Europace. 2025;27(10):8267820.
Direct oral anticoagulants in very elderly and high-bleeding-risk patients with atrial fibrillation often excluded from oral anticoagulation therapy: a nationwide population-based cohort study.
제1저자 고영혜, 이소령 · 교신저자 최의근
소속 (5)
- Department of Internal Medicine, Seoul National University College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea.
- Department of Internal Medicine, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea.
- Statistics and Actuarial Science, Soongsil University, Seoul, Republic of Korea.
- Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Chest and Heart Hospital, Liverpool, UK.
- Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Abstract
AIMS In the Edoxaban Low-Dose for Elder Care Atrial Fibrillation Patients (ELDERCARE-AF) trial, very low-dose edoxaban (15 mg once daily) showed better efficacy and positive net clinical benefit compared with placebo in very elderly, high-bleeding-risk patients with atrial fibrillation (AF). However, there are limited data to generalize these results into daily practice. We aimed to investigate the optimal oral anticoagulant (OAC) strategy for the best net clinical benefit in ELDERCARE-AF-like patients.
METHODS AND RESULTS We used the Korean nationwide claims database to identify AF patients aged ≥80 years from 2014 to 2017 who had one or more ELDERCARE-AF trial inclusion criteria. The risks of ischaemic stroke, major bleeding, all-cause death, and net clinical outcome were evaluated. Primarily, we compared patients without OAC therapy (non-OAC group) to patients with direct OAC (DOAC) therapy (DOAC group), using a propensity score weighting method. A total of 23 858 patients were included (no OAC: 16 575; warfarin: 2390; DOAC: 4893). Among the DOAC group, 69% used low dose, and 9% used very low dose. Compared with the non-OAC group, the DOAC group showed lower risks of ischaemic stroke (hazard ratio, 95% confidence interval: 0.81, 0.68-0.96) and all-cause death (0.91, 0.86-0.96) and a higher risk of major bleeding (1.44, 1.21-1.70). The DOAC group was associated with a lower risk of net clinical outcome compared with the non-OAC group (0.93, 0.88-0.98).
CONCLUSION In very elderly, high-bleeding-risk patients with AF, DOACs that were prescribed in usual clinical practice showed better effectiveness and positive net clinical benefit compared with no OAC treatment.
© The Author(s) 2025. Published by Oxford University Press on behalf of the European Society of Cardiology.
Keywords
Atrial fibrillationBleedingDirect oral anticoagulantStrokeVery elderly
Figures
그림 출처: PubMed Central 공개 논문 (PMC12510312)
Conflict of interest statement
Conflict of interest: E.-K.C.: Research grants or speaking fees from Bayer, BMS/Pfizer, Biosense Webster, Chong Kun Dang, Daiichi-Sankyo, Dreamtech Co., Ltd, Medtronic, Samjinpharm, Sanofi-Aventis, Seers Technology, Skylabs, and Yuhan. G.Y.H.L.: Consultant and speaker for BMS/Pfizer, Boehringer Ingelheim, and Daiichi-Sankyo, but no fees are received personally. No other relationships or activities that could appear to have influenced the submitted work. All remaining authors have declared no conflicts of interest.
그 밖의 정보
- 출판 형태
- Journal Article
- 저널
- Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · eISSN 1532-2092
- MeSH
- Humans · Atrial Fibrillation* / drug therapy / complications / diagnosis / mortality · Aged, 80 and over · Male · Female · Hemorrhage* / chemically induced / epidemiology · Administration, Oral · Anticoagulants* / administration & dosage / adverse effects · Republic of Korea / epidemiology · Factor Xa Inhibitors* / administration & dosage / adverse effects · Risk Assessment · Risk Factors · Ischemic Stroke* / prevention & control / epidemiology / diagnosis / mortality · Thiazoles* / administration & dosage / adverse effects · Treatment Outcome · Age Factors · Pyridines* / administration & dosage / adverse effects
- Substances
- Anticoagulants · edoxaban · Factor Xa Inhibitors · Thiazoles · Pyridines
- 연구비
- Patient-Centered Clinical Research Coordinating Center · PACEN · Ministry of Health & Welfare RS-2021-KH119931 · National Research Foundation of Korea · NRF · Korea government IRIS RS-2024-00340590
- 참고문헌
- 53편