Matsumura Jon S, Cambria Richard P, Dake Michael D, Moore Randy D, Svensson Lars G, Snyder Scott
Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
J Vasc Surg. 2008 Feb;47(2):247-257; discussion 257. doi: 10.1016/j.jvs.2007.10.032.
This trial evaluated the safety and effectiveness of thoracic endovascular aortic repair (TEVAR) with a contemporary endograft system compared with open surgical repair (open) of descending thoracic aortic aneurysms and large ulcers.
Forty-two international trial sites enrolled 230 subjects with descending thoracic aortic aneurysms or ulcers. The study compared 160 TEVAR subjects treated with the Zenith TX2 Endovascular Graft (William Cook Europe, ApS, Bjaeverskov, Denmark) with 70 open subjects. Subjects were evaluated preprocedure, predischarge, 1, 6, and 12 months, and yearly through 5 years with medical examination, laboratory testing, chest radiographs, and computed tomography scans. Mortality rates, prespecified severe morbidity composite index, major morbidity, clinical utility, aneurysm rupture, and secondary interventions were compared. The TEVAR subjects were evaluated by a core laboratory for device performance, including change in aneurysm size, endoleak, migration, and device integrity.
The 30-day survival rate was noninferior (P < .01) for the TEVAR group compared with the open group (98.1% vs 94.3%). The severe morbidity composite index was lower for TEVAR (0.2 +/- 0.7 vs 0.7 +/- 1.2; P < .01). Cumulative major morbidity scores were significantly lower at 30 days for the TEVAR group compared with the open group (1.3 +/- 3.0 vs 2.9 +/- 3.6, P < .01). The TEVAR patients had fewer cardiovascular, pulmonary, and vascular adverse events, although neurologic events were not significantly different. Clinical utility for the TEVAR patients was superior to that of the open patients. No ruptures or conversions occurred in the first year. Reintervention rates were similar in both groups. At 12 months, aneurysm growth was identified in 7.1% (8/112), endoleak in 3.9% (4/103), migration (>10 mm) in 2.8% (3/107), and other device issues were rare. None of the patients with migration experienced endoleak, aneurysm growth, or required a secondary intervention.
Thoracic endovascular aortic repair with the TX2 is a safer and effective alternative to open surgical repair for the treatment of anatomically suitable descending thoracic aortic aneurysms and ulcers at 1 year of follow-up. Device performance issues are infrequent, but careful planning and regular follow-up with imaging remain a necessity.
本试验评估了使用当代血管内移植物系统进行胸主动脉腔内修复术(TEVAR)与开放性手术修复(开放手术)治疗降主动脉瘤和大溃疡的安全性和有效性。
42个国际试验点招募了230例降主动脉瘤或溃疡患者。该研究将160例接受Zenith TX2血管内移植物(威廉库克欧洲公司,丹麦比耶沃斯考夫)治疗的TEVAR患者与70例接受开放手术的患者进行了比较。在术前、出院前、术后1、6和12个月以及直至5年每年对患者进行评估,评估内容包括医学检查、实验室检测、胸部X线片和计算机断层扫描。比较了死亡率、预先设定的严重并发症综合指数、主要并发症、临床实用性、动脉瘤破裂和二次干预情况。由一个核心实验室对TEVAR患者进行器械性能评估,包括动脉瘤大小变化、内漏、移位和器械完整性。
与开放手术组相比,TEVAR组30天生存率不劣于开放手术组(P <.01)(98.1%对94.3%)。TEVAR组的严重并发症综合指数更低(0.2±0.7对0.7±1.2;P <.01)。与开放手术组相比,TEVAR组30天时的累积主要并发症评分显著更低(1.3±3.0对2.9±3.6,P <.01)。TEVAR患者的心血管、肺部和血管不良事件较少,尽管神经事件无显著差异。TEVAR患者的临床实用性优于开放手术患者。第一年未发生破裂或中转手术情况。两组的再次干预率相似。在12个月时,7.1%(8/112)的患者出现动脉瘤生长,3.9%(4/103)的患者出现内漏,2.8%(3/107)的患者出现移位(>10 mm),其他器械问题罕见。没有移位患者出现内漏、动脉瘤生长或需要二次干预。
在随访1年时,使用TX2进行胸主动脉腔内修复术是治疗解剖结构合适的降主动脉瘤和溃疡的一种比开放性手术修复更安全有效的替代方法。器械性能问题不常见,但仍需要仔细规划并定期进行影像学随访。