School of Pharmacy, Nanjing Medical University, Nanjing, China.
School of Health Policy and Management, Nanjing Medical University, Nanjing, China.
Br J Clin Pharmacol. 2024 Feb;90(2):483-492. doi: 10.1111/bcp.15921. Epub 2023 Nov 8.
The study aimed to estimate the cost-effectiveness of CYP2C19 genotype-guided antiplatelet therapy using cilostazol and ticagrelor as an alternative to clopidogrel, compared to conventional antiplatelet therapy with clopidogrel and aspirin.
A 90-day decision tree and 30-year Markov model were employed to assess the costs and quality-adjusted life years (QALYs) of personalized antiplatelet therapy for patients with minor ischemic stroke and high-risk transient ischemic attack, compared to conventional antiplatelet therapy in the Chinese healthcare system. The primary outcome was the incremental cost-effectiveness ratio (ICER). The data sources included clinical trials, published literature, official documents and local prices. One-way sensitivity analysis and probabilistic sensitivity analysis were performed to confirm the robustness of the findings.
The base-case analysis indicated that the CYP2C19 genotype-guided antiplatelet strategy was cost-effective, and cilostazol group and ticagrelor group yielded an ICER of 3327.40 US dollars (USD)/QALY and 3426.92 USD/QALY, respectively, which were less than threshold. The one-way sensitivity analysis showed the results were robust, where the most sensitive parameter was the disability distribution in the modified Rankin scale 3-5. The probabilistic analysis showed that the CYP2C19 genotype-guided antiplatelet therapy with either cilostazol or ticagrelor was 100% cost-effective under the willingness-to-pay threshold.
CYP2C19 genotype-guided antiplatelet therapy using cilostazol and ticagrelor as an alternative to clopidogrel appeared to be more cost-effective than conventional antiplatelet therapy for acute minor ischemic stroke and high-risk transient ischemic attack patients over 30 years in China.
本研究旨在评估 CYP2C19 基因型指导的抗血小板治疗(以西洛他唑和替格瑞洛替代氯吡格雷)相较于常规抗血小板治疗(氯吡格雷加阿司匹林)的成本效果。
采用 90 天决策树和 30 年 Markov 模型,评估 CYP2C19 基因型指导的抗血小板治疗(西洛他唑和替格瑞洛)与中国医疗体系中常规抗血小板治疗(氯吡格雷加阿司匹林)对有轻度缺血性卒中和高危短暂性脑缺血发作风险的患者的成本和质量调整生命年(QALY)。主要结局是增量成本效果比(ICER)。数据来源包括临床试验、已发表文献、官方文件和当地价格。进行了单因素敏感性分析和概率敏感性分析,以确认结果的稳健性。
基础情况分析表明,CYP2C19 基因型指导的抗血小板策略具有成本效果,西洛他唑组和替格瑞洛组的 ICER 分别为 3327.40 美元/QALY 和 3426.92 美元/QALY,均低于阈值。单因素敏感性分析显示结果稳健,最敏感的参数是改良 Rankin 量表 3-5 残疾分布。概率分析表明,在支付意愿阈值下,CYP2C19 基因型指导的抗血小板治疗(西洛他唑或替格瑞洛)对急性轻度缺血性卒中和高危短暂性脑缺血发作患者在 30 年内有 100%的成本效果。
在中国,对于 30 年以上的急性轻度缺血性卒中和高危短暂性脑缺血发作患者,CYP2C19 基因型指导的抗血小板治疗(以西洛他唑和替格瑞洛替代氯吡格雷)相较于常规抗血小板治疗(氯吡格雷加阿司匹林)具有更高的成本效果。