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在州医疗补助计划中全面管理丙型肝炎病毒药物治疗概述。

Overview of Comprehensive Hepatitis C Virus Medication Management in a State Medicaid Program.

机构信息

1 Clinical Pharmacy Services, University of Massachusetts Medical School, Shrewsbury, Massachusetts.

2 Office of Clinical Affairs, University of Massachusetts Medical School, Quincy, Massachusetts.

出版信息

J Manag Care Spec Pharm. 2016 Oct;22(10):1161-6. doi: 10.18553/jmcp.2016.22.10.1161.

Abstract

BACKGROUND

Breakthrough direct-acting antivirals set a new standard in the management of hepatitis C virus (HCV) with regard to cure rates and improved tolerability; however, the health care system is challenged by the cost of these medications.

OBJECTIVE

To describe the effect of a comprehensive HCV medication management program on optimized regimen use, prior authorization (PA) modifications, and medication cost avoidance in a state Medicaid program.

METHODS

This program consists of a 2-tiered prescriber outreach: (1) regimen outreach to promote optimized regimen selection and (2) refill outreach to support medication adherence. PA criteria were developed to identify optimized regimens, taking into account member- and virus-specific factors as well as cost. Prescriber outreach was conducted to recommend the use of an optimized regimen as applicable. Successful regimen outreach was defined as the number of members for whom a recommendation was accepted. A refill report identified members without a subsequent paid HCV medication claim within 25 days of the previous claim and outreach to the prescriber's office was performed. The outcome measure for refill outreach was the number and type of PA modifications made secondary to outreach (closure or extension). Cost avoidance was calculated for members who completed treatment with an optimized regimen. Return on investment (ROI) was calculated for the program.

RESULTS

Between December 18, 2013, and January 31, 2015, 911 members had PA requests approved for simeprevir, sofosbuvir, or ledipasvir/ sofosbuvir. Of these members, 223 (24.5%) met the criteria for regimen outreach. Pharmacist interventions to treat with an optimized regimen were accepted for 135 members (60.5%). Following implementation of prescriber outreach to promote refills, between March 10, 2014, and January 31, 2015, offices were informed of an upcoming refill for 515 members. As a result of outreach, 19.6% of members had a subsequent PA modification. Sixty-nine approved PAs (for 68 members) were closed after correspondence with the prescriber, and 33 approved PAs (for 33 members) were extended. The total projected cost avoidance was $3,770,097. The comprehensive HCV medication management program demonstrated an ROI of $10.28 for every $1 spent.

CONCLUSIONS

A comprehensive HCV medication management program can help contain costs while ensuring that members have access to most clinically appropriate regimens.

DISCLOSURES

No outside funding supported this study. Lavitas reports personal fees and nonfinancial support from University of Tennessee, Advanced Studies in Medicine and grant funding from Bristol-Myers Squibb, outside the submitted work. All other authors report no conflicts of interest. The poster "Overview of a Hepatitis C Medication Monitoring Program in a State Medicaid Program" was presented October 8, 2014, by Lavitas at the AMCP Nexus 2014 meeting in Boston, Massachusetts. A program update was presented at the 2015 American Drug Utilization Review Society Meeting on February 27, 2015. Study concept and design were contributed by Price, Lenz, and Jeffrey, with assistance from Lavitas, Tesell, and Hydery. Lavitas, Tesell, and Hydery collected the data, assisted by Price, Lenz, and Jeffrey, and data interpretation was performed by all authors. The manuscript was written by Greenwood, Lavitas, Tesell, and Hydery, with assistance from the other authors, and was revised by all authors.

摘要

背景

突破性的直接作用抗病毒药物在丙型肝炎病毒 (HCV) 的治疗方面创造了新的标准,在治愈率和改善耐受性方面取得了突破;然而,医疗保健系统面临着这些药物成本的挑战。

目的

描述 HCV 药物管理综合计划在优化方案使用、预先授权 (PA) 修改和避免药物费用方面对州医疗补助计划的影响。

方法

该计划由两层次的医生外联组成:(1) 方案外联,以促进优化方案的选择;(2) 补充外联,以支持药物依从性。制定了 PA 标准,以根据成员和病毒的具体因素以及成本来确定优化方案。进行医生外联以推荐适用的优化方案。成功的方案外联被定义为被接受推荐的成员数量。补充报告确定了在之前的索赔后 25 天内没有随后的 HCV 药物索赔的成员,并对医生办公室进行了外联。补充外联的结果衡量标准是由于外联而进行的 PA 修改的数量和类型(关闭或延长)。为完成优化方案治疗的成员计算成本避免。为该计划计算投资回报率 (ROI)。

结果

在 2013 年 12 月 18 日至 2015 年 1 月 31 日期间,有 911 名成员的西美瑞韦、索非布韦或 ledipasvir/索非布韦的 PA 请求获得批准。在这些成员中,223 名 (24.5%) 符合方案外联的标准。药剂师干预治疗优化方案被 135 名成员 (60.5%) 接受。在实施促进补充方案的医生外联之后,在 2014 年 3 月 10 日至 2015 年 1 月 31 日期间,办公室收到了 515 名成员即将进行的补充通知。由于外联,19.6%的成员随后进行了 PA 修改。在与医生沟通后,有 69 份批准的 PA (68 名成员) 被关闭,有 33 份批准的 PA (33 名成员) 被延长。预计总成本避免额为 3770097 美元。综合 HCV 药物管理计划的投资回报率为每 1 美元投入 10.28 美元。

结论

综合 HCV 药物管理计划可以帮助控制成本,同时确保成员能够获得最符合临床的方案。

披露

这项研究没有外部资金支持。Lavitas 报告了来自田纳西大学的个人酬金和非财务支持,以及 Bristol-Myers Squibb 的赠款资金,这些都与提交的工作无关。所有其他作者均未报告利益冲突。海报“州医疗补助计划中丙型肝炎药物监测计划概述”于 2014 年 10 月 8 日由 Lavitas 在波士顿举行的 AMCP Nexus 2014 会议上展示。在 2015 年美国药物利用审查学会会议上于 2015 年 2 月 27 日展示了该计划的更新。Price、Lenz 和 Jeffrey 提出了研究的概念和设计,Lavitas、Tesell 和 Hydery 提供了协助。Lavitas、Tesell 和 Hydery 收集了数据,并得到了 Price、Lenz 和 Jeffrey 的协助,数据解释由所有作者完成。手稿由 Greenwood、Lavitas、Tesell 和 Hydery 撰写,其他作者提供了协助,并由所有作者进行了修订。

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