Incidence and Predictors of Worsening Renal Function in Edoxaban-Treated Atrial Fibrillation Patients Within ETNA-AF-Europe Registry.

ETNA-AF-Europe atrial fibrillation direct acting oral anticoagulant edoxaban worsening renal function

Journal

JACC. Advances
ISSN: 2772-963X
Titre abrégé: JACC Adv
Pays: United States
ID NLM: 9918419284106676

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 26 06 2023
revised: 27 11 2023
accepted: 20 12 2023
medline: 28 6 2024
pubmed: 28 6 2024
entrez: 28 6 2024
Statut: epublish

Résumé

Managing patients with atrial fibrillation (AF) and worsening renal function (WRF) remains a clinical challenge due to the need of dose adjustment of non-vitamin K antagonist oral anticoagulants. To determine the incidence of WRF in patients with AF treated with edoxaban, the association of WRF with clinical outcomes, and predictors of WRF and clinical outcomes in these patients. This is a subanalysis of the Edoxaban Treatment in routiNe clinical prActice for patients with non-valvular Atrial Fibrillation in Europe study (NCT02944019), an observational study of edoxaban-treated patients with AF. WRF was defined as a ≥25% reduction in creatinine clearance between baseline and 2 years. Of the 9,054 patients included (69% of the total 13,133 enrolled), most did not experience WRF (90.3%) during the first 2 years of follow-up. WRF occurred in 9.7% of patients. Patients with WRF had significantly higher rates of all-cause death (3.88%/y vs 1.88%/y; WRF occurred in approximately 10% of edoxaban-treated AF patients. Rates of death and major bleeding were significantly higher in patients with WRF than without. Stroke events were low in both subgroups.

Sections du résumé

Background UNASSIGNED
Managing patients with atrial fibrillation (AF) and worsening renal function (WRF) remains a clinical challenge due to the need of dose adjustment of non-vitamin K antagonist oral anticoagulants.
Objectives UNASSIGNED
To determine the incidence of WRF in patients with AF treated with edoxaban, the association of WRF with clinical outcomes, and predictors of WRF and clinical outcomes in these patients.
Methods UNASSIGNED
This is a subanalysis of the Edoxaban Treatment in routiNe clinical prActice for patients with non-valvular Atrial Fibrillation in Europe study (NCT02944019), an observational study of edoxaban-treated patients with AF. WRF was defined as a ≥25% reduction in creatinine clearance between baseline and 2 years.
Results UNASSIGNED
Of the 9,054 patients included (69% of the total 13,133 enrolled), most did not experience WRF (90.3%) during the first 2 years of follow-up. WRF occurred in 9.7% of patients. Patients with WRF had significantly higher rates of all-cause death (3.88%/y vs 1.88%/y;
Conclusions UNASSIGNED
WRF occurred in approximately 10% of edoxaban-treated AF patients. Rates of death and major bleeding were significantly higher in patients with WRF than without. Stroke events were low in both subgroups.

Identifiants

pubmed: 38939675
doi: 10.1016/j.jacadv.2024.100880
pii: S2772-963X(24)00058-9
pmc: PMC11198551
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100880

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

This study was funded by 10.13039/501100022274Daiichi Sankyo Europe GmbH, Munich, Germany. Dr Gwechenberger has received personal fees (lectures, advisory boards, research grants) and travel grants from Daiichi Sankyo, Boehringer Ingelheim, Bayer, Abbott, Biotronik, Boston, Medtronic, and Sorin. Dr Barón-Esquivias has received honoraria for presentations and/or consultancy fees and/or research grants from Boehringer Ingelheim, Bayer, Daiichi Sankyo, Pfizer-Bristol-Myers-Squibb, and Biotronik. Dr de Vries has received nonfinancial support from Daiichi Sankyo for other research projects related to the ETNA-AF-Europe registry, and speaker fees from Bristol Myers Squibb. He is also being considered for the adjudication committee of the LIMIT & DANCE trials, which are sponsored by the Population Health Research Institute (PHRI). Dr Siller-Matula has received speaker or consultant fees from Chiesi, Biosensors, Boston Scientific, P&F, Boehringer Ingelheim, and Daiichi Sankyo not related to the submitted work. Dr de Groot reports personal fees from Daiichi Sankyo during the conduct of the study; grants from Abbott, Atricure, Bayer, Boston Scientific, Daiichi Sankyo, Johnson & Johnson, and Medtronic; personal fees from Atricure, Bayer, berlin-Chemie, Daiichi Sankyo, Johnson & Johnson, Medtronic, Menarini, Novartis, and Servier; and other from RhythmCARE outside the submitted work. Dr Manu was an employee of Daiichi Sankyo Europe GmbH, Munich, Germany (at the time of development of the manuscript). Dr Souza is an employee of Daiichi Sankyo Europe GmbH, Munich, Germany. Dr Wienerroither is an employee of Daiichi Sankyo Austria GmbH, Vienna, Austria. Dr Pecen has received fees and honoraria from Daiichi-Sankyo, SOTIO, and Beckman Coulter. Dr De Caterina reports grants, personal fees and nonfinancial support from Daiichi Sankyo, during the conduct of the study; and reports consulting fees, honoraria and research funding from: AstraZeneca, Boehringer Ingelheim, Bayer, BMS/Pfizer, Daiichi Sankyo, Janssen, Milestone, Novartis, Merck, Portola, Sanofi, Menarini, Guidotti, and Roche, outside the submitted work. Dr Kirchhof receives research support for basic, translational, and clinical research projects from European Union Big-Data@Heart (grant agreement EU IMI 116 074); CATCH ME (grant agreement ID: 633 196); AFFECT-EU (grant agreement ID: 847 770); Leducq foundation, Medical Research Council (UK); German Centre for Cardiovascular Research supported by the German Ministry of Education and Research; from several drug and device companies active in atrial fibrillation and has received honoraria from several such companies in the past but not in the last 3 years. He is listed as inventor on 2 patents held by University of Birmingham (Atrial Fibrillation Therapy WO 2 015 140 571, Markers for Atrial Fibrillation WO 2 016 012 783) and is employed as Director of the Department of Cardiology, University Heart and Vascular Centre UKE Hamburg and Professor of Cardiovascular Medicine (part-time), University of Birmingham, UK. He is also Speaker of the board of AFNET, Germany, and Board member of the ESC.

Auteurs

Marianne Gwechenberger (M)

Department of Cardiology, Medical University of Vienna, Vienna, Austria.

Gonzalo Barón-Esquivias (G)

Virgen del Rocio University Hospital, University of Seville, Seville, Spain.

Tim A C de Vries (TAC)

Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Amsterdam Cardiovascular Sciences, Heart Failure and Arrhythmias, Amsterdam, the Netherlands.
Department of Cardiology, Rijnstate Hospital, Arnhem, the Netherlands.

Jolanta M Siller-Matula (JM)

Department of Cardiology, Medical University of Vienna, Vienna, Austria.

Marius C Manu (MC)

Daiichi Sankyo Europe GmbH, Munich, Germany.

José A G Souza (JAG)

Daiichi Sankyo Europe GmbH, Munich, Germany.

Sebastian Wienerroither (S)

Daiichi Sankyo Austria GmbH, Vienna, Austria.

Ladislav Pecen (L)

Institute of Computer Science of the Czech Academy of Sciences, Prague, Czech Republic.
Department of Immunochemistry Diagnostics, University Hospital Pilsen, Pilsen, Czech Republic.

Joris R de Groot (JR)

Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands.
Amsterdam Cardiovascular Sciences, Heart Failure and Arrhythmias, Amsterdam, the Netherlands.

Raffaele De Caterina (R)

Cardiology Division, University of Pisa, Pisa, Italy.
Fondazione VillaSerena per la Ricerca, Pescara, Italy.

Paulus Kirchhof (P)

Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.
University Heart and Vascular Centre Hamburg, University Medical Centre Hamburg Eppendorf, Hamburg, Germany.
German Center for Cardiovascular Sciences (DZHK) Partner Site Hamburg/Kiel/Lübeck, Hamburg/Kiel/Lübeck, Germany.

Classifications MeSH