Conrad Mark F, Tuchek James, Freezor Robert, Bavaria Joseph, White Rodney, Fairman Ronald
Massachusetts General Hospital, Harvard Medical School, Boston, Mass.
Loyola University, Maywood, Ill.
J Vasc Surg. 2017 Aug;66(2):335-342. doi: 10.1016/j.jvs.2016.12.136. Epub 2017 Mar 30.
The 1-year results of endovascular exclusion of degenerative descending thoracic aortic aneurysms (DTA) with the Valiant Thoracic Stent Graft (Medtronic Vascular, Santa Rosa, Calif) have been previously reported. With long-term follow-up now complete, the 5-year results are reported.
The VALOR II trial (Evaluation of the Clinical Performance of the Valiant Thoracic Stent Graft System in the Treatment of Descending Thoracic Aneurysms of Degenerative Etiology in Subjects Who Are Candidates for Endovascular Repair) was a prospective, nonrandomized trial of the Valiant Thoracic Stent Graft system in patients with degenerative DTA. The trial involved 24 sites in the United States and enrolled patients between December 2006 and September 2009. Standard follow-up included physical examination, computed tomography, and chest radiography through 5 years.
The study enrolled 160 patients. The average age was 72.2 years (range, 36-85 years), 95 (59%) were men, 150 (94%) had hypertension, and 26 (16%) had renal insufficiency. There were 50 patients (31%) who presented with symptoms; back pain was the most common (34 [68%]). The average aneurysm diameter was 57 mm (range, 32-96 mm). There were 103 patients (64%) with a fusiform aneurysm and 57 (36%) with a saccular aneurysm or penetrating ulcer. Two or more devices were implanted in 126 patients (79%), and the maximum number of grafts implanted was four. There were 54 deaths during the study. The 5-year actuarial survival was 64%. There were eight aneurysm-related deaths (5 deaths ≤30 days of implant), and the 5-year freedom from aneurysm-related death was 95%. There was one conversion to open repair at 36 months. Eleven patients underwent 13 secondary procedures (9 for endoleak, 3 for aneurysm expansion, and 1 rupture). Follow-up imaging was available at 5 years for 56 patients. The average aortic diameter decreased >5 mm in 27 patients (48%), increased >5 mm in 6 patients (11%), and remained unchanged in 23 (41%).
The VALOR II 5-year results demonstrate that the reintervention and aneurysm-related death rates are low. The Valiant Thoracic Stent Graft is an effective treatment of degenerative DTA.
此前已有关于使用维兰特胸主动脉覆膜支架(美敦力血管公司,加利福尼亚州圣罗莎)对退行性降主动脉瘤(DTA)进行血管腔内隔绝术的1年结果报道。随着长期随访的完成,现将5年结果报告如下。
VALOR II试验(维兰特胸主动脉覆膜支架系统治疗适合血管腔内修复的退行性病因降主动脉瘤患者的临床性能评估)是一项针对维兰特胸主动脉覆膜支架系统治疗退行性DTA患者的前瞻性、非随机试验。该试验在美国的24个地点开展,于2006年12月至2009年9月纳入患者。标准随访包括5年的体格检查、计算机断层扫描和胸部X线检查。
该研究共纳入160例患者。平均年龄为72.2岁(范围36 - 85岁),95例(59%)为男性,150例(94%)患有高血压,26例(16%)患有肾功能不全。有50例患者(31%)出现症状;背痛最为常见(34例[68%])。动脉瘤平均直径为57毫米(范围32 - 96毫米)。103例患者(64%)为梭形动脉瘤,57例(36%)为囊状动脉瘤或穿透性溃疡。126例患者(79%)植入了两个或更多装置,植入移植物的最大数量为4个。研究期间有54例死亡。5年精算生存率为64%。有8例与动脉瘤相关的死亡(5例死亡发生在植入后≤30天),5年无动脉瘤相关死亡的概率为95%。36个月时1例转为开放修复。11例患者接受了13次二次手术(9次用于治疗内漏,3次用于治疗动脉瘤扩张,1次用于治疗破裂)。56例患者有5年的随访影像学资料。27例患者(48%)的主动脉平均直径减小>5毫米,6例患者(11%)增大>5毫米,23例患者(41%)保持不变。
VALOR II试验的5年结果表明,再次干预率和与动脉瘤相关的死亡率较低。维兰特胸主动脉覆膜支架是治疗退行性DTA的有效方法。