Key result
Combined low-dose warfarin and aspirin reduced activated factor VII levels by 26% on average during 8 weeks of treatment (P<0.001), with a rebound to 122% two weeks after stopping.
Why the study?
Does combined low-dose warfarin and aspirin reduce activated factor VII levels in patients with clinically stable coronary artery disease?
Does combined low-dose warfarin and aspirin reduce activated factor VII levels in patients with clinically stable coronary artery disease?
p-value: p=<.001
Low-dose warfarin combined with aspirin reduces factor VIIa levels in stable coronary artery disease, but abrupt cessation is associated with a significant rebound effect.
May trigger factor VIIa rebound after abrupt cessation in stable CAD; leaves open whether this raises ischemic risk.
Factor VII is an independent risk factor for ischemic heart disease. We performed a prospective study to evaluate the effect of combined low-dose warfarin-aspirin on activated factor VII (factor VIIa) and to determine if abruptly stopping this treatment is associated with a rebound in the level of factor VIIa. Thirty-three patients with clinically stable coronary artery disease were treated with combined 3 mg warfarin and 80 mg aspirin daily for 8 weeks. The factor VIIa level was measured before treatment, weekly during treatment, and 2 weeks after stopping treatment. The mean percent of pretreatment levels of factor VIIa for weeks 1 through 8 of treatment were 60%, 60%, 72%, 70%, 71%, 70%, 74%, and 87%, respectively (P < .05 compared with pretreatment for weeks 1 through 7 inclusive); 2 weeks after stopping treatment, the level was 122% (95% confidence interval [CI]; 111% to 133%; P < .001 compared with pretreatment). The mean percent level of factor VIIa on-treatment was 74% (P < .001). Factor VIIa is reduced by 26% on average during treatment. This finding provides further rationale for the antithrombotic effect of low-dose warfarin. The results suggest a rebound in the factor VIIa level may occur after treatment is stopped. The potential rebound and its clinical importance should be evaluated by further studies.
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Ge et al. (1995) studied clinically stable coronary artery disease (n=33). combined low-dose warfarin-aspirin vs. pretreatment baseline was evaluated on mean percent level of factor VIIa on-treatment (p=<.001). Combined low-dose warfarin and aspirin reduced activated factor VII levels by 26% on average during 8 weeks of treatment (P<0.001), with a rebound to 122% two weeks after stopping.
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