首页> 外文期刊>Circulation. Cardiovascular interventions >Long-Term Effect of Ultrathin-Strut Versus Thin-Strut Drug-Eluting Stents in Patients With Small Vessel Coronary Artery Disease Undergoing Percutaneous Coronary Intervention A Subgroup Analysis of the BIOSCIENCE Randomized Trial
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Long-Term Effect of Ultrathin-Strut Versus Thin-Strut Drug-Eluting Stents in Patients With Small Vessel Coronary Artery Disease Undergoing Percutaneous Coronary Intervention A Subgroup Analysis of the BIOSCIENCE Randomized Trial

机译:超薄 - 支柱与薄管冠状动脉疾病患者对薄管冠状动脉疾病患者的长期影响,经皮冠状动脉介入冠状动脉介入的亚组分析对随机试验

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Background: Randomized trials evaluating the Orsiro biodegradable polymer sirolimus-eluting stent (BP-SES; 60 and 80 mu m strut thickness for stent diameters 3 mm, respectively) did not stratify according to vessel size and failed to specify the impact of ultrathin-strut thickness on long-term clinical outcomes compared with durable polymer everolimus-eluting stents (DP-EES). We sought to assess the long-term effect of ultrathin-strut (60 mu m) BP-SES versus thin-strut (81 mu m) DP-EES on long-term outcomes in patients undergoing percutaneous coronary revascularization for small vessel disease. Methods: In a subgroup analysis of the randomized, multicenter, noninferiority BIOSCIENCE trial, patients with stable coronary artery disease or acute coronary syndrome randomly assigned to treatment with BP-SES or DP-EES were stratified according to vessel size ( 3 mm) as a surrogate to compare patients treated with ultrathin-strut versus thin-strut drug-eluting stent. The primary end point was target lesion failure, a composite of cardiac death, target vessel myocardial infarction, and clinically indicated target lesion revascularization, within 5 years. Results: Among 2109 patients, 1234 (59%) were treated for small vessel disease. At 5 years, target lesion failure occurred in 124 patients (cumulative incidence, 22.3%) treated with ultrathin-strut BP-SES and 109 patients (18.3%) treated with thin-strut DP-EES (rate ratio, 1.22; 95% CI, 0.94-1.58; P=0.13). Cumulative incidences of cardiac death, target vessel myocardial infarction, and clinically indicated target lesion revascularization and definite stent thrombosis at 5 years were similar in patients treated with ultrathin-strut BP-SES and thin-strut DP-EES. After adjustment for potential confounders, there was no significant interaction between vessel size and treatment effect of BP-SES versus DP-EES. Conclusions: We found no significant difference in clinical outcomes throughout 5 years between patients with small vessel disease treated with ultrathin-strut BP-SES versus thin-strut DP-EES.
机译:背景:评估orsiro可生物降解的聚合物Siroverimus洗脱支架的随机试验(BP-SES;分别用于支架直径的60和80μm支柱厚度)没有根据容器尺寸分层并未指定超薄 - 支柱的影响与耐用的聚合物维生铝洗脱支架(DP-EES)相比,长期临床结果的厚度。我们试图评估超薄 - 支柱(60μm)BP-SE与薄壁(81μm)dp-ees对小血管疾病进行经皮冠状动脉血型血管化的长期结果的长期效果。方法:在随机,多中心,非事实体生物科学试验的亚组分析中,根据血管尺寸(3mm),分层与BP-SES或DP-EES随机分配稳定的冠状动脉疾病或急性冠状动脉综合征的患者。替代试剂比较用超薄 - 支柱对薄管溶液洗脱支架进行比较患者。主要终点是目标病变失败,心脏死亡,靶血管心肌梗死和临床指出的目标病变血运重建于5年内。结果:2109例患者中,对小血管疾病进行1234名(59%)。在5年后,用超薄 - 支柱BP-SES处理的124名患者(累积发病率,22.3%)发生靶病变失败,用薄溶液DP-EES处理(率比,1.22; 95%CI)治疗(18.3%) ,0.94-1.58; p = 0.13)。用超薄 - 支柱BP-SES和薄型DP-EES处理的患者,心脏死亡,靶血管心肌梗死和临床表明目标病变血体化和明确支架血栓形成的累积发病率相似。调整潜在混凝剂后,BP-SES对DP-EES的血管尺寸和治疗效果之间没有显着的相互作用。结论:我们发现,用超薄 - 支柱患者与薄管DP-EES处理的小血管疾病患者在患有小血管疾病的患者之间的临床结果差异没有显着差异。

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