Reducing the Out-of-Pocket Costs of Disease-Modifying Therapies for Medicare Beneficiaries With Multiple Sclerosis.

IF 3.2 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-12-01 Epub Date: 2025-09-16 DOI:10.1212/CPJ.0000000000200536
Pengxiang Li, John K Lin, Matthew J Klebanoff, Riya Palkar, Salim Chahin, Jalpa A Doshi
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引用次数: 0

Abstract

Background and objectives: The Inflation Reduction Act (IRA) introduced major reforms to Medicare Part D, including an annual out-of-pocket (OOP) maximum and the Medicare Prescription Payment Plan (MPPP), which allows beneficiaries to spread OOP costs over monthly payments. The IRA's Part D provisions, as well as wider use of direct-to-consumer (DTC) pharmacies, could reduce OOP costs for self-administered disease-modifying therapies (DMTs) among Medicare beneficiaries with multiple sclerosis (MS). This study estimated OOP costs for self-administered DMTs under the IRA's Part D provisions and through DTC pharmacies.

Methods: We calculated OOP costs for brand-name and generic DMTs under Part D in the pre-IRA (2023) and post-IRA (2025) periods. We also assessed the impact of voluntary enrollment in the MPPP in 2025. Finally, we examined OOP costs for generic DMTs purchased through DTC pharmacies.

Results: Before the IRA (2023), annual OOP costs ranged from $6,275 to $8,883 for brand-name DMTs; after the IRA (2025), annual OOP costs decreased by 68%-77% because all brand-name DMT users reached the annual OOP maximum ($2,000 in 2025). OOP costs were heavily frontloaded as lumpsum payments unless beneficiaries enrolled in the MPPP, which could lead to monthly payments as low as $167 for DMTs in 2025 (a reduction of over 90% in monthly OOP costs for January). Generic DMTs had annual OOP costs ranging from $212 to $7,855 before the IRA (2023) and $212 to $2,000 after the IRA (2025). Purchasing generic DMTs through DTC pharmacies resulted in annual OOP costs ranging from $133 to $39,984 and could lead to lower costs for some beneficiaries.

Discussion: Annual OOP costs for self-administered DMTs among Medicare beneficiaries with MS decreased significantly beginning January 1, 2025, because of the IRA's annual OOP maximum. Beneficiaries who voluntarily enroll in the MPPP will also be able to spread OOP costs over more manageable monthly payments. Direct cash purchase of some generic DMTs through DTC pharmacies could lead to lower OOP costs, but these payments will not count toward beneficiaries' deductible or annual OOP maximum. Neurologists have a critical role in ensuring that their Medicare patients with MS are aware of the option to enroll in the MPPP and the possibility of obtaining generic DMTs through DTC pharmacies.

减少患有多发性硬化症的医疗保险受益人的疾病修饰疗法的自付费用。
背景和目标:《减少通货膨胀法》(IRA)对医疗保险D部分进行了重大改革,包括年度自付(OOP)最高限额和医疗保险处方支付计划(MPPP),该计划允许受益人将自付费用分摊到每月付款中。IRA的D部分规定,以及直接面向消费者(DTC)药店的广泛使用,可以降低患有多发性硬化症(MS)的医疗保险受益人自我管理的疾病改善疗法(dmt)的OOP成本。本研究估计了根据IRA的D部分规定和通过DTC药房自行管理的dmt的OOP成本。方法:我们计算了D部分在ira前(2023年)和ira后(2025年)期间的品牌和仿制药dmt的OOP成本。我们还评估了2025年自愿加入MPPP的影响。最后,我们考察了通过DTC药店购买非专利dmt的OOP成本。结果:在IRA(2023)之前,品牌dmt的年度OOP成本从6,275美元到8,883美元不等;在IRA(2025)之后,年度OOP成本下降了68%-77%,因为所有品牌DMT用户都达到了年度OOP最大值(2025年为2,000美元)。除非受益人参加了MPPP计划,否则OOP的费用都是一次性支付,这可能导致2025年DMTs的月付款低至167美元(1月份每月OOP费用减少90%以上)。通用dmt的年度OOP成本在IRA之前(2023年)为212美元至7,855美元,IRA之后(2025年)为212美元至2,000美元。通过DTC药房购买非专利dmt导致每年OOP费用从133美元到39,984美元不等,并可能降低一些受益人的费用。讨论:自2025年1月1日起,由于IRA的年度OOP最大值,医疗保险受益人中MS自我管理的dmt的年度OOP成本显著下降。自愿参加MPPP计划的受益人还可以将OOP费用分摊到更易于管理的每月付款中。通过DTC药房直接现金购买一些非专利dmt可能会降低OOP成本,但这些付款将不计入受益人的免赔额或年度OOP最高限额。神经科医生在确保他们的医疗保险多发性硬化症患者了解参加MPPP的选择以及通过DTC药房获得通用dmt的可能性方面发挥着关键作用。
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
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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