Molenaar I Q, Legnani C, Groenland T H, Palareti G, Begliomini B, Terpstra O T, Porte R J
Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Liver Transpl. 2001 Oct;7(10):896-903. doi: 10.1053/jlts.2001.27854.
Aprotinin reduces blood transfusion requirements in orthotopic liver transplantation (OLT). Concern has been voiced about the potential risk for thrombotic complications when aprotinin is used. The aim of this study is to evaluate the effects of aprotinin on the two components of the hemostatic system (coagulation and fibrinolysis) in patients undergoing OLT. As part of a larger, randomized, double-blind, placebo-controlled study, we compared coagulation (fibrinogen level, activated partial thromboplastin time [aPTT], prothrombin time, and platelet count) and fibrinolytic variables (tissue-type plasminogen activator [tPA] antigen and activity, plasminogen activator inhibitor activity, and D-dimer), as well as thromboelastography (reaction time [r], clot formation time, and maximum amplitude) in 27 patients administered either high-dose aprotinin (2 x 10(6) kallikrein inhibitor units [KIU] at induction, continuous infusion of 1 x 10(6) KIU/h, and 1 x 10(6) KIU before reperfusion; n = 10), regular-dose aprotinin (2 x 10(6) KIU at induction and continuous infusion of 0.5 x 10(6) KIU/h; n = 8), or placebo (n = 9) during OLT. Blood samples were drawn at seven standardized intraoperative times. Baseline characteristics were similar for the three groups. During the anhepatic and postreperfusion periods, fibrinolytic activity (plasma D-dimer and tPA antigen levels) was significantly lower in aprotinin-treated patients compared with the placebo group. Interestingly, coagulation times (aPTT and r) were significantly more prolonged in aprotinin-treated patients than the placebo group. No difference was seen in the incidence of perioperative thrombotic complications in the entire study population (n = 137). Aprotinin has an anticoagulant rather than a procoagulant effect. Its blood-sparing (prohemostatic) effect appears to be the overall result of a strong antifibrinolytic and a weaker anticoagulant effect. These findings argue against a prothrombotic effect of aprotinin in patients undergoing OLT.
抑肽酶可减少原位肝移植(OLT)中的输血需求。有人对使用抑肽酶时血栓形成并发症的潜在风险表示担忧。本研究的目的是评估抑肽酶对接受OLT患者止血系统的两个组成部分(凝血和纤溶)的影响。作为一项更大规模的随机、双盲、安慰剂对照研究的一部分,我们比较了27例在OLT期间接受高剂量抑肽酶(诱导时2×10⁶激肽释放酶抑制单位[KIU],持续输注1×10⁶KIU/h,再灌注前1×10⁶KIU;n = 10)、常规剂量抑肽酶(诱导时2×10⁶KIU,持续输注0.5×10⁶KIU/h;n = 8)或安慰剂(n = 9)治疗的患者的凝血指标(纤维蛋白原水平、活化部分凝血活酶时间[aPTT]、凝血酶原时间和血小板计数)、纤溶指标(组织型纤溶酶原激活物[tPA]抗原和活性、纤溶酶原激活物抑制剂活性和D-二聚体)以及血栓弹力图指标(反应时间[r]、凝血形成时间和最大振幅)。在七个标准化的术中时间点采集血样。三组的基线特征相似。在无肝期和再灌注期,与安慰剂组相比,抑肽酶治疗的患者纤溶活性(血浆D-二聚体和tPA抗原水平)显著降低。有趣的是,抑肽酶治疗的患者凝血时间(aPTT和r)比安慰剂组显著延长。在整个研究人群(n = 137)中,围手术期血栓形成并发症的发生率没有差异。抑肽酶具有抗凝而非促凝作用。其血液保护(促止血)作用似乎是强烈的抗纤溶作用和较弱的抗凝作用的总体结果。这些发现反对抑肽酶在接受OLT患者中具有促血栓形成作用的观点。