Jubelirer S J, Koenig B A, Bates M C
Charleston Area Medical Center, West Virginia University, Charleston Division, Robert C. Byrd Health Sciences Center, Charleston, West Virginia, USA.
Am J Hematol. 1999 Jul;61(3):205-8. doi: 10.1002/(sici)1096-8652(199907)61:3<205::aid-ajh8>3.0.co;2-9.
Platelets play a crucial role in the ischemic complications of percutaneous coronary procedures. The recent availability of C7E3 Fab (Abxiximab or ReoProtrade mark), a chimeric monoclonal antibody Fab fragment directed against the platelet glycoprotein IIb/IIIa receptor, has reduced abrupt closure and other adverse events and lessened the need for revascularization procedures. As the use for this drug has increased, rare cases of severe thrombocytopenia have been revealed. From August 1995 to June 1997, 452 patients at Charleston Area Medical Center who underwent percutaneous coronary revascularization procedures and were treated with abciximab were evaluated for the development of severe thrombocytopenia (i.e., platelet count less than 20,000 within 48 hr of treatment). A review of published reports of severe thrombocytopenia was also reviewed. A review of published reports of abciximab-induced severe thrombocytopenia, as well as our three cases, reveals that: 1) the incidence is less than 0.7%; 2) the nadir platelet count (range 1, 000-16,000) was noted within 2-31 hr after abciximab infusion; 3) the platelet count increases to greater than 100,000 within 12 days in all patients; 4) bleeding episodes were treated with platelet transfusion with an improvement in platelet count within 24 hr in all patients in whom they were given; and 5) in the one patient treated with gamma globulin alone, no significant rise in platelet count was noted. Acute severe thrombocytopenia can occur after ReoProtrade mark administration. Its development is not predictable and may occur within 2 hr of administration. Thrombocytopenia, therefore, requires consideration in every patient treated with this drug. It appears prudent to obtain a platelet count 2 hr after initiating ReoProtrade mark. If thrombocytopenia develops, then the drug can be stopped in a timely manner and platelet transfusion can be given.
血小板在经皮冠状动脉介入治疗的缺血性并发症中起关键作用。最近可获得的C7E3 Fab(阿昔单抗或商品名ReoPro),一种针对血小板糖蛋白IIb/IIIa受体的嵌合单克隆抗体Fab片段,已减少了急性血管闭塞和其他不良事件,并减少了血管重建手术的需求。随着这种药物使用的增加,已发现罕见的严重血小板减少病例。1995年8月至1997年6月,对查尔斯顿地区医疗中心452例行经皮冠状动脉血管重建术并接受阿昔单抗治疗的患者进行了严重血小板减少(即治疗后48小时内血小板计数低于20,000)情况的评估。还回顾了已发表的严重血小板减少报告。对已发表的阿昔单抗诱导的严重血小板减少报告以及我们的3例病例的回顾显示:1)发生率低于0.7%;2)阿昔单抗输注后2 - 31小时内出现最低血小板计数(范围1,000 - 16,000);3)所有患者在12天内血小板计数增加至大于100,000;4)出血发作通过输注血小板治疗,所有接受输注的患者血小板计数在24小时内得到改善;5)仅接受γ球蛋白治疗的1例患者,未观察到血小板计数有显著升高。使用ReoPro后可发生急性严重血小板减少。其发生不可预测,可能在给药后2小时内出现。因此,对于接受此药治疗的每位患者都需要考虑血小板减少的情况。在开始使用ReoPro 2小时后进行血小板计数似乎是谨慎的做法。如果发生血小板减少,可及时停药并给予血小板输注。