预防

Elliott Currie
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摘要

【一级标题】背景:HMG-CoA还原酶抑制剂(他汀类)治疗心血管疾病的临床疗效已在临床试验中得到确立。然而,就心血管疾病的总体绝对风险降低和长期他汀类药物治疗的成本效益而言,对于没有心血管疾病的患者,他汀类药物应该在何时向谁开始治疗尚不清楚。目的:利用来自日本队列研究的冠心病风险预测的心脏危险因素,研究普伐他汀10mg /天与无药物治疗在冠心病一级预防中的成本-效果。方法:采用马尔可夫转移模型评价普伐他汀治疗与无药物治疗的成本-效果。在日本,使用CAD的风险预测来估计急性心肌梗死的发生率。使用心脏危险因素对45 - 75岁的假设人群进行了检查。从支付者的角度估计了整个生命周期的质量调整生命年(QALYs)和增量成本效益比(ICER)。结果:患有糖尿病、高血压(II级)和吸烟的55岁男性患者,与无药物治疗相比,普伐他汀治疗的ICERs为9,677,000日元/ QALY; 65岁男性患者的ICERs为8,648,000日元/ QALY。在所有评估的亚组中,普伐他汀治疗与无药物治疗相比没有成本效益。结论:使用基于无心血管事件史的日本队列的CAD风险预测,普伐他汀用于冠心病一级预防的成本效益可能在低和高心脏病风险人群中都不具有成本效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevention
[First-level Header] Background: The clinical efficacy of HMG-CoA reductase inhibitor (statin) therapy in cardiovascular disease has been established in clinical trials. Nonetheless, it is unclear to whom and when statin treatment should be initiated for patients without cardiovascular disease with regard to overall absolute risk reduction of cardiovascular disease and the cost-effectiveness of long-term statin therapy. Objectives: To examine the cost-effectiveness of pravastatin 10 mg/day compared with no drug therapy for primary prevention of coronary artery disease (CAD), using cardiac risk factors from risk predictions for CAD from Japanese cohort studies. Methods: A Markov transition model was used to evaluate the cost-effectiveness of pravastatin compared with no drug therapy. The incidence of acute myocardial infarction was estimated using risk predictions for CAD in Japan. A hypothetical population from 45 to 75 years old was examined using the cardiac risk factors. Quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratio (ICER) over a lifetime horizon were estimated from a perspective of payers. Results: ICERs of pravastatin therapy compared with no drug therapy were 9,677,000 yen per QALY in 55-year-old men and 8,648,000 yen per QALY in 65-year-old men with diabetes mellitus, hypertension (grade II), and smoking as cardiac risk factors. Pravastatin therapy was not cost-effective compared with no drug therapy in all subgroups evaluated. Conclusions: Using risk prediction for CAD based on a Japanese cohort with no history of cardiovascular events, the cost-effectiveness of pravastatin for primary prevention of CAD may not be cost-effective in populations at both low and high cardiac risk.
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