Anticoagulation management in haemodialysis patients with atrial fibrillation: evidence and opinion

被引:36
作者
De Vriese, An S. [1 ]
Heine, Gunnar [2 ]
机构
[1] Univ Ghent, Div Nephrol & Infect Dis, AZ Sint Jan Brugge, Ghent, Belgium
[2] Saarland Univ, Fac Med, Agaplesion Markus Krankenhaus, Homburg, Germany
关键词
antiplatelet agent; atrial fibrillation; bleeding; CHA2DS2-VASc score; direct oral anticoagulant; haemodialysis; left atrial appendage occlusion; low molecular weight heparin; mortality; oral anticoagulation; risk stratification; stroke; vitamin K antagonist; CHRONIC KIDNEY-DISEASE; VITAMIN-K ANTAGONISTS; WARFARIN USE; ORAL ANTICOAGULATION; ISCHEMIC-STROKE; DIALYSIS; RISK; RIVAROXABAN; OUTCOMES; SAFETY;
D O I
10.1093/ndt/gfab060
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
In the absence of robust evidence to guide clinical decision-making, the optimal approach to prevent stroke and systemic embolism in haemodialysis (HD) patients with atrial fibrillation (AF) remains moot. In this position paper, studies on oral anticoagulation (OAC) in HD patients with AF are highlighted, followed by an evidence-based conclusion, a critical analysis to identify sources of bias and practical opinion-based suggestions on how to manage anticoagulation in this specific population. It remains unclear whether AF is a true risk factor for embolic stroke in HD. The currently employed cut-off values for the CHA(2)DS(2)-VASc score do not adequately discriminate dialysis patients deriving a net benefit from those suffering a net harm from OAC. Anticoagulation initiation should probably be more restrictive than currently advocated by official guidelines. Recent evidence reveals that the superior benefit-risk profile of direct oral anticoagulants (DOACs) versus vitamin K antagonists (VKAs) observed in the general population and in moderate chronic kidney disease can be extended to the HD population. VKA may be especially harmful in dialysis patients and should therefore be avoided, in particular in patients with a high bleeding risk and labile international normalized ratio. Dose-finding studies of DOACs suggest that rivaroxaban 10 mg daily and apixaban 2.5 mg twice daily are appropriate choices in dialysis patients. Combined treatment with oral anticoagulants and antiplatelet agents should be reserved for strong indications and limited in time. Left atrial appendage occlusion is a potential attractive solution to reduce the risk of stroke without increasing bleeding propensity, but it has not been properly studied in dialysis patients.
引用
收藏
页码:2072 / 2079
页数:8
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