首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Initial clinical experience with the modified zenith 'Pro-Form' TX2 thoracic endograft.
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Initial clinical experience with the modified zenith 'Pro-Form' TX2 thoracic endograft.

机译:改良天顶“ Pro-Form” TX2胸腔内移植物的初步临床经验。

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PURPOSE: To assess the safety and efficacy of thoracic aortic endovascular repair (TEVAR) with the newly introduced Zenith TX2 thoracic stent-graft with Pro-Form. METHODS: From March 2009 to present, the Zenith TX2 with Pro-Form was used to treat 27 patients (23 men; median age 65 years, range 22-77) suffering from descending thoracic aortic disease: 20 degenerative aneurysms, 3 chronic type B dissections, 2 type I endoleaks following previous endograft repair, 1 aortic ulcer, and 1 traumatic isthmic rupture. According to Ishimaru's classification, the distribution of the proximal landing zone was zone 0 in 4 cases, zone 1 in 2 cases, zone 2 in 9 cases, zone 3 in 7 cases, and zone 4 in 5 cases. One aneurysm distally involved the thoracoabdominal aorta. An acutely angulated (<90 degrees ) proximal landing zone was found in 9 patients. RESULTS: The device was safely and effectively deployed in all cases, with no problems during sheath retrieval. The postoperative course was free from major complications in all cases, and there was no perioperative mortality. Postoperative morbidity included respiratory failure in 1 case, transient acute renal failure in 3 cases, and post-implantation syndrome in 2 cases. Postoperative computed tomography at 1 and 6 months confirmed 100% clinical success with the absence of device-related complications. No type I endoleak was documented. The proximal sealing stent fitted well with the aortic profile in all cases except one, in which malapposition was seen in a severely angulated aorta at 6-month follow-up. CONCLUSION: Based on this preliminary experience, the TX2 thoracic stent-graft with Pro-Form can be safely and effectively deployed to satisfactorily repair thoracic aortic pathology, including lesions in the arch. Stent-graft conformance to the aorta was excellent even in cases with unfavorable anatomy. These encouraging results will need to be confirmed in larger series with larger follow-up.
机译:目的:通过采用Pro-Form的新推出的Zenith TX2胸腔支架移植术评估胸主动脉血管内修复术(TEVAR)的安全性和有效性。方法:从2009年3月至今,Zenith TX2 Pro-Form用于治疗27例胸降主动脉疾病患者(23名男性,中位年龄65岁,范围22-77):变性动脉瘤20例,慢性B型3例。解剖,2次I型内漏,先前的内移植修复,1次主动脉溃疡和1次外伤性峡部破裂。根据Ishimaru的分类,近端着陆区的分布为0区4例,1区2例,2区9例,3区7例和4区5例。一个动脉瘤远端累及胸腹主动脉。在9例患者中发现了一个锐角(<90度)近端着陆区。结果:该设备在所有情况下均安全有效地部署,在护套取回过程中没有问题。在所有情况下,术后过程均无重大并发症,并且没有围手术期死亡。术后发病包括呼吸衰竭1例,短暂性急性肾衰竭3例,植入后综合征2例。术后1个月和6个月的计算机体层摄影术在没有设备相关并发症的情况下证实了100%的临床成功。没有记录我的内漏型。在所有情况下,除一种情况外,近端密封支架均与主动脉吻合良好,其中一种情况是在随访6个月时在严重成角度的主动脉中出现错位。结论:基于此初步经验,可以安全有效地部署带有Pro-Form的TX2胸廓支架,以令人满意地修复胸主动脉病变,包括牙弓病变。即使在解剖学不利的情况下,支架移植物对主动脉的顺应性也非常好。这些令人鼓舞的结果将需要在更大范围的后续行动中得到进一步证实。

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