Zhao Xin, Ai Guannan, Qiu Miaohan, Wang Xiaozeng, Zhang Lei, Yang Xiaoxu, Liu Yifei, Xu Pei, Zhang Jiyuan, Gu Chonghuai, Zhou Mengge, Hao Yongchen, Zhao Dong, Han Yaling
Department of Cardiology, General Hospital of Northern Theater Command, Shenyang, Liaoning 110016, China.
Department of Cardiology, General Hospital of Northern Theater Command, Shenyang, Liaoning 110016, China; Jinzhou Medical University, Jinzhou, Liaoning 121001, China.
Int J Cardiol. 2020 Jul 1;310:1-8. doi: 10.1016/j.ijcard.2020.04.004. Epub 2020 Apr 7.
Risk stratification with specific biomarkers is proposed for tailored P2Y12 inhibitor therapy in patients with STEMI.
This nationwide registry and quality improvement study is from November 1, 2014, to June 30, 2017. In total, 11,512 STEMI patients received aspirin and P2Y12 receptor inhibitor (clopidogrel or ticagrelor) and underwent PCIs in hospitals. Of the patients, 2992 were prescribed ticagrelor and 8520 clopidogrel. The primary effectiveness outcome was major adverse cardiovascular and cerebrovascular events (MACCE: cardiac death, myocardial infarction, stent thrombosis, in-hospital ischemic stroke). The primary safety outcome was in-hospital major bleeding.
MACCE incidence was lower in the ticagrelor group than in the clopidogrel group (0.8% versus 1.2%; P=0.046), but under different NT-proBNP levels, cumulative hazards of MACCE were without statistical significance. Bleeding rates were higher in the ticagrelor group than in the clopidogrel group (all bleeding: 9.9% versus 6.9%, P<0.001; major bleeding: 4.0% versus 2.7%, P<0.001). The higher cumulative hazard of bleeding could be identified in the Kaplan-Meier curves. In the multivariate analysis, ticagrelor increased bleeding events, compared with clopidogrel, at NT-proBNP >1800 ng/L patients (all bleeding: HR 1.46; 95%CI, 1.07-2.01; major bleeding: HR 1.68, 95%CI, 1.03-2.74), but a low effect was found in those with lower NT-proBNP level. Subgroup analyses show that ticagrelor increased major bleeding in patients with left ventricular ejection fraction (LVEF) <0.50 (HR 3.29; 95% CI 1.61-6.74) (interaction p=0.03).
We found that ticagrelor, compared with clopidogrel, increased bleeding complications in hospitalized patients with NT-proBNP>1800 ng/L, especially in patients with EF < 0.50.
对于ST段抬高型心肌梗死(STEMI)患者,建议使用特定生物标志物进行危险分层,以制定个性化的P2Y12抑制剂治疗方案。
这项全国性登记和质量改进研究的时间范围是2014年11月1日至2017年6月30日。共有11512例STEMI患者在医院接受了阿司匹林和P2Y12受体抑制剂(氯吡格雷或替格瑞洛)治疗并接受了经皮冠状动脉介入治疗(PCI)。其中,2992例患者使用替格瑞洛,8520例使用氯吡格雷。主要有效性结局是主要不良心血管和脑血管事件(MACCE:心源性死亡、心肌梗死、支架血栓形成、院内缺血性卒中)。主要安全性结局是院内大出血。
替格瑞洛组的MACCE发生率低于氯吡格雷组(0.8%对1.2%;P = 0.046),但在不同NT-proBNP水平下,MACCE的累积风险无统计学意义。替格瑞洛组的出血率高于氯吡格雷组(所有出血:9.9%对6.9%,P < 0.001;大出血:4.0%对2.7%,P < 0.001)。在Kaplan-Meier曲线中可以发现出血的累积风险更高。在多变量分析中,与氯吡格雷相比,NT-proBNP>1800 ng/L的患者使用替格瑞洛会增加出血事件(所有出血:HR 1.46;95%CI,1.07 - 2.01;大出血:HR 1.68,95%CI,1.03 - 2.74),但在NT-proBNP水平较低的患者中影响较小。亚组分析表明,替格瑞洛会增加左心室射血分数(LVEF)<0.50的患者的大出血风险(HR 3.29;95%CI 1.61 - 6.74)(交互作用p = 0.03)。
我们发现,与氯吡格雷相比,替格瑞洛会增加NT-proBNP>1800 ng/L的住院患者的出血并发症,尤其是LVEF < 0.50的患者。