对美国 65 岁以上未接种疫苗的成人接种 21 价肺炎球菌结合疫苗 V116 的成本效益分析。

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES Infectious Diseases and Therapy Pub Date : 2024-12-01 Epub Date: 2024-11-08 DOI:10.1007/s40121-024-01067-1
Zinan Yi, Kwame Owusu-Edusei, Elamin Elbasha
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引用次数: 0

摘要

简介:鉴于美国最近批准并推荐使用 21 价肺炎球菌结合疫苗 (PCV)--V116,我们评估了在美国年龄≥ 65 岁、之前从未接种过 PCV 的成年人中使用 V116 与 20 价 PCV (PCV20) 或 15 价 PCV (PCV15) 和 23 价肺炎球菌多糖疫苗 (PPSV23) 系列的成本效益:方法:建立了一个静态多队列状态转换马尔可夫模型,从社会角度估算 V116 与 PCV20 或 PCV15 + PPSV23 的终生增量临床和经济影响。所有模型输入均基于已发表的文献、公开数据库和/或报告。模型结果包括未贴现的临床病例:侵袭性肺炎球菌疾病 (IPD)、住院和门诊非细菌性肺炎球菌肺炎 (NBPP)、脑膜炎后遗症 (PMS)、IPD 和住院非细菌性肺炎球菌肺炎死亡病例、贴现质量调整生命年 (QALY) 以及贴现总成本(2023 年美元),其中包括疫苗采购和管理成本、与疾病相关的直接和间接成本以及接种疫苗的差旅费用。最后的总结性指标是增量成本效益比 (ICER),以美元/QALY 的形式报告。年贴现率为 3%:根据所使用的输入和假设,结果表明,与 PCV20 和 PCV15 + PPSV23 策略相比,V116 策略可分别预防 27,766 例和 32,387 例疾病病例/死亡,并为年龄≥ 65 岁的未接种疫苗的成年人节省 2.39 亿美元和 18 亿美元的总成本。两种方案(即 V116 与 PCV20 或 PCV15 + PPSV23)的估计 ICER 均可节省成本。情景分析以及确定性和概率敏感性分析也证明了定性结果的稳健性:这些结果表明,在美国,对年龄≥ 65 岁的成年人使用 V116 可预防大量白内障病例和死亡病例的发生,同时在各种投入和情景下仍具有很高的经济效益。
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Cost-Effectiveness Analysis of the Use of V116, a 21-Valent Pneumococcal Conjugate Vaccine, in Vaccine-Naïve Adults Aged ≥ 65 Years in the United States.

Introduction: Given the recent approval and recommendation of V116, a 21-valent pneumococcal conjugate vaccine (PCV), in the United States (US), we evaluated the cost-effectiveness of using V116 versus the 20-valent PCV (PCV20) or the 15-valent PCV (PCV15) in series with the 23-valent pneumococcal polysaccharide vaccine (PPSV23) among adults aged ≥ 65 years in the US who had never received a PCV previously.

Methods: A static multi-cohort state-transition Markov model was developed to estimate the lifetime incremental clinical and economic impact of V116 vs. PCV20 or PCV15 + PPSV23 from the societal perspective. All model inputs were based on published literature and publicly available databases and/or reports. Model outcomes included undiscounted clinical cases: invasive pneumococcal disease (IPD), inpatient and outpatient non-bacteremic pneumococcal pneumonia (NBPP), post-meningitis sequelae (PMS), deaths from IPD and inpatient NBPP, discounted quality-adjusted life years (QALYs) as well as the discounted total cost (in 2023 USD), which consisted of vaccine acquisition and administration costs, direct and indirect costs associated with the disease, and travel costs for vaccination. The final summary measure was the incremental cost-effectiveness ratio (ICER), reported as $/QALY gained. Three percent was used for the annual discounting rate.

Results: Based on the inputs and assumptions used, the results indicated that the V116 strategy prevented 27,766 and 32,387 disease cases/deaths and saved $239 million and $1.8 billion in total costs when compared to the PCV20 and PCV15 + PPSV23 strategies, respectively, in vaccine-naïve adults aged ≥ 65 years. The estimated ICERs were cost saving in both regimens (i.e., V116 vs. PCV20 or vs. PCV15 + PPSV23). The scenario analysis and deterministic and probabilistic sensitivity analyses also demonstrated the robustness of the qualitative results.

Conclusions: These results demonstrated that using V116 in adults aged ≥ 65 years in the US can prevent a substantial number of PD cases and deaths while remaining highly favorable economically over a wide range of inputs and scenarios.

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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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