Huang Sheng-Wei, Chen Po-Wei, Feng Wen-Han, Hsieh I-Chang, Ho Ming-Yun, Cheng Chung-Wei, Yeh Hung-I, Chen Ching-Pei, Huang Wei-Chun, Fang Ching-Chang, Lin Hui-Wen, Lin Sheng-Hsiang, Tsai Chin-Feng, Su Chun-Hung, Li Yi-Heng
School of Medicine, Chung Shan Medical University Hospital, Chung Shan Medical University, Taichung, Taiwan.
College of Medicine, National Cheng Kung University Hospital, National Cheng Kung University, Tainan, Taiwan.
Front Cardiovasc Med. 2022 Feb 24;8:772820. doi: 10.3389/fcvm.2021.772820. eCollection 2021.
Dual antiplatelet therapy (DAPT) score is used to stratify ischemic and bleeding risk for antiplatelet therapy after percutaneous coronary intervention (PCI). This study assessed the association between the DAPT score and clinical outcomes in acute coronary syndrome (ACS) patients who were treated with P2Y12 inhibitor monotherapy.
A total of 498 ACS patients, with early aspirin discontinuation for various reasons and who received P2Y12 inhibitor monotherapy after PCI, were enrolled during the period from January 1, 2014 to December 31, 2018. The efficacy and safety between those with low (<2) and high (≥2) DAPT scores were compared during a 12-month follow-up after PCI. Inverse probability of treatment weighting was used to balance the covariates between the two groups. The primary endpoint was a composite outcome of all-cause mortality, recurrent ACS or unplanned revascularization, and stroke within 12 months. The safety endpoint was major bleeding, defined as Bleeding Academic Research Consortium (BARC) 3 or 5 bleeding.
The primary composite endpoint occurred in 11.56 and 14.38% of the low and high DAPT score groups, respectively. Although there was no significant difference in the primary composite endpoint between the two groups in the multivariate Cox proportional hazards models, the risk of recurrent ACS or unplanned revascularization was significantly higher in the high DAPT score group (adjusted hazard ratio [HR]: 1.900, 95% confidence interval [CI]: 1.095-3.295). The safety outcome for BARC 3 or 5 bleeding was similar between the two groups.
Our results indicate that ACS patients receiving P2Y12 monotherapy with high DAPT score had an increased risk of recurrent ACS or unplanned revascularization.
双联抗血小板治疗(DAPT)评分用于对经皮冠状动脉介入治疗(PCI)后抗血小板治疗的缺血和出血风险进行分层。本研究评估了DAPT评分与接受P2Y12抑制剂单药治疗的急性冠状动脉综合征(ACS)患者临床结局之间的关联。
2014年1月1日至2018年12月31日期间,共纳入498例因各种原因早期停用阿司匹林且PCI后接受P2Y12抑制剂单药治疗的ACS患者。在PCI后12个月的随访期间,比较DAPT评分低(<2)和高(≥2)的患者之间的疗效和安全性。采用治疗权重逆概率法平衡两组之间的协变量。主要终点是12个月内全因死亡、复发性ACS或计划外血运重建以及卒中的复合结局。安全终点是大出血,定义为出血学术研究联盟(BARC)3级或5级出血。
低DAPT评分组和高DAPT评分组的主要复合终点发生率分别为11.56%和14.38%。虽然在多变量Cox比例风险模型中两组之间的主要复合终点无显著差异,但高DAPT评分组复发性ACS或计划外血运重建的风险显著更高(调整后风险比[HR]:1.900,95%置信区间[CI]:1.095 - 3.295)。两组之间BARC 3级或5级出血的安全结局相似。
我们的结果表明,接受P2Y12单药治疗且DAPT评分高的ACS患者复发性ACS或计划外血运重建的风险增加。