Department of Vascular Surgery, St. Franziskus Hospital and University Hospital of Muenster, Germany.
J Endovasc Ther. 2013 Oct;20(5):672-7. doi: 10.1583/13-4400MR.1.
To assess the anatomical suitability of the new off-the-shelf multibranched endograft (t-branch) in patients with thoracoabdominal aortic aneurysms (TAAA) previously treated by means of custom-made multibranched endografts.
Clinical and radiological data of 43 consecutive patients (34 men; mean age 72 years) with Crawford types I (n=1), II (n=16), III (n=18), or IV (n=8) TAAAs treated with custom-made multibranched endografts between June 2008 and February 2013 were retrospectively reviewed. Primary anatomical suitability of the t-branch device was assessed using 3-dimensional computed tomographic angiograms. Assisted suitability referred to the ability to use adjuvant procedures to eliminate anatomical obstacles that did not hinder the custom-made devices.
Among the study group, 21 (49%) patients were suitable for treatment using the t-branch device. Another 6 (14%) would have been suitable with the assistance of additional maneuvers, such as thoracic endografting with (n=3) or without (n=3) left carotid-subclavian bypass. Sixteen (37%) patients violated the eligibility criteria due to a distance >56 cm between the celiac trunk and the most caudal renal artery (9, 60%), insufficient diameter (<25 mm) at the level of the visceral arteries (5, 33%), upward orientation of a renal artery (3, 20%), inadequate (>40 mm) proximal landing zone (2, 13%), and a distance <67 mm between the most caudal renal artery and aortic bifurcation (1, 7%).
The t-branch stent-graft system would have been primarily suitable for implantation in half of the patients. With additional maneuvers, the assisted suitability reached 63%. Further optimization and refinement of the device will probably lead to a shift toward off-the-shelf multibranched stent-graft exclusion of TAAAs.
评估新的即市分支型覆膜支架(t-branch)在先前使用定制分支型覆膜支架治疗的胸腹主动脉瘤(TAAA)患者中的解剖学适用性。
回顾性分析 2008 年 6 月至 2013 年 2 月期间,43 例连续接受定制分支型覆膜支架治疗的 Crawford Ⅰ型(n=1)、Ⅱ型(n=16)、Ⅲ型(n=18)或Ⅳ型(n=8)TAAA 的患者的临床和影像学资料。使用三维 CT 血管造影评估 t-branch 装置的原发性解剖学适用性。辅助适用性是指能够使用辅助手术来消除不影响定制设备的解剖学障碍的能力。
在研究组中,21 例(49%)患者适合使用 t-branch 装置进行治疗。另外 6 例(14%)患者需要通过额外的手术来增加辅助适用性,例如胸主动脉覆膜支架置入术(n=3)或不进行该手术(n=3)加左侧颈动脉-锁骨下旁路术。16 例(37%)患者因腹腔干与最下肾动脉之间的距离>56cm(9 例,60%)、内脏动脉水平的直径<25mm(5 例,33%)、肾动脉向上走行(3 例,20%)、近端锚定区不足(>40mm,2 例,13%)和最下肾动脉与主动脉分叉之间的距离<67mm(1 例,7%)而不符合入选标准。
t-branch 支架移植物系统在一半的患者中原本适合植入。通过额外的手术,辅助适用性达到 63%。该装置的进一步优化和改进可能会导致采用即市分支型覆膜支架治疗 TAAA 的比例增加。