Vos Nicola S, Amoroso Giovanni, Vink Maarten A, Maarse Moniek, Adams Rob, Herrman Jean-Pau R, Patterson Mark S, van der Schaaf Renè J, Slagboom Ton, de Winter Robbert J
Department of Interventional Cardiology, OLVG Hospital, Oosterpark 9, 1091 AC, Amsterdam, The Netherlands.
J Invasive Cardiol. 2018 Dec;30(12):431-436. Epub 2018 Oct 15.
Pretreatment with P2Y12 inhibitors before primary percutaneous coronary intervention (PPCI) can reduce the incidence of major adverse cardiovascular event (MACE) rate in ST-segment elevation myocardial infarction (STEMI) patients. We investigated differences in coronary reperfusion and clinical outcomes between prehospital administration of prasugrel vs ticagrelor in a historical cohort analysis.
We conducted a retrospective analysis of prospectively collected data of 533 STEMI patients, directly referred by the ambulance for PPCI, and pretreated with either prasugrel (2013-2014) or ticagrelor (2015-2016). The primary outcome measurement was coronary and myocardial reperfusion prior to and after intervention. Secondary outcome measurements included MACE and stent thrombosis (ST) at 30 days. The median time from first medical contact to balloon was 82 minutes. There was no significant difference in preprocedural and postprocedural coronary reperfusion (TIMI flow grade 3) and postprocedural ST-segment elevation resolution between the prasugrel and ticagrelor groups. No significant differences in MACE and ST rates were found between the groups. No fatal or intracranial bleedings were reported up to 30-day follow-up.
Prehospital administration of both prasugrel and ticagrelor in STEMI patients is safe, without differences in preprocedural and postprocedural reperfusion and short-term clinical outcomes.
在直接经皮冠状动脉介入治疗(PPCI)前使用P2Y12抑制剂预处理,可降低ST段抬高型心肌梗死(STEMI)患者主要不良心血管事件(MACE)发生率。我们在一项历史性队列分析中研究了院前给予普拉格雷与替格瑞洛在冠状动脉再灌注和临床结局方面的差异。
我们对533例STEMI患者前瞻性收集的数据进行了回顾性分析,这些患者由救护车直接转诊接受PPCI,并分别在2013 - 2014年或2015 - 2016年接受了普拉格雷或替格瑞洛预处理。主要结局指标是干预前后的冠状动脉和心肌再灌注情况。次要结局指标包括30天时的MACE和支架血栓形成(ST)。从首次医疗接触到球囊扩张的中位时间为82分钟。普拉格雷组和替格瑞洛组在术前和术后冠状动脉再灌注(TIMI血流3级)以及术后ST段抬高缓解方面无显著差异。两组在MACE和ST发生率方面未发现显著差异。在30天随访期内未报告致命或颅内出血事件。
STEMI患者院前给予普拉格雷和替格瑞洛均安全,在术前和术后再灌注及短期临床结局方面无差异。