Association of Oral Anticoagulation With Stroke in Atrial Fibrillation or Heart Failure: A Comparative Meta-Analysis
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Updated: Oct 27, 2025

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Catriona Reddin1,2, Conor Judge1,3,2,4, Elaine Loughlin1,2
1HRB-Clinical Research Facility (C.R., C.J., E.L., R.M., M. Costello, A.A., J.F., A.S., M. Canavan, M.J.O.), National University of Ireland Galway.
Insights
Oral anticoagulation shows similar stroke risk reduction for atrial fibrillation and heart failure with reduced ejection fraction (HFrEF). Differences in trial outcomes may explain varied guideline recommendations for HFrEF patients.
Area of Science:
- Cardiology
- Clinical Trials
- Evidence-Based Medicine
Background:
- Atrial fibrillation and heart failure with reduced ejection fraction (HFrEF) are significant causes of cardioembolic events.
- Oral anticoagulation is standard for atrial fibrillation, but its use in HFrEF is debated due to uncertain net clinical benefit.
Purpose of the Study:
- To systematically review and meta-analyze the comparative association of oral anticoagulation with stroke and cardiovascular risk in patients with atrial fibrillation versus HFrEF.
- To identify factors influencing the perceived net clinical benefit of oral anticoagulation in these populations.
Main Methods:
- A systematic search of PubMed and Embase for randomized clinical trials comparing oral anticoagulation to control.
- Random-effects meta-analysis to pool treatment effects, assessing differences between atrial fibrillation and HFrEF populations.
- Primary outcome: all stroke; Secondary outcomes: ischemic stroke, hemorrhagic stroke, mortality, myocardial infarction, major hemorrhage.
Main Results:
- Twenty-one trials (15 in AF, 6 in HFrEF) were included.
- Oral anticoagulation demonstrated a consistent association with reduced all-stroke risk in both atrial fibrillation (OR, 0.51) and HFrEF (OR, 0.61), with no significant interaction (P=0.31).
- No statistically significant differences were found in the association with cardiovascular events, mortality, or bleeding between the two patient groups.
Conclusions:
- The relative benefit of oral anticoagulation in reducing stroke risk is comparable for patients with atrial fibrillation and HFrEF.
- Discrepancies in primary outcome measures used in HFrEF trials compared to atrial fibrillation trials may account for differing conclusions on oral anticoagulation efficacy.
Background And Purpose:
Atrial fibrillation and heart failure with reduced ejection fraction (HFrEF) are common sources of cardioembolism. While oral anticoagulation is strongly recommended for atrial fibrillation, there are marked variations in guideline recommendations for HFrEF due to uncertainty about net clinical benefit. This systematic review and meta-analysis evaluates the comparative association of oral anticoagulation with stroke and other cardiovascular risk in populations with atrial fibrillation or HFrEF in sinus rhythm and identify factors mediating different estimates of net clinical benefit.
Methods:
PubMed and Embase were searched from database inception to November 20, 2019 for randomized clinical trials comparing oral anticoagulation to control. A random-effects meta-analysis was used to estimate a pooled treatment-effect overall and within atrial fibrillation and HFrEF trials. Differences in treatment effect were assessed by estimating I2 among all trials and testing the between-trial-population P-interaction. The primary outcome measure was all stroke. Secondary outcome measures were ischemic stroke, hemorrhagic stroke, mortality, myocardial infarction, and major hemorrhage.
Results:
Twenty-one trials were eligible for inclusion, 15 (n=19 332) in atrial fibrillation (mean follow-up: 23.1 months), and 6 (n=9866) in HFrEF (mean follow-up: 23.9 months). There were differences in primary outcomes between trial populations, with all-cause mortality included for 95.2% of HFrEF trial population versus 0.38% for atrial fibrillation. Mortality was higher in controls groups of HFrEF populations (19.0% versus 9.6%) but rates of stroke lower (3.1% versus 7.0%) compared with atrial fibrillation. The association of oral anticoagulation with all stroke was consistent for atrial fibrillation (odds ratio, 0.51 [95% CI, 0.42–0.63]) and HFrEF (odds ratio, 0.61 [95% CI, 0.47–0.79]; I2=12.4%; P interaction=0.31). There were no statistically significant differences in the association of oral anticoagulation with cardiovascular events, mortality or bleeding between populations.
Conclusions:
The relative association of oral anticoagulation with stroke risk, and other cardiovascular outcomes, is similar for patients with atrial fibrillation and HFrEF. Differences in the primary outcomes employed by trials in HFrEF, compared with atrial fibrillation, may have contributed to differing conclusions of the relative efficacy of oral anticoagulation.
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