Gandhi Sanjay K, Jensen Marie M, Fox Kathleen M, Smolen Lee, Olsson Anders G, Paulsson Thomas
AstraZeneca LP, Wilmington, DE, USA.
Clinicoecon Outcomes Res. 2012;4:1-11. doi: 10.2147/CEOR.S26621. Epub 2012 Jan 10.
To assess the long-term cost-effectiveness of rosuvastatin therapy compared with generic simvastatin and generic atorvastatin in reducing the incidence of cardiovascular events and mortality in a Swedish population with Framingham risk ≥20%.
A PROBABILISTIC MONTE CARLO SIMULATION MODEL BASED ON DATA FROM JUPITER (THE JUSTIFICATION FOR THE USE OF STATINS IN PREVENTION: an Intervention Trial Evaluating Rosuvastatin) was used to estimate the long-term cost-effectiveness of rosuvastatin 20 mg daily versus simvastatin or atorvastatin 40 mg for the prevention of cardiovascular death and morbidity. The three- stage model included cardiovascular event prevention simulating the 4 years of JUPITER, initial prevention beyond the trial, and subsequent cardiovascular event prevention. A Swedish health care payer perspective (direct costs only) was modeled for a lifetime horizon, with 2008/2009 as the costing period. Univariate and probabilistic sensitivity analyses were performed.
The incremental cost per quality-adjusted life-year (QALY) gained with rosuvastatin 20 mg over simvastatin or atorvastatin 40 mg ranged from SEK88,113 (rosuvastatin 20 mg versus simvastatin 40 mg; Framingham risk ≥30%; net avoidance of 34 events/1000 patients) to SEK497,542 (versus atorvastatin 40 mg: Framingham risk ≥20%; net avoidance of 11 events/1000 patients) over a lifetime horizon. Probabilistic sensitivity analyses indicated that at a willingness-to-pay threshold of SEK500,000/QALY, rosuvastatin 20 mg would be cost-effective for approximately 75%-85% of simulations relative to atorvastatin or simvastatin 40 mg. Sensitivity analyses indicated the findings to be robust.
Rosuvastatin 20 mg is cost-effective over a lifetime horizon compared with generic simvastatin or atorvastatin 40 mg in patients at high cardiovascular risk in Sweden.
评估瑞舒伐他汀治疗与普通辛伐他汀和普通阿托伐他汀相比,在降低瑞典弗明汉风险≥20%人群心血管事件发生率和死亡率方面的长期成本效益。
基于JUPITER(瑞舒伐他汀在预防中的应用理由:一项评估瑞舒伐他汀的干预试验)的数据,使用概率蒙特卡罗模拟模型来估计每日20毫克瑞舒伐他汀与40毫克辛伐他汀或阿托伐他汀在预防心血管死亡和发病方面的长期成本效益。三阶段模型包括模拟JUPITER的4年心血管事件预防、试验后的初始预防以及随后的心血管事件预防。从瑞典医疗保健支付者的角度(仅直接成本)建立了终身模型,以2008/2009年作为成本计算期。进行了单变量和概率敏感性分析。
与40毫克辛伐他汀或阿托伐他汀相比,每日20毫克瑞舒伐他汀每获得一个质量调整生命年(QALY)的增量成本在终身范围内从88,113瑞典克朗(瑞舒伐他汀20毫克与辛伐他汀40毫克相比;弗明汉风险≥30%;每1000名患者净避免34起事件)到497,542瑞典克朗(与阿托伐他汀40毫克相比:弗明汉风险≥20%;每1000名患者净避免11起事件)不等。概率敏感性分析表明,在支付意愿阈值为500,000瑞典克朗/QALY时,相对于40毫克阿托伐他汀或辛伐他汀,约75%-85%的模拟显示20毫克瑞舒伐他汀具有成本效益。敏感性分析表明研究结果具有稳健性。
在瑞典心血管风险高的患者中,与普通40毫克辛伐他汀或阿托伐他汀相比,终身服用20毫克瑞舒伐他汀具有成本效益。