i3 Innovus, Stockholm, Sweden.
Osteoporos Int. 2011 Mar;22(3):955-65. doi: 10.1007/s00198-010-1291-5. Epub 2010 Jun 8.
The cost-effectiveness of bazedoxifene was compared to placebo in France, Germany, Italy, Spain, Sweden and the UK from a healthcare perspective using FRAX® for both fracture risks and for treatment efficacy. Cost/QALY differences were explained to a large extent by differences in fracture risk.
In cost-effectiveness modelling of osteoporosis treatments, the fracture risk has traditionally been calculated with risk adjustments based on age, bone mineral density and prior fracture. However, knowledge of additional clinical risk factors contributes to fracture risk assessment as demonstrated by the FRAX® tool. Bazedoxifene, a new selective estrogen receptor modulator for the treatment and prevention of osteoporosis, has been shown in a phase III clinical trial to reduce the risk of osteoporotic fractures in women. In an analysis using FRAX®, the efficacy of bazedoxifene was greater in patients with higher fracture risk.
The aim of this study was to evaluate the cost-effectiveness of bazedoxifene compared to placebo in France, Germany, Italy, Spain, Sweden and the UK from a healthcare perspective using FRAX®. A Markov cohort model was adapted to incorporate the FRAX® risk factors. FRAX® produces relative risks for hip fractures and major osteoporotic fractures. Patients were given a 5-year intervention, reducing the risk of fractures in a risk-dependent manner. The effect of treatment on fractures was assumed to decline linearly over 5 years after the intervention.
There are large cost/quality-adjusted life year variations between countries in the European setting studied. The base case values ranged from cost saving (Sweden) to EUR 105,450 (Spain) in 70-year-old women with a T-score of -2.5 SD and a prior fracture.
Bazedoxifene can be a cost-effective treatment for postmenopausal osteoporosis. The variability between countries was explained to a large extent by differences in fracture risk, and the estimated cost-effectiveness was highly dependent on the population's FRAX®-estimated probability of major osteoporotic fracture.
从医疗保健角度出发,使用 FRAX®评估骨折风险和治疗效果,比较了巴泽多昔芬与安慰剂在法国、德国、意大利、西班牙、瑞典和英国的成本效益。成本/QALY 差异在很大程度上可以用骨折风险的差异来解释。
在骨质疏松症治疗的成本效益建模中,传统上使用基于年龄、骨密度和既往骨折的风险调整来计算骨折风险。然而,如 FRAX®工具所示,更多的临床风险因素知识有助于评估骨折风险。巴泽多昔芬是一种新的选择性雌激素受体调节剂,用于治疗和预防骨质疏松症,一项 III 期临床试验表明,它可以降低女性骨质疏松性骨折的风险。在使用 FRAX®的分析中,巴泽多昔芬在骨折风险较高的患者中的疗效更大。
本研究旨在使用 FRAX®从医疗保健角度评估巴泽多昔芬与安慰剂在法国、德国、意大利、西班牙、瑞典和英国的成本效益。适应了一个马尔可夫队列模型,以纳入 FRAX®风险因素。FRAX®产生髋部骨折和主要骨质疏松性骨折的相对风险。患者接受了为期 5 年的干预,以风险依赖的方式降低骨折风险。假设治疗对骨折的影响在干预后 5 年内呈线性下降。
在所研究的欧洲环境中,70 岁 T 评分为-2.5 SD 且有既往骨折的女性,国家之间的成本/质量调整生命年存在很大差异。基本情况值从节省成本(瑞典)到 105450 欧元(西班牙)不等。
巴泽多昔芬可作为绝经后骨质疏松症的一种具有成本效益的治疗方法。国家之间的差异在很大程度上可以用骨折风险的差异来解释,并且估计的成本效益高度依赖于人群的 FRAX®估计的主要骨质疏松性骨折概率。