Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Institute of Public Health, Medical Decision Making and Health Technology Assessment, Department of Public Health, Health Services Research and Health Technology Assessment, UMIT -University for Health Sciences, Medical Informatics and Technology, Hall in Tirol, Austria.
Int J Stroke. 2023 Apr;18(4):416-425. doi: 10.1177/17474930221111898. Epub 2022 Aug 24.
The CHANCE-2 study compared 3 weeks of aspirin-ticagrelor to aspirin-clopidogrel in CYP2C19 loss-of-function (LOF) allele carriers following a transient ischemic attack (TIA)/minor stroke and demonstrated a modestly lower risk of stroke recurrence with aspirin-ticagrelor. This stroke protection was largely for minor stroke and came at an increased risk of bleeding. The cost-effectiveness of implementing testing for LOF allele status to personalize antiplatelet regimen for secondary stroke prevention after a TIA/minor stroke in the Canadian health care context is unknown.
Cost-effectiveness analysis using a decision-analytic Markov cohort model with a lifetime horizon was performed to determine the costs and health benefits of testing for LOF allele status compared with no testing (current standard of care). The population of interest was patients living in Canada who suffered a TIA/minor stroke. Outcomes of interest were life-years gained (LYG), quality-adjusted life years (QALY) gained, costs (reported in 2022 Canadian dollars), and the incremental cost-effectiveness ratio (ICER). We adopted the perspective of the Federal, Provincial, and Territorial Ministries of Health and used a 1.5% annual discount rate. Sensitivity analyses were performed to assess uncertainty.
Compared to standard of care, LOF allele testing leads to 0.14 LYG (undiscounted), 0.12 QALYs gained (undiscounted), and additional lifetime costs of CAD$432 (discounted) per patient. The ICER of the LOF allele testing strategy is CAD$4310 per QALY gained compared with standard of care. The probabilistic sensitivity analyses demonstrated that LOF allele testing was cost-effective in more than 99.99% of simulations using a willingness-to-pay threshold of CAD$50,000 per QALY.
Based on available evidence, testing for LOF allele followed by short duration 3 weeks of aspirin-ticagrelor compared to standard-of-care aspirin-clopidogrel can lead to prolonged life and improved quality of life and can be considered very cost-effective when compared with other well-accepted technologies in health and medicine.
CHANCE-2 研究比较了 CYP2C19 功能丧失(LOF)等位基因携带者在短暂性脑缺血发作(TIA)/小卒中后使用 3 周阿司匹林-替格瑞洛与阿司匹林-氯吡格雷的疗效,结果显示阿司匹林-替格瑞洛可适度降低卒中复发风险。这种卒中保护主要针对小卒中,但出血风险增加。在加拿大医疗保健背景下,对于 TIA/小卒中后的二级卒中预防,实施 LOF 等位基因状态检测以制定个体化抗血小板治疗方案的成本效益尚不清楚。
使用具有终生时间范围的决策分析马尔可夫队列模型进行成本效益分析,以确定与不检测(当前的标准护理)相比,检测 LOF 等位基因状态的成本和健康效益。感兴趣的人群是在加拿大遭受 TIA/小卒中的患者。主要结局是获得的生命年(LYG)、获得的质量调整生命年(QALY)、成本(以 2022 加元报告)和增量成本效益比(ICER)。我们采用联邦、省和地区卫生部门的观点,并使用 1.5%的年度贴现率。进行了敏感性分析以评估不确定性。
与标准护理相比,LOF 等位基因检测可导致每个患者无折扣的 0.14 LYG、0.12 QALY 增加和终生额外成本 432 加元(贴现)。与标准护理相比,LOF 等位基因检测策略的 ICER 为每个 QALY 增加 4310 加元。概率敏感性分析表明,在使用每 QALY 50000 加元的意愿支付阈值时,LOF 等位基因检测在超过 99.99%的模拟中具有成本效益。
基于现有证据,与标准护理相比,检测 LOF 等位基因后使用 3 周短疗程阿司匹林-替格瑞洛治疗可延长寿命并提高生活质量,与卫生和医学领域的其他公认技术相比,可被认为具有很高的成本效益。