Wheatley Grayson H, Gurbuz Ahmet Tayfun, Rodriguez-Lopez Julio A, Ramaiah Venkatesh G, Olsen Dawn, Williams James, Diethrich Edward B
Department of Cardiovascular Surgery, Arizona Heart Institute, Phoenix, Arizona 85006, USA.
Ann Thorac Surg. 2006 May;81(5):1570-7; discussion 1577. doi: 10.1016/j.athoracsur.2005.06.068.
Despite recent improvements in surgical technique, some patients with descending thoracic aortic pathologies are unable to undergo open surgical repair due to significant comorbidities and/or unfavorable thoracic aortic anatomy. Some of these patients might be able to tolerate a less invasive approach, such as endoluminal grafting. We reviewed our consecutive clinical experience with the Gore TAG endoprosthesis (W. L. Gore & Assoc, Flagstaff, AZ) for the endovascular exclusion of assorted descending thoracic aortic pathologies in higher surgical risk patients.
After obtaining institutional review board approval, 158 high surgical risk patients underwent attempted delivery of a Gore TAG thoracic endoprosthesis between February 2000 and July 2004. Indications for study enrollment were atherosclerotic aneurysm (n = 76), aortic dissection (n = 36), penetrating aortic ulcer (n = 15), contained rupture (n = 11), pseudoaneurysm (n = 10), traumatic aortic injury (n = 5), aortobronchial fistula (n = 4), and aortic coarctation (n = 1).
The device was successfully delivered in 156 (98.7%) patients. Mean patient age was 72 +/- 12.1 years. Three (1.9%) patients developed transient paraparesis after graft deployment and 1 (0.6%) patient developed paraplegia. While postimplantation endoleaks were observed in 18 (11.5%) patients, only 12 patients required reintervention. Thirty-day mortality was 3.8% (6 of 156). Mean follow-up was 21.5 +/- 18.8 months, and the overall mortality was 17.3% (27 of 156).
Endoluminal grafting of multiple types of descending thoracic aorta pathologies with the Gore TAG thoracic endoprosthesis is feasible and safe in higher surgical risk patients. Additional studies and long-term follow-up of these patients are warranted.
尽管近期手术技术有所改进,但一些降主动脉病变患者由于严重的合并症和/或降主动脉解剖结构不佳,无法接受开放手术修复。其中一些患者可能能够耐受侵入性较小的方法,如腔内移植术。我们回顾了我们连续使用Gore TAG血管内移植物(W.L.Gore & Assoc,弗拉格斯塔夫,亚利桑那州)对手术风险较高的患者进行各种降主动脉病变血管腔内排除的临床经验。
在获得机构审查委员会批准后,158例手术风险较高的患者在2000年2月至2004年7月期间尝试植入Gore TAG胸主动脉内移植物。纳入研究的指征包括动脉粥样硬化性动脉瘤(n = 76)、主动脉夹层(n = 36)、穿透性主动脉溃疡(n = 15)、局限性破裂(n = 11)、假性动脉瘤(n = 10)、创伤性主动脉损伤(n = 5)、主动脉支气管瘘(n = 4)和主动脉缩窄(n = 1)。
该装置在156例(98.7%)患者中成功植入。患者平均年龄为72±12.1岁。3例(1.9%)患者在植入移植物后出现短暂性截瘫,1例(0.6%)患者出现截瘫。虽然18例(11.5%)患者在植入后观察到内漏,但只有12例患者需要再次干预。30天死亡率为3.8%(156例中的6例)。平均随访时间为21.5±18.8个月,总死亡率为17.3%(156例中的27例)。
对于手术风险较高的患者,使用Gore TAG胸主动脉内移植物对多种类型的降主动脉病变进行腔内移植是可行且安全的。对这些患者进行进一步研究和长期随访是必要的。