Trish Erin, Kaiser Katrina M, Celestin Jeanai, Joyce Geoffrey
University of Southern California.
J Health Polit Policy Law. 2022 Dec 1;47(6):853-877. doi: 10.1215/03616878-10041233.
Reforming the Medicare Part D program-which provides prescription drug coverage to 49 million beneficiaries-has emerged as a key policy priority.
The authors evaluate prescription drug claims from a 100% sample of Medicare Part D beneficiaries to evaluate the current spending distribution across different payers for different types of beneficiaries across different benefit phases. They then model how these estimates would change under a proposal to redesign the Medicare Part D standard benefit.
Spending patterns differ for beneficiaries who do and do not qualify for low-income subsidies. Part D plans face limited liability for total spending under the current standard benefit design, amounting to 36% of total spending for beneficiaries who do not receive low-income subsidies and 28% of total spending for those who do. Proposed reforms would increase plan liability and significantly change the distribution of liability across plans, drug manufacturers, and the federal government.
Though the original goal of the Part D program was to create a market of competing private plans that provide prescription drug coverage to Medicare beneficiaries, the standard benefit design that was included in the original legislation reflected significant political compromises. Reforming the standard benefit design to give plans more skin in the game could significantly affect competition in the market, with differential impact across drug classes and types of beneficiaries.
改革医疗保险D部分计划(该计划为4900万受益人提供处方药保险)已成为一项关键的政策优先事项。
作者评估了医疗保险D部分受益人的100%样本的处方药报销申请,以评估不同类型受益人在不同受益阶段跨不同支付方的当前支出分布情况。然后,他们模拟了在重新设计医疗保险D部分标准福利的提案下,这些估计将如何变化。
符合和不符合低收入补贴资格的受益人的支出模式有所不同。在当前的标准福利设计下,D部分计划面临的总支出责任有限,对于未获得低收入补贴的受益人,这一比例为总支出的36%,对于获得补贴的受益人,这一比例为总支出的28%。拟议的改革将增加计划责任,并显著改变责任在各计划、药品制造商和联邦政府之间的分配。
尽管D部分计划的最初目标是创建一个由相互竞争的私人计划组成的市场,为医疗保险受益人提供处方药保险,但原始立法中包含的标准福利设计反映了重大的政治妥协。改革标准福利设计以使各计划承担更多风险,可能会显著影响市场竞争,对不同药品类别和受益人类别产生不同影响。