“…Ticlopidine is a new antiplatelet drug that can interrupt platelet aggregation induced by adenosine diphos phate, arachidonic acid, thrombin, adrena line and thromboxane Aj [19,22,23], In vivo, this drug increases platelet survival in recent Dacron grafts, decreases labeled platelet deposition on tetrafluorethylene grafts, and reduces the thrombus develop ment in polyethylene arteriovenous shunt [24][25][26]. In humans, it reduces the rate of aortocoronary bypass graft occlusion [27], but it does not inhibit platelet deposition on Dacron aortic prostheses [12], Indobufen is a new platelet inhibitor commonly used in Europe, and the mecha nism by which this drug exerts its action is similar to ASA. In vitro, indobufen inter rupts platelet aggregation induced by adeno sine diphosphate and collagen, and seems to be more effective than the association ASAdipyridamole or ASA alone [28,29], A re cent study suggests that indobufen improves symptoms in patients with ischemic cardiac disease [30], but no data are available on the deposition of the platelets on thrombus sur face.…”