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Duration of dual antiplatelet therapy after implantation of the first-generation and second-generation drug-eluting stents

机译:植入第一代和第二代药物洗脱支架后双重抗血小板治疗的持续时间

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OBJECTIVE: This study was carried out to determine the effect of the use of dual antiplatelet therapy (DAPT) for more than 12 months on long-term clinical outcomes in patients who had undergone a percutaneous coronary intervention with the first and second generations of drug-eluting stents (DES). BACKGROUND: The potential benefits of the use of DAPT beyond a 12-month period in patients receiving DES have not been established clearly. Moreover, it is also unclear whether the optimal duration of DAPT is similar for all DES types. METHODS: A total of 2141 patients with coronary artery disease treated exclusively with Cypher sirolimus-eluting stents (SES) or Endeavor zotarolimus-eluting stents (ZES) were considered for retrospective analysis. The primary endpoint [a composite of all-cause mortality, nonfatal myocardial infarction (MI), and stroke] was compared between the 12-month DAPT and the >12-month DAPT group. RESULTS: A total of 1870 event-free patients on DAPT at 12 months were identified. The average follow-up was 28.2±7.4 months. The primary outcomes were similar between the two groups (4.1% 12-month DAPT vs. 1.9% >12-month DAPT; P=0.090). Incidences of death, MI, stroke, and target vessel revascularization did not differ significantly between the two groups. Subgroup analysis showed that in the patients with hypertension, >12-month DAPT significantly reduced the occurrence of death/MI/stroke compared with that in the 12-month DAPT group (P=0.04). In patients implanted with SES, the primary outcome was significantly lower with the >12-month DAPT group (5.2% 12-month DAPT vs. 1.6% >12-month DAPT; P=0.016), whereas in patients with ZES, the primary outcome was comparable between the two groups (2.3% 12-month DAPT vs. 2.0% >12-month DAPT; P=0.99). CONCLUSION: In our study, for all patients, >12-month DAPT in patients who had received DES was not significantly more effective than 12-month DAPT in reducing the rate of death/MI/stroke. Our findings, that patients who received SES benefit from >12-month DAPT whereas extended use of DAPT was not significantly more effective in those implanted with ZES, implied that the optimal duration of DAPT was different depending on different types of DES.
机译:目的:本研究旨在确定在接受第一代和第二代药物治疗的经皮冠状动脉介入治疗的患者中,使用双重抗血小板治疗(DAPT)超过12个月对长期临床结局的影响洗脱支架(DES)。背景:在接受DES的患者中使用DAPT超过12个月的潜在益处尚未明确。此外,还不清楚DAPT的最佳持续时间是否对所有DES类型都相似。方法:回顾性分析了总共2141例仅使用Cypher西罗莫司洗脱支架(SES)或Endeavor佐他莫司洗脱支架(ZES)治疗的冠心病患者。比较了12个月DAPT组和12个月以上DAPT组的主要终点[全因死亡率,非致命性心肌梗塞(MI)和中风的综合]。结果:在12个月时,共鉴定了1870例DAPT无事件患者。平均随访28.2±7.4个月。两组之间的主要结局相似(4.1%的12个月DAPT对比1.9%的12个月DAPT; P = 0.090)。两组之间的死亡,心梗,中风和靶血管血运重建的发生率无显着差异。亚组分析显示,与12个月DAPT组相比,高血压患者中,> 12个月DAPT显着降低了死亡/心梗/中风的发生率(P = 0.04)。在植入SES的患者中,> 12个月的DAPT组的主要结局明显较低(5.2%的12个月的DAPT对1.6%的> 12个月的DAPT; P = 0.016),而在ZES的患者中,主要结局是两组之间的预后相当(2.3%的12个月DAPT对比2.0%的12个月DAPT; P = 0.99)。结论:在我们的研究中,对于所有患者,在接受DES的患者中,> 12个月DAPT在降低死亡率/ MI /中风方面并不比12个月DAPT显着更有效。我们的发现表明,接受SES的患者受益于> 12个月的DAPT,而长期使用DAPT在植入ZES的患者中并没有明显更有效,这表明DAPT的最佳持续时间取决于不同类型的DES。

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