Department of Cardiology, Jinshan Hospital of Fudan University, Shanghai, 201500, China.
BMC Pharmacol Toxicol. 2024 Sep 27;25(1):67. doi: 10.1186/s40360-024-00796-w.
The ideal single antiplatelet therapy for long-term maintenance after coronary stenting remains uncertain. In a head-to-head comparison, we aimed to evaluate the efficacy and safety profile of aspirin and clopidogrel as monotherapies in this patient cohort.
We reviewed 1044 patients who underwent percutaneous coronary intervention (PCI) with drug-eluting stents (DES) at the Department of Cardiovascular Medicine, Jinshan Hospital of Fudan University, between January 2019 and December 2021 and completed a 12-month Dual Antiplatelet Therapy (DAPT) treatment. They were divided into two groups: 582 were assigned to the aspirin group (100 mg/day) and 422 to the clopidogrel group (75 mg/day). The primary endpoint was the composite cardiac death, ischemic stroke, myocardial infarction, and Bleeding Academic Research Consortium (BARC) bleeding type 3 or greater. Secondary endpoint events included all-cause death, ischemic stroke, myocardial infarction, bleeding (defined as a BARC type ≥ 2 bleeding), and gastrointestinal complications.
After a mean observation period of 25 ± 8.4 months, the primary endpoint event occurred in 29 (6.8%) patients in the clopidogrel group and 30 (5.1%) in the aspirin group, with no difference between the two groups (P = 0.253). In BARC type 2 or greater bleeding events, there were 9 (1.5%) in the aspirin group compared to 7 (1.7%) in the clopidogrel group, with no difference between the two groups (P = 0.160).
After 12-month DAPT in Chinese patients undergoing DES implantation, aspirin monotherapy versus clopidogrel monotherapy showed no significant difference between the two drugs in terms of safety and efficacy in terms of hemorrhage, myocardial infarction, ischemic stroke, cardiac death, and bleeding with BARC type 2 or greater.
经皮冠状动脉介入治疗(PCI)后长期应用单一抗血小板治疗的理想药物仍不明确。我们旨在进行头对头比较,评估阿司匹林和氯吡格雷单药治疗在该患者人群中的疗效和安全性。
我们回顾了 2019 年 1 月至 2021 年 12 月在复旦大学附属金山医院心血管内科接受药物洗脱支架(DES)PCI 并完成 12 个月双联抗血小板治疗(DAPT)的 1044 例患者。他们被分为两组:582 例患者分配至阿司匹林组(100mg/天),422 例患者分配至氯吡格雷组(75mg/天)。主要终点是复合终点事件,包括心源性死亡、缺血性卒中和心肌梗死以及出血学术研究联合会(BARC)出血 3 级或更高。次要终点事件包括全因死亡、缺血性卒中和心肌梗死、出血(定义为 BARC 类型≥2 级出血)和胃肠道并发症。
平均随访 25±8.4 个月后,氯吡格雷组有 29 例(6.8%)患者和阿司匹林组有 30 例(5.1%)患者发生主要终点事件,两组间无差异(P=0.253)。在 BARC 类型 2 级或更高出血事件中,阿司匹林组有 9 例(1.5%),氯吡格雷组有 7 例(1.7%),两组间无差异(P=0.160)。
在中国接受 DES 植入的患者中,DAPT 治疗 12 个月后,阿司匹林单药治疗与氯吡格雷单药治疗在出血、心肌梗死、缺血性卒中心脏性死亡和 BARC 类型 2 级或更高出血方面,两种药物的安全性和疗效无显著差异。