Budgetary Impact of 20-Valent Pneumococcal Conjugate Vaccine Use for Adult Expatriates Living in Dubai

IF 1.6 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Current Therapeutic Research-clinical and Experimental Pub Date : 2023-01-01 DOI:10.1016/j.curtheres.2023.100698
Mostafa Zayed MSc , Jean Joury BS Pharm, CMD , Mohamed Farghaly FRCGP , Sara Al Dallal MD, MSc , Bassam Mahboub MD , Emily Kutrieb BA , Ahuva Averin MPP
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Abstract

Background

Dubai Health Authority currently recommends sequential administration of 13-valent pneumococcal conjugate vaccine (PCV13) followed by (→) 23-valent pneumococcal polysaccharide vaccine (PPV23) to prevent pneumococcal disease among adults at elevated risk of illness. Despite recommendations, disease burden and associated costs remain substantial. A new 20-valent pneumococcal conjugate vaccine (PCV20) recently received regulatory approval in the United Arab Emirates and has the potential to further reduce burden of pneumococcal disease.

Objectives

To evaluate budget impact of use of novel PCV20 compared with current recommendations (ie, PCV13→PPV23) among expatriates in Dubai aged 50 to 99 years and those aged 19 to 49 years with risk factors.

Methods

A deterministic model depicted 5-year risks and costs of invasive pneumococcal disease and all-cause nonbacteremic pneumonia. Each year of the modeling horizon, persons could be vaccinated with either PCV20 or PCV13→PPV23 or remain unvaccinated; persons vaccinated during the modeling horizon were not eligible for vaccination in subsequent years. Annual vaccine uptake was assumed to be 5% in base cases analyses; higher uptake was considered in scenario analyses. Costs were discounted at 3.5% annually and reported in US dollars.

Results

In base case, use of PCV20 alone would prevent an additional 13 cases of invasive pneumococcal disease, 31 cases of inpatient all-cause nonbacteremic pneumonia, 139 cases of outpatient all-cause nonbacteremic pneumonia, and 5 disease-related deaths compared with PCV13→PPV23. Medical care costs would be reduced by $354,000, and total vaccination costs would decrease by $4.4 million. PCV20 would therefore yield net budgetary impact of –$4.8 million, resulting in savings of $2.47 per-person per-year over 5 years. In scenarios with higher vaccine uptake, PCV20 prevented more cases and deaths and yielded greater budget savings (vs PCV13→PPV23).

Conclusions

PCV20 would reduce burden and economic costs of pneumococcal disease among expatriates in Dubai compared with PCV13→PPV23 and would therefore be budget saving for private health insurers who cover the majority of this population.

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20价肺炎球菌结合疫苗对居住在迪拜的成年侨民的预算影响
背景迪拜卫生局目前建议依次接种13价肺炎球菌结合疫苗(PCV13),然后(→) 23价肺炎球菌多糖疫苗(PPV23),用于在患病风险较高的成年人中预防肺炎球菌疾病。尽管提出了建议,但疾病负担和相关费用仍然很大。一种新的20价肺炎球菌结合疫苗(PCV20)最近在阿拉伯联合酋长国获得了监管部门的批准,有可能进一步减轻肺炎球菌疾病的负担。目的与目前的建议(即PCV13)相比,评估新型PCV20的使用对预算的影响→PPV23)。方法一个确定性模型描述了侵袭性肺炎球菌疾病和全因非细菌性肺炎的5年风险和费用。在建模期的每一年,人们都可以接种PCV20或PCV13疫苗→PPV23或保持未接种疫苗;在建模期间接种疫苗的人在随后几年没有资格接种疫苗。在基本病例分析中,假设年疫苗接种率为5%;在情景分析中考虑了更高的吸收率。成本以每年3.5%的价格贴现,并以美元计价。结果在基础病例中,与PCV13相比,单独使用PCV20可预防13例侵袭性肺炎球菌疾病、31例住院全因非细菌性肺炎、139例门诊全因非病毒性肺炎和5例疾病相关死亡→PPV23.医疗费用将减少354000美元,疫苗接种总费用将减少440万美元。因此,PCV20将产生480万美元的净预算影响,从而在5年内每人每年节省2.47美元。在疫苗接种率较高的情况下,PCV20预防了更多的病例和死亡,并节省了更多的预算(与PCV13相比→PPV23)。结论与PCV13相比,PCV20将减轻迪拜外籍人士患肺炎球菌疾病的负担和经济成本→PPV23,因此将为覆盖大多数人口的私人医疗保险公司节省预算。
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CiteScore
3.50
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0.00%
发文量
31
审稿时长
3 months
期刊介绍: We also encourage the submission of manuscripts presenting preclinical and very preliminary research that may stimulate further investigation of potentially relevant findings, as well as in-depth review articles on specific therapies or disease states, and applied health delivery or pharmacoeconomics. CTR encourages and supports the submission of manuscripts describing: • Interventions designed to understand or improve human health, disease treatment or disease prevention; • Studies that focus on problems that are uncommon in resource-rich countries; • Research that is "under-published" because of limited access to monetary resources such as English language support and Open Access fees (CTR offers deeply discounted English language editing); • Republication of articles previously published in non-English journals (eg, evidence-based guidelines) which could be useful if translated into English; • Preclinical and clinical product development studies that are not pursued for further investigation based upon early phase results.
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