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活性位点阻断的凝血因子IXa用于无肝素体外循环:犬的初步研究

Heparinless cardiopulmonary bypass with active-site blocked factor IXa: a preliminary study on the dog.

作者信息

Spanier T B, Oz M C, Minanov O P, Simantov R, Kisiel W, Stern D M, Rose E A, Schmidt A M

机构信息

Department of Surgery, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.

出版信息

J Thorac Cardiovasc Surg. 1998 May;115(5):1179-88. doi: 10.1016/S0022-5223(98)70419-2.

Abstract

OBJECTIVE

Cardiopulmonary bypass is a potent stimulus for activation of procoagulant pathways. Heparin, the traditional antithrombotic agent, however, is often associated with increased perioperative blood loss because of its multiple sites of action in the coagulation cascade and its antiplatelet and profibrinolytic effects. Furthermore, heparin-mediated immunologic reactions (that is, heparin-induced thrombocytopenia) may contraindicate its use. Cardiopulmonary bypass with a selective factor IXa inhibitor was tested to see whether it could effectively limit bypass circuit/intravascular space thrombosis while decreasing extravascular bleeding, thereby providing an alternative anticoagulant strategy when heparin may not be safely administered.

METHODS

Active site-blocked factor IXa, a competitive inhibitor of the assembly of factor IXa into the factor X activation complex, was prepared by modification of the enzyme's active site by the use of dansyl glutamic acid-glycine-arginine-chlormethylketone. Twenty mongrel dogs (five were given standard heparin/protamine; 15 were given activated site-blocked factor IXa doses ranging from 300 to 600 microg/kg) underwent 1 hour of hypothermic cardiopulmonary bypass, and blood loss was monitored for 3 hours after the procedure.

RESULTS

Use of activated site-blocked factor IXa as an anticoagulant in cardiopulmonary bypass limited fibrin deposition within the extracorporeal circuit as assessed by scanning electron microscopy, comparable with the antithrombotic effect seen with heparin. In contrast to heparin, effective antithrombotic doses of activated site-blocked factor IXa significantly diminished blood loss in the thoracic cavity and in an abdominal incisional bleeding model.

CONCLUSION

These initial studies on the dog suggest that administration of activated site-blocked factor IXa may be an effective alternative anticoagulant strategy in cardiopulmonary bypass when heparin is contraindicated, affording inhibition of intravascular/extracorporeal circuit thrombosis with enhanced hemostasis in the surgical wound.

摘要

目的

体外循环是激活促凝血途径的一种强效刺激因素。然而,传统的抗血栓药物肝素,由于其在凝血级联反应中的多个作用位点以及抗血小板和促纤溶作用,常与围手术期失血增加有关。此外,肝素介导的免疫反应(即肝素诱导的血小板减少症)可能使其使用成为禁忌。对使用选择性因子IXa抑制剂进行体外循环进行了测试,以观察其是否能有效限制体外循环回路/血管内血栓形成,同时减少血管外出血,从而在肝素可能无法安全使用时提供一种替代抗凝策略。

方法

通过使用丹磺酰谷氨酸 - 甘氨酸 - 精氨酸 - 氯甲基酮修饰酶的活性位点,制备了活性位点被阻断的因子IXa,它是因子IXa组装到因子X激活复合物中的竞争性抑制剂。20只杂种犬(5只给予标准肝素/鱼精蛋白;15只给予活性位点被阻断的因子IXa,剂量范围为300至600微克/千克)接受1小时的低温体外循环,并在术后监测3小时的失血量。

结果

通过扫描电子显微镜评估,使用活性位点被阻断的因子IXa作为体外循环中的抗凝剂可限制体外循环回路内的纤维蛋白沉积,与肝素的抗血栓作用相当。与肝素相反,有效抗血栓剂量的活性位点被阻断的因子IXa显著减少了胸腔内和腹部切口出血模型中的失血量。

结论

这些对犬的初步研究表明,当肝素禁忌时,给予活性位点被阻断的因子IXa可能是体外循环中一种有效的替代抗凝策略,可抑制血管内/体外循环回路血栓形成,并增强手术伤口的止血效果。

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