首页> 外文期刊>Circulation: An Official Journal of the American Heart Association >Risk of bleeding with 2 doses of dabigatran compared with warfarin in older and younger patients with atrial fibrillation: an analysis of the randomized evaluation of long-term anticoagulant therapy (RE-LY) trial.
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Risk of bleeding with 2 doses of dabigatran compared with warfarin in older and younger patients with atrial fibrillation: an analysis of the randomized evaluation of long-term anticoagulant therapy (RE-LY) trial.

机译:与华法林相比,在房颤的老年患者和年轻患者中,与华法林相比,服用2剂量达比加群有出血的风险:长期抗凝治疗(RE-LY)试验的随机评估分析。

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BACKGROUND: Dabigatran 150 and 110 mg twice a day and warfarin are effective for stroke prevention in atrial fibrillation. The purpose of this study was to compare their risks of bleeding in the Randomized Evaluation of Long-Term Anticoagulant Therapy (RE-LY) trial. METHODS AND RESULTS: The RE-LY trial randomized 18 113 patients to receive dabigatran 110 or 150 mg twice a day or warfarin dose adjusted to an international normalized ratio of 2.0 to 3.0 for a median follow-up of 2.0 years. Compared with warfarin, dabigatran 110 mg twice a day was associated with a lower risk of major bleeding (2.87% versus 3.57%; P=0.002), whereas dabigatran 150 mg twice a day was associated with a similar risk of major bleeding (3.31% versus 3.57%; P=0.32). There was a significant treatment-by-age interaction, such that dabigatran 110 mg twice a day compared with warfarin was associated with a lower risk of major bleeding in patients aged <75 years (1.89% versus 3.04%; P<0.001) and a similar risk in those aged >/=75 years (4.43% versus 4.37%; P=0.89; P for interaction <0.001), whereas dabigatran 150 mg twice a day compared with warfarin was associated with a lower risk of major bleeding in those aged <75 years (2.12% versus 3.04%; P<0.001) and a trend toward higher risk of major bleeding in those aged >/=75 years (5.10% versus 4.37%; P=0.07; P for interaction <0.001). The interaction with age was evident for extracranial bleeding, but not for intracranial bleeding, with the risk of the latter being consistently reduced with dabigatran compared with warfarin irrespective of age. CONCLUSIONS: In patients with atrial fibrillation at risk for stroke, both doses of dabigatran compared with warfarin have lower risks of both intracranial and extracranial bleeding in patients aged <75 years. In those aged >/=75 years, intracranial bleeding risk is lower but extracranial bleeding risk is similar or higher with both doses of dabigatran compared with warfarin. CLINICAL TRIAL REGISTRATION: http://www.clinicaltrials.gov. Unique identifier: NCT00262600.
机译:背景:达比加群每天150和110 mg两次,华法林对房颤的中风预防有效。这项研究的目的是在长期抗凝治疗(RE-LY)试验的随机评估中比较他们的出血风险。方法和结果:RE-LY试验将18113例患者随机分为两组,每天接受两次达比加群110或150 mg或华法林剂量调整为国际标准化比2.0至3.0,中位随访时间为2.0年。与华法林相比,每天两次110毫克的达比加群发生大出血的风险较低(2.87%对3.57%; P = 0.002),而每天两次150毫克的达比加群发生类似的大出血风险(3.31%对比3.57%; P = 0.32)。年龄之间存在显着的相互作用,因此达比加群110 mg每天两次与华法林相比,在75岁以下患者中发生大出血的风险较低(1.89%对3.04%; P <0.001),并且> / = 75岁的人群具有相似的风险(4.43%比4.37%; P = 0.89; P相互作用<0.001),而达比加群150 mg每天两次与华法林相比,与那些年龄较大的人群发生大出血的风险较低<75岁(2.12%对3.04%; P <0.001),并且在> / = 75岁年龄组中有更大的大出血风险趋势(5.10%对4.37%; P = 0.07;交互作用P <0.001)。与年龄的相互作用对于颅外出血很明显,但对于颅内出血却没有,因为与华法林相比,无论年龄大小,达比加群均可以持续降低颅内出血的风险。结论:在发生卒中风险的心房颤动患者中,达比加群和华法林相比,两种剂量的75岁以下患者发生颅内和颅外出血的风险均较低。在年龄≥75岁的人群中,两种剂量的达比加群与华法林相比,颅内出血的风险较低,但颅外出血的风险相似或较高。临床试验注册:http://www.clinicaltrials.gov。唯一标识符:NCT00262600。

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