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首页> 外文期刊>European heart journal. Acute cardiovascular care >Duration of eptifibatide infusion after percutaneous coronary intervention and outcomes among high-risk patients with non-ST-segment elevation acute coronary syndrome: insights from EARLY ACS
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Duration of eptifibatide infusion after percutaneous coronary intervention and outcomes among high-risk patients with non-ST-segment elevation acute coronary syndrome: insights from EARLY ACS

机译:非ST段抬高的急性冠脉综合征高危患者经皮冠状动脉介入治疗后依替巴肽的输注持续时间和结果:来自EARLY ACS的见解

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Background and Objectives: Eptifibatide is indicated during percutaneous coronary intervention (PCI) with continuation for 18-24 hours post procedure but is associated with bleeding. We examined the efficacy and safety of shorter post-PCI eptifibatide infusions in high-risk non-ST-segment elevation acute coronary syndrome (NSTE ACS) patients. Methods: EARLY ACS patients treated with PCI and eptifibatide were grouped by post-procedure infusion duration: <10, 10-13, 13-17, and 17-25 (per protocol) hours. Adjusted estimated event rates for 96-hour death/myocardial infarction (Ml)/recurrent ischaemia requiring urgent revascularization (RIUR), 30-day death/Ml, post-PCI packed red blood cell (PRBC) transfusion, and GUSTO (Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries) moderate/severe bleeding were obtained using inverse-propensity weighting to account for informative censoring of infusions. Results: Among 3271 eptifibatide-treated PCI patients, there were 66 96-hour death/MI/RlUR events, 94 30-day death/ Ml events, 127 PRBC transfusions, and 115 GUSTO moderate/severe bleeds. Compared with per protocol, patients receiving post-PCI infusions < 10 hours had similar adjusted estimated rates of 96-hour death/MI/RlUR (absolute difference 0.021 higher; 0.040 vs. 0.019, 95% Cl -0.023 to 0.064; p=035) and 30-day death/Ml (0.020 higher; 0.046 vs. 0.026, 95% Cl -0.021 to 0.062; p=0.34). There were also no differences in ischaemic outcomes between infusions of 10-17 hours and per-protocol infusions. Adjusted estimated rates of PRBC transfusion were higher for the < 10-hour infusion group compared with per protocol (0.048 higher; 0.079 vs. 0.03, 95% Cl 0.005 to 0.09, p=0.03) but were similar for other groups. Adjusted GUSTO moderate/severe bleeding rates were similar to per-protocol rates for all groups. Conclusions: In high-risk NSTE ACS patients, post-PCI eptifibatide infusions
机译:背景与目的:依替非巴肽在经皮冠状动脉介入治疗(PCI)期间使用,术后持续18-24小时,但与出血有关。我们研究了在高危非ST段抬高的急性冠状动脉综合征(NSTE ACS)患者中较短的PCI后埃替非巴肽输注的有效性和安全性。方法:按PCI方案和依替巴肽治疗的早期ACS患者按手术后输注时间:<10、10-13、13-17和17-25(按方案)小时分组。调整后的估计事件发生率,用于96小时死亡/心肌梗塞(Ml)/需要缺血性血运重建(RIUR)的反复缺血,30天死亡/ Ml,PCI后包装的红细胞(PRBC)输血和GUSTO(全球使用率)使用倾向加权法对输注进行有益的检查,获得中度/重度出血的链激酶和组织阻塞性冠状动脉的纤溶酶原激活剂。结果:在3271例接受艾替非巴肽治疗的PCI患者中,有66例96小时死亡/ MI / RlUR事件,94例30天死亡/ MI事件,127例PRBC输血和115例GUSTO中度/重度出血。与每个方案相比,接受PCI后输注<10小时的患者的96小时死亡/ MI / RlUR调整后估计比率相似(绝对差异高0.021; 0.040对0.019,95%Cl -0.023至0.064; p = 035) )和30天死亡率/毫升(0.020较高; 0.046对0.026; 95%Cl -0.021至0.062; p = 0.34)。输注10-17小时与按方案输注之间的缺血结局也没有差异。与10小时输注组相比,调整后的PRBC输注估计速率高于每个方案(0.048较高; 0.079对0.03,95%Cl 0.005至0.09,p = 0.03),但其他组相似。调整后的GUSTO中度/重度出血率与所有组的按方案发生率相似。结论:在高危NSTE ACS患者中,PCI后ipifibatide输注

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