Martens L L, Guibert R
Abt Associates Inc., Cambridge, Massachusetts.
Clin Ther. 1994 Nov-Dec;16(6):1052-62; discussion 1036.
This study estimated the cost-effectiveness of the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors available in Canada for the primary prevention of coronary heart disease (CHD). A model of the cost-effectiveness of therapy used to modify low-density lipoprotein (LDL) cholesterol and high-density lipoprotein cholesterol levels was developed in the primary prevention of CHD based on risk functions from the Framingham Heart Study and Canadian data on coronary risk factors and the cost of treating the leading manifestations of CHD. Relative to no treatment, discounted gains in life expectancy range from 0.174 year for fluvastatin 40 mg to 0.215 year for simvastatin 10 mg. Costs per year-of-life-saved range from $38,800 for fluvastatin 40 mg to $56,200 for pravastatin 20 mg. In the incremental analysis relative to fluvastatin 40 mg, additional gains in life expectancy range from 0.011 year for pravastatin 20 mg to 0.041 year for simvastatin 10 mg, and incremental cost-effectiveness ratios range from $88,200 for simvastatin, 10 mg to $330,300 for pravastatin 20 mg. Our analysis showed that the cost-effectiveness of cholesterol-lowering therapy is sensitive to pretreatment risk of CHD, as expressed by pretreatment cholesterol levels and the presence of additional risk factors such as hypertension, diabetes, and smoking. The results of the analysis suggest that it is more cost-effective to initiate treatment with fluvastatin than with pravastatin, simvastatin, or lovastatin. Sensitivity analysis showed the results to be stable even if the lipid-lowering effect of fluvastatin is varied by 23% from the original assumption of 25% LDL reduction (ie, from 19.3% to 30.8%). Limitations of the study are recognized and discussed. A head-to-head comparison of these HMG-CoA reductase inhibitors could provide further evidence that therapy initiated with fluvastatin may be the most cost-effective way to treat patients with hypercholesterolemia who are eligible for treatment with HMG-CoA reductase inhibitors.
本研究评估了加拿大可用的3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂在冠心病(CHD)一级预防中的成本效益。基于弗雷明汉心脏研究的风险函数以及加拿大关于冠心病危险因素和治疗冠心病主要表现的成本数据,建立了一个用于改变低密度脂蛋白(LDL)胆固醇和高密度脂蛋白胆固醇水平的治疗成本效益模型。相对于不治疗,预期寿命的贴现收益范围从氟伐他汀40毫克的0.174年到辛伐他汀10毫克的0.215年。每挽救一年生命的成本范围从氟伐他汀40毫克的38,800美元到普伐他汀20毫克的56,200美元。在相对于氟伐他汀40毫克的增量分析中,预期寿命的额外增加范围从普伐他汀20毫克的0.011年到辛伐他汀10毫克的0.041年,增量成本效益比范围从辛伐他汀10毫克的88,200美元到普伐他汀20毫克的330,300美元。我们的分析表明,降低胆固醇治疗的成本效益对冠心病的治疗前风险敏感,治疗前风险由治疗前胆固醇水平以及高血压、糖尿病和吸烟等其他危险因素的存在来表示。分析结果表明起始使用氟伐他汀治疗比使用普伐他汀、辛伐他汀或洛伐他汀更具成本效益。敏感性分析表明,即使氟伐他汀的降脂效果与最初假设的降低25%的LDL(即从19.3%到30.8%)相差23%,结果仍然稳定。本研究的局限性已得到认识和讨论。对这些HMG-CoA还原酶抑制剂进行直接比较可能会提供进一步的证据,表明起始使用氟伐他汀治疗可能是治疗符合HMG-CoA还原酶抑制剂治疗条件的高胆固醇血症患者的最具成本效益的方法。