Cogar Bryan D, Wayangankar Siddharth A, Abu-Fadel Mazen, Hennebry Thomas A, Ghani Mohammad K, Kipperman Robert M, Chrysant George S
Integris Baptist Medical Center, University of Oklahoma, Oklahoma City, Oklahoma 73112, USA.
J Invasive Cardiol. 2012 May;24(5):202-5.
Prior to June 2011, carotid artery stenting (CAS) had been limited to patients deemed high risk for surgical revascularization due to medical or anatomic reasons. Intraprocedural anticoagulation for CAS has traditionally been carried out with unfractionated heparin (UFH). The direct thrombin inhibitor bivalirudin has emerged as a possible alternative choice for anticoagulation in this patient population. In patients undergoing coronary interventions, bivalirudin has been shown in large prospective analysis to reduce major adverse events and hemorrhagic complications (TIMI major bleeding rates, 0.6%-3.1%; TIMI minor bleeding rates, 1.3%-3.7%). As of now, the safety and efficacy of bivalirudin for use during carotid stenting has not been rigorously evaluated. To date, the published evidence in favor of bivalirudin for CAS exists in small retrospective analyses and two prospective studies.
We present a retrospective analysis of 331 patients with a total of 365 carotid artery lesions undergoing CAS between February 2007 and September 2010. The procedures were performed by five experienced operators from four separate sites within the same metropolitan area. Patients were included who received bivalirudin as the anticoagulation strategy and underwent CAS. The primary endpoints of the study were 30-day incidence of death, stroke, TIMI major bleeding (defined as ≥5 g/dL Hgb drop or intracranial hemorrhage), TIMI minor bleeding (defined as ≥3 g/dL Hgb drop), and blood transfusion. All data were collected by retrospective chart review.
A total of 365 CAS procedures were performed. There were no deaths, strokes, or TIMI major bleeds. There was a 2.19% incidence of TIMI minor bleeding (8/365) and a 1.64% rate of blood transfusion (6/365).
In our patient population, the major endpoints of stroke, death, MI, major and minor bleeding rates were well within those previously reported overall for carotid artery revascularization. Hence, we conclude that bivalirudin may be safe for use in CAS procedures with a safety profile similar to that validated in percutaneous coronary interventions.
在2011年6月之前,由于医学或解剖学原因,颈动脉支架置入术(CAS)仅限于那些被认为手术血运重建风险高的患者。传统上,CAS术中抗凝一直使用普通肝素(UFH)。直接凝血酶抑制剂比伐芦定已成为该患者群体抗凝的一种可能替代选择。在接受冠状动脉介入治疗的患者中,大型前瞻性分析表明比伐芦定可减少主要不良事件和出血并发症(TIMI大出血发生率为0.6% - 3.1%;TIMI小出血发生率为1.3% - 3.7%)。截至目前,比伐芦定在颈动脉支架置入术中使用的安全性和有效性尚未得到严格评估。迄今为止,支持比伐芦定用于CAS的已发表证据存在于小型回顾性分析和两项前瞻性研究中。
我们对2007年2月至2010年9月期间共365处颈动脉病变的331例接受CAS的患者进行了回顾性分析。这些手术由来自同一大都市区四个不同地点的五名经验丰富的操作人员进行。纳入接受比伐芦定作为抗凝策略并接受CAS的患者。该研究的主要终点是30天内的死亡、中风、TIMI大出血(定义为血红蛋白下降≥5 g/dL或颅内出血)、TIMI小出血(定义为血红蛋白下降≥3 g/dL)和输血发生率。所有数据均通过回顾性病历审查收集。
共进行了365例CAS手术。无死亡、中风或TIMI大出血发生。TIMI小出血发生率为2.19%(8/365),输血率为1.64%(6/365)。
在我们的患者群体中,中风、死亡、心肌梗死、大出血和小出血发生率等主要终点均在先前报道的颈动脉血运重建总体发生率范围内。因此,我们得出结论,比伐芦定在CAS手术中使用可能是安全的,其安全性与经皮冠状动脉介入治疗中验证的安全性相似。