Ten tips to manage oral anticoagulation in hemodialysis patients with atrial fibrillation
- PMID: 39439440
- PMCID: PMC11495411
- DOI: 10.1093/ckj/sfae270
Ten tips to manage oral anticoagulation in hemodialysis patients with atrial fibrillation
Abstract
Patients with chronic kidney disease (CKD) have a high incidence and prevalence of atrial fibrillation (AF). While general treatment strategies for AF may largely be transferred to patients with mild to moderate CKD, patients with advanced CKD-particularly hemodialysis (HD) patients-with AF pose substantial therapeutical challenges to cardiologists and nephrologists. The arguably greatest dilemma is the very limited evidence on appropriate strategies for prevention of stroke and systemic embolism in HD patients with AF, since the risk for both thromboembolic events without oral anticoagulation and severe bleeding events with oral anticoagulation are substantially increased in advanced CKD, compared with the general population. Thus, the benefit to risk ratio of either vitamin K antagonists or direct oral anticoagulants is less evident in HD than in non-CKD patients with AF. As a multidisciplinary panel of clinicians, we here propose 10 tips that may help our colleagues to navigate between the risk of undertreatment-exposing CKD patients with AF to a high stroke risk-and overtreatment-exposing the very same patients to a prohibitively high bleeding risk. These tips include ideas on alternative risk stratification strategies and novel treatment approaches that are currently in clinical studies-such as factor XI inhibitors or left atrial appendage closure-and may become game-changers for HD patients with AF.
Keywords: FXI inhibition; atrial fibrillation; hemodialysis; oral anticoagulation; risk stratification.
© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.
Conflict of interest statement
G.H.H. and A.D.V. have no conflicts of interests related to this publication. C.S. has received honoraria as speaker from AstraZeneca and support for meeting and traveling from Boehringer Ingelheim. R.B. has received honoraria from Bayer, Bristol Meyers Squibb, LEO-Pharma and Pfizer. I.E. has received grants from ABBOTT, consulting fees from Daiichi-Sanyko and Boehringer Ingelheim, speaker honoraria from ABBOTT, Boston Scientific, Bayer, Bristo-Myers Squibb, Daiichi-Sankyo and Boehringer-Ingelheim, and received support for traveling and meetings from ABBOTT, Boston Scientific, Bayer, Bristo-Myers Squibb, Daiichi-Sankyo and Boehringer-Ingelheim. B.N. has received fees for advisory boards, scientific presentations, continuing education, steering committee roles and travel from AstraZeneca, Alexion, Bayer, Boehringer Ingelheim, Cambridge Healthcare, Cornerstone Medical Education, the Limbic, Medscape, Novo Nordisk and Travere Pharmaceuticals, with all honoraria paid to his institution. C.T.R. has received research grants through institution from Athos, AstraZeneca, Daiichi Sankyo, Janssen and Novartis, and honoraria for scientific ad boards and consulting from Anthos, Bayer, Bristol Myers Squibb, Daiichi Sankyo, Janssen and Pfizer. S.H.S. has received personal consulting fees from Boehringer Ingelheim, Bristol Myers Squibb (BMS) and Daiichi-Sankyo, lecture fees from Boehringer Ingelheim, BMS, Daiichi-Sankyo, Bayer, AstraZeneca, and support for meeting and travels from Boehringer Ingelheim, BMS, Daiichi-Sankyo, Bayer and AstraZeneca. He has stocks from Bayer, FMC and possible others through indirect stakeholding via funds.
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References
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- De Vriese AS, Caluwé R, Pyfferoen L et al. Multicenter randomized controlled trial of vitamin K antagonist replacement by rivaroxaban with or without vitamin K2 in hemodialysis patients with atrial fibrillation: the Valkyrie Study. J Am Soc Nephrol 2020;31:186–96. 10.1681/ASN.2019060579 - DOI - PMC - PubMed
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