Department of Cardiac Surgery, University of Heidelberg, Heidelberg, Germany.
J Thorac Cardiovasc Surg. 2010 Jan;139(1):181-8; discussion 188. doi: 10.1016/j.jtcvs.2009.09.019.
Although aprotinin has been widely used to reduce perioperative blood loss after cardiopulmonary bypass, recent concerns have led to its withdrawal. This study investigated effects of the novel synthetic serine protease inhibitors CU-2010 and CU-2020 on blood loss, coagulation parameters, and coronary relaxation in a canine model.
Thirty-seven dogs were divided into 5 groups: control (n = 5), aprotinin (n = 8, Hammersmith scheme of intravenous bolus, prime, and continuous infusion), Hammersmith CU-2010 (n = 8, 1.6 mg/kg Hammersmith scheme), continuous CU-2010 (n = 8, 1.6 mg/kg continuous infusion), and CU-2020 (n = 8, 8.9 mg/kg Hammersmith scheme). All animals underwent 90-minute cardiopulmonary bypass. End points were blood loss during first 2 hours after protamine and activated clotting, partial thromboplastin, and prothrombin times. At end of experiments, coronary rings were removed for in vitro testing of relaxation to acetylcholine and sodium nitroprusside.
Hammersmith and continuous CU-2010, CU-2020, and aprotinin groups all had reduced blood loss (43 + or - 4, 43 + or - 8, 52 + or - 7, 61 + or - 7, respectively, vs control 149 + or - 24 mL, P < .05). After protamine, activated clotting time and partial thromboplastin time normalized in control, aprotinin, and Hammersmith CU-2010 groups but remained elevated in continuous CU-2010 and CU-2020 groups. Prothrombin time and vascular relaxation did not differ between groups.
CU-2010 and CU-2020 significantly reduced blood loss after cardiac surgery, with prolonged partial thromboplastin and activated clotting times, demonstrating improved antithrombotic profile. Neither aprotinin nor the novel serine protease inhibitors influenced vascular relaxation.
尽管抑肽酶已被广泛用于减少体外循环后的围手术期失血,但最近的一些担忧已导致其被停用。本研究旨在探讨新型合成丝氨酸蛋白酶抑制剂 CU-2010 和 CU-2020 在犬模型中对失血、凝血参数和冠状动脉舒张的影响。
37 只狗分为 5 组:对照组(n=5)、抑肽酶组(n=8,采用静脉推注、首剂和持续输注的哈默史密斯方案)、哈默史密斯 CU-2010 组(n=8,采用哈默史密斯方案 1.6mg/kg)、持续 CU-2010 组(n=8,采用持续输注 1.6mg/kg)和 CU-2020 组(n=8,采用哈默史密斯方案 8.9mg/kg)。所有动物均接受 90 分钟体外循环。终点为鱼精蛋白和激活凝血时间、部分凝血活酶时间和凝血酶原时间后前 2 小时的失血量。实验结束时,取出冠状动脉环进行乙酰胆碱和硝普钠松弛的离体检测。
哈默史密斯和持续 CU-2010、CU-2020 和抑肽酶组的失血量均减少(分别为 43±4、43±8、52±7、61±7 比对照组 149±24mL,P<.05)。在鱼精蛋白后,对照组、抑肽酶组和哈默史密斯 CU-2010 组的激活凝血时间和部分凝血活酶时间恢复正常,但持续 CU-2010 和 CU-2020 组的这些时间仍升高。各组凝血酶原时间和血管舒张无差异。
CU-2010 和 CU-2020 显著减少心脏手术后的失血,同时延长部分凝血活酶时间和激活凝血时间,显示出改善的抗血栓形成特性。抑肽酶和新型丝氨酸蛋白酶抑制剂均不影响血管舒张。