Key result
Argatroban plus DAPT fails to reduce 7-day mortality or 90-day stroke readmission versus DAPT alone.
Why the study?
Although DAPT is frequently combined with argatroban for acute atherosclerotic stroke in Japan, the safety and effectiveness of this combination compared with DAPT alone remains unclear.
Does argatroban added to DAPT improve outcomes or increase bleeding in patients with acute atherothrombotic stroke?
Cohort (n=59,983)
Yes
Does argatroban added to DAPT improve outcomes or increase bleeding in patients with acute atherothrombotic stroke?
The addition of argatroban to DAPT for acute atherothrombotic stroke does not significantly improve mortality or stroke recurrence, nor does it significantly increase hemorrhagic complications compared to DAPT alone.
Answers are grounded in this paper and cite their sources.
Argatroban addition to DAPT warrants no practice change in acute atherothrombotic stroke; leaves open benefit or harm in randomized trials.
BACKGROUND: Dual antiplatelet therapy (DAPT) is more effective than aspirin alone in preventing early recurrences of non-cardioembolic strokes. In Japan, DAPT is often combined with argatroban, a direct thrombin inhibitor, for treating acute atherosclerotic stroke. However, the safety and effectiveness of this combination compared with those of DAPT alone remains unclear. METHODS: We identified patients with acute atherothrombotic stroke treated with DAPT between April 2016 and March 2022, using the Diagnostic Procedure Combination database, a large national inpatient database in Japan. Patients were divided into two groups: those receiving DAPT plus argatroban and those receiving DAPT alone. We compared 7-day mortality, hemorrhagic complications, and readmission for stroke recurrence within 90 days between the groups using propensity-score overlap weighting analyses. RESULTS: Of 59,983 eligible patients, 47,213 received DAPT plus argatroban, while 12,770 received DAPT alone. In the propensity-score overlap weighting analyses, no significant differences in 7-day mortality (0.2% vs 0.2%; adjusted risk ratio [aRR], 0.77; 95% confidence interval [CI], 0.49-1.21), the proportions of hemorrhagic complications (2.3% vs 2.1%; aRR, 1.12; 95% CI, 0.99-1.27), or 90-day readmission for stroke recurrence (1.2% vs 1.2%; aRR, 0.99; 95%CI, 0.84-1.17) were observed between the DAPT plus argatroban and DAPT alone groups. CONCLUSIONS: The outcomes did not differ significantly between DAPT alone and argatroban combined with DAPT for acute atherothrombotic stroke.
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Nakashima et al. (2025) conducted a cohort in acute atherothrombotic stroke (n=59,983). DAPT plus argatroban vs. DAPT alone was evaluated on 7-day mortality (aRR 0.77, 95% CI 0.49-1.21). Argatroban plus DAPT did not significantly reduce 7-day mortality (aRR 0.77; 95% CI 0.49-1.21) or 90-day stroke readmission (aRR 0.99; 95% CI 0.84-1.17) compared to DAPT alone.
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