Key result
DOACs linked to ~22% higher ischemic stroke risk versus warfarin in AF and mitral stenosis.
Why the study?
Whether direct oral anticoagulants are a safe and effective alternative to warfarin in patients with atrial fibrillation and mitral stenosis remains controversial.
Do DOACs improve clinical outcomes compared to warfarin in patients with atrial fibrillation and mitral stenosis?
Cohort
Yes
Do DOACs improve clinical outcomes compared to warfarin in patients with atrial fibrillation and mitral stenosis?
Relative Risk: 1.22 (95% CI 1.05–1.41)
In Asian patients with atrial fibrillation and mitral stenosis, DOACs are associated with an increased 1-year risk for stroke but a decreased risk for MI compared with warfarin.
Captured external expert commentary on this paper, strongest first. Original sources are linked where available.
“In atrial fibrillation with mital stenosis warerin still looks safer for stroke prevention than a direct oral anti-coagulant... it addresses a decision many of us face without randomized data and it argues against a switch that is very tempting to make.”
DOACs may warrant caution versus warfarin in AF-MS; leaves open optimal choice pending randomized trials.
BACKGROUND: Whether direct oral anticoagulants (DOACs) are a safe and effective alternative to warfarin in patients with atrial fibrillation and mitral stenosis (AF-MS) remains controversial. OBJECTIVE: To evaluate the effectiveness and safety of DOACs versus warfarin in patients with AF-MS. DESIGN: Observational cohort study using target trial emulation. SETTING: Population-wide insurance claims data in Taiwan. PARTICIPANTS: Patients diagnosed with AF-MS and prescribed either DOACs or warfarin between 1 January 2011 and 31 December 2021 were included in the study. INTERVENTION: DOACs or warfarin. MEASUREMENTS: Absolute risk differences (RDs) and risk ratios (RRs) at 1 year and 5 years of follow-up for ischemic stroke, systemic embolism, composite stroke, myocardial infarction (MI), intracranial hemorrhage, gastrointestinal bleeding, bleeding at other critical sites, and all-cause death. RESULTS: Compared with warfarin, DOACs were associated with an increased risk for ischemic stroke (RD, 4.97 percentage points [95% CI, 1.27 to 8.57 percentage points]; RR, 1.22 [CI, 1.05 to 1.41]) and composite stroke (RD, 5.56 percentage points [CI, 1.77 to 8.97 percentage points]; RR, 1.23 [CI, 1.07 to 1.42]) and a decreased risk for MI (RD, -1.61 percentage points [CI, -3.17 to -0.03 percentage points]; RR, 0.61 [CI, 0.37 to 0.99]) at the 1-year follow-up. Rivaroxaban increased the risk for ischemic stroke during both short- and long-term follow-up periods. The 2 groups did not differ in risks for bleeding or all-cause death. LIMITATION: Limited sample size, lack of detailed information on MS severity, and lack of international normalized ratio measurements. CONCLUSION: In Asian patients with AF-MS, DOACs were associated with an increased 1-year risk for stroke but a decreased risk for MI compared with warfarin. PRIMARY FUNDING SOURCE: Research Grants Council of Hong Kong.
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Yang et al. (2026) conducted a cohort in Atrial fibrillation and mitral stenosis. Direct oral anticoagulants (DOACs) vs. Warfarin was evaluated on Ischemic stroke at 1 year (RR 1.22, 95% CI 1.05 to 1.41). In patients with atrial fibrillation and mitral stenosis, DOACs were associated with an increased 1-year risk for ischemic stroke compared with warfarin (RR 1.22; 95% CI 1.05-1.41).
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