Arrhythmias & electrophysiology

Antithrombotic therapy for stable coronary artery disease and atrial fibrillation in patients with and without revascularisation: the AFIRE trial

EuroInterventionPublished Post hoc subgroup analysis of the AFIRE randomised trial

Authors' conclusion

In high-risk thrombosis patients with a history of prior revascularisation, rivaroxaban monotherapy versus combination therapy demonstrated favourable safety and efficacy outcomes.

Study context

Population
Patients with AF and stable CAD, with or without prior revascularisation1,697 with prior revascularisation · with 1,697 · or without 518
Participants
2,215 patients
Comparison
Rivaroxaban monotherapy vs combination therapy (rivaroxaban plus a single antiplatelet), by prior revascularisation
Primary endpoint
Efficacy: composite of stroke, systemic embolism, MI, unstable angina requiring revascularisation, or all-cause death; safety: major bleeding

Primary result

As reported in the abstract

Primary efficacy (composite of stroke, systemic embolism, MI, unstable angina requiring revascularisation or all-cause death) and primary safety (major bleeding) endpoints, by prior revascularisation
Monotherapy vs Combination therapyHazard ratio (95% CI)P value
Efficacy; prior revascularisation (n=1,697)
0.62(0.45–0.85)
P = 0.003
Safety (major bleeding); prior revascularisation (n=1,697)
0.62(0.39–0.98)
P = 0.042
No prior revascularisation (n=518): no significant difference in efficacy endpoint (HR 1.19, 95% CI 0.67-2.12)
P = 0.554
No prior revascularisation (n=518): no significant difference in safety endpoint (HR 0.47, 95% CI 0.18-1.26)
P = 0.134

Safety

OutcomeHR (95% CI)P value
Any bleeding, no prior revascularisation0.59 (0.38–0.93)P = 0.022

Original publication

Antithrombotic therapy for stable coronary artery disease and atrial fibrillation in patients with and without revascularisation: the AFIRE trial. EuroIntervention. Published 1 April 2024. doi:10.4244/eij-d-23-00396

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