Cardiovascular Branch, Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.
Center for Structural Heart Disease, Division of Cardiology, and Division of Cardiac Surgery, Henry Ford Health System, Detroit, Michigan; Structural Heart and Valve Center, Emory University Hospital, Atlanta, Georgia.
JACC Cardiovasc Interv. 2019 Jul 8;12(13):1240-1252. doi: 10.1016/j.jcin.2019.03.035. Epub 2019 Jun 12.
The BASILICA (Bioprosthetic or native Aortic Scallop Intentional Laceration to prevent Iatrogenic Coronary Artery obstruction during TAVR) investigational device exemption trial was a prospective, multicenter, single-arm safety and feasibility study.
Coronary artery obstruction is a rare but devastating complication of transcatheter aortic valve replacement (TAVR). Current stent-based preventative strategies are suboptimal. Bioprosthetic or native aortic scallop intentional laceration to prevent iatrogenic coronary artery obstruction during TAVR (BASILICA) is a novel transcatheter technique performed immediately before TAVR to prevent coronary artery obstruction.
Subjects with severe native or bioprosthetic aortic valve disease at high or extreme risk for surgery, and at high risk of coronary artery obstruction, were included. The primary success endpoint was successful BASILICA and TAVR without coronary obstruction or reintervention. The primary safety endpoint was freedom from major adverse cardiovascular events. Data were independently monitored. Endpoints were independently adjudicated. A core laboratory analyzed computed tomography images.
Between February 2018 and July 2018, 30 subjects were enrolled. Primary success was met in 28 (93%) subjects. BASILICA traversal and laceration was successful in 35 of 37 (95%) attempted leaflets. There was 100% freedom from coronary obstruction and reintervention. Primary safety was met in 21 (70%), driven by 6 (20%) major vascular complications related to TAVR but not BASILICA. There was 1 death at 30 days. There was 1 (3%) disabling stroke and 2 (7%) nondisabling strokes. Transient hemodynamic compromise was rare (7%) and resolved promptly with TAVR.
BASILICA was feasible in both native and bioprosthetic valves. Hemodynamic compromise was uncommon. Safety was acceptable and needs confirmation in larger studies. BASILICA appears effective in preventing coronary artery obstruction from TAVR in subjects at high risk.
BASILICA(经导管主动脉瓣置换术中预防医源性冠状动脉阻塞的生物瓣或原生主动脉瓣叶蓄意撕裂)研究性器械豁免试验是一项前瞻性、多中心、单臂安全性和可行性研究。
冠状动脉阻塞是经导管主动脉瓣置换术(TAVR)罕见但具有破坏性的并发症。目前基于支架的预防策略并不理想。生物瓣或原生主动脉瓣叶蓄意撕裂以预防 TAVR 期间的医源性冠状动脉阻塞(BASILICA)是一种新型经导管技术,在 TAVR 之前立即进行,以预防冠状动脉阻塞。
纳入严重的原生或生物瓣主动脉瓣疾病患者,这些患者手术风险高或极高,且存在冠状动脉阻塞高风险。主要成功终点是成功进行 BASILICA 和 TAVR,且无冠状动脉阻塞或再次介入。主要安全性终点是无重大不良心血管事件。数据由独立监测人员进行监测。终点由独立裁决人员进行裁决。一个核心实验室分析了计算机断层扫描图像。
在 2018 年 2 月至 2018 年 7 月期间,共纳入 30 例患者。28 例(93%)患者达到了主要成功。在 37 个尝试的瓣叶中,有 35 个(95%)成功进行了 BASILICA 穿越和撕裂。100%的患者无冠状动脉阻塞和再次介入。21 例(70%)达到了主要安全性,这主要是由 6 例(20%)与 TAVR 相关而非 BASILICA 相关的大血管并发症导致的。有 1 例患者在 30 天时死亡。有 1 例(3%)致残性中风和 2 例(7%)非致残性中风。短暂的血液动力学障碍很少见(7%),并通过 TAVR 迅速解决。
BASILICA 在原生和生物瓣中均可行。血液动力学障碍并不常见。安全性可以接受,需要在更大的研究中证实。BASILICA 似乎可有效预防高危患者 TAVR 中的冠状动脉阻塞。