Robert S, Miller A J, Fagan S C
College of Pharmacy, Wayne State University, Detroit, MI 48076.
Pharmacotherapy. 1991;11(4):317-22; discussion 322-5.
Ticlopidine is a new prototype antiplatelet drug chemically unrelated to currently available agents. It causes an alteration in platelet membrane reactivity to a variety of aggregating stimuli and a marked prolongation of bleeding time, the mechanism of which remains unclear. Two major phase III multicenter trials, the ticlopidine-aspirin stroke study (TASS) and the Canadian-American ticlopidine study (CATS) reported that the agent may reduce the occurrence of stroke, myocardial infarction, or vascular death in patients of both sexes who have had recent cerebral ischemia. Ticlopidine has been well tolerated in preliminary studies, with the most commonly described adverse effects being rash and gastrointestinal complaints. The most important adverse effect is neutropenia, which was reported in both TASS and CATS, approximating a frequency of 0.9% and 0.8%, respectively. Ticlopidine holds considerable promise as adjunctive therapy in selected patients.
噻氯匹定是一种新型的抗血小板药物原型,在化学结构上与现有的药物无关。它会改变血小板膜对各种聚集刺激的反应性,并显著延长出血时间,其机制尚不清楚。两项主要的III期多中心试验,即噻氯匹定-阿司匹林中风研究(TASS)和加拿大-美国噻氯匹定研究(CATS)报告称,该药物可能会降低近期发生脑缺血的男女患者中风、心肌梗死或血管性死亡的发生率。在初步研究中,噻氯匹定的耐受性良好,最常描述的不良反应是皮疹和胃肠道不适。最重要的不良反应是中性粒细胞减少,TASS和CATS均有报告,发生率分别约为0.9%和0.8%。噻氯匹定作为特定患者的辅助治疗具有很大的前景。