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Ultrasound enhanced prehospital thrombolysis using microbubbles infusion in patients with acute st elevation myocardial infarction: Pilot of the sonolysis study

机译:超声对急性ST段抬高型心肌梗死患者使用微泡输注进行院前溶栓治疗:声波消融研究的先驱

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摘要

In animal studies, transthoracic ultrasound and microbubbles have shown to dissolve thrombi in ST elevation myocardial infarction (STEMI). To examine this effect in patients, we have initiated the Sonolysis trial. In this pilot study of 10 patients with a first acute STEMI, we investigated the safety and feasibility of this trial. After pretreatment in the ambulance, five patients were randomized to receive microbubbles with three-dimensional (3-D) guided high mechanical index impulses (1.18) for 15 min, whereas the control group received placebo without ultrasound. Subsequently, primary percutaneous coronary intervention (PPCI) was performed, if indicated. All patients successfully underwent study treatment and PPCI. No significant difference between treatment and control group in safety (minor adverse events 2/5 vs. 2/5, p= NS) and outcome (TIMI III flow 3/5 vs. 1/5 respectively, p= 0.23) was recorded. These results demonstrate that the study protocol is feasible in the acute cardiac care setting and safe during treatment and follow-up.
机译:在动物研究中,经胸超声和微泡显示可溶解ST抬高型心肌梗死(STEMI)中的血栓。为了检查对患者的这种作用,我们已经开始进行声波溶解试验。在这项针对10例首发急性STEMI患者的初步研究中,我们调查了该试验的安全性和可行性。在救护车中进行预处理后,五名患者被随机分配接受三维(3-D)引导的高机械指数脉冲(1.18)的微泡,持续15分钟,而对照组则接受了无超声的安慰剂。随后,如果有指示,则进行初次经皮冠状动脉介入治疗(PPCI)。所有患者均成功接受了研究治疗和PPCI。治疗组和对照组在安全性(次要不良事件2/5 vs. 2/5,p = NS)和结局(TIMI III血流分别为3/5 vs. 1/5,p = 0.23)之间没有显着差异。这些结果表明,该研究方案在急性心脏护理环境中是可行的,并且在治疗和随访期间是安全的。

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