Cardiocenter, Third Faculty of Medicine, Charles University, Prague, Czech Republic.
Int J Cardiol. 2013 Oct 9;168(4):3522-6. doi: 10.1016/j.ijcard.2013.04.209. Epub 2013 May 22.
Outcome data are limited in patients with ST-segment elevation acute myocardial infarction (STEMI) or other acute coronary syndromes (ACSs) who receive a drug-eluting stent (DES). Data suggest that first generation DES is associated with an increased risk of stent thrombosis when used in STEMI. Whether this observation persists with newer generation DES is unknown. The study objective was to analyze the two-year safety and effectiveness of Resolute™ zotarolimus-eluting stents (R-ZESs) implanted for STEMI, ACS without ST segment elevation (non-STEACS), and stable angina (SA).
Data from the Resolute program (Resolute All Comers and Resolute International) were pooled and patients with R-ZES implantation were categorized by indication: STEMI (n=335), non-STEACS (n=1416), and SA (n=1260).
Mean age was 59.8±11.3 years (STEMI), 63.8±11.6 (non-STEACS), and 64.9±10.1 (SA). Fewer STEMI patients had diabetes (19.1% vs. 28.5% vs. 29.2%; P<0.001), prior MI (11.3% vs. 27.2% vs. 29.4%; P<0.001), or previous revascularization (11.3% vs. 27.9% vs. 37.6%; P<0.001). Two-year definite/probable stent thrombosis occurred in 2.4% (STEMI), 1.2% (non-STEACS) and 1.1% (SA) of patients with late/very late stent thrombosis (days 31-720) rates of 0.6% (STEMI and non-STEACS) and 0.4% (SA) (P=NS). The two-year mortality rate was 2.1% (STEMI), 4.8% (non-STEACS) and 3.7% (SA) (P=NS). Death or target vessel re-infarction occurred in 3.9% (STEMI), 8.7% (non-STEACS) and 7.3% (SA) (P=0.012).
R-ZES in STEMI and in other clinical presentations is effective and safe. Long term outcomes are favorable with an extremely rare incidence of late and very late stent thrombosis following R-ZES implantation across indications.
在接受药物洗脱支架(DES)治疗的 ST 段抬高型急性心肌梗死(STEMI)或其他急性冠脉综合征(ACS)患者中,结局数据有限。数据表明,第一代 DES 在用于 STEMI 时与支架血栓形成的风险增加相关。在使用新一代 DES 时,这种观察结果是否仍然存在尚不清楚。本研究的目的是分析 Resolute™佐他莫司洗脱支架(R-ZES)用于 STEMI、非 ST 段抬高型 ACS(non-STEACS)和稳定型心绞痛(SA)的两年安全性和有效性。
汇总 Resolute 计划(Resolute All Comers 和 Resolute International)的数据,并根据适应证将接受 R-ZES 植入的患者进行分类:STEMI(n=335)、非 ST 段抬高型 ACS(n=1416)和稳定型心绞痛(n=1260)。
平均年龄为 59.8±11.3 岁(STEMI)、63.8±11.6 岁(非 ST 段抬高型 ACS)和 64.9±10.1 岁(SA)。STEMI 患者中糖尿病(19.1% vs. 28.5% vs. 29.2%;P<0.001)、既往心肌梗死(11.3% vs. 27.2% vs. 29.4%;P<0.001)或既往血运重建(11.3% vs. 27.9% vs. 37.6%;P<0.001)的比例较低。两年内明确/可能的支架血栓形成发生率分别为 2.4%(STEMI)、1.2%(非 ST 段抬高型 ACS)和 1.1%(SA),晚期/极晚期支架血栓形成(31-720 天)发生率分别为 0.6%(STEMI 和非 ST 段抬高型 ACS)和 0.4%(SA)(P=NS)。两年死亡率分别为 2.1%(STEMI)、4.8%(非 ST 段抬高型 ACS)和 3.7%(SA)(P=NS)。死亡或靶血管再梗死发生率分别为 3.9%(STEMI)、8.7%(非 ST 段抬高型 ACS)和 7.3%(SA)(P=0.012)。
R-ZES 在 STEMI 和其他临床表现中是有效和安全的。在不同适应证中,R-ZES 植入后晚期和极晚期支架血栓形成的发生率极低,长期结局良好。