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首页> 外文期刊>European heart journal. Acute cardiovascular care >Radial versus femoral access in patients with acute coronary syndrome undergoing invasive management: A prespecified subgroup analysis from VALIDATE-SWEDEHEART
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Radial versus femoral access in patients with acute coronary syndrome undergoing invasive management: A prespecified subgroup analysis from VALIDATE-SWEDEHEART

机译:急性冠状动脉综合征患者接受侵袭性管理的桡动脉患者:验证 - 瑞典语的预先确定的亚组分析

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Aims: In the Bivalirudin versus Heparin in ST-Segment and Non-ST-Segment Elevation Myocardial Infarction in Patients on Modern Antiplatelet Therapy in the Swedish Web System for Enhancement and Development of Evidence-based Care in Heart Disease Evaluated according to Recommended Therapies Registry Trial (VALIDATE-SWEDEHEART), bivalirudin was not superior to unfractionated heparin in patients with acute coronary syndrome undergoing invasive management. We assessed whether the access site had an impact on the primary endpoint of death, myocardial infarction or major bleeding at 180 days and whether it interacted with bivalirudin/unfractionated heparin.Methods and results: A total of 6006 patients with acute coronary syndrome planned for percutaneous coronary intervention were randomised to either bivalirudin or unfractionated heparin. Arterial access was left to the operator discretion. Overall, 90.5% of patients underwent transradial access and 9.5% transfemoral access. Baseline risk was higher in transfemoral access. The unadjusted hazard ratio for the primary outcome was lower with transradial access (hazard ratio 0.53, 95% confidence interval 0.43-0.67, £><0.00l) and remained lower after multivariable adjustment (hazard ratio 0.56, 95% confidence interval 0.52-0.84, p<0.00l). Transradial access was associated,with lower risk of death (hazard ratio 0.41, 95% confidence interval 0.28-0.60, p<0.00) and major bleeding (hazard ratio 0.57, 95% confidence interval 0.44-0.75, £><0.00l). There was no interaction between treatment with bivalirudin and access site for the primary endpoint (p=0.976) or major bleeding (p=0.80).
机译:目的:在瑞典抗血小板治疗中的瑞典抗血小板治疗中的瑞典抗血小板治疗中的肝素和非ST段抬高心肌梗死中的生物素和非ST段抬高肝素。根据推荐的疗法评估,评估了瑞典网络系统的瑞典抗血小板治疗。 (验证 - 瑞典语),双戊突不优于急性冠状动脉综合征患者侵入性管理的患者中未被释放的肝素。我们评估了接入部位是否对死亡,心肌梗死或在180天的重大出血的主要终点产生影响,以及它是否与双戊毛蛋白/联合肝素相互作用。方法和结果:共有6006例急性冠状动脉综合征患者进行经皮冠状动脉干预被随机化为双valirudin或未分叉的肝素。动脉接入留给运营商自行决定。总体而言,90.5%的患者接受了跨越跨行机和9.5%的经纪进入。跨罚款通道的基线风险较高。主要结果的未调整危险比率较低,颅内进入(危险比0.53,95%置信区间0.43-0.67,£> <0.00L),多变量调节后仍然较低(危险比0.56,95%置信区间0.52-0.84 ,p <0.00l)。颅代进入较低的死亡风险较低(危险比0.41,95%置信区间0.28-0.60,P <0.00℃)和重大出血(危险比0.57,95%置信区间0.44-0.75,£> <0.00l) 。对初级终点(P = 0.976)或主要出血的双胞苷儿和接入部位之间没有相互作用(P = 0.976)或重大出血(P = 0.80 )。

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