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为新的阿尔茨海默病药物支付做好医疗体系准备。

Preparing the health-care system to pay for new Alzheimer's drugs.

机构信息

Center for the Evaluation of Value and Risk in Health, Tufts Medical Center, Institute for Clinical Research and Health Policy Studies, Boston, Massachusetts, USA.

出版信息

Alzheimers Dement. 2020 Nov;16(11):1568-1570. doi: 10.1002/alz.12155. Epub 2020 Aug 18.

Abstract

Biogen's announcement last fall that it will seek U.S. Food and Drug Administration approval for its Alzheimer's disease (AD) treatment, aducanumab, 7 months after the drug was declared a failure, buoyed patients and families, but put health payers and policymakers on alert. Whether aducanumab succeeds, other disease-modifying therapies for AD will follow, and the health-care system is unprepared for the reimbursement and access challenges. Novel AD therapies are much needed, but we cannot assume substantial cost offsets. With forethought and preparation, however, the health-care system can accommodate new AD drugs. First, we urge the use of cost-effectiveness of new Alzheimer's treatments as a starting point for setting value-based prices. Second, payments for new AD therapies should ideally incorporate a performance warranty, which helps apportion risk associated with initial therapy value estimates between drug manufacturers and payers. Third, we urge consideration of "subscription" payment agreements to address system affordability issues.

摘要

去年秋天,渤健公司宣布将寻求美国食品和药物管理局 (FDA) 批准其治疗阿尔茨海默病(AD)的药物 aducanumab,距离该药物被宣布失败仅 7 个月。这一消息令患者和家属欢欣鼓舞,但也引起了医疗支付方和政策制定者的警惕。无论 aducanumab 是否成功,其他用于治疗 AD 的疾病修饰疗法都将随之而来,而医疗保健系统尚未为报销和准入挑战做好准备。新型 AD 疗法是非常需要的,但我们不能假设它们会带来实质性的成本节约。然而,只要有远见和准备,医疗保健系统就能适应新的 AD 药物。首先,我们敦促将新的阿尔茨海默病治疗方法的成本效益作为制定基于价值的价格的起点。其次,新的 AD 疗法的支付最好纳入绩效保证,以帮助在制药商和支付方之间分摊与初始治疗价值估计相关的风险。第三,我们敦促考虑“订阅”支付协议,以解决系统的负担能力问题。

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