Department of Cardiology, Centre Hospitalier Régional Universitaire (CHRU) Lille and Unité Mixte de Recherche (UMR1011), Lille, France.
Deutsches Herzzentrum München, Technische Universität München, Munich, Germany; Deutsches Zentrum für Herz-Kreislauf-Forschung E.V. (DZHK), partner site Munich Heart Alliance, Munich, Germany.
J Am Coll Cardiol. 2016 Aug 9;68(6):589-599. doi: 10.1016/j.jacc.2016.05.006. Epub 2016 May 18.
Cerebral embolization is a frequent complication after transcatheter aortic valve replacement (TAVR). We hypothesized that cerebral embolization may be reduced by anticoagulation with bivalirudin during TAVR.
This study sought to determine the proportion of patients with new cerebral embolus after TAVR and to investigate whether parenteral procedural anticoagulation strategies affect cerebral embolization.
The BRAVO (Effect of Bivalirudin on Aortic Valve Intervention Outcomes)-3 randomized trial compared bivalirudin with unfractionated heparin in patients undergoing transfemoral TAVR. A prospective cerebral magnetic resonance imaging (MRI) substudy was conducted in 4 sites; 60 patients were imaged with brain MRI after TAVR. Primary endpoint was proportion of patients with new cerebral emboli on MRI. Secondary endpoints included quantitative MRI analyses of cerebral lesions and neurological outcomes at 48 h and 30 days.
Patients were randomized to bivalirudin (n = 29) versus heparin (n = 31). The proportion of patients with new cerebral emboli on MRI did not differ between bivalirudin and heparin groups (65.5% vs. 58.1%; p = 0.55). Groups were similar for median number of emboli per patient (1 [interquartile range (IQR): 0 to 3] vs. 1 [IQR: 0 to 1]; p = 0.08), total volume of emboli (45 [IQR: 0 to 175] mm(3) vs. 33 [IQR: 0 to 133] mm(3); p = 0.86), or proportion of patients with a clinical neurological deficit at 48 h or 30 days. All patients who presented clinically with stroke had evidence of new emboli on MRI.
This study documented cerebral embolization in nearly two-thirds of patients during contemporary TAVR. There were no significant differences in cerebral embolization for bivalirudin versus heparin anticoagulation during TAVR. (Open-Label, Randomized Trial in Patients Undergoing TAVR to Determine Safety and Efficacy of Bivalrudin vs. UFH [BRAVO-2/3]; NCT01651780).
经导管主动脉瓣置换术(TAVR)后,脑栓塞是一种常见的并发症。我们假设,在 TAVR 期间使用比伐芦定进行抗凝治疗可以减少脑栓塞。
本研究旨在确定 TAVR 后新发脑栓塞患者的比例,并探讨是否经导管主动脉瓣置换术(TAVR)时的抗凝策略影响脑栓塞。
BRAVO(比伐芦定对主动脉瓣介入治疗结局的影响)-3 是一项随机试验,比较了比伐芦定与普通肝素在经股动脉 TAVR 患者中的疗效。在 4 个地点进行了前瞻性脑磁共振成像(MRI)子研究;60 例患者在 TAVR 后进行脑 MRI 检查。主要终点是 MRI 上新发脑栓塞患者的比例。次要终点包括 48 小时和 30 天时脑损伤的定量 MRI 分析和神经学结局。
患者随机分为比伐芦定组(n=29)和肝素组(n=31)。MRI 上有新发脑栓塞的患者比例在比伐芦定组和肝素组之间无差异(65.5%比 58.1%;p=0.55)。两组患者的平均栓塞数(中位数[四分位距]:1[0 至 3]比 1[0 至 1];p=0.08)、栓塞总体积(45[0 至 175]mm3比 33[0 至 133]mm3;p=0.86)或 48 小时或 30 天有临床神经功能缺损的患者比例相似。所有临床表现为中风的患者 MRI 上均有新的栓塞证据。
本研究记录了当代 TAVR 中近三分之二患者的脑栓塞。与肝素抗凝相比,TAVR 期间比伐芦定抗凝并未显著降低脑栓塞的发生。(在接受 TAVR 的患者中进行的以比伐芦定为对照的开放性随机试验,以确定比伐芦定与 UFH 的安全性和疗效[BRAVO-2/3];NCT01651780)。