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首页> 外文期刊>Journal of thrombosis and thrombolysis >A real world data of dabigatran etexilate: multicenter registry of oral anticoagulants in nonvalvular atrial fibrillation
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A real world data of dabigatran etexilate: multicenter registry of oral anticoagulants in nonvalvular atrial fibrillation

机译:达比加群酯的真实世界数据:非瓣膜性心房颤动中口服抗凝剂的多中心注册

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摘要

Atrial fibrillation (AF) is a common cardiac arrhythmia. Dabigatran etixalate (DE) is one of the new oral anticoagulant drugs being used in nonvalvular AF (NVAF). There is no adequate real world data in different populations about DE. The aim of this registry was to evaluate the efficacy and safety of DE Consecutive NVAF patients treated with warfarin or both DE doses were enrolled during 18 months study period. The patients were re-evaluated at regular 6-month intervals during the follow-up period. During the follow-up period outcomes were documented according to RELY methodology A total of 555 patients were analyzed. There was no significant difference in ischemic stroke rates (p = 0.73), death rates (p = 0.15) and MI rates (p = 0.56) between groups. The rate of major bleeding was significantly higher in warfarin and dabigatran 150 mg group than dabigatran 110 mg (p < 0.001). Intracranial bleeding rate and relative risk were significantly lower in dabigatran 110 mg group than warfarin group (p = 0.004). Dyspepsia was significantly higher in both DE doses than warfarin (p = 0.004) Both DE doses are as effective as warfarin in reducing stroke rates in NVAF patients, without increasing MI rates. Intracranial bleeding rates are significantly lower in warfarin than both doses of DE and gastrointestinal bleeding risk increases with increased DE doses.
机译:心房颤动(AF)是常见的心律不齐。达比加群依替沙酸酯(DE)是用于非瓣膜性AF(NVAF)的新型口服抗凝药之一。在不同人群中,没有足够的关于DE的真实世界数据。该注册的目的是评估在18个月研究期间接受华法林治疗的DE连续NVAF患者的疗效和安全性,或同时接受两种DE剂量。在随访期间,每隔6个月定期对患者进行重新评估。在随访期间,根据RELY方法记录结果,共分析了555例患者。两组之间的缺血性卒中发生率(p = 0.73),死亡率(p = 0.15)和MI发生率(p = 0.56)没有显着差异。华法林和达比加群150 mg组的主要出血率显着高于达比加群110 mg(p <0.001)。达比加群110 mg组的颅内出血率和相对风险显着低于华法林组(p = 0.004)。两种DE剂量的消化不良均显着高于华法林(p = 0.004)。两种DE剂量在降低NVAF患者卒中发生率方面均与华法林一样有效,而不会增加MI发生率。华法林的颅内出血率显着低于DE剂量,胃肠道出血风险随DE剂量增加而增加。

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