Cost-effectiveness of rosuvastatin in comparison with generic atorvastatin and simvastatin in a Swedish population at high risk of cardiovascular events

被引:16
作者
Gandhi, Sanjay K. [1 ]
Jensen, Marie M. [2 ]
Fox, Kathleen M. [3 ]
Smolen, Lee [4 ]
Olsson, Anders G. [5 ,6 ]
Paulsson, Thomas [7 ]
机构
[1] AstraZeneca LP, Wilmington, DE USA
[2] AstraZeneca, Lund, Sweden
[3] Strateg HealthCare Solut, Monkton, MD USA
[4] Med Decis Modeling Inc, Indianapolis, IN USA
[5] Linkoping Univ, Dept Med & Hlth Sci, Linkoping, Sweden
[6] Stockholm Heart Ctr, Stockholm, Sweden
[7] AstraZeneca, Sodertalje, Sweden
关键词
cardiovascular disease; cost-benefit analysis; cost-effectiveness; rosuvastatin; simvastatin; atorvastatin; generic; high risk;
D O I
10.2147/CEOR.S26621
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: 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%. Methods: 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. Results: 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. Conclusion: 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.
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页码:1 / 11
页数:11
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