Poston Robert S, White Charles, Gu Junyan, Brown James, Gammie James, Pierson Richard N, Lee Andrew, Connerney Ingrid, Avari Thrity, Christenson Robert, Tandry Udaya, Griffith Bartley P
Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Ann Thorac Surg. 2006 Jan;81(1):104-10; discussion 110-1. doi: 10.1016/j.athoracsur.2005.05.085.
Hemostatic drugs are widely thought to be unnecessary and potentially detrimental in off-pump coronary artery bypass graft surgery (OPCABG), despite well-established use in on-pump surgery. In a randomized, prospective OPCABG trial, we assessed efficacy and safety of aprotinin through a comprehensive assessment of graft patency and hematologic function.
Sixty patients were randomly assigned to full-dose aprotinin or placebo. Heparin was titrated to a kaolin-based activated clotting time of greater than 300 seconds. Exclusionary criteria included creatinine greater than 2 mg/dL, conversion to on-pump CABG, and preoperative GPIIb/IIIa inhibition. Hematologic assessments were obtained preoperatively, at the end of surgery, and on days 1 and 3: mean platelet volume, thrombin generation (prothrombin fragment 1.2 assay), and aspirin resistance using a modified thrombelastography, whole blood aggregometry, 11-dehydro-thromboxane B2 levels, and flow cytometry. Thrombotic events were defined as postoperative myocardial infarction by electrocardiography or elevated troponin I, clinical stroke by examination and head computed tomography, and bypass graft failure by multichannel computed tomography angiography on day 5.
Aprotinin was associated with a significant reduction in intraoperative and postoperative blood loss compared with placebo but had no effect on transfusion rates. Patients treated with aprotinin had significantly fewer thrombotic events (3% versus 23%, p < 0.05, Fisher's exact test) and less postoperative aspirin resistance (20% versus 46%, respectively, p < 0.05, Fisher's exact test). Postoperative prothrombin fragment 1.2 level was reduced by aprotinin use.
Aprotinin reduced perioperative bleeding after OPCABG. Preserved aspirin sensitivity in the aprotinin group may explain the observed reduction in thrombotic events and might be related to the suppression of perioperative and transmyocardial thrombin formation.
尽管止血药物在体外循环心脏手术中已被广泛应用,但人们普遍认为在非体外循环冠状动脉旁路移植术(OPCABG)中使用止血药物是不必要的,而且可能有害。在一项随机、前瞻性OPCABG试验中,我们通过全面评估移植血管通畅情况和血液学功能,评估了抑肽酶的疗效和安全性。
60例患者被随机分配至接受全剂量抑肽酶或安慰剂治疗组。将肝素滴定至基于高岭土的活化凝血时间大于300秒。排除标准包括肌酐大于2mg/dL、转为体外循环CABG以及术前使用糖蛋白IIb/IIIa抑制剂。在术前、手术结束时以及术后第1天和第3天进行血液学评估:平均血小板体积、凝血酶生成(凝血酶原片段1.2测定),并使用改良血栓弹力图、全血凝集试验、11-脱氢血栓素B2水平以及流式细胞术评估阿司匹林抵抗情况。血栓形成事件定义为术后通过心电图或肌钙蛋白I升高诊断的心肌梗死、通过体格检查和头部计算机断层扫描诊断的临床中风以及术后第5天通过多通道计算机断层扫描血管造影诊断的旁路移植血管失败。
与安慰剂相比,抑肽酶可显著减少术中和术后失血,但对输血率无影响。接受抑肽酶治疗的患者血栓形成事件显著减少(分别为3%和23%,p<0.05,Fisher精确检验),术后阿司匹林抵抗也较轻(分别为20%和46%,p<0.05,Fisher精确检验)。使用抑肽酶可降低术后凝血酶原片段1.2水平。
抑肽酶可减少OPCABG术后围手术期出血。抑肽酶组中阿司匹林敏感性得以保留,这可能解释了观察到的血栓形成事件减少的现象,并且可能与围手术期和经心肌凝血酶形成的抑制有关。