Urgent endovascular treatment of symptomatic or contained ruptured aneurysms with modified stent grafts.

Gustavo S Oderich, Mark A Farber, Luis A Sanchez
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引用次数: 20

Abstract

Anatomical constraints limit the utility of endovascular therapy with infrarenal stent grafts in approximately 40% of the patients. Fenestrated and branched stent grafts that incorporate the visceral and renal arteries are currently not approved for commercial use in the United States and require at least 6 to 8 weeks for customization. These devices are not currently available as an "off-the-shelf" option to treat complex aneurysms, although recent publications suggest that standardization will be possible in 70% to 80% of patients. Modification of aortic stent grafts with creation of reinforced fenestrations or side branches has been reported and may have a future role in the compassionate treatment of high-risk patients with complex aneurysms who otherwise would not have access to a manufactured device, or for those in need of urgent or emergent repair as in the case of a patient with an impending or contained ruptured aneurysm. This article summarizes the current principles applied for device design, procedure planning, and potential applications of modified stent grafts for urgent treatment of symptomatic or contained ruptured aortic aneurysms.

改良支架移植对有症状或包含的破裂动脉瘤的紧急血管内治疗。
解剖学上的限制限制了大约40%的患者使用肾下支架进行血管内治疗。包含内脏和肾动脉的开窗和分支支架目前在美国尚未被批准用于商业用途,并且需要至少6至8周的定制时间。这些设备目前还不能作为治疗复杂动脉瘤的“现成”选择,尽管最近的出版物表明,标准化将有可能在70%到80%的患者中实现。有报道称,改良的主动脉支架植入物可以产生加强的开窗或侧分支,这可能在未来的复杂动脉瘤高危患者的同情治疗中发挥作用,否则这些患者将无法获得制造设备,或者对于那些需要紧急或紧急修复的患者,如即将发生或包含破裂的动脉瘤。本文综述了目前用于紧急治疗症状性或包含性破裂主动脉瘤的改良支架设计、手术计划和潜在应用的原则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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