Department of Pharmacy and Clinical Pharmacology, Health Division, Maccabi Healthcare Services, Tel Aviv, Israel.
Institute of Clinical Pharmacology, Sheba Medical Center, Tel Hashomer & Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Isr J Health Policy Res. 2024 Jul 15;13(1):30. doi: 10.1186/s13584-024-00617-9.
In Israel, coverage of health needs is delivered by four health maintenance organizations (HMOs), which are budgeted by the government according to the recommendations of the National Drug Formulary (NDF) Committee. For medications not listed in the NDF, individuals may request to cover the costs by the HMO Exemptions Committee (DEC). The objectives of the current study, a first of its kind, are to document the DEC decision process, to identify its components and to determine the decisions' clinical outcome.
This retrospective cohort study included all members (≥ age 18) of the Maccabi Healthcare Service (MHS) who submitted a request to the DEC between June 2017 and December 2018. Collected data include patient demographics, clinical information and components of the decision process. Decision success (i.e., clinical outcome correlated with DEC decision) was determined by clinical outcome over at least one-year follow-up.
A total of 335 requests were included. Strong evidence and rare disease were positively associated with approvals, while the availability of alternative treatments and costs were negatively associated. The majority of decisions (75%) met predicted clinical outcomes. Only estimated costs were found to be associated with decision success.
Factors that reduce the potential costs of a requested drug are significantly associated with higher odds for drug approval, but only when the evidence supports potential benefit.
在以色列,四项健康维护组织(HMO)提供医疗需求保障,政府根据国家药物处方集(NDF)委员会的建议为其分配预算。对于 NDF 中未列出的药物,个人可以通过 HMO 豁免委员会(DEC)申请覆盖费用。本研究旨在记录 DEC 的决策过程,识别其组成部分,并确定决策的临床结果,这在同类研究中尚属首次。
本回顾性队列研究纳入了 2017 年 6 月至 2018 年 12 月期间向 DEC 提交申请的 Maccabi 医疗保健服务(MHS)的所有成员(≥18 岁)。收集的数据包括患者人口统计学信息、临床信息和决策过程的组成部分。通过至少一年的随访确定决策的临床结果(即与 DEC 决策相关的临床结果)来判断决策的成功与否。
共纳入 335 份申请。充分的证据和罕见疾病与批准呈正相关,而替代治疗方法的可及性和成本与批准呈负相关。大多数决策(75%)符合预测的临床结果。仅估计成本与决策成功相关。
降低申请药物潜在成本的因素与更高的药物批准几率显著相关,但前提是证据支持潜在获益。