Robertson Teisha, Wong-Flores Jessica, Raisor Thomas Scott, Shakes Leighcraft
Defense Health Agency, Falls Church, VA.
Defense Health Agency, Bethesda, MD.
J Manag Care Spec Pharm. 2025 Jun;31(6):537-542. doi: 10.18553/jmcp.2025.31.6.537.
Over the past decade, the TRICARE pharmacy benefit has undergone significant changes, particularly in the management and utilization of compound drugs. Compound drugs are customized formulations that combine 2 or more pharmaceutical ingredients to meet specific patient needs and can offer therapeutic alternatives when standard US Food and Drug Administration-approved medications are ineffective. However, concerns regarding the safety, clinical effectiveness, and rising costs have necessitated increased oversight. Between 2013 and 2015, TRICARE experienced a drastic surge in compound drug expenditures, escalating from 4% of total pharmacy outpatient drug costs to 13% (more than $1.6 billion), despite representing only 0.4% of total outpatient prescription volume. This rapid increase highlighted the need for stricter controls to manage spending and ensure appropriate utilization. In response, the Defense Health Agency implemented a compound drug screening process in 2015, applying utilization management tools such as quantity limits, prior authorization, and step therapy. These measures aim to balance cost containment with maintaining access to clinically necessary compounded medications. This article provides a comprehensive review of the evolution of compound drugs within the TRICARE pharmacy benefit, examining safety concerns, spending trends, and management strategies.
在过去十年中,TRICARE药房福利计划经历了重大变革,尤其是在复方药物的管理和使用方面。复方药物是定制配方,将两种或更多药物成分组合在一起,以满足特定患者的需求,并且在标准的美国食品药品监督管理局批准的药物无效时可以提供治疗选择。然而,对安全性、临床有效性和成本上升的担忧使得加强监管成为必要。在2013年至2015年期间,TRICARE的复方药物支出急剧飙升,从药房门诊药品总成本的4%升至13%(超过16亿美元),尽管其仅占门诊处方总量的0.4%。这种快速增长凸显了需要更严格的控制措施来管理支出并确保合理使用。作为回应,国防卫生局在2015年实施了复方药物筛查程序,采用了数量限制、预先授权和阶梯治疗等利用管理工具。这些措施旨在在控制成本与确保获得临床必需的复方药物之间取得平衡。本文全面回顾了TRICARE药房福利计划中复方药物的演变,审视了安全问题、支出趋势和管理策略。