Neovius M, Narbro K
Department of Medicine, Centre for Pharmacoepidemiology, Karolinska Institute, Stockholm, Sweden.
Int J Obes (Lond). 2008 Dec;32(12):1752-63. doi: 10.1038/ijo.2008.189. Epub 2008 Nov 4.
To review economic evaluations of weight loss drugs and compare reported incremental cost-effectiveness ratios (ICERs).
A literature search was conducted for cost-effectiveness (CEAs) and cost-utility analyses (CUAs) of sibutramine, orlistat and rimonabant.
Fourteen unique articles were identified (11 CUAs and 3 CEAs; 9 orlistat, 4 sibutramine and 1 rimonabant). All used diet and exercise as comparator, whereas none included indirect costs. Time horizons varied from treatment period only (1-4 years) to 80 years (median 7.5 years). Longer studies modeled effects on diabetes, micro- and macrovascular complications, coronary heart disease and death. Of the CUAs, the median ICER was 16,000 euro(2007)/QALY (quality-adjusted life-year; range 10,000-88,000), with the worst cost-effectiveness when recommended stop rules for non-responding patients were not applied. All studies but three were funded by the manufacturing company, and the median ICER was considerably higher for independent than for sponsored analyses (62,000 euro vs 15,000 euro/QALY). However, two of the three independent CUAs did not use recommended stop rules, as compared with one of eight manufacturer-sponsored analyses. The results were most sensitive to assumptions regarding weight loss sustainability and utility per kilogram lost. Side effects and dropout because of reasons other than lack of efficacy were generally not incorporated.
Published economic evaluations indicate that orlistat, sibutramine and rimonabant are within the range of what is generally regarded as cost-effective. Uncertainty remains about weight loss sustainability, utility gain associated with weight loss and extrapolations from transient weight loss to long-term health benefits. Modeling of head-to-head comparisons and attrition is needed, as are analyses conducted independently of manufacturing companies.
回顾减肥药物的经济学评价,并比较报告的增量成本效益比(ICER)。
对西布曲明、奥利司他和利莫那班的成本效益分析(CEA)和成本效用分析(CUA)进行文献检索。
共识别出14篇独特的文章(11篇CUA和3篇CEA;9篇关于奥利司他,4篇关于西布曲明,1篇关于利莫那班)。所有研究均将饮食和运动作为对照,无一纳入间接成本。时间跨度从仅治疗期(1 - 4年)到80年(中位数7.5年)不等。较长时间的研究模拟了对糖尿病、微血管和大血管并发症、冠心病及死亡的影响。在CUA中,ICER的中位数为16,000欧元(2007年)/质量调整生命年(QALY)(范围为10,000 - 88,000),当未应用针对无反应患者的推荐停药规则时,成本效益最差。除3项研究外,所有研究均由制药公司资助,独立分析的ICER中位数显著高于受资助分析(62,000欧元对15,000欧元/QALY)。然而,3项独立CUA中有2项未使用推荐停药规则,而8项制造商资助的分析中有1项未使用。结果对减肥可持续性及每减轻1千克体重所获效用的假设最为敏感。一般未纳入因缺乏疗效以外的原因导致的副作用和退出情况。
已发表的经济学评价表明,奥利司他、西布曲明和利莫那班在通常认为具有成本效益的范围内。减肥的可持续性、与减肥相关的效用增加以及从短暂减肥到长期健康益处的外推仍存在不确定性。需要进行直接比较和损耗的建模,以及独立于制药公司进行的分析。