Lamotte Mark, Annemans Lieven, Kawalec Pawel, Zoellners York
HEDM-IMS, Bruxelles, Belgium.
Herz. 2006 Dec;31 Suppl 3:74-82.
Patients who survive an acute myocardial infarction (MI) are at increased risk of subsequent major cardiovascular events and cardiac (often sudden) death. The use of highly concentrated and purified omega-3 polyunsaturated fatty acids (n-3 PUFAs), in addition to standard secondary prevention after MI, results in a significant reduction in the risk of sudden death. This study assessed the cost-effectiveness of adding n-3 PUFAs to the current secondary prevention treatment after acute MI in 5 countries: Australia, Belgium, Canada, Germany, Poland. Based on the clinical outcomes of GISSI-Prevenzione (MI, stroke, revascularisation rate and mortality), a decision-model was built in DataPROTM. The implications of adding n-3 PUFAs to standard treatment in patients with a recent history of MI were analysed from the health care payer's perspective. The time horizon was 3.5 years (identical to GISSI-Prevenzione). Event costs were based on literature data. Life expectancy data for survivors of cardiac disease were taken from the Saskatchewan database and then country-adjusted. Results are expressed as extra cost (Euro) per life-year gained (LYG). Annual discounting of 5% was applied to health effects and costs. Treatment with highly concentrated n-3 PUFAs yielded between 0.260 (Poland) and 0.284 (Australia) LYG, at an additional cost of Euro 807 (Canada) to Euro 1,451 (Belgium). The incremental cost-effectiveness ratio (ICER) varied between Euro 2,867 (Canada) and Euro 5,154 (Belgium) per LYG. Sensitivity analyses on effectiveness, cost of complications and discounting proved the robustness of the results. A 2nd order Monte Carlo simulation based on the 95% CIs obtained from GISSI showed that highly concentrated n-3 PUFAs are cost-effective in more than 99% of patients (assuming societal willingness to pay threshold of Euro 20,000/LYG). Including health care costs incurred during the remaining life-years considerably increased total costs, but had no impact on the ICER-based treatment recommendation. Adding highly concentrated n-3 PUFAs to standard treatment in the secondary prevention after MI appears to be cost-effective in the 5 countries studied.
急性心肌梗死(MI)幸存者发生后续重大心血管事件和心脏性(通常为猝死)死亡的风险会增加。在MI后的标准二级预防基础上,使用高浓度、纯化的ω-3多不饱和脂肪酸(n-3 PUFAs)可显著降低猝死风险。本研究评估了在澳大利亚、比利时、加拿大、德国、波兰这5个国家,在急性MI后的当前二级预防治疗中添加n-3 PUFAs的成本效益。基于GISSI-Prevenzione研究的临床结果(MI、中风、血运重建率和死亡率),在DataPROTM中构建了一个决策模型。从医疗保健支付方的角度分析了在近期有MI病史的患者中,在标准治疗基础上添加n-3 PUFAs的影响。时间跨度为3.5年(与GISSI-Prevenzione相同)。事件成本基于文献数据。心脏病幸存者的预期寿命数据取自萨斯喀彻温省数据库,然后进行国家调整。结果以每获得一个生命年(LYG)的额外成本(欧元)表示。对健康效果和成本应用5%的年度贴现率。使用高浓度n-3 PUFAs治疗每获得0.260(波兰)至0.284(澳大利亚)个LYG,额外成本为807欧元(加拿大)至1451欧元(比利时)。增量成本效益比(ICER)在每LYG 2867欧元(加拿大)至5154欧元(比利时)之间。对有效性、并发症成本和贴现率的敏感性分析证明了结果的稳健性。基于从GISSI获得的95%置信区间进行的二阶蒙特卡罗模拟表明,高浓度n-3 PUFAs在超过99%的患者中具有成本效益(假设社会支付意愿阈值为20000欧元/LYG)。纳入余生所产生的医疗保健成本会大幅增加总成本,但对基于ICER的治疗建议没有影响。在MI后的二级预防中,在标准治疗基础上添加高浓度n-3 PUFAs在所研究的5个国家似乎具有成本效益。