单吸入器三联疗法与ICS/LABA治疗COPD的成本效益比较

Alan A Martin, D. Shah, E. Goodall, M. Schroeder, N. Risebrough, K. Ndirangu, A. Ismaila
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摘要

背景:IMPACT(通知慢性阻塞性肺病治疗途径,NCT02164513)显示,对于中/重度慢性阻塞性肺病患者,每日一次氟替卡松/乌莫替尼/维兰特罗(FF/UMEC/VI) 100/62.5/22μg与每日一次FF/VI 100/22μg相比,使用单一吸入器可显著减少急性加重和改善肺功能。目的:从加拿大公共支付者的角度评估FF/UMEC/VI与FF/VI的成本效益。方法:一个经过验证的关联风险方程模型(Briggs, Med Decis Making 37;4 2017),预测COPD疾病进展、相关医疗成本和健康结果,并填充IMPACT的基线特征、疗效和药物使用。采用加拿大医疗资源单位成本和药品成本,未来成本和健康结果每年折现1.5%。分析是概率性的,其生命周期和输出包括恶化率、成本(2017年CAD)、获得的质量调整生命年(QALYs)和每个QALY的增量成本效益比(ICER)。结果:与FF/VI相比,FF/UMEC/VI治疗导致的中度和重度恶化较少(10.52和3.38 vs 11.13和3.48),平均(95% CI)增量成本和QALY分别为2,598美元(2,010美元,3,268美元)和0.13美元(0.09,0.18),ICER为每个QALY 19,649美元(15,406美元,26,454美元)。FF/UMEC/VI与FF/VI相比具有成本效益的可能性为100%,每个QALY的支付意愿阈值为50,000美元。结果对停药后治疗的时间范围和疗效最为敏感。结论:在加拿大,与FF/VI相比,FF/UMEC/VI预计可以改善健康结果,并且是治疗中/重度COPD的一种具有成本效益的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cost-effectiveness of a single inhaler triple therapy versus ICS/LABA in COPD
Background: IMPACT (InforMing the PAthway of COPD Treatment, NCT02164513), showed superior exacerbation reduction and lung function improvement with single inhaler, once-daily fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) 100/62.5/22μg vs once-daily FF/VI 100/22μg, for patients with moderate/severe COPD. Objectives: The cost-effectiveness of FF/UMEC/VI vs FF/VI was assessed, from a Canadian public payer perspective. Methods: A validated linked risk equation model (Briggs, Med Decis Making 37;4 2017), which predicts COPD disease progression, associated healthcare costs and health outcomes, was populated with baseline characteristics, efficacy and medication use from IMPACT. Canadian healthcare resource unit costs and drug costs were applied, with future costs and health outcomes discounted at 1.5% annually. Analysis was probabilistic, with a lifetime horizon and outputs including exacerbation rates, costs (2017 CAD), quality-adjusted life years (QALYs) gained and incremental cost effectiveness ratio (ICER) per QALY. Results: Compared with FF/VI, FF/UMEC/VI treatment resulted in fewer moderate and severe exacerbations (10.52 and 3.38 vs 11.13 and 3.48), mean (95% CI) incremental costs and QALYs of $2,598 ($2,010, $3,268) and 0.13 (0.09, 0.18), and an ICER of $19,649 per QALY ($15,406, $26,454). The probability of FF/UMEC/VI being cost-effective vs FF/VI was 100% at a willingness-to-pay threshold of $50,000 per QALY. Results were most sensitive to time horizon, and efficacy of treatment post-discontinuation. Conclusions: FF/UMEC/VI was predicted to improve health outcomes and to be a cost-effective option for treatment of moderate/severe COPD compared with FF/VI, in Canada.
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