Cost-Effectiveness of Baloxavir Marboxil Versus Oseltamivir or no Treatment for the Management of Influenza in the United States.

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES Infectious Diseases and Therapy Pub Date : 2024-09-01 Epub Date: 2024-08-16 DOI:10.1007/s40121-024-01027-9
Svenn Alexander Kommandantvold, Shih-Chen Chang, Andy Surinach, Vincent Yau, Jennie H Best, Hassan Zaraket, Hao Zhou, Jeff Frimpter, Marie-Helene Blanchet Zumofen
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Abstract

Introduction: This study sought to evaluate the cost-effectiveness of baloxavir marboxil compared with oseltamivir or no antiviral treatment from a US payer perspective using data from a real-world US administrative claims study. Given baloxavir's ability to rapidly stop viral shedding, the potential health economic implications of a baloxavir-induced population-level reduction in viral transmission was also explored.

Methods: A decision tree cost-effectiveness model was developed for seasonal influenza (2018-2020) using a lifetime time horizon with 3.0% discounting for costs and quality-adjusted life-years (QALYs). Patients aged ≥ 12 years could receive baloxavir, oseltamivir or no antiviral treatment. Patient characteristics, complications, and costs were derived from the Merative™ MarketScan® Research Databases including US commercial claims and Medicare and Medicaid Supplemental databases. A scenario analysis explored the impact of reduced viral transmission with baloxavir.

Results: In the base case analysis, baloxavir was cost-effective within a willingness-to-pay threshold of US$100,000/QALY compared with oseltamivir [incremental cost-effectiveness ratio (ICER), $6813/QALY gained] or no antiviral treatment (ICER, $669/QALY gained). The net monetary benefit (NMB) of baloxavir was $1180 and $6208 compared with oseltamivir and no treatment, respectively. The NMB of baloxavir increased linearly with reductions in viral transmission, where a 5% transmission reduction yielded an NMB of $2592 versus oseltamivir and $7621 versus no treatment. Baloxavir became dominant (more effective and less costly, with ICERs < 0) starting with a 12.0% reduction in viral transmission versus oseltamivir and 6.0% versus no antiviral treatment.

Conclusion: Baloxavir was cost-effective compared with oseltamivir or no antiviral treatment. The potential of baloxavir to reduce viral transmission offers a substantial economic benefit from a US payer perspective.

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在美国,治疗流感时使用 Baloxavir Marboxil 与使用奥司他韦或不使用奥司他韦治疗的成本效益。
简介:本研究试图从美国支付方的角度,利用一项真实的美国行政索赔研究数据,评估巴洛沙韦 marboxil 与奥司他韦或无抗病毒治疗相比的成本效益。鉴于巴洛沙韦能迅速阻止病毒脱落,我们还探讨了由巴洛沙韦引起的病毒传播率下降对健康经济的潜在影响:方法:针对季节性流感(2018-2020 年)开发了一个决策树成本效益模型,该模型采用终生时间跨度,成本和质量调整生命年(QALYs)的贴现率为 3.0%。年龄≥12岁的患者可接受巴洛沙韦、奥司他韦或不接受抗病毒治疗。患者特征、并发症和成本来自 Merative™ MarketScan® 研究数据库,包括美国商业索赔和医疗保险及医疗补助补充数据库。一项情景分析探讨了使用巴洛沙韦减少病毒传播的影响:在基础病例分析中,与奥司他韦[增量成本效益比(ICER)为 6813 美元/QALY gained]或无抗病毒治疗(ICER 为 669 美元/QALY gained)相比,巴洛沙韦在 100,000 美元/QALY 的支付意愿阈值内具有成本效益。与奥司他韦和不治疗相比,巴洛沙韦的净货币效益(NMB)分别为 1180 美元和 6208 美元。随着病毒传播率的降低,巴洛沙韦的净货币收益呈线性增长,与奥司他韦相比,病毒传播率降低 5%,净货币收益为 2592 美元;与不治疗相比,净货币收益为 7621 美元。巴洛沙韦成为主导药物(更有效、成本更低,ICERs 结论:巴洛沙韦与奥司他韦相比具有成本效益:与奥司他韦或不进行抗病毒治疗相比,巴洛沙韦具有成本效益。从美国付款人的角度来看,巴洛沙韦减少病毒传播的潜力带来了巨大的经济效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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