Department of Cardiology, Helsinki University Central Hospital, Finland.
Eur Heart J Acute Cardiovasc Care. 2013 Dec;2(4):371-8. doi: 10.1177/2048872613501985. Epub 2013 Aug 21.
Current guidelines prefer primary percutaneous coronary intervention (pPCI) over fibrinolysis in the treatment of acute ST-elevation myocardial infarction (STEMI). Pre-hospital fibrinolysis followed by early invasive evaluation is an alternative that we have used in patients presenting within three hours of symptom onset. We made a survey of patients suffering an acute STEMI over one year to assess mortality and adverse events following either pPCI or fibrinolysis.
Of the 448 consecutive STEMI patients, 194 were treated with pPCI and 176 underwent fibrinolysis; 78 patients received no reperfusion treatment within 12 hours (NRT group). The median TIMI risk scores were 4.0, 3.0 and 4.0 in the pPCI, fibrinolysis and NRT groups, respectively (p<0.001). Mortality at one year was 14.4% following pPCI, 5.1% following fibrinolysis and 12.8% in the NRT group (p=0.011 across all groups and p=0.003 between pPCI and fibrinolysis, adjusted for differences in risk factors). The one-year composite of cardiovascular death, stroke, reinfarction and new revascularization was 20.1%, 18.2% and 26.9% for the pPCI, fibrinolysis and NRT groups, respectively (p=NS). In patients presenting within three hours of symptom onset, one-year mortality was 3.7% in the fibrinolysis group (n=163) and 15.3% in the pPCI group (n=118) (adjusted p =0.001), while the composite of adverse events was 16.6% in the former group and 19.5% in the latter (p=NS).
Pre-hospital fibrinolysis followed by routine early invasive evaluation provides an excellent reperfusion strategy for low-risk STEMI patients presenting early after symptom onset.
目前的指南更倾向于在急性 ST 段抬高型心肌梗死(STEMI)的治疗中采用经皮冠状动脉介入治疗(pPCI)而非纤溶治疗。在症状发作后 3 小时内,我们采用了一种替代方法,即先进行院前纤溶治疗,然后进行早期有创评估。我们对一年中患有急性 STEMI 的患者进行了一项调查,以评估接受 pPCI 或纤溶治疗后的死亡率和不良事件。
在 448 例连续的 STEMI 患者中,194 例接受了 pPCI 治疗,176 例接受了纤溶治疗;78 例患者在 12 小时内未接受再灌注治疗(NRT 组)。pPCI、纤溶和 NRT 组的中位 TIMI 风险评分分别为 4.0、3.0 和 4.0(p<0.001)。pPCI 组一年死亡率为 14.4%,纤溶组为 5.1%,NRT 组为 12.8%(各组间差异有统计学意义,p=0.011;pPCI 组与纤溶组之间差异有统计学意义,p=0.003,校正了危险因素的差异)。pPCI、纤溶和 NRT 组一年心血管死亡、卒中和再梗死及新血运重建的复合终点发生率分别为 20.1%、18.2%和 26.9%(p=NS)。在症状发作后 3 小时内就诊的患者中,纤溶组一年死亡率为 3.7%(n=163),pPCI 组为 15.3%(n=118)(校正后 p=0.001),而前者的不良事件复合终点发生率为 16.6%,后者为 19.5%(p=NS)。
对于早期症状发作的低危 STEMI 患者,院前纤溶治疗后常规进行早期有创评估提供了一种出色的再灌注策略。