Merz Pharmaceuticals, Raleigh, NC.
School of Pharmacy and Pharmaceutical Sciences, University of California, Irvine.
J Manag Care Spec Pharm. 2021 Apr;27(4):478-487. doi: 10.18553/jmcp.2021.20346. Epub 2021 Jan 29.
The Centers for Medicare & Medicaid Services (CMS) is the single largest payer for health care in the United States and the largest payer by spending globally. Medicare Part B, with more than 50 million beneficiaries, currently has no broad mechanisms in place for promoting cost-effective care of injectable drugs. To conduct a real-world utilization and cost analysis comparing botulinum toxins in movement disorders. The 2017 Medicare Provider Utilization and Payment Data: Physician and Other Supplier dataset from CMS was used for this claims level analysis. Neurologists, ophthalmologists, or physiatrists who injected predominantly for movement disorders (defined as blepharospasm, cervical dystonia, sialorrhea, and/or spasticity) were included along with their patients. Botulinum toxins with FDA indications spanning these 3 specialties were included. A total of 891 physicians (406 ophthalmologists, 338 neurologists, and 147 physiatrists) along with their 29,954 botulinum toxin (27,441 onabotulinumtoxinA and 2,513 incobotulinumtoxinA) patients were included in the analysis. The average total drug cost per patient per year (PPPY) was significantly lower for incobotulinumtoxinA versus onabotulinumtoxinA ($2,099 vs. $3,115; < 0.001), for an average savings of 32.6%. Annual average out-of-pocket costs were also significantly less expensive for incobotulinumtoxinA versus onabotulinumtoxinA ($486 vs. $719; < 0.001), for an average savings of 32.4%. Across 74,346 total injection visits, there was no significant difference in dosing between the agents, with an average dosing ratio of 0.94 incobotulinumtoxinA to 1.0 onabotulinumtoxinA. Injections PPPY were 2.42 for onabotulinumtoxinA and 2.29 for incobotulinumtoxinA. Average reported wastage was 64% higher for onabotulinumtoxinA than it was for incobotulinumtoxinA. A budget impact analysis estimated that increasing incobotulinumtoxinA use in the movement disorder space to attain an overall 20% botulinum toxin market share would save Medicare $32.9 million over a 3-year period versus current use. IncobotulinumtoxinA was shown to be a less costly alternative than onabotulinumtoxinA with similar dosing in real-world practice in this large national Medicare population. Policies to increase use of agents that promote cost-effective evidence-based care should be further explored and implemented for this fundamental federal payer. This research received no external funding. Kazerooni was an employee of Merz Pharmaceuticals at the time of the analysis. Watanabe received no compensation or funding for this research project. Watanabe is a member of the National Academies of Sciences, Engineering, and Medicine Forum on Drug, Discovery, Development, and Translation. This information, content, and conclusions are those of the authors and should not be construed as the official position or policy of, nor should any endorsements be inferred by the U.S. government or the National Academies of Sciences, Engineering.
医疗保险和医疗补助服务中心(CMS)是美国最大的医疗保健支付方,也是全球最大的支付方。医疗保险 B 部分拥有超过 5000 万的受益人群,但目前没有广泛的机制来促进注射用药物的具有成本效益的治疗。本研究旨在比较运动障碍患者中使用肉毒毒素的真实世界利用情况和成本。本分析使用了 CMS 的 2017 年医疗保险提供者利用和支付数据:医师和其他供应商数据集。本研究纳入了主要治疗运动障碍(定义为眼睑痉挛、颈部肌张力障碍、涎液过多和/或痉挛)的神经科医生、眼科医生或理疗医生及其患者。纳入了具有跨越这 3 个专业的 FDA 适应证的肉毒毒素。共纳入了 891 名医生(406 名眼科医生、338 名神经科医生和 147 名理疗医生)及其 29954 名肉毒毒素(27441 例注射用肉毒毒素 A 和 2513 例注射用利斯美妥毒素 A)患者。每患者每年的平均总药物成本(PPPY),与注射用肉毒毒素 A 相比,利斯美妥毒素 A 显著降低(2099 美元对 3115 美元;<0.001),平均节省 32.6%。与注射用肉毒毒素 A 相比,利斯美妥毒素 A 的年平均自付费用也显著降低(486 美元对 719 美元;<0.001),平均节省 32.4%。在 74346 次总注射就诊中,两种药物的剂量没有显著差异,平均剂量比为 0.94 利斯美妥毒素 A 对 1.0 注射用肉毒毒素 A。注射用肉毒毒素 A 的 PPPY 为 2.42,利斯美妥毒素 A 为 2.29。平均报告的损耗率注射用肉毒毒素 A 比利斯美妥毒素 A 高 64%。预算影响分析估计,在运动障碍领域增加利斯美妥毒素 A 的使用,以达到整体 20%的肉毒毒素市场份额,与目前的使用相比,在 3 年内可为医疗保险节省 3290 万美元。在这项大型全国医疗保险人群的真实世界研究中,利斯美妥毒素 A 与注射用肉毒毒素 A 相比,具有相似的剂量,且成本更低。应该进一步探索和实施增加使用促进具有成本效益的循证护理的药物的政策,这对这一基本联邦支付方至关重要。本研究没有外部资金支持。Kazerooni 在分析时是 Merz 制药公司的员工。Watanabe 没有因这项研究项目获得任何报酬或资金。Watanabe 是美国国家科学院、工程院和医学研究院药物发现、开发和翻译论坛的成员。作者的信息、内容和结论仅代表作者,不应被视为美国政府或美国国家科学院、工程院的官方立场或政策,也不应推断任何背书。