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PCV13 疫苗接种在比利时 65-84 岁高风险肺炎球菌感染成人中的成本效益。

Cost-effectiveness of PCV13 vaccination in Belgian adults aged 65-84 years at elevated risk of pneumococcal infection.

机构信息

Pfizer NV/SA, Brussels, Belgium.

Department of Internal Medicine, University Hospital Leuven, Leuven, Belgium.

出版信息

PLoS One. 2018 Jul 6;13(7):e0199427. doi: 10.1371/journal.pone.0199427. eCollection 2018.

Abstract

BACKGROUND

The Belgian Superior Health Council (SHC) recently added a 13-valent pneumococcal conjugate vaccine (PCV13) to its recommendations for adult pneumococcal vaccination. This study addresses the policy question regarding whether a single dose of PCV13 should be reimbursed among Belgian adults aged 65-84 years with chronic comorbidities ("moderate-risk") or immunosuppression ("high-risk").

METHODS

A cohort model was developed to project lifetime risks, consequences, and costs of invasive pneumococcal disease (IPD) and pneumococcal community-acquired pneumonia (CAP). Parameter values were estimated using published literature and available databases, and were reviewed by Belgian experts. PCV13 effectiveness was assumed to be durable during the first 5 years following receipt, and to progressively decline thereafter with 15 years protection. The Belgian National Health Insurance perspective was employed.

RESULTS

Use of PCV13 (vs. no vaccine) in moderate/high-risk persons aged 65-84 years (n = 861,467; 58% vaccination coverage) would be expected to prevent 527 cases of IPD, 1,744 cases of pneumococcal CAP and 176 pneumococcal-related deaths, and reduce medical care costs by €20.1 million. Vaccination costs, however, would increase by €36.9 million and thus total overall costs would increase by €16.8 million. Cost per QALY gained was €17,126. In probabilistic sensitivity analyses, use of PCV13 was cost-effective in 97% of 1,000 simulations.

CONCLUSIONS

Reimbursement of PCV13 in moderate/high-risk Belgian adults aged 65-84 years would be cost-effective from the Belgian healthcare perspective.

摘要

背景

比利时高级卫生理事会(SHC)最近将 13 价肺炎球菌结合疫苗(PCV13)纳入其成人肺炎球菌疫苗接种建议。本研究针对的政策问题是,对于 65-84 岁患有慢性合并症(“中度风险”)或免疫抑制(“高风险”)的比利时成年人,是否应报销一剂 PCV13。

方法

开发了一个队列模型,以预测侵袭性肺炎球菌病(IPD)和肺炎球菌社区获得性肺炎(CAP)的终生风险、后果和成本。使用已发表的文献和可用数据库估计参数值,并由比利时专家进行审查。假设 PCV13 在接种后的前 5 年内有效,此后保护作用逐渐下降,15 年后保护作用下降。采用比利时国家健康保险的观点。

结果

在 65-84 岁的中度/高风险人群(n=861467;58%疫苗接种覆盖率)中使用 PCV13(与不接种疫苗相比)预计将预防 527 例 IPD、1744 例肺炎球菌 CAP 和 176 例肺炎球菌相关死亡,并降低 2010 万欧元的医疗费用。然而,疫苗接种成本将增加 3690 万欧元,因此总费用将增加 1680 万欧元。每获得一个质量调整生命年的成本为 17126 欧元。在概率敏感性分析中,在 1000 次模拟中的 97%情况下,使用 PCV13 具有成本效益。

结论

从比利时医疗保健的角度来看,为 65-84 岁的中度/高风险比利时成年人报销 PCV13 是具有成本效益的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a73f/6034794/efcd3fb9fa3d/pone.0199427.g001.jpg

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