Mernick Francesca, Akrap Antonia, MacCormack-Gagnon Jacqueline
Massachusetts General Hospital, Boston, MA, USA.
Am J Health Syst Pharm. 2023 Jan 1;80(1):e46-e52. doi: 10.1093/ajhp/zxac259.
Healthcare systems are challenged with implementing high-cost, high-impact medication therapies with increasing frequency. Pharmacy & therapeutics (P&T) committees may struggle to integrate requests for these medications into their existing formulary review process. This article describes one large academic medical center's experience with creating a new P&T subcommittee that addresses the clinical, operational, and financial challenges these medications present.
The High-Impact Medication Therapy Subcommittee was established to optimize the institution's process for reviewing formulary requests for medications that are defined as "high impact"-nononcology medications that are extremely expensive and/or have complex operational or clinical challenges. The multidisciplinary subcommittee has 3 chairs-a physician, a nurse, and a pharmacist-and includes representation from all areas of pharmacy practice (clinical pharmacy, operations, supply chain, finance, and informatics), as well as medical and nursing leadership, hospital finance, and patient access services. Additional relevant stakeholders are invited as needed. The first medication to be reviewed at this subcommittee was afamelanotide, a melanocortin receptor agonist indicated for treatment of erythropoietic protoporphyria. The subcommittee addressed cost-efficacy concerns and operational challenges, and the final recommendation was for formulary addition, with clearly defined restriction criteria and the creation of a new workflow to meet the unique operational considerations with this drug.
As medication costs continue to rise at unprecedented rates and reimbursement requirements continue to increase in complexity, the High-Impact Medication Therapy Subcommittee provides a necessary venue for reviewing high-cost medications with complex clinical or operational considerations and proactively addressing implementation challenges.
医疗保健系统面临着越来越频繁地实施高成本、高影响力药物治疗的挑战。药学与治疗学(P&T)委员会可能难以将这些药物的申请纳入其现有的处方集审查流程。本文介绍了一家大型学术医疗中心创建一个新的P&T小组委员会的经验,该小组委员会应对这些药物带来的临床、运营和财务挑战。
成立了高影响力药物治疗小组委员会,以优化该机构审查被定义为“高影响力”药物(非肿瘤学药物,极其昂贵和/或具有复杂的运营或临床挑战)的处方申请流程。这个多学科小组委员会有三名主席——一名医生、一名护士和一名药剂师——成员包括药学实践各个领域(临床药学、运营、供应链、财务和信息学)的代表,以及医学和护理领导层、医院财务和患者准入服务部门的代表。根据需要邀请其他相关利益相关者。该小组委员会审查的第一种药物是阿法美拉肽,一种用于治疗红细胞生成性原卟啉症的黑皮质素受体激动剂。该小组委员会解决了成本效益问题和运营挑战,最终建议将其纳入处方集,并明确规定限制标准,创建新的工作流程以满足该药物独特的运营考虑因素。
随着药物成本以前所未有的速度持续上涨,报销要求的复杂性不断增加,高影响力药物治疗小组委员会为审查具有复杂临床或运营考虑因素的高成本药物并积极应对实施挑战提供了一个必要的场所。