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Predictors and outcomes of no-reflow phenomenon in patients with acute ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention

机译:急性ST段升高患者急性心肌梗死患者无回流现象的预测和结果

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Aim The aim of this study is to identify the predictors of angiographic no-reflow development in patients who underwent primary percutaneous coronary intervention and to investigate the long-term (median follow-up time=59 months) clinical endpoints. Patients and methods We retrospectively evaluated 3205 patients (824 females, mean age: 58.6 years) with acute myocardial infarction (ST-segment elevation myocardial infarction) admitted within the first 12 h of chest pain and treated with primary percutaneous coronary intervention between January 2006 and January 2010. The patients were divided into angiographic no-reflow [final Thrombolysis In Myocardial Infarction (TIMI) = 2 (OR=1.99, 95% CI: 1.30-3.04, P=0.002), pain-to-balloon time more than 4 h (OR=3.98, 95% CI: 2.50-6.32, P<0.001), baseline TIMI <= 1 flow (OR=2.55, 95% CI: 1.05-6.22, P=0.038), lesion length of at least 15 mm (OR=4.31, 95% CI: 2.89-6.41, P<0.001), reference vessel diameter of at least 3.5 mm (OR=2.83, 95% CI: 1.87-4.27, P<0.001), cutoff occlusion pattern (OR=1.93, 95% CI: 1.03-3.62, P=0.04), and SYNTAX score of at least 19 (OR=1.76, 95% CI: 1.1.23-3.07, P<0.001)] were found as significant predictors for the development of no-reflow phenomenon. In no-reflow patients, in-hospital mortality (10.8 vs. 2.9%), heart failure (32.1 vs. 8.7%), and severe arrhythmias (23.1 vs. 9.3%) were significantly more common (P<0.001), for all. In the long-term follow-up, death (33.3 vs. 13.4%, P<0.001), advanced heart failure (12.5 vs. 5.4%, P<0.001), and stroke (3.5 vs. 1.7%, P=0.035) rates were significantly higher in the no-reflow group. Conclusion The no-reflow predictors that were identified in this study might be useful in the determination of the patients who could benefit from aggressive pharmaco-invasive therapy. Development of no-reflow is associated with both in-hospital and long-term very high morbidity and mortality rates.
机译:目的这项研究的目的是鉴定经过一次经皮冠状动脉干预的患者的血管造影无回流发育的预测因子,并调查长期(中位随访时间= 59个月)临床终点。患者和方法我们回顾性评估了3205名患者(824名女性,平均年龄:58.6岁),急性心肌梗死(ST段抬高心肌梗死)在胸痛的前12小时内接受,并在2006年1月至1月和初步经皮冠状动脉干预治疗2010年1月。患者分为血管造影无回流[心肌梗死的最终溶栓(TIMI)= 2(或= 1.99,95%CI:1.30-3.04,P = 0.002),疼痛到气球时间超过4 h(或= 3.98,95%CI:2.50-6.32,P <0.001),基线TIMI <= 1流量(或= 2.55,95%CI:1.05-6.22,P = 0.038),损伤长度至少为15毫米(或= 4.31,95%CI:2.89-6.41,P <0.001),参考容器直径至少为3.5毫米(或= 2.83,95%CI:1.87-4.27,P <0.001),截止闭塞模式(或= 1.93,95%CI:1.03-3.62,P = 0.04),并且在开发的重要预测因子中发现了至少19(或= 1.76,95%CI:1.1.23-3.07,P <0.001)的语法得分无回流现象。在无回流患者中,住院死亡率(10.8 vs.2.9%),心力衰竭(32.1与8.7%),严重的心律失常(23.1节与9.3%)明显更常见(P <0.001),所有。在长期随访中,死亡(33.3与13.4%,P <0.001),晚期心力衰竭(12.5 vs.5.4%,P <0.001)和中风(3.5 vs.1.7%,P = 0.035) No-Reshow组的速率显着高。结论本研究中鉴定的无回流预测因子可能是可用于测定可以受益于侵略性药物侵袭治疗的患者。无回流的发展与医院内和长期非常高的发病率和死亡率相关。

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