Angelis Aris, Tordrup David, Kanavos Panos
Medical Technology Research Group, LSE Health, London School of Economics and Political Science, Houghton Street, WC2A 2AE London, United Kingdom.
Medical Technology Research Group, LSE Health, London School of Economics and Political Science, Houghton Street, WC2A 2AE London, United Kingdom.
Health Policy. 2015 Jul;119(7):964-79. doi: 10.1016/j.healthpol.2014.12.016. Epub 2014 Dec 30.
Cost-of-illness studies, the systematic quantification of the economic burden of diseases on the individual and on society, help illustrate direct budgetary consequences of diseases in the health system and indirect costs associated with patient or carer productivity losses. In the context of the BURQOL-RD project ("Social Economic Burden and Health-Related Quality of Life in patients with Rare Diseases in Europe") we studied the evidence on direct and indirect costs for 10 rare diseases (Cystic Fibrosis [CF], Duchenne Muscular Dystrophy [DMD], Fragile X Syndrome [FXS], Haemophilia, Juvenile Idiopathic Arthritis [JIA], Mucopolysaccharidosis [MPS], Scleroderma [SCL], Prader-Willi Syndrome [PWS], Histiocytosis [HIS] and Epidermolysis Bullosa [EB]). A systematic literature review of cost of illness studies was conducted using a keyword strategy in combination with the names of the 10 selected rare diseases. Available disease prevalence in Europe was found to range between 1 and 2 per 100,000 population (PWS, a sub-type of Histiocytosis, and EB) up to 42 per 100,000 population (Scleroderma). Overall, cost evidence on rare diseases appears to be very scarce (a total of 77 studies were identified across all diseases), with CF (n=29) and Haemophilia (n=22) being relatively well studied, compared to the other conditions, where very limited cost of illness information was available. In terms of data availability, total lifetime cost figures were found only across four diseases, and total annual costs (including indirect costs) across five diseases. Overall, data availability was found to correlate with the existence of a pharmaceutical treatment and indirect costs tended to account for a significant proportion of total costs. Although methodological variations prevent any detailed comparison between conditions and based on the evidence available, most of the rare diseases examined are associated with significant economic burden, both direct and indirect.
疾病成本研究是对疾病给个人和社会造成的经济负担进行系统量化,有助于说明疾病在卫生系统中的直接预算后果以及与患者或护理人员生产力损失相关的间接成本。在“欧洲罕见病患者的社会经济负担与健康相关生活质量”(BURQOL-RD)项目背景下,我们研究了10种罕见病(囊性纤维化[CF]、杜氏肌营养不良症[DMD]、脆性X综合征[FXS]、血友病、幼年特发性关节炎[JIA]、黏多糖贮积症[MPS]、硬皮病[SCL]、普拉德-威利综合征[PWS]、组织细胞增多症[HIS]和大疱性表皮松解症[EB])的直接和间接成本证据。我们采用关键词策略结合10种选定罕见病的名称,对疾病成本研究进行了系统的文献综述。欧洲已知的疾病患病率在每10万人1至2例(普拉德-威利综合征、组织细胞增多症的一种亚型和大疱性表皮松解症)到每10万人42例(硬皮病)之间。总体而言,关于罕见病的成本证据似乎非常稀少(所有疾病共识别出77项研究),与其他疾病相比,囊性纤维化(n = 29)和血友病(n = 22)的研究相对充分,而其他疾病的疾病成本信息非常有限。在数据可得性方面,仅在四种疾病中发现了终生总成本数据,在五种疾病中发现了年度总成本(包括间接成本)。总体而言,发现数据可得性与药物治疗的存在相关,间接成本往往占总成本的很大比例。尽管方法上的差异妨碍了对不同疾病进行任何详细比较,且基于现有证据,大多数所研究的罕见病都与重大的直接和间接经济负担相关。