替格瑞洛负荷治疗st段抬高型心肌梗死:与前驱心绞痛对梗死面积和临床事件的相互作用

IF 2.5 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
João Pedro Faria, Pedro Oliveira, André Alexandre, David Sá Couto, Ricardo Costa, Andreia Campinas, André Frias, Bruno Brochado, Raquel Santos, João Silveira, Severo Torres, André Luz
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引用次数: 0

摘要

在st段抬高型心肌梗死(STEMI)患者中,替格瑞洛可能通过发挥更有效的抗血小板作用或促进潜在的调节刺激来减小梗死面积。梗死前心绞痛(PIA)是一种有效的预处理刺激,可减轻缺血再灌注损伤。由于对替格瑞洛负荷的stemi患者PIA的相互作用知之甚少,我们试图确定与氯吡格雷相比,替格瑞洛负荷的患者是否有改善的临床结果,并研究PIA是否受到PIA的调节。方法:2008年1月至2018年12月,1272例STEMI患者接受了经皮冠状动脉介入治疗,并接受氯吡格雷或替格瑞洛治疗,其中826例进行倾向评分匹配分析。通过峰值肌酸激酶(CK)和肌钙蛋白T (TnT)估计梗死面积,并通过1年随访累积主要心脑血管事件(MACCE)评估临床影响。分析匹配的患者及其与PIA的相互作用。结果:与PIA无关,替格瑞洛患者CK峰值[1405.50 U/L (730.25-2491.00), P < 0.001]和TnT峰值[3.58 ng/mL (1.73-6.59), P < 0.001)]较低。PIA的存在与较低的CK相关(P = 0.030),而与TnT无关(P = 0.097)。替格瑞洛负荷与PIA无交互作用(TnT为P = .788, CK为P = .555)。负荷氯吡格雷和替格瑞洛的MACCE发生率无差异(P = 0.129)。无论PIA如何,氯吡格雷和替格瑞洛的累积生存期也相似(P = .103)。结论:替格瑞洛可独立降低梗死面积,与PIA无协同作用。尽管减少了梗死面积,但两组的临床结果相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ticagrelor Loading on ST-Elevation Myocardial Infarction: Interaction With Prodromal Angina on Infarct Size and Clinical Events.

Introduction: Ticagrelor might reduce infarct size by exerting a more potent antiplatelet effect or by promoting a potential conditioning stimulus in ST-elevation myocardial infarction (STEMI) patients. Pre-infarction angina (PIA) is an effective preconditioning stimulus that reduces ischemia-reperfusion injury. Because little is known on the interaction of PIA in STEMI-patients loaded with ticagrelor, we sought to determine if patients loaded with ticagrelor had improved clinical outcomes as compared to clopidogrel and to study if it is modulated by the presence of PIA.

Methods: From 1272 STEMI patients submitted to primary percutaneous coronary intervention and treated with clopidogrel or ticagrelor from January 2008 to December 2018, 826 were analyzed after propensity score matching. Infarct size was estimated using peak creatine kinase (CK) and troponin T (TnT), and clinical impact was evaluated through cumulative major cardiac and cerebrovascular events (MACCE) at 1-year follow-up. Matched patients and their interaction with PIA were analyzed.

Results: Patients loaded with ticagrelor had lower peak CK [1405.50 U/L (730.25-2491.00), P < .001] and TnT [3.58 ng/mL (1.73-6.59), P < .001)], regardless of PIA. The presence of PIA was associated with lower CK (P = .030), but not TnT (P = .097). There was no interaction between ticagrelor loading and PIA (P = .788 for TnT and P = .555 for CK). There was no difference in MACCE incidence between clopidogrel or ticagrelor loading (P = .129). Cumulative survival was also similar between clopidogrel or ticagrelor, regardless of PIA (P = .103).

Conclusion: Ticagrelor reduced infarct sizes independently and without a synergic effect with PIA. Despite reducing infarct size, clinical outcomes were similar across both groups.

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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
33
审稿时长
6-12 weeks
期刊介绍: Journal of Cardiovascular Pharmacology and Therapeutics (JCPT) is a peer-reviewed journal that publishes original basic human studies, animal studies, and bench research with potential clinical application to cardiovascular pharmacology and therapeutics. Experimental studies focus on translational research. This journal is a member of the Committee on Publication Ethics (COPE).
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