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首页> 外文期刊>Circulation journal >Factors Affecting Platelet Reactivity 2 Hours After P2Y12 Receptor Antagonist Loading in Primary Percutaneous Coronary Intervention for ST-Elevation Myocardial Infarction – Impact of Pain-to-Loading Time –
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Factors Affecting Platelet Reactivity 2 Hours After P2Y12 Receptor Antagonist Loading in Primary Percutaneous Coronary Intervention for ST-Elevation Myocardial Infarction – Impact of Pain-to-Loading Time –

机译:P2Y 12 受体拮抗剂负荷后2小时在ST抬高型心肌梗死的经皮冠状动脉介入治疗中影响血小板反应性的因素–负荷时间对负荷的影响–

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Background: Delay in the onset of antiplatelet action occurs in patients with ST-elevation myocardial infarction (STEMI) and is likely due to disturbed absorption. We hypothesized that patients presenting relatively late after the onset of symptoms would have faster antiplatelet action. Methods?and?Results: We analyzed patient-level data from 5 studies of 207 P2Y12receptor antagonist-na?ve patients with STEMI undergoing primary percutaneous coronary intervention (PCI). All patients had available platelet reactivity (PR) assessment with the VerifyNow assay (in P2Y12reaction units; PRU) prior to and 2 h after loading. High PR (HPR) was defined as ≥208 PRU. Pain-to-antiplatelet loading time independently predicted PR at 2 h after loading: every 1-h increase in pain-to-antiplatelet loading time produced a 7% decrease in PR (P=0.001). Pretreatment PR, body mass index, morphine and novel P2Y12receptor antagonist also affected PR 2 h after loading. Novel P2Y12receptor antagonist use and per hour increase in pain-to-antiplatelet loading time were independently associated with lower probability for HPR with an OR (95% CI) of 0.145 (0.095–0.220) and 0.776 (0.689–0.873), P12receptor antagonist loading, according to patient-level data pooled analysis. ( Circ J 2016; 80: 442–449)
机译:背景:ST抬高型心肌梗死(STEMI)患者的抗血小板作用起效延迟,可能是由于吸收不良所致。我们假设症状出现后相对较晚出现的患者将具有更快的抗血小板作用。方法和结果:我们分析了207例初发STEMI的初次经皮冠状动脉介入治疗(PCI)的P2Y 12 受体拮抗剂初治患者的5项研究的患者水平数据。所有患者在加载前和加载后2小时均通过VerifyNow测定法(以P2Y 12 反应单位; PRU)进行血小板反应性(PR)评估。高PR(HPR)被定义为≥208PRU。疼痛至抗血小板加载时间独立预测加载后2 h的PR:疼痛至抗血小板加载时间每增加1 h,PR降低7%(P = 0.001)。预处理PR,体重指数,吗啡和新型P2Y 12 受体拮抗剂也可在负荷后2小时影响PR。新型P2Y 12 受体拮抗剂的使用以及每小时疼痛至抗血小板负荷时间的增加与HPR的可能性较低相关,OR(95%CI)为0.145(0.095–0.220)和0.776 (0.689–0.873),根据患者水平的数据汇总分析,P12 受体拮抗剂的负载量。 (Circ J 2016; 80:442–449)

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