Optimal antithrombotic therapy for post-ischemic stroke patients with atrial fibrillation and atherosclerotic cardiovascular disease: A frequentist network meta-analysis

Authors

Ahmed Ibrahim, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Elsayed Balbaa, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Ameer Awashra, Department of Medicine, An Najah National University, Nablus, Palestine.
Abdalhakim Shubietah, Advocate Health - MidwestFollow
Giulia Cavolina, Azienda Ospedaliera Papardo, Messina, and Department of Clinical and Experimental Medicine, University of Messina, Italy.
Alessio Villari, Azienda Ospedaliera Papardo, Messina, and Department of Clinical and Experimental Medicine, University of Messina, Italy.
Giuseppe Andò, Azienda Ospedaliera Papardo, Messina, and Department of Clinical and Experimental Medicine, University of Messina, Italy. Electronic address: giuseppe.ando@unime.it.
Pierre Sabouret, Heart Institute and Action Group, Pitié-Salpétrière, Sorbonne University, 75013 Paris, France.

Recommended Citation

Ibrahim A, Balbaa E, Awashra A, et al. Optimal antithrombotic therapy for post-ischemic stroke patients with atrial fibrillation and atherosclerotic cardiovascular disease: A frequentist network meta-analysis. J Neurol Sci. Published online March 3, 2026. doi:10.1016/j.jns.2026.125852

Affiliations

Advocate Illinois Masonic Medical Center

Abstract

Background: The optimal antithrombotic strategy for secondary prevention in patients with atrial fibrillation (AF) and concomitant atherosclerotic cardiovascular disease (ASCVD) following acute ischemic stroke (IS) remains undefined. This network meta-analysis aimed to compare the efficacy and safety of oral anticoagulant (OAC) monotherapy, antiplatelet therapy (APT), and their combination in this population.

Methods: We systematically searched major electronic databases through October 2025 for relevant randomized and non-randomized studies. A frequentist network meta-analysis was performed using random-effects models to calculate pooled hazard ratios (HRs) with 95% confidence intervals (CIs). Treatment hierarchies were ranked using P-scores. The primary outcome was a composite of all-cause mortality, major bleeding, and any ischemic event.

Results: Ten studies (1 randomized trial, 9 observational) involving 14,104 patients were included. Compared to combination therapy, OAC monotherapy ranked most favorable for the primary composite endpoint (HR 0.82, 95% CI: 0.53-1.27; P-score: 0.90) and for recurrent IS (HR 0.77, 95% CI: 0.50-1.20; P-score: 0.88). Regarding major bleeding, both APT (HR 0.64, 95% CI: 0.28-1.46; P-score: 0.75) and OAC monotherapy (HR 0.74, 95% CI: 0.35-1.55; P-score: 0.57) showed a trend toward reduced major bleeding compared to combination therapy, though neither reached statistical significance. For mortality, OAC monotherapy was comparable to combination therapy (HR 1.11, 95% CI: 0.66-1.87), whereas APT showed a trend toward higher risk (HR 1.78, 95% CI: 0.97-3.29; P-score: 0.05).

Conclusion: In patients with IS, AF, and ASCVD, OAC monotherapy appears to be the most favorable strategy for secondary prevention, offering an optimal balance between efficacy and safety. Adding APT confers no additional clinical benefit while potentially increasing bleeding risk. However, given the predominance of observational data, these findings should be interpreted with caution and confirmed through dedicated randomized controlled trials.

Type

Article

PubMed ID

41797114