Sakai M, Ohteki H, Narita Y, Naitoh K, Natsuaki M, Itoh T
Department of Thoracic-Cardiovascular Surgery, Saga Medical School, Saga City, Japan.
Cardiovasc Surg. 1999 Mar;7(2):187-94. doi: 10.1016/s0967-2109(98)00119-7.
Argatroban is a selective thrombin inhibitor synthesized in Japan. Argatroban, which has a high affinity for thrombin, and markedly inhibits thrombin-induced reactions, has been used in patients with artherosclerosis obliterans. The efficiency of argatroban, instead of heparin, as an anticoagulant in dog models of cardiopulmonary bypass was explored. In the first study, argatroban was administered as a bolus plus infusion for 1 h during cardiopulmonary bypass at doses of 1.0 mg + 10 microg/kg per min, 2.0 mg + 10 microg/kg per min and 3.0 mg + 10 microg/kg per min (n = 2 per group). Activated clotting time and arterial gas analyses were performed beforehand and 10 min thereafter. In the second study, there were four groups. In the first group (n = 5), no coated extracorporeal circuit was used and heparin (2 mg/kg) was used as an anticoagulant. In the second group (n = 5), a coated extracorporeal circuit was used and heparin was used (2 mg/kg) as an anticoagulant. In the third group (n = 3), no coated extracorporeal circuit was used and argatroban (2.0 mg + 10 microg/kg per min) was used as an anticoagulant. In the fourth group (n = 5), a coated extracorporeal circuit was used and argatroban was used (2.0 mg + 10 microg/kg per min) as an anticoagulant. All animals were perfused for 120 min at 40 ml/kg per minute. Platelet count, activated clotting time, thrombin-antithrombin III complex, antithrombin III, fibrinogen, fibrinogen degradation products and C3a were measured to evaluate platelet, coagulofibrinolytic and the complement system. Activated clotting time values and the effect of argatroban during cardiopulmonary bypass indicated a dose-dependent response. The next highest dosing group (2.0 mg + 10 microg/kg per minute) had activated clotting time values of 250-300 seconds during cardiopulmonary bypass, and fell after reaching near-normal levels within 60 minutes. No clots were noted in the extracorporeal circuit. The argatroban group showed lower levels in their coagulofibrinolytic system compared with the heparin group. The platelet count remained at a high level in the argatroban group. It is concluded that the combination of heparinized cardiopulmonary bypass circuits, and the use of argatroban as an anticoagulant, is safe and reduces the activation of coagulation and fibrinolytic systems and preserves platelet count.
阿加曲班是一种在日本合成的选择性凝血酶抑制剂。阿加曲班对凝血酶具有高亲和力,并能显著抑制凝血酶诱导的反应,已被用于治疗闭塞性动脉硬化症患者。本研究探讨了在犬体外循环模型中,用阿加曲班替代肝素作为抗凝剂的效果。在第一项研究中,在体外循环期间,阿加曲班以推注加输注的方式给药1小时,剂量分别为1.0mg + 10μg/kg每分钟、2.0mg + 10μg/kg每分钟和3.0mg + 10μg/kg每分钟(每组n = 2)。在体外循环前及之后10分钟进行活化凝血时间和动脉血气分析。在第二项研究中,分为四组。第一组(n = 5),未使用涂层体外循环回路,使用肝素(2mg/kg)作为抗凝剂。第二组(n = 5),使用涂层体外循环回路,使用肝素(2mg/kg)作为抗凝剂。第三组(n = 3),未使用涂层体外循环回路,使用阿加曲班(2.0mg + 10μg/kg每分钟)作为抗凝剂。第四组(n = 5),使用涂层体外循环回路,使用阿加曲班(2.0mg + 10μg/kg每分钟)作为抗凝剂。所有动物以每分钟40ml/kg的流量灌注120分钟。检测血小板计数、活化凝血时间、凝血酶 - 抗凝血酶III复合物、抗凝血酶III、纤维蛋白原、纤维蛋白原降解产物和C3a,以评估血小板、凝血纤维蛋白溶解和补体系统。体外循环期间活化凝血时间值及阿加曲班的作用呈剂量依赖性反应。剂量次高组(2.0mg + 10μg/kg每分钟)在体外循环期间活化凝血时间值为250 - 300秒,并在60分钟内达到接近正常水平后下降。体外循环回路中未发现血栓。与肝素组相比,阿加曲班组的凝血纤维蛋白溶解系统水平较低。阿加曲班组的血小板计数维持在较高水平。结论是,肝素化体外循环回路与使用阿加曲班作为抗凝剂相结合是安全的,可减少凝血和纤维蛋白溶解系统的激活,并维持血小板计数。