Why the study?
Do antiplatelet agents (ticlopidine or aspirin/dipyridamole) improve platelet function and hemodynamics in patients with intermittent claudication compared to xanthinol nicotinate?
Do antiplatelet agents (ticlopidine or aspirin/dipyridamole) improve platelet function and hemodynamics in patients with intermittent claudication compared to xanthinol nicotinate?
Antiplatelet therapy with ticlopidine or aspirin/dipyridamole improves surrogate hemodynamic and hematologic markers in patients with intermittent claudication.
Supports antiplatelet choice in intermittent claudication based on surrogates; extends RCT evidence versus xanthinol nicotinate.
In a double-blind study, 296 patients with intermittent claudication (Fontaine stage II) were treated with 250 mg ticlopidine twice daily, 500 mg aspirin every third day plus 75 mg dipyridamole three times daily, or 300 mg xanthinol nicotinate three times daily for 6 months. Ticlopidine and aspirin/dipyridamole, but not xanthinol nicotinate, improved platelet aggregation, reduced beta-thromboglobulin, platelet factor IV and fibrinopeptide A concentrations, and increased antithrombin III concentrations and red blood cell filterability. No changes in lipid profiles, platelet count or fibrinogen were recorded following any treatment. The doppler systolic blood pressure ratio was improved in patients treated with ticlopidine or aspirin/dipyridamole, but not with xanthinol nicotinate. It is concluded that antiplatelet treatment is useful for the treatment of limb arteriopathy.
No takes yet. Share an insight, caveat, or question.
Giansante et al. (1990) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: