An Ta, Liping Huang, Warisa Wannaadisai, Aleksandar Ilic, Kyla Hayford, Ayman Sabra
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引用次数: 0

Abstract

Introduction: Despite the approval of a 20-valent pneumococcal conjugate vaccine (PCV20) for pediatric use in many regions globally, integration of PCV20 into national immunization programs (NIPs) is delayed in some countries. We explored the public health and economic benefits forfeited by postponing transitions from lower-valent pneumococcal conjugate vaccines (PCVs) to PCV20.

Methods: A targeted literature review (TLR) identified modeling studies comparing the public health and economic impact of PCV20 versus 13-valent PCV (PCV13) or 15-valent PCV (PCV15) in pediatric NIPs. Only studies with accessible models underwent data extraction and analysis. Foregone public health (pneumococcal disease cases/disease-related deaths) and economic (medical/non-medical costs) outcomes, defined as the projected incremental differences between the outcomes associated with PCV20 and lower-valent PCVs, were calculated over 2 years following PCV20 implementation (per year and month). Discount rates for all outcomes were adjusted to 0% given the short time horizon and for consistency across analyses.

Results: The TLR identified models from 13 countries globally. The monthly health benefits forgone due to delayed transitions from PCV13 to PCV20 ranged between 40 (Slovakia) and 1740 (Canada) pneumococcal disease cases averted in the first year of delay across populations, increasing by between 1.5 (Sweden) and 15-16 times (Germany and Mexico) in the second year. Forgone cumulative disease-related deaths averted ranged from 18 (Spain) to 2657 (Germany) and forgone cumulative direct medical cost-savings ranged from 930 thousand Euros (Portugal) to 146 million Euros (Germany) due to delayed transitions from PCV13 to PCV20 over 2 years. Similar, but slightly reduced, benefits were forfeited with delayed transitions from PCV15 to PCV20.

Conclusion: Delays in implementing PCV20 into pediatric NIPs were projected to have substantial negative public health and economic consequences. These results underscore the necessity for national immunization technical advisory groups, policymakers, health organizations, and manufacturers to accelerate replacement of lower-valent standard-of-care PCVs with PCV20.

在儿童国家免疫规划中延迟过渡到20价肺炎球菌结合疫苗:放弃公共卫生和经济利益。
导论:尽管全球许多地区批准了用于儿科的20价肺炎球菌结合疫苗(PCV20),但在一些国家,将PCV20纳入国家免疫规划(NIPs)的工作被推迟。我们探讨了推迟从低价肺炎球菌结合疫苗(PCVs)向PCV20过渡所丧失的公共卫生和经济效益。方法:一项针对性的文献综述(TLR)确定了模型研究,比较了PCV20与13价PCV (PCV13)或15价PCV (PCV15)在儿科NIPs中的公共卫生和经济影响。只有具有可访问模型的研究才进行数据提取和分析。预先的公共卫生(肺炎球菌疾病病例/疾病相关死亡)和经济(医疗/非医疗费用)结果,定义为与PCV20和低价pcv相关的结果之间预计的增量差异,在PCV20实施后的2年内计算(每年和每月)。考虑到较短的时间范围和分析的一致性,所有结果的贴现率调整为0%。结果:TLR识别了全球13个国家的模型。由于延迟从PCV13过渡到PCV20而放弃的每月健康福利在延迟的第一年避免了40例(斯洛伐克)和1740例(加拿大)肺炎球菌疾病病例,第二年增加了1.5倍(瑞典)和15-16倍(德国和墨西哥)。由于在2年内延迟从PCV13过渡到PCV20,因此避免的累计疾病相关死亡人数从18人(西班牙)到2657人(德国)不等,而节省的累计直接医疗费用从93万欧元(葡萄牙)到1.46亿欧元(德国)不等。从PCV15到PCV20的延迟过渡与此相似,但略有减少,益处丧失。结论:在儿科NIPs中延迟实施PCV20预计会对公共卫生和经济产生重大负面影响。这些结果强调了国家免疫技术咨询小组、政策制定者、卫生组织和制造商加速用PCV20替代低价标准pcv的必要性。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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