Fairman Ronald M, Criado Frank, Farber Mark, Kwolek Christopher, Mehta Manish, White Rodney, Lee Anthony, Tuchek J Michael
Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
J Vasc Surg. 2008 Sep;48(3):546-54. doi: 10.1016/j.jvs.2008.03.061. Epub 2008 Jun 24.
This report summarizes the 30-day and 12-month results of endovascular treatment using the Medtronic Vascular Talent Thoracic Stent Graft System (Medtronic Vascular, Santa Rosa, Calif) for patients with thoracic aortic aneurysms (TAA) who are considered candidates for open surgical repair.
The study was a prospective, nonrandomized, multicenter, pivotal trial conducted at 38 sites. Enrollment occurred between December 2003 and June 2005. Standard follow-up interval examinations were prescribed at 1 month, 6 months, 1 year, and annually thereafter. These endovascular results were compared with retrospective open surgical data from three centers of excellence.
The Evaluation of the Medtronic Vascular Talent Thoracic Stent Graft System for the Treatment of Thoracic Aortic Aneurysms (VALOR) trial enrolled 195 patients, and 189 were identified as retrospective open surgical subjects. Compared with the open surgery group, the VALOR test group had similar age and sex distributions, but had a smaller TAA size. Patients received a mean number of 2.7 +/- 1.3 stent graft components. The diameters of 25% of the proximal stent graft components implanted were <26 mm or >40 mm. Left subclavian artery revascularization was performed before the initial stent graft procedure in 5.2% of patients. Iliac conduits were used in 21.1% of patients. In 33.5% of patients, the bare spring segment of the most proximally implanted device was in zones 1 or 2 of the aortic arch. In 194 patients (99.5%), vessel access and stent graft deployment were successful at the intended site. The 30-day VALOR results included perioperative mortality, 2.1%; major adverse advents, 41%; incidence of paraplegia, 1.5%; paraparesis, 7.2%; and stroke, 3.6%. The 12-month VALOR results included all-cause mortality, 16.1%; aneurysm-related mortality, 3.1%; conversion to open surgery, 0.5%; target aneurysm rupture, 0.5%; stent graft migration >10 mm, 3.9%; endoleak (12.2%), stent graft patency, 100%; stable or decreasing aneurysm diameter, 91.5%; and loss of stent graft integrity, four patients. No deployment-related events or perforation of the aorta by a graft component occurred. The Talent Thoracic Stent Graft showed statistically superior performance with respect to acute procedural outcomes (P < .001), 30-day major adverse events (41% vs 84.4%, P < .001), perioperative mortality (2% vs 8%, P < .01), and 12-month aneurysm-related mortality (3.1% vs 11.6%, P < .002) vs open surgery.
The pivotal VALOR 12-month trial results demonstrate that the Medtronic Talent Thoracic Stent Graft System is a safe and effective endovascular therapy as an alternative to open surgery in patients with TAA who were considered candidates for open surgical repair.
本报告总结了使用美敦力血管Talent胸主动脉覆膜支架系统(美敦力血管,加利福尼亚州圣罗莎)对被视为开放手术修复候选者的胸主动脉瘤(TAA)患者进行血管内治疗的30天和12个月结果。
该研究是一项在38个地点进行的前瞻性、非随机、多中心关键试验。入组时间为2003年12月至2005年6月。规定在1个月、6个月、1年及此后每年进行标准的随访间隔检查。将这些血管内治疗结果与来自三个卓越中心的回顾性开放手术数据进行比较。
美敦力血管Talent胸主动脉覆膜支架系统治疗胸主动脉瘤(VALOR)试验纳入了195例患者,其中189例被确定为回顾性开放手术对象。与开放手术组相比,VALOR试验组的年龄和性别分布相似,但TAA尺寸较小。患者平均接受2.7±1.3个覆膜支架组件。植入的近端覆膜支架组件中25%的直径<26 mm或>40 mm。5.2%的患者在初次覆膜支架手术前进行了左锁骨下动脉血运重建。21.1%的患者使用了髂血管导管。33.5%的患者中,最近端植入装置的裸弹簧段位于主动脉弓的1区或2区。194例患者(99.5%)在预期部位成功进行了血管入路和覆膜支架置入。VALOR试验的30天结果包括围手术期死亡率2.1%;主要不良事件41%;截瘫发生率1.5%;轻截瘫7.2%;中风3.6%。VALOR试验的12个月结果包括全因死亡率16.1%;动脉瘤相关死亡率3.1%;转为开放手术0.5%;目标动脉瘤破裂0.5%;覆膜支架移位>10 mm 3.9%;内漏(12.2%),覆膜支架通畅率100%;动脉瘤直径稳定或缩小91.5%;覆膜支架完整性丧失4例。未发生与置入相关的事件或移植物组件对主动脉的穿孔。与开放手术相比,Talent胸主动脉覆膜支架在急性手术结果(P<.001)、30天主要不良事件(41%对84.4%,P<.001)、围手术期死亡率(2%对8%,P<.01)和12个月动脉瘤相关死亡率(3.1%对11.6%,P<.002)方面显示出统计学上更优的性能。
关键的VALOR 12个月试验结果表明,美敦力Talent胸主动脉覆膜支架系统是一种安全有效的血管内治疗方法,可作为开放手术修复候选者的TAA患者开放手术的替代方案。