首页> 外文期刊>International Journal of Cardiology >Long-term outcomes of patients receiving zotarolimus-eluting stents in ST elevation myocardial infarction, non-ST elevation acute coronary syndrome, and stable angina: Data from the Resolute program
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Long-term outcomes of patients receiving zotarolimus-eluting stents in ST elevation myocardial infarction, non-ST elevation acute coronary syndrome, and stable angina: Data from the Resolute program

机译:在ST抬高型心肌梗死,非ST抬高型急性冠状动脉综合征和稳定型心绞痛中接受佐他莫司洗脱支架的患者的长期预后:Resolute程序的数据

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Background 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). Methods 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). Results 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). Conclusion 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.
机译:背景ST段抬高的急性心肌梗塞(STEMI)或其他接受药物洗脱支架(DES)的急性冠状动脉综合征(ACS)的患者的结果数据有限。数据表明,当用于STEMI时,第一代DES与支架血栓形成的风险增加相关。这种观察是否与新一代DES一起持续存在尚不清楚。研究目的是分析Resolute?的两年安全性和有效性。佐他莫司洗脱支架(R-ZESs)植入用于STEMI,无ST段抬高的ACS(non-STEACS)和稳定型心绞痛(SA)。方法汇总来自Resolute计划(Resolute All Comers和Resolute International)的数据,并对R-ZES植入患者按以下适应症进行分类:STEMI(n = 335),非STEACS(n = 1416)和SA(n = 1260) )。结果平均年龄为59.8±11.3岁(STEMI),63.8±11.6(非STEACS)和64.9±10.1(SA)。较少的STEMI患者患有糖尿病(19.1%vs.28.5%vs.29.2%; P <0.001),MI前(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)。晚期/非常晚期支架血栓形成(第31-720天)的发生率为0.6%(STEMI)的患者中,两年期明确/可能的支架血栓形成发生率为2.4%(STEMI),1.2%(非STEACS)和1.1%(SA)和非STEACS)和0.4%(SA)(P = NS)。两年死亡率为2.1%(STEMI),4.8%(非STEACS)和3.7%(SA)(P = NS)。死亡或目标血管再梗死发生率为3.9%(STEMI),8.7%(非STEACS)和7.3%(SA)(P = 0.012)。结论STEMI和其他临床表现中的R-ZES是安全有效的。 R-ZES植入适应症后,长期预后良好,晚期和晚期支架血栓形成的发生率极少发生。

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