Medicines Management Programme, Health Service Executive, Trinity Centre for Health Sciences, St James's Hospital, Dublin 8, Ireland.
Department of Pharmacology and Therapeutics, Trinity College Dublin, St James's Hospital, Dublin 8, Ireland.
Appl Health Econ Health Policy. 2024 Nov;22(6):771-781. doi: 10.1007/s40258-024-00904-1. Epub 2024 Aug 12.
The Health Service Executive, responsible for operating the Irish health service, has introduced health technology management (HTM) initiatives to manage expenditure on medicines. One such approach is managed access protocols (MAPs) to support access to high-cost medicines, while providing oversight, governance and budgetary certainty to the payer. Herein we describe the development and operation of MAPs, using case studies of liraglutide (Saxenda), dupilumab (Dupixent) and calcitonin gene-related peptide monoclonal antibodies. A MAP imposes the eligibility criteria attached to reimbursement support of a medicine. Criteria applied include controls on prescribing authority, clinical diagnostic and severity criteria, previous lines of treatment, concomitant treatments, outcome data collection, and validations within the reimbursement claims system. The choice of criteria are specific to each medicine, dictated by the areas of uncertainty highlighted in the health technology assessment report, such as the place in treatment, population, duration of treatment, etc., the commercial arrangements reached with the marketing authorisation holder, and specific recommendations made by the decision maker. By December 2023, there were 28 medicines reimbursed subject to a MAP in Ireland. Across the three case studies outlined, over 3000 patients were accessing novel treatments for chronic illnesses in September 2023. Managed access protocols can provide some cost certainty for the payer by aligning utilisation and expenditure with committed funds, while enabling access where unmet need is highest. Managed access protocols are now established in the drug reimbursement process in Ireland, meeting the needs of both payers, patients and industry, and are likely to remain a feature of the reimbursement landscape.
爱尔兰卫生服务执行局负责运营爱尔兰的卫生服务,该局采取了医疗技术管理(HTM)措施来管理药品支出。其中一种方法是采用管理准入协议(MAP)来支持高价药品的准入,同时为支付方提供监督、治理和预算确定性。本文通过利拉鲁肽(Saxenda)、度普利尤单抗(Dupixent)和降钙素基因相关肽单克隆抗体的案例研究,介绍了 MAP 的制定和运行情况。MAP 规定了药品报销支持所附的资格标准。适用的标准包括处方权控制、临床诊断和严重程度标准、先前的治疗线、伴随治疗、结果数据收集以及报销索赔系统内的验证。标准的选择特定于每种药物,取决于卫生技术评估报告中突出的不确定性领域,例如治疗中的地位、人群、治疗持续时间等,与营销授权持有人达成的商业安排,以及决策者提出的具体建议。截至 2023 年 12 月,爱尔兰有 28 种药品需要经过 MAP 才能报销。在概述的三个案例研究中,截至 2023 年 9 月,超过 3000 名患者正在接受慢性疾病的新治疗方法。通过使利用和支出与承诺资金保持一致,管理准入协议可以为支付方提供一些成本确定性,同时在未满足的需求最高的情况下实现准入。管理准入协议现在已在爱尔兰的药物报销流程中确立,满足支付方、患者和行业的需求,并且可能仍然是报销格局的一个特征。