Smart A J, Walters L
Department of Pharmacology, University of Cape Town.
S Afr Med J. 1994 Dec;84(12):834-7.
To perform a comparative pharmaco-economic assessment of two HMG-CoA reductase inhibitors.
A cost-effectiveness analysis was employed using comparative efficacy data from selected clinical trials. A comprehensive international literature search formed the basis for this selection. Criteria for inclusion of clinical trial results in the analysis were set a priori. Acquisition costs used were the recommended reimbursement prices as at September 1994.
Two outcome measures are reported: (i) the comparative cost-effectiveness in lowering blood lipid concentrations; and (ii) the comparative cost-effectiveness of the medicines when used to achieve a predetermined therapeutic goal.
The average cost per 1% decrease in total cholesterol is 21.9% higher on 10 mg pravastatin daily than on 10 mg simvastatin daily. Similarly the average cost per 1% decrease in low-density lipoprotein (LDL) cholesterol is 23.1% higher on 10 mg pravastatin than on 10 mg simvastatin daily. This difference is consistent throughout the dosage range. The use of incremental doses of simvastatin monotherapy in order to reach a predetermined therapeutic goal (LDL < or = 4.14 mmol/l) is more cost-effective than an equivalent pravastatin dosage regimen. Total treatment costs for simvastatin-treated patients are 3.5% less than for pravastatin-treated patients. More patients on simvastatin are successfully treated; the difference in overall treatment costs per successfully treated patient is 27.9% in favour of simvastatin. Sensitivity analysis shows these results to be stable under extreme scenarios.
This analysis employed objective comparative efficacy data obtained from peer-reviewed sources to compare the economic and clinical outcomes of simvastatin and pravastatin in the treatment of hypercholesterolaemia. The acquisition cost of simvastatin is 10.3-22.8% higher than an equivalent milligram dose of pravastatin, depending on the dosage used. However, because of the greater milligram potency of simvastatin, it is a more cost-effective alternative. Simvastatin therefore provides better value for money than pravastatin in lowering lipid levels in clinical practice.
对两种HMG-CoA还原酶抑制剂进行药物经济学比较评估。
采用成本效益分析,使用从选定临床试验中获取的比较疗效数据。全面的国际文献检索构成了此次选择的基础。分析中纳入临床试验结果的标准事先设定。所使用的购置成本为截至1994年9月的推荐报销价格。
报告了两项观察指标:(i)降低血脂浓度方面的比较成本效益;(ii)用于实现预定治疗目标时药物的比较成本效益。
每日服用10mg普伐他汀使总胆固醇每降低1%的平均成本比每日服用10mg辛伐他汀高21.9%。同样,每日服用10mg普伐他汀使低密度脂蛋白(LDL)胆固醇每降低1%的平均成本比每日服用10mg辛伐他汀高23.1%。在整个剂量范围内这种差异是一致的。使用递增剂量的辛伐他汀单药治疗以达到预定治疗目标(LDL≤4.14mmol/l)比同等剂量的普伐他汀治疗方案更具成本效益。辛伐他汀治疗患者的总治疗成本比普伐他汀治疗患者低3.5%。更多服用辛伐他汀的患者得到成功治疗;每例成功治疗患者的总体治疗成本差异中,辛伐他汀占优27.9%。敏感性分析表明这些结果在极端情况下是稳定的。
本分析采用从同行评审来源获得的客观比较疗效数据,比较辛伐他汀和普伐他汀治疗高胆固醇血症的经济和临床结果。根据所用剂量,辛伐他汀的购置成本比同等毫克剂量的普伐他汀高10.3 - 22.8%。然而,由于辛伐他汀的毫克效力更高,它是一种更具成本效益的选择。因此,在临床实践中降低血脂水平方面,辛伐他汀比普伐他汀性价比更高。