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Sarpogrelate Based Triple Antiplatelet Therapy Improved Left Ventricular Systolic Function in Acute Myocardial Infarction: Retrospective Study

机译:萨普格雷酯三联抗血小板疗法改善急性心肌梗塞左室收缩功能:回顾性研究

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Purpose The purpose of this study was to assess the potential benefit of a 5-hydroxytryptamine receptor antagonist, sarpogrelate-based triple antiplatelet therapy (TAPT) in comparison with dual antiplatelet therapy (DAPT) in patients undergoing primary percutaneous coronary intervention (PCI) for ST-elevation myocardial infarction (STEMI). Materials and Methods 119 patients of STEMI were retrospectively assessed. All patients received aspirin and clopidogrel per standard of care. Among them, 53 patients received an additional loading dose of sarpogrelate and a maintenance dose for 6 months post-PCI (TAPT group), while others did not (DAPT group). Results The rates of complete ST-segment resolution at 30 minutes post-PCI and post-procedural thrombolysis in myocardial infarction flow were not significantly different between the two groups (52.8% vs. 48.5%, p =0.200; 92.5% vs. 89.4%, p =0.080). In addition, no significant differences were observed between the two groups with regard to 30-day and 12-month clinical outcomes (cardiac death, myocardial infarction, stent thrombosis, target vessel revascularization, and severe bleeding). Meanwhile, improvement in left ventricular (LV) systolic function was observed in the TAPT group [ΔLV ejection fraction (LVEF)=17.1±9.4%, p Conclusion Sarpogrelate-based TAPT improved LV systolic function at 6 months in STEMI patients undergoing primary PCI.
机译:目的本研究的目的是评估在接受经皮冠状动脉介入治疗(PCI)的患者中,5-羟基色胺受体拮抗剂,基于沙格雷酯的三重抗血小板治疗(TAPT)与双重抗血小板治疗(DAPT)的潜在获益高度心肌梗死(STEMI)。材料与方法回顾性分析119例STEMI患者。所有患者均按标准接受阿司匹林和氯吡格雷治疗。其中53例患者在PCI后6个月接受了另一剂量的沙普格雷酯和维持剂量的治疗(TAPT组),而其他患者则没有(DAPT组)。结果两组在PCI后30分钟的ST段完全消退率和心肌梗死过程中溶栓后的两组之间无显着差异(52.8%vs. 48.5%,p = 0.200; 92.5%vs. 89.4%) ,p = 0.080)。此外,在30天和12个月的临床结局(心脏死亡,心肌梗塞,支架血栓形成,靶血管血运重建和严重出血)方面,两组之间没有观察到显着差异。同时,在TAPT组中观察到左心室(LV)收缩功能的改善[ΔLV射血分数(LVEF)= 17.1±9.4%,p]结论基于Sarpogrelate的TAPT在接受原发PCI的STEMI患者中在6个月时改善了LV收缩功能。

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