Ximelagatran was noninferior to warfarin for preventing stroke and systemic embolic events in patients with atrial fibrillation and prior stroke or TIA (absolute difference -0.44%; 95% CI -1.88 to 1.01).
RCT (n=7,329)
Does ximelagatran prevent ischemic and hemorrhagic strokes and systemic embolic events in patients with nonvalvular atrial fibrillation and prior stroke or TIA compared to warfarin?
Ximelagatran is noninferior to warfarin for secondary stroke prevention in patients with nonvalvular atrial fibrillation, though concomitant aspirin increases bleeding risk.
Estimación del efecto: absolute difference -0.44% (95% CI -1.88 to 1.01)
Tasa de eventos absoluta: 2.83% vs 3.27%
valor p: p=0.625
BACKGROUND AND PURPOSE: Patients with nonvalvular atrial fibrillation and prior stroke or transient ischemic attack (TIA) are at high risk for recurrent stroke. We investigated whether ximelagatran was noninferior to warfarin in patients with prior stroke or TIA. METHODS: We analyzed pooled data from the SPORTIF III and V trials in patients with prior stroke/TIA. The primary outcome was the composite annual rate of both ischemic and hemorrhagic strokes and systemic embolic events. Secondary analyses considered ischemic and hemorrhagic strokes separately, bleeding, and nonrandomized, concomitant therapy with aspirin < or =100 mg/d. RESULTS: Patients from SPORTIF III (n=3407) and SPORTIF V (n=3922) trials were categorized by prior stroke/TIA (21%) versus no prior stroke/TIA (79%) and by treatment group (ximelagatran vs warfarin). The primary event rate in patients with prior stroke/TIA was 2.83%/y with ximelagatran and 3.27%/y with warfarin (absolute difference, -0.44%; 95% CI, -1.88 to1.01; P=0.625). In those without prior stroke/TIA, the primary event rate was 1.31%/y with ximelagatran and 1.26%/y with warfarin (P=NS). Ischemic strokes outnumbered cerebral hemorrhages with both warfarin (31 of 36) and ximelagatran (30 of 32) treatment (difference between treatments was not significant). Combining aspirin with either anticoagulant was associated with higher rates of major bleeding (1.5%/y with warfarin and 4.95%/y with warfarin plus aspirin, P=0.004; 2.35%/y with ximelagatran and 5.09%/y with ximelagatran plus aspirin, P=0.046) but not lower rates of primary events. CONCLUSIONS: Ximelagatran was at least as effective as well-controlled warfarin for the secondary prevention of stroke. The nonrandomized, concomitant treatment with aspirin and anticoagulation was associated with increased bleeding without evidence of a reduction in primary outcome events.
Akins et al. (Fri,) conducted a rct in nonvalvular atrial fibrillation and prior stroke or transient ischemic attack (TIA) (n=7,329). ximelagatran vs. warfarin was evaluated on composite annual rate of both ischemic and hemorrhagic strokes and systemic embolic events (absolute difference -0.44%, 95% CI -1.88 to 1.01, p=0.625). Ximelagatran was noninferior to warfarin for preventing stroke and systemic embolic events in patients with atrial fibrillation and prior stroke or TIA (absolute difference -0.44%; 95% CI -1.88 to 1.01).
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