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引入每 6 个月给药一次的棕榈酸帕利哌酮在美国医保计划中的预算影响。

Budget impact of introducing once-every-6-months paliperidone palmitate in US health care plans.

机构信息

Janssen Global Services, LLC, Raritan, NJ.

Janssen Scientific Affairs, LLC, Titusville, NJ.

出版信息

J Manag Care Spec Pharm. 2023 Mar;29(3):303-313. doi: 10.18553/jmcp.2023.29.3.303.

Abstract

In the United States, most patients with schizophrenia have Medicaid coverage. Antipsychotic treatments are the cornerstone of schizophrenia management; most patients are treated with daily oral antipsychotics but struggle with medication adherence. Evidence suggests that medication adherence is inversely correlated with dosing frequency. Once-monthly paliperidone palmitate (PP) has been demonstrated to improve adherence compared with oral antipsychotics; transitioning to once-every-3-months PP (PP3M) further improved adherence. In 2021, once-every-6-months PP (PP6M) was approved by the US Food and Drug Administration to provide even longer between-dose intervals. Public health stakeholders who aim to improve medication adherence are interested in understanding how introducing PP6M to the formulary will impact the budget. To evaluate the budget impact of introducing PP6M to the formulary from the perspectives of a hypothetical US multistate health care payer and state Medicaid programs using California, Georgia, and Ohio as examples. The budget impact model was developed from a payer perspective, comparing the reference scenario (without PP6M in the market) with a new scenario (with PP6M). The study population included patients with schizophrenia who were eligible to receive PP6M. Market shares were assigned to the reference and new market scenarios. Efficacy was measured by the relative risk of relapse while receiving treatment. Adherence effects were included in the model and affected costs of treatment and relapse rates. A deterministic 1-way sensitivity analysis was performed. Base-case results for a multistate payer with 1 million members demonstrate that adding PP6M to the market results in total incremental plan-level costs ranging from $7,747 in year 1 to $11,501 in year 5. Increased drug costs were offset by administration and relapse cost savings ($105 and $881 in year 5, respectively). The average incremental cost per treated patient per year was stable at $180.06 for each year, and the incremental cost per member per month stayed below $0.01 for each year. The results of the model from the state-level Medicaid scenarios are broadly similar to those of the multistate base-case perspective. The 1-way sensitivity analysis demonstrated the model is most sensitive to the per-package costs of PP6M and PP3M, along with the proportion of patients fully adherent with PP3M. The budget impact of introducing PP6M as a treatment option is minimal. With the expected cost offsets from reduced administration and relapse costs due to adherence benefits, these results suggest that PP6M can be a viable treatment option from a clinical and a budgetary perspective. This study was funded by Janssen Scientific Affairs, LLC. The study sponsor provided funds to Xcenda and ApotheCom for medical writing, editorial support, and submission of the manuscript. Hilary Phelps was an employee of Janssen Global Services, LLC, at the time of the development and finalization of the manuscript. Alex Keenan is an employee of Janssen Global Services, LLC, and holds stock in Johnson & Johnson, Inc. Dee Lin and Carmela Benson are employees of Janssen Scientific Affairs, LLC, and hold stock in Johnson & Johnson, Inc. Aditya Raju was an employee of Xcenda at the time of the development and finalization of the manuscript, and Danmeng Huang is an employee of Xcenda, a health care consulting firm that was contracted by Janssen Scientific Affairs, LLC. Chih-Yuan Cheng is an employee of Janssen NV.

摘要

在美国,大多数精神分裂症患者都有医疗补助保险。抗精神病药物治疗是精神分裂症管理的基石;大多数患者接受每日口服抗精神病药物治疗,但在用药依从性方面存在困难。有证据表明,用药依从性与给药频率呈反比。每月一次的棕榈酸帕利哌酮(PP)已被证明与口服抗精神病药物相比能提高用药依从性;将其转换为每 3 个月一次的 PP(PP3M)进一步提高了用药依从性。2021 年,美国食品和药物管理局批准了每 6 个月一次的 PP(PP6M),以提供更长的给药间隔。旨在提高用药依从性的公共卫生利益相关者有兴趣了解将 PP6M 纳入处方集将如何影响预算。为了从假设的美国多州医疗保健支付方和州医疗补助计划的角度评估将 PP6M 纳入处方集的预算影响,我们以加利福尼亚州、佐治亚州和俄亥俄州为例。预算影响模型是从支付方的角度开发的,将参考方案(市场上没有 PP6M)与新方案(有 PP6M)进行比较。研究人群包括有资格接受 PP6M 的精神分裂症患者。市场份额被分配给参考和新的市场方案。疗效通过接受治疗时复发的相对风险来衡量。依从性影响被纳入模型,影响治疗和复发率的成本。进行了确定性单因素敏感性分析。针对一个拥有 100 万成员的多州支付方的基础案例结果表明,将 PP6M 添加到市场中,将导致计划层面的总增量成本从第 1 年的 7747 美元增加到第 5 年的 11501 美元。药品成本的增加被管理和复发成本的节省所抵消(第 5 年分别为 105 美元和 881 美元)。每年每治疗患者的平均增量成本稳定在每年 180.06 美元,每年每个成员的增量成本保持在每月 0.01 美元以下。州级医疗补助方案的模型结果与多州基础案例的结果基本相似。单因素敏感性分析表明,该模型对 PP6M 和 PP3M 的每个包装成本以及完全依从 PP3M 的患者比例最为敏感。引入 PP6M 作为治疗选择的预算影响很小。由于依从性带来的管理和复发成本的降低,预计会带来成本节约,这些结果表明,从临床和预算的角度来看,PP6M 可以成为一种可行的治疗选择。本研究由杨森科学事务有限责任公司资助。研究赞助商为 Xcenda 和 ApotheCom 提供了医学写作、编辑支持和手稿提交方面的资金。希拉里·菲尔普斯(Hilary Phelps)在制定和最终确定稿件时是杨森全球服务有限责任公司的员工。阿德里亚·拉朱(Aditya Raju)是 Xcenda 的员工,在制定和最终确定稿件时,丹梦·黄(Danmeng Huang)是 Xcenda 的员工,Xcenda 是一家医疗保健咨询公司,受杨森科学事务有限责任公司委托。齐豫·程(Chih-Yuan Cheng)是杨森 NV 的员工。

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