Haemostasis in Patients with Behçet's Disease

AbstractAim to determine whether Behçet's disease affects haemostatic function.Setting University Hospital, Turkey. Patients one hundred and twenty-seven consecutive patients with Behçet's disease, 34 of whom with a history of vascular involvement. Methods prothrombin fragment 1+2 tissue plasminogen activator, protein S and C, antithrombin, fibrinogen, von Willebrand factor, thrombomodulin and prothrombin time (PT) were measured in patient plasma. Results soluble thrombomodulin was significantly lower and von Willebrand factor (vWF) and tissue plasminogen activator (tPA) significantly higher in Behçet's patients. Patients with vascular involvement showed the highest levels of vWF and tPA. There was no activation of coagulation, not even in patients with an active disease at the time of sampling. Conclusion there were indirect signs of endothelial activity or damage, particularly in patients with vascular involvement. Coagulation was not activated