Alfred Hospital, Melbourne, Australia (J.Z., D.L., D.K., S.Z., D.S.).
School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia (D.L., S.Z., D.S.).
Circ Cardiovasc Qual Outcomes. 2022 Oct;15(10):e008638. doi: 10.1161/CIRCOUTCOMES.121.008638. Epub 2022 Oct 11.
Empagliflozin is the first medication to demonstrate clinical benefit in patients with heart failure with preserved ejection fraction, but its cost-effectiveness is unknown. We aimed to evaluate the cost-effectiveness of adding empagliflozin to standard therapy in patients with heart failure with preserved ejection fraction.
A Markov model from the perspective of the Australian health care system was constructed to compare empagliflozin plus standard care to standard care alone among a hypothetical cohort of patients with heart failure with preserved ejection fraction. Clinical probabilities were derived from The EMPEROR-Preserved (Empagliflozin Outcome Trial in Patients with Chronic Heart Failure with Preserved Ejection Fraction). Costs and utilities were derived from published sources. The main outcome was the incremental cost-effectiveness ratio per quality-adjusted life-year gained. Deterministic and probabilistic sensitivity analyses were performed to assess model uncertainty. Costs and benefits were discounted at 5% annually.
Over a lifetime, the addition of empagliflozin to standard care prevented 167 heart failure hospitalizations and 155 heart failure-related urgent care visits for every 1000 patients treated and increased mean quality-adjusted survival by 0.16 quality adjusted life-years per patient. Mean lifetime costs in the empagliflozin and standard care groups were AUD$63 218 and AUD$58 478 per patient, respectively. This resulted in an incremental cost-effectiveness ratio of AUD$29 202 per quality adjusted life-year gained. In probabilistic sensitivity analyses, empagliflozin was cost-effective in 85% of 10 000 Monte Carlo simulations at a willingness-to-pay threshold of AUD$50 000 per quality adjusted life-year gained.
In patients with heart failure with preserved ejection fraction, adding empagliflozin to standard care is likely to be cost-effective when compared with standard care alone in the Australian health care setting.
恩格列净是首个在射血分数保留的心力衰竭患者中显示出临床获益的药物,但它的成本效益尚不清楚。我们旨在评估在射血分数保留的心力衰竭患者中,将恩格列净添加到标准治疗中的成本效益。
从澳大利亚医疗保健系统的角度构建了一个马尔可夫模型,以比较恩格列净加标准治疗与单独标准治疗在射血分数保留的心力衰竭患者中的情况。临床概率来自 EMPEROR-Preserved(恩格列净在射血分数保留的慢性心力衰竭患者中的疗效试验)。成本和效用来自已发表的资料。主要结果是每获得一个质量调整生命年的增量成本效益比。进行了确定性和概率敏感性分析以评估模型不确定性。成本和效益以每年 5%贴现。
在一生中,每 1000 名接受治疗的患者中,加用恩格列净可预防 167 例心力衰竭住院和 155 例心力衰竭相关的紧急护理就诊,并使每位患者的平均质量调整生存时间增加 0.16 个质量调整生命年。恩格列净组和标准治疗组的平均终生成本分别为每位患者 63218 澳元和 58478 澳元。这导致每获得一个质量调整生命年的增量成本效益比为 29202 澳元。在概率敏感性分析中,在 10000 次蒙特卡罗模拟中,在愿意支付的阈值为 50000 澳元/质量调整生命年的情况下,恩格列净在 85%的模拟中是成本有效的。
在澳大利亚的医疗保健环境中,与单独标准治疗相比,在射血分数保留的心力衰竭患者中,加用恩格列净可能具有成本效益。