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首页> 外文期刊>Annals of Internal Medicine >Risks for stroke, bleeding, and death in patients with atrial fibrillation receiving dabigatran or warfarin in relation to the CHADS2 score: a subgroup analysis of the RE-LY trial.
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Risks for stroke, bleeding, and death in patients with atrial fibrillation receiving dabigatran or warfarin in relation to the CHADS2 score: a subgroup analysis of the RE-LY trial.

机译:接受达比加群或华法林治疗的房颤患者卒中,出血和死亡的风险与CHADS2得分相关:RE-LY试验的亚组分析。

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BACKGROUND: CHADS(2) is a simple, validated risk score for predicting the risk for stroke in patients with atrial fibrillation not treated with anticoagulants. There are sparse data on the risk for thrombotic and bleeding complications according to the CHADS(2) score in patients receiving anticoagulant therapy. OBJECTIVE: To evaluate the prognostic importance of CHADS(2) risk score in patients with atrial fibrillation receiving oral anticoagulants, including the vitamin K antagonist warfarin and the direct thrombin inhibitor dabigatran. DESIGN: Subgroup analysis of a randomized, controlled trial. (ClinicalTrials.gov registration number: NCT00262600) SETTING: Multinational study setting. PATIENTS: 18 112 patients with atrial fibrillation who were receiving oral anticoagulants. MEASUREMENTS: Baseline CHADS(2) score, which assigns 1 point each for congestive heart failure, hypertension, age 75 years or older, and diabetes mellitus and 2 points for stroke. RESULTS: Distribution of CHADS(2) scores were as follows: 0 to 1-5775 patients; 2-6455 patients; and 3 to 6-5882 patients. Annual rates of the primary outcome of stroke or systemic embolism among all participants were 0.93% in patients with a CHADS(2) score of 0 to 1, 1.22% in those with a score of 2, and 2.24% in those with a score of 3 to 6. Annual rates of other outcomes among all participants with CHADS(2) scores of 0 to 1, 2, and 3 to 6, respectively, were the following: major bleeding, 2.26%, 3.11%, and 4.42%; intracranial bleeding, 0.31%, 0.40%, and 0.61%; and vascular mortality, 1.35%, 2.39%, and 3.68% (P < 0.001 for all comparisons). Rates of stroke or systemic embolism, major and intracranial bleeding, and vascular and total mortality each increased in the warfarin and dabigatran groups as CHADS(2) score increased. The rates of stroke or systemic embolism with dabigatran, 150 mg twice daily, and of intracranial bleeding with dabigatran, 150 mg or 110 mg twice daily, were lower than those with warfarin; there was no significant heterogeneity in subgroups defined by CHADS(2) scores. LIMITATION: These analyses were not prespecified and should be deemed exploratory. CONCLUSION: Higher CHADS(2) scores were associated with increased risks for stroke or systemic embolism, bleeding, and death in patients with atrial fibrillation receiving oral anticoagulants. Primary Funding Source: Boehringer Ingelheim.
机译:背景:CHADS(2)是一个简单且经过验证的风险评分,用于预测未经抗凝剂治疗的房颤患者中风的风险。根据CHADS(2)评分,接受抗凝治疗的患者中血栓形成和出血并发症风险的稀疏数据。目的:评估CHADS(2)风险评分在房颤患者中接受口服抗凝剂(包括维生素K拮抗剂华法林和直接凝血酶抑制剂达比加群)的预后重要性。设计:一项随机对照试验的亚组分析。 (ClinicalTrials.gov注册号:NCT00262600)设置:跨国学习设置。患者:18 112例房颤患者正在接受口服抗凝剂治疗。测量:基线CHADS(2)得分,该得分为充血性心力衰竭,高血压,年龄75岁或以上,糖尿病和中风各得1分。结果:CHADS(2)得分分布如下:0至1-5775例患者; 2-6455位患者; 3至6-5882名患者。在CHADS(2)评分为0到1的患者中,所有参与者中风或全身性栓塞的主要结局的年发生率为0.93%,在2分的患者中为1.22%,在2分的患者中为2.24% 3至6。CHADS(2)得分分别为0、1、2和3至6的所有参与者的其他结局的年发生率分别为:大出血,2.26%,3.11%和4.42%;颅内出血0.31%,0.40%和0.61%;血管死亡率分别为1.35%,2.39%和3.68%(所有比较的P <0.001)。随着CHADS(2)评分的增加,华法林和达比加群组的卒中或全身性栓塞,大出血和颅内出血以及血管和总死亡率均增加。每日两次两次达比加群150 mg的中风或全身性栓塞发生率,每天两次达150毫克或110 mg达比加群的颅内出血率均低于华法林。 CHADS(2)评分定义的亚组中没有明显的异质性。限制:这些分析未预先指定,应视为探索性的。结论:较高的CHADS(2)分数与接受口服抗凝剂的房颤患者发生中风或全身性栓塞,出血和死亡的风险增加相关。主要资金来源:勃林格殷格翰。

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