Section of Cardiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Chronic Disease Innovation Center, Seven Oaks General Hospital, Winnipeg, Manitoba, Canada.
Am J Cardiol. 2023 Jul 1;198:26-32. doi: 10.1016/j.amjcard.2023.03.012. Epub 2023 May 15.
Dual antiplatelet therapy with acetylsalicylic acid and a P2Y12 inhibitor has become a mainstay of therapy after percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS). Although higher-potency P2Y12 inhibitors are preferred over clopidogrel in major society guidelines, recent evidence has questioned the extent of the benefit. It is important to evaluate the relative efficacy and safety of P2Y12 inhibitors in a real-world setting. This is a retrospective cohort study of all patients who underwent PCI for ACS in a Canadian province from January 1, 2015 to March 31, 2020. Baseline characteristics, including co-morbidities, medications, and bleeding risk, were obtained. Propensity matching was used to compare patients who received ticagrelor versus clopidogrel. The primary outcome was occurrence of major adverse cardiovascular events (MACEs) at 12 months, defined as death, nonfatal myocardial infarction, or unplanned revascularization. Secondary outcomes included all-cause mortality, major bleeding, stroke, and all-cause hospitalization. A total of 6,665 patients were included; 2,108 received clopidogrel and 4,214 received ticagrelor. Patients who received clopidogrel were older, had more co-morbidities, including cardiovascular risk factors, and had a higher bleeding risk. In 1.925 propensity score-matched pairs, ticagrelor was associated with a significantly lower risk of MACE (hazard ratio 0.79, 0.67 to 0.93, p <0.01) and hospitalization (hazard ratio 0.85, 0.77 to 0.95, p <0.01). No difference was observed in the risk of major bleeding. A statistically nonsignificant trend toward reduced risk of all-cause mortality was noted. In conclusion, in a real-world high-risk cohort, ticagrelor was associated with decreased risk of MACE and all-cause hospitalization compared with clopidogrel after PCI for ACS.
双联抗血小板治疗,即阿司匹林联合 P2Y12 抑制剂,已成为急性冠脉综合征(ACS)经皮冠状动脉介入治疗(PCI)后的主要治疗方法。虽然在主要的社会指南中,高选择性 P2Y12 抑制剂优于氯吡格雷,但最近的证据对其获益程度提出了质疑。因此,在真实世界环境中评估 P2Y12 抑制剂的相对疗效和安全性非常重要。
这是一项回顾性队列研究,纳入了 2015 年 1 月 1 日至 2020 年 3 月 31 日期间在加拿大一个省接受 PCI 治疗的所有 ACS 患者。研究收集了基线特征,包括合并症、药物使用和出血风险。采用倾向评分匹配比较接受替格瑞洛和氯吡格雷的患者。主要结局为 12 个月时主要不良心血管事件(MACE)的发生,定义为死亡、非致死性心肌梗死或计划外血运重建。次要结局包括全因死亡率、大出血、卒中和全因住院治疗。
共纳入 6665 例患者,其中 2108 例接受氯吡格雷治疗,4214 例接受替格瑞洛治疗。接受氯吡格雷治疗的患者年龄较大,合并症更多,包括心血管危险因素,且出血风险更高。在 1925 对倾向评分匹配的患者中,替格瑞洛治疗与 MACE 风险显著降低相关(风险比 0.79,0.67 至 0.93,p<0.01)和住院风险(风险比 0.85,0.77 至 0.95,p<0.01)。两组大出血风险无差异。全因死亡率风险呈降低趋势,但无统计学意义。
总之,在现实世界的高危人群中,与氯吡格雷相比,替格瑞洛在 ACS 患者 PCI 后可降低 MACE 和全因住院风险。