Boinot C, Lanquetot H, Macchi L, Charrière J M, Menu P
Laboratoire d'hématologie, CHU de Poitiers, BP 577, 86021 Poitiers, France.
Ann Fr Anesth Reanim. 2003 Jul;22(7):635-8. doi: 10.1016/s0750-7658(03)00217-x.
Lepirudin is an alternative anticoagulant therapy in heparin-induced thrombocytopenia (HIT) during cardiopulmonary bypass (CPB). We report a case of a female patient with HIT referred for aortocoronary bypass graft despite persistence of antibodies to platelet factor 4-heparin complexes. Anticoagulation management is described. Whole blood hirudin concentration attempted during CPB was above 4 microg ml(-1). To obtain this concentration, lepirudin administration was managed as follows: 0.1 mg kg(-1) h(-1) lepirudin during preoperative course, 0.2 mg kg(-1) bolus just before CPB and 0.2 mg kg(-1) in the priming solution, complementary boluses of 5 and 10 mg during procedure (according to whole blood ecarin clotting time). Aprotinin was administered simultaneously according to Royston protocol. Anticoagulation was monitored with whole blood ecarin time performed in the operation room (patient's whole blood was diluted one half and one third with normal whole blood; in vitro calibration curve was constructed using normal whole blood spiked with lepirudin). CPB duration was 73 min. When measured, whole blood hirudin concentration was 3.8-5.8 microg ml(-1). Total lepirudin administration was 44 mg. No haemorrhagic or thrombotic events were observed during surgical procedure and postoperative course. Despite lepirudin administration is not yet clearly precise for CPB procedure, its use seems adapted and safe in subjects without renal insufficiency but requiring precise coordination for anaesthesiological, surgical and biological teams.
在体外循环(CPB)期间,比伐卢定是肝素诱导的血小板减少症(HIT)的一种替代抗凝疗法。我们报告了一例患有HIT的女性患者,尽管其仍存在针对血小板因子4 - 肝素复合物的抗体,但仍被转诊进行主动脉冠状动脉搭桥术。本文描述了抗凝管理情况。CPB期间尝试达到的全血比伐卢定浓度高于4μg/ml。为达到该浓度,比伐卢定的给药管理如下:术前过程中以0.1mg/kg/h的速度输注比伐卢定,CPB前即刻给予0.2mg/kg的静脉推注剂量,并在预充液中加入0.2mg/kg,术中根据全血蛇静脉酶凝血时间给予5mg和10mg的补充静脉推注。同时按照罗伊斯顿方案给予抑肽酶。在手术室通过全血蛇静脉酶时间监测抗凝情况(患者全血用正常全血稀释一半和三分之一;使用添加了比伐卢定的正常全血构建体外校准曲线)。CPB持续时间为73分钟。测量时,全血比伐卢定浓度为3.8 - 5.8μg/ml。比伐卢定的总给药量为44mg。在手术过程和术后过程中未观察到出血或血栓形成事件。尽管比伐卢定在CPB过程中的给药尚未明确精确,但在没有肾功能不全但需要麻醉、手术和生物团队精确协调的患者中,其使用似乎是合适且安全的。