Wagner Monika, Goetghebeur Mireille, Merikle Elizabeth, Pandya Ankur, Chu Paula, Taylor Douglas C A
BioMedCom Consultants Inc, Montreal, Canada.
Can J Clin Pharmacol. 2009 Summer;16(2):e331-45. Epub 2009 Jun 16.
The TNT study compared high dose atorvastatin (80 mg) versus moderate atorvastatin (10 mg) treatment in 10,001 patients with stable coronary heart disease (CHD), over 4.9 years. Intensive lipid-lowering with atorvastatin (80 mg) reduced major cardiovascular events by 22%.
To assess the cost-effectiveness of intensive lipid-lowering versus moderate lipid lowering treatment from the perspective of the Canadian Ministries of Health.
A lifetime Markov model was developed to predict cardiovascular (CV) events, costs, survival, and quality-adjusted life years (QALYs) for CHD patients receiving 80 mg versus 10 mg of atorvastatin. Predictions were also made for 10- and 5-year horizons. Treatment-specific event risks were used until five years. Beyond year five, equivalent CV risks were assumed for all patients. Medical-care costs and post-event survival were estimated using Canadian data. Health utility scores were obtained from published studies. Benefits and costs were discounted 5% annually. Probabilistic and deterministic sensitivity analyses were performed.
Treatment with atorvastatin (80 mg) over a lifetime horizon resulted in increased costs (Can$16,542 vs. Can$15,365), survival (10.12 vs. 10.03 life years), and QALYs (7.71 vs. 7.61) per patient compared with atorvastatin (10 mg), yielding an incremental cost-effectiveness of Can$12,946 per life year gained and Can$11,969 per QALY. The incremental cost per QALY remained below Can$50,000 in 98.1% of 1000 simulations. Results were robust to variations in event hazard ratios, costs, health utility values, and discount rate.
Intensive atorvastatin (80 mg) treatment is predicted to be cost-effective versus atorvastatin (10 mg) for CHD patients in Canada.
TNT研究在10001例稳定性冠心病(CHD)患者中对比了高剂量阿托伐他汀(80毫克)与中等剂量阿托伐他汀(10毫克)治疗,随访4.9年。阿托伐他汀(80毫克)强化降脂使主要心血管事件减少了22%。
从加拿大卫生部的角度评估强化降脂与中等强度降脂治疗的成本效益。
构建一个终生马尔可夫模型,以预测接受80毫克与10毫克阿托伐他汀治疗的CHD患者的心血管(CV)事件、成本、生存率和质量调整生命年(QALY)。还对10年和5年的时间范围进行了预测。使用特定治疗的事件风险直至5年。5年后,假定所有患者的CV风险相等。使用加拿大数据估算医疗成本和事件后生存率。健康效用评分来自已发表的研究。效益和成本按每年5%进行贴现。进行了概率性和确定性敏感性分析。
与阿托伐他汀(10毫克)相比,终生使用阿托伐他汀(80毫克)治疗使每位患者的成本增加(16542加元对15365加元)、生存率提高(10.12个生命年对10.03个生命年)、QALY增加(7.71对7.61),每获得一个生命年的增量成本效益为12946加元,每获得一个QALY的增量成本为11969加元。在1000次模拟中,98.1%的情况下每QALY的增量成本仍低于50000加元。结果对于事件风险比、成本、健康效用值和贴现率的变化具有稳健性。
预计在加拿大,对于CHD患者,阿托伐他汀(80毫克)强化治疗比阿托伐他汀(10毫克)治疗更具成本效益。