首页> 外文期刊>Journal of thrombosis and haemostasis: JTH >Incidence of chronic kidney disease in patients with atrial fibrillation and its relevance for prescribing new oral antithrombotic drugs.
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Incidence of chronic kidney disease in patients with atrial fibrillation and its relevance for prescribing new oral antithrombotic drugs.

机译:心房颤动患者慢性肾脏疾病的发生率及其与开具新的口服抗血栓药物的相关性。

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摘要

Atrial fibrillation (AF) is one of the major indications for therapy with direct thrombin (dabigatran etexilate) or factor Xa inhibitors (rivaroxaban). Both Dabigatran (80%) and Rivaroxaban (65%) are primarily excreted via the kidney [1]. Therefore, prescribing these drugs in patients with chronic kidney disease (CKD) could lead to accumulation and hence potentially to more bleeding complications [2]. Importantly, patients with an estimated glomerular filtration rate (eGFR) of < 30 mL min~-1 have been excluded from trials with new antithrombotics [2-4]. However, patients with severe CKD are at increased risk of AF due to structural and electrical atrial remodeling [5,6]. Dabigatran has been approved by the Food and Drug Administration in an oral dose of 150 mg twice daily in AF patients with eGFR > 30 mL min~-1 and in a dose of 75 mg twice daily in patients with eGFR 15-30 mL min~-1 [7].
机译:心房颤动(AF)是直接凝血酶(达比加群酯)或Xa因子抑制剂(利伐沙班)治疗的主要适应症之一。达比加群(80%)和利伐沙班(65%)均主要通过肾脏排泄[1]。因此,在患有慢性肾脏病(CKD)的患者中开这些药可能会导致积聚,从而可能导致更多的出血并发症[2]。重要的是,估计肾小球滤过率(eGFR)<30 mL min〜-1的患者已被排除在新抗栓剂的试验之外[2-4]。然而,由于结构和电心房重构,患有严重CKD的患者发生房颤的风险增加[5,6]。食品药品监督管理局已批准达比加群对eGFR> 30 mL min〜-1的AF患者每日两次口服剂量为150 mg,对eGFR 15-30 mL min〜的患者每日两次口服剂量为75 mg -1 [7]。

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