首页> 外文期刊>The American heart journal >Stent thrombosis up to 3 years after stenting for ST-segment elevation myocardial infarction versus for stable angina--comparison of the effects of drug-eluting versus bare-metal stents.
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Stent thrombosis up to 3 years after stenting for ST-segment elevation myocardial infarction versus for stable angina--comparison of the effects of drug-eluting versus bare-metal stents.

机译:ST段抬高型心肌梗死与稳定型心绞痛相比,支架置入后长达3年的支架内血栓形成比较药物洗脱支架与裸金属支架的效果。

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BACKGROUND: The long-term safety of drug-eluting stents (DES) for the treatment of ST-segment elevation myocardial infarction (STEMI) is unclear and may differ from that in stable angina (stable) patients as noted in autopsy studies. METHODS: To assess this problem, 210 consecutive STEMI and 323 stable patients, randomized 2:1 to DES versus bare-metal stents (BMS), were followed up for 3 years for definite/probable stent thrombosis (ST) and cardiac death/myocardial infarction. Events occurring during the initial 6 months were separated from later events. RESULTS: The 3-year rate of ST was 8.1% in STEMI vs 3.4% in stable patients (P = .02), with corresponding rates of 9.4% vs 2.9% (P = .01) for DES and of 5.6% vs 4.3% (P = .71) for BMS patients, respectively. This difference appeared only after 6 months: 4.6% in STEMI vs 1.7% in stable patients (P = .05) and in DES-treated patients (6.2% vs 2.0%, P = .05). Results of ST were paralleled by findings of clinical events, although here differences were less pronounced, but also seen only late after stenting. Thus, in STEMI patients, late events occurred more frequently after DES vs BMS implantation (11.6% vs 3.0%, P = .04), compared to results in stable patients (DES 6.4%, BMS 1.9%, P = .08). CONCLUSIONS: In this pilot study, we observed an increased rate of late ST and a trend to more related clinical events in patients after stenting for STEMI vs for stable angina, particularly if treated with DES. This may explain outcome differences between results of pivotal trials in stable patients vs those of real-world
机译:背景:目前尚不清楚药物洗脱支架(DES)用于治疗ST段抬高型心肌梗塞(STEMI)的长期安全性,并且可能与稳定型心绞痛(稳定)患者的尸检研究中所述的安全性不同。方法:为评估该问题,对210例连续的STEMI患者和323例稳定的患者进行了3年的随访,随访时间为2:1 DES与裸金属支架(BMS)对比,以明确/可能的支架血栓形成(ST)和心源性死亡/心肌病梗塞。在最初的6个月内发生的事件与以后的事件分开。结果:STEMI的3年ST发生率为8.1%,而稳定患者为3.4%(P = .02),DES的3年ST发生率分别为9.4%vs 2.9%(P = .01),而5.6%vs 4.3分别为BMS患者的%(P = .71)。这种差异仅在6个月后才出现:STEMI为4.6%,而稳定患者(P = .05)和DES治疗患者(6.2%vs 2.0%,P = .05)为1.7%。 ST的结果与临床事件的发现相平行,尽管此处差异不那么明显,但也仅在置入支架后才看到。因此,与稳定患者的结果相比,在STEMI患者中,DES和BMS植入后的晚期事件发生频率更高(11.6%vs 3.0%,P = .04),而稳定患者的结果则较稳定患者(DES 6.4%,BMS 1.9%,P = .08)。结论:在这项前瞻性研究中,我们观察到STEMI支架置入术后与稳定型心绞痛相比,尤其是用DES治疗的患者,晚期ST发生率增加,并且发生更多相关临床事件的趋势。这可以解释稳定患者与现实世界中关键性试验结果之间的差异

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