Kaló Zoltán, Muszbek Noémi, Bodrogi József, Bidló Judit
Novartis Hungary Ltd, Budapest, Hungary.
Health Policy. 2007 Mar;80(3):402-12. doi: 10.1016/j.healthpol.2006.04.002. Epub 2006 May 30.
Therapeutic reference pricing is one of the potential cost containment methods for pharmaceuticals. The most critical question of reference pricing is how to select reference product(s) if their efficacy is different, especially if different strengths of the same substance are available. Authors describe the Hungarian experience related to the introduction of therapeutic reference pricing for statin therapies as of 1 September 2003. The National Health Insurance Fund selected the reference products based on their low price per DDD. Therapeutic reference pricing was expected to reduce the expenditure on statins by switching therapy to cheaper alternatives and therefore decreasing the average price per prescribed unit. The National Health Insurance Fund expected price erosion not only for branded products directly affected by generics but even for patented ones. Despite generic price erosion of simvastatin, the average unit price of statins was reduced by only 3% at 7 months after the introduction of the reference pricing system. During the same period the average DDD per prescription was increased from 1.14 to 1.65. The price of patented statins did not change over this period. Introduction of therapeutic reference pricing neglected evidence-based medicine results and ultimately increased the expenditure on statins in Hungary. Selection of the cheapest DDD per unit as the reference product resulted in growth of DDD per prescription, and consequently increased price per prescribed unit of statins. The failure of the system could have been even more dramatic if increased utilisation of generic statins had not reduced the negative effect of therapeutic reference pricing. Based upon the first experiences of the Hungarian implementation, the method described in this paper for the extension of generic reference pricing to therapeutic categories is not justifiable.
治疗参考定价是药品潜在的成本控制方法之一。参考定价最关键的问题是,如果参考产品的疗效不同,尤其是同一物质有不同规格时,如何选择参考产品。作者描述了匈牙利自2003年9月1日起引入他汀类药物治疗参考定价的经验。国家健康保险基金根据每限定日剂量(DDD)的低价来选择参考产品。治疗参考定价预计通过将治疗转换为更便宜的替代品来降低他汀类药物的支出,从而降低每个处方单位的平均价格。国家健康保险基金预计不仅受仿制药直接影响的品牌产品会出现价格下降,甚至专利产品也会如此。尽管辛伐他汀出现了仿制药价格下降,但在引入参考定价系统7个月后,他汀类药物的平均单价仅降低了3%。在此期间,每张处方的平均DDD从1.14增加到了1.65。专利他汀类药物的价格在此期间没有变化。治疗参考定价的引入忽视了循证医学的结果,最终增加了匈牙利他汀类药物的支出。选择每单位最便宜的DDD作为参考产品导致每张处方的DDD增加,从而增加了他汀类药物每个处方单位的价格。如果增加仿制药他汀类药物的使用没有减少治疗参考定价的负面影响,该系统的失败可能会更加严重。基于匈牙利实施的首次经验,本文中描述的将仿制药参考定价扩展到治疗类别的方法是不合理的。