Chen D K, Kim J S, Sutton D M
Department of Medicine, Toronto Hospital, University of Toronto, Ontario, Canada.
Arch Intern Med. 1999 Feb 8;159(3):311-4. doi: 10.1001/archinte.159.3.311.
Ticlopidine hydrochloride is an antiplatelet agent used for an increasing number of indications, including cerebrovascular disease, unstable angina, coronary artery stenting, and peripheral vascular bypass grafting. It has uncommon but severe hematologic effects, including thrombotic thrombocytopenic purpura. We report 3 new cases of ticlopidine-associated thrombotic thrombocytopenic purpura and review the English-language literature. Of the 13 patients described (10 from published articles), an equal number were women and men. The median age of the women was 50 years, and that of the men was 72 years. Thrombotic thrombocytopenic purpura occurred within 2 to 8 weeks of starting ticlopidine therapy. Survivors received plasma therapy, but of the 4 who died, 3 had received platelet transfusions. With discontinuation of the drug and prompt plasma exchange therapy, mortality was comparable to that seen with idiopathic thrombotic thrombocytopenic purpura, and relapse was uncommon. Physicians and patients should be aware of this potentially fatal but treatable complication of ticlopidine therapy.
盐酸噻氯匹定是一种抗血小板药物,其应用于越来越多的适应症,包括脑血管疾病、不稳定型心绞痛、冠状动脉支架置入术和外周血管搭桥术。它具有罕见但严重的血液学效应,包括血栓性血小板减少性紫癜。我们报告3例新的与噻氯匹定相关的血栓性血小板减少性紫癜病例,并回顾英文文献。在所描述的13例患者中(10例来自已发表文章),男女数量相等。女性的中位年龄为50岁,男性为72岁。血栓性血小板减少性紫癜在开始噻氯匹定治疗的2至8周内发生。幸存者接受了血浆治疗,但在4例死亡患者中,有3例接受了血小板输注。随着药物停用和及时进行血浆置换治疗,死亡率与特发性血栓性血小板减少性紫癜相当,且复发罕见。医生和患者应意识到噻氯匹定治疗的这种潜在致命但可治疗的并发症。