首页> 外文OA文献 >Efficacy and safety of tenecteplase in combination with the low-molecular-weight heparin enoxaparin or unfractionated heparin in the prehospital setting: the Assessment of the Safety and Efficacy of a New Thrombolytic Regimen (ASSENT)-3 PLUS randomized trial in acute myocardial infarction
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Efficacy and safety of tenecteplase in combination with the low-molecular-weight heparin enoxaparin or unfractionated heparin in the prehospital setting: the Assessment of the Safety and Efficacy of a New Thrombolytic Regimen (ASSENT)-3 PLUS randomized trial in acute myocardial infarction

机译:替奈普酶与低分子量肝素依诺肝素或普通肝素联合治疗在院前环境中的疗效和安全性:急性心肌梗死新溶栓剂(ASSENT)-3 PLUS随机试验的安全性和有效性评估

摘要

BACKGROUND: The combination of a single-bolus fibrinolytic and a low-molecular-weight heparin may facilitate prehospital reperfusion and further improve clinical outcome in patients with ST-elevation myocardial infarction. METHODS AND RESULTS: In the prehospital setting, 1639 patients with ST-elevation myocardial infarction were randomly assigned to treatment with tenecteplase and either (1) intravenous bolus of 30 mg enoxaparin (ENOX) followed by 1 mg/kg subcutaneously BID for a maximum of 7 days or (2) weight-adjusted unfractionated heparin (UFH) for 48 hours. The median treatment delay was 115 minutes after symptom onset (53% within 2 hours). ENOX tended to reduce the composite of 30-day mortality or in-hospital reinfarction, or in-hospital refractory ischemia to 14.2% versus 17.4% for UFH (P=0.080), although there was no difference for this composite end point plus in-hospital intracranial hemorrhage or major bleeding (18.3% versus 20.3%, P=0.30). Correspondingly, there were reductions in in-hospital reinfarction (3.5% versus 5.8%, P=0.028) and refractory ischemia (4.4% versus 6.5%, P=0.067) but increases in total stroke (2.9% versus 1.3%, P=0.026) and intracranial hemorrhage (2.20% versus 0.97%, P=0.047). The increase in intracranial hemorrhage was seen in patients >75 years of age. CONCLUSIONS: Prehospital fibrinolysis allows 53% of patients to receive reperfusion treatment within 2 hours after symptom onset. The combination of tenecteplase with ENOX reduces early ischemic events, but lower doses of ENOX need to be tested in elderly patients. At present, therefore, tenecteplase and UFH are recommended as the routine pharmacological reperfusion treatment in the prehospital setting.
机译:背景:单次大剂量纤溶酶和低分子量肝素的组合可促进ST抬高型心肌梗死患者的院前再灌注并进一步改善临床结局。方法和结果:在院前环境中,将1639例ST抬高型心肌梗死患者随机分配到替奈普酶治疗下,或者(1)静脉推注30 mg依诺肝素(ENOX),然后1 mg / kg皮下BID,最大剂量为7天或(2)重量调整后的普通肝素(UFH),持续48小时。中位治疗延迟为症状发作后115分钟(2小时内为53%)。 ENOX倾向于将30天死亡率或院内再梗塞或院内难治性缺血的复合物降低至14.2%,而UFH降低至17.4%(P = 0.080),尽管该复合物终点与入院时无差异。医院颅内出血或大出血(18.3%对20.3%,P = 0.30)。相应地,院内再梗塞减少(3.5%对5.8%,P = 0.028)和难治性缺血(4.4%对6.5%,P = 0.067),但总卒中增加(2.9%对1.3%,P = 0.026) )和颅内出血(2.20%对0.97%,P = 0.047)。大于75岁的患者可见颅内出血的增加。结论:院前纤维蛋白溶解可使53%的患者在症状发作后2小时内接受再灌注治疗。替奈普酶与ENOX的组合可减少早期缺血事件,但老年患者需要测试较低剂量的ENOX。因此,目前推荐将替奈普酶和UFH作为院前环境中的常规药物再灌注治疗。

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