The UK National Haemophilia Database, Manchester University Department of Haematology, Manchester Royal Infirmary, Oxford Road, Manchester, UK.
Haemophilia. 2013 Sep;19(5):660-7. doi: 10.1111/hae.12169. Epub 2013 May 28.
The increasing intensity of treatment, the widespread adoption of factor VIII and IX prophylaxis and increasing usage over the past decade have led to haemophilia becoming an almost uniquely expensive condition to treat. The average adult with severe haemophilia A in the UK used 250,000 IU of factor VIII in 2011/2012, at a cost in excess of £ 100,000 p.a. The cost to the end-user may be considerably higher than this for some US patients supplied by home care companies with high on-costs. This has led to a high level of administrative scrutiny of treatment and an imperative to procure clotting factor concentrates more efficiently and collectively. National procurement schemes have run successfully in various countries and will become commoner. The UK system of procurement is described. This system, following EU procurement rules, evaluated products technically and by price. The price of bioequivalent products was determined by reverse e-auction. Considerable cost reductions were achieved whilst retaining all suppliers and maintaining a degree of prescribing freedom. Elements of this system could be more widely applied.
治疗强度的增加、因子 VIII 和 IX 预防性治疗的广泛采用以及过去十年中用量的增加,使得血友病成为一种治疗费用极高的疾病。英国 2011/2012 年,每一位重度甲型血友病成年患者的因子 VIII 用量为 25 万国际单位,每年的费用超过 10 万英镑。对于一些由高附加成本的家庭护理公司供应的美国患者来说,最终用户的费用可能比这还要高。这导致对治疗的高度行政审查,并迫切需要更有效地集体采购凝血因子浓缩物。在不同国家,国家采购计划已成功运行,并将变得更加普遍。本文介绍了英国的采购系统。该系统遵循欧盟采购规则,从技术和价格两方面对产品进行评估。生物等效产品的价格通过反向电子拍卖确定。在保留所有供应商并保持一定程度的处方自由的同时,实现了相当大的成本降低。该系统的某些要素可以更广泛地应用。