Abadi-Korek Ifat, Shemer Joshua
Harefuah. 2012 Jun;151(6):362-3, 377, 376.
Healthcare systems worldwide are dealing with the uncertainty characterizing new and expensive health technoLogies, particularly aspects involving drug effectiveness and the extent and doses required for utilization. Reducing this uncertainty can be achieved mainly by using either coverage with evidence development methods or risk-sharing schemes (RSS). In 2011, the first phenylketonuria (PKU) risk-sharing scheme was set up in Israel, through the public funding health services updating process. This was done in order to ensure that people with PKU could access PKU sole treatment--sapropterin dihydrochloride, Kuvan. The apparent effectiveness of the treatment, on one hand, and the uncertainty regarding the number of patients and average treatment dosage, on the other hand, dictated the RRS. This scheme determined a ceiling number of tablets to be funded by the insurer, above this ceiling the manufacturer would finance Kuvan. Furthermore, it was agreed that after 3 years Kuvan would be brought to the public committee for updating reimbursement decisions. It is inevitable that risk sharing and conditional coverage agreements will become a common practice in the reimbursement process in the future. This will allow competent authorities and pharmaceutical companies to build clinical experience and other required data with medicines which might normally not be eLigible for reimbursement. Before it becomes the common practice in Israel, the RSS for Kuvan, process and outcomes, should be monitored and analyzed by the Ministry of Health, to ensure patients access to treatment, the effective collection of the research data and the effective interaction between Israel's four health funds and the manufacturer.
全球医疗保健系统都在应对新型昂贵医疗技术所具有的不确定性,尤其是涉及药物疗效以及使用所需的范围和剂量等方面。减少这种不确定性主要可以通过采用有证据支持的覆盖范围扩展方法或风险分担计划(RSS)来实现。2011年,以色列通过公共资助医疗服务更新程序设立了首个苯丙酮尿症(PKU)风险分担计划。这样做是为了确保苯丙酮尿症患者能够获得PKU唯一的治疗药物——盐酸沙丙蝶呤,商品名Kuvan。一方面是该治疗方法明显的有效性,另一方面是患者数量和平均治疗剂量的不确定性,这就决定了要实施风险分担计划。该计划确定了保险公司资助药片的上限数量,超过这个上限后制造商将为Kuvan提供资金。此外,各方还商定,3年后Kuvan将提交给公共委员会以更新报销决定。风险分担和有条件覆盖协议在未来报销过程中成为常见做法是不可避免的。这将使主管当局和制药公司能够积累通常可能不符合报销条件的药物的临床经验和其他所需数据。在其在以色列成为常见做法之前,卫生部应对Kuvan的风险分担计划、过程和结果进行监测和分析,以确保患者能够获得治疗、有效收集研究数据以及以色列四大医疗基金与制造商之间的有效互动。