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下肢旁路手术患者中直接凝血酶抑制剂比伐卢定(Angiomax)的初步前瞻性评估

A pilot, prospective evaluation of a direct thrombin inhibitor, bivalirudin (Angiomax), in patients undergoing lower extremity bypass.

机构信息

Department of Vascular Surgery, Cleveland Clinic, Cleveland, Ohio 44195, USA.

出版信息

J Vasc Surg. 2010 Aug;52(2):369-74. doi: 10.1016/j.jvs.2010.02.276. Epub 2010 May 15.

Abstract

OBJECTIVE

Replacing heparin with bivalirudin has been beneficial in patients undergoing coronary intervention and coronary artery bypass. The use of this alternative anticoagulant during peripheral bypass operations has not been studied. Concerns over distal thrombosis using this direct thrombin inhibitor (DTI) prompted a single-arm, open-label, pilot prospective trial of bivalirudin in patients undergoing lower extremity bypass to assess perioperative safety and efficacy.

METHODS

Between 2006 and 2007, 18 patients met criteria for enrollment and underwent primary lower extremity bypass using bivalirudin. All patients had severe symptomatic atherosclerotic disease requiring lower extremity bypass. Bivalirudin at a bolus dose of 0.75 mg/kg and continuous infusion of 1.75 mg/kg/hr was used as the sole anticoagulant.

RESULTS

Patients (mean age, 67 years) underwent femoral-popliteal (n = 14) or femoral-tibial (n = 4) bypass preferentially using saphenous vein (83%). Mean operative time was 261 minutes, with bivalirudin infusion time of 95 +/- 26 minutes (mean +/- standard deviation). Reliable anticoagulation was achieved with weight-based dosing with activated clotting time values at baseline (systemic) of 131 +/- 92 seconds, during infusion (systemic) of 347 +/- 36 seconds, and from the distal vasculature (limb) of 345 +/- 66 seconds. Distal limb bivalirudin levels were stable at 9755 +/- 3860 ng/mL during clamp occlusion. Mean estimated blood loss was 332 +/- 191 mL with four patients (22%) requiring blood products. One patient required revision of the proximal anastomosis during the initial hospitalization. At 30 days, all bypass operations were patent with improvement of mean ankle-brachial index from 0.57 to 0.81. There were no deaths, myocardial infarctions, or amputations in the 30-day postoperative period. Based on the Thrombolysis in Myocardial Infarction classification for bleeding, one patient had major bleeding (>2 units of packed red blood cells), and three patients had minor bleeding within the first 30 days.

CONCLUSIONS

Bivalirudin is a safe and effective anticoagulant for lower extremity bypass operations. Thrombosis beyond the distal clamp was not seen. A comparative trial to standard anticoagulation is warranted.

摘要

目的

在接受冠状动脉介入和冠状动脉旁路手术的患者中,肝素替代物比伐卢定已显示有益。在周围旁路手术中使用这种替代抗凝剂尚未得到研究。由于对这种直接凝血酶抑制剂(DTI)引起的远端血栓形成的担忧,我们进行了一项单臂、开放标签、前瞻性研究,评估比伐卢定在下肢旁路手术中的围手术期安全性和疗效,入组标准为下肢旁路手术的患者。

方法

在 2006 年至 2007 年期间,18 名患者符合入组标准并接受了下肢旁路手术的比伐卢定治疗。所有患者均患有严重的有症状的动脉粥样硬化疾病,需要进行下肢旁路手术。使用 0.75mg/kg 的首剂量和 1.75mg/kg/hr 的持续输注量的比伐卢定为唯一抗凝剂。

结果

患者(平均年龄,67 岁)接受了股腘旁路(n=14)或股胫旁路(n=4)手术,主要使用隐静脉(83%)。平均手术时间为 261 分钟,比伐卢定输注时间为 95±26 分钟(平均值±标准差)。通过体重剂量实现了可靠的抗凝,基础(全身)激活凝血时间值为 131±92 秒,输注(全身)时为 347±36 秒,从远端血管(肢体)为 345±66 秒。在夹闭时,远端肢体的比伐卢定水平稳定在 9755±3860ng/mL。平均估计出血量为 332±191mL,有 4 名患者(22%)需要输血。一名患者在初次住院期间需要重新吻合近端吻合口。在 30 天时,所有旁路手术均通畅,平均踝肱指数从 0.57 改善至 0.81。在术后 30 天内无死亡、心肌梗死或截肢。根据血栓溶解治疗心肌梗死出血分类,有 1 名患者发生大出血(>2 单位浓缩红细胞),3 名患者在术后 30 天内发生轻微出血。

结论

比伐卢定为下肢旁路手术提供了一种安全有效的抗凝选择。未观察到远端夹闭处以外的血栓形成。有必要进行与标准抗凝比较的临床试验。

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