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Review
. 2018 Nov;38(6):618-628.
doi: 10.1016/j.semnephrol.2018.08.006.

Oral Anticoagulation in Patients With End-Stage Kidney Disease on Dialysis and Atrial Fibrillation

Affiliations
Review

Oral Anticoagulation in Patients With End-Stage Kidney Disease on Dialysis and Atrial Fibrillation

Austin Hu et al. Semin Nephrol. 2018 Nov.

Abstract

Patients with end-stage kidney disease (ESKD) have an elevated incidence of atrial fibrillation (AF) and are at increased risk for thromboembolic events. However, these patients are also at increased risk for bleeding and it is unclear whether they benefit from an oral anticoagulant. Point prevalent on July 1, 2015, only ~28% of dialysis patients with AF were on oral anticoagulation. Warfarin was the most commonly used oral anticoagulant, followed by apixaban, while dabigatran and rivaroxaban were rarely used. This article reviews the current evidence regarding each oral anticoagulant especially as they relate to patients with ESKD.

Keywords: Hemodialysis; arrhythmia; drug safety; outcomes; peritoneal dialysis.

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Figures

Figure 1:
Figure 1:. The inter-relationship between chronic kidney disease and atrial fibrillation risk factors.
Note: This figure depicts the inter-relationship between CKD and AF. Both diseases share multiple risk factors, disease states, and pathological processes that can predispose or cause both CKD and AF. Patients with CKD also tend to be more exposed to the health care system, which increases the chances of diagnosing paroxysmal AF and vice-versa.
Figure 2:
Figure 2:. Period prevalence of any oral anticoagulant, or specific agents, between July and December 2015, among patients with ESKD on dialysis, by dialysis modality.
HD – hemodialysis; PD – peritoneal dialysis
Figure 3:
Figure 3:. Patterns of new initiation of individual oral anticoagulants in patients with ESKD on dialysis, July to December 2015.
Note: All point prevalent patients on dialysis on July 1 2015 in the USRDS previously diagnosed with atrial fibrillation. Anticoagulation use was assessed between July and December 2015, with new use ascertained by absence of a filled prescription for the same anticoagulant in the previous 6 month period. All patients had Medicare A, B, and D coverage.

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