Servicio de Farmacia, Hospital Universitario Virgen Macarena, Seville, Spain.
Omakase Consulting S.L., Barcelona, Spain.
Int J Technol Assess Health Care. 2022 May 20;38(1):e48. doi: 10.1017/S0266462322000332.
The reimbursement of medicines by the Spanish National Health System (NHS) is based on a set of criteria included in the Royal Legislative Decree 1/2015 (RDL 1/2015). The Interministerial Committee on Pricing of Medicines and Healthcare Products (CIPM) is responsible for the final price and reimbursement (P&R) decision, including on its resolutions the criteria listed in the law by which the reimbursement of a drug is approved or denied. Nevertheless, the information behind its reasoning is not provided. The present study aims to characterize the P&R criteria of the RDL 1/2015 through criteria definitions from other countries to improve the P&R evaluation in Spain.
A multidisciplinary experts panel with relevant experience in drug evaluation and decision making at national, regional, and local level in Spain was selected for this study. A literature review to characterize the criteria listed in the RDL 1/2015 was performed based on the most relevant and recognized Health Technology Assessment (HTA) agencies in Europe, UK, and Canada. Eventually, a feasibility study was performed to evaluate the novel drug cefiderocol using the characterized criteria, including a reflective discussion of the results.
Consensus was reached among the multidisciplinary experts on the characterization of the criteria set by the law. The feasibility of their application to a new drug was exploratory, notwithstanding it showed the potential to improve the transparency as well as to offer a more structured rationale for the CIPM to evaluate the inclusion of new drugs in the Spanish NHS.
西班牙国家卫生系统(NHS)的药品报销基于包括在皇家法令 1/2015(RDL 1/2015)中的一系列标准。药品价格和医疗产品联委会(CIPM)负责最终价格和报销(P&R)决策,包括在法律规定的范围内,列出了批准或拒绝药品报销的标准。然而,其决策背后的信息并未提供。本研究旨在通过其他国家的标准定义来描述 RDL 1/2015 的 P&R 标准,以改善西班牙的 P&R 评估。
选择了具有在西班牙国家、地区和地方层面评估和决策药物相关经验的多学科专家小组进行本研究。根据欧洲、英国和加拿大最相关和公认的卫生技术评估(HTA)机构,对 RDL 1/2015 中列出的标准进行了文献综述,以对其进行特征描述。最终,使用特征化的标准对新型药物头孢地尔进行了可行性研究,包括对结果进行反思性讨论。
多学科专家就法律规定的标准特征达成了共识。尽管对新药头孢地尔的应用具有探索性,但表明有可能提高透明度,并为 CIPM 提供更具结构性的理由,以评估新药物在西班牙 NHS 中的纳入。