Brinster Clayton J, Milner Ross
Section of Vascular Surgery and Endovascular Therapy, Department of Surgery, Ochsner Clinic Foundation, New Orleans, LA, USA.
Division of Vascular Surgery and Endovascular Therapy, Department of Surgery, University of Chicago Medicine, Chicago, IL, USA -
J Cardiovasc Surg (Torino). 2018 Jun;59(3):342-359. doi: 10.23736/S0021-9509.18.10460-5. Epub 2018 Mar 19.
Endovascular aortic repair (EVAR) has revolutionized the treatment of infrarenal abdominal aortic aneurysm (AAA), with consistently low reported perioperative morbidity and mortality. Universal applicability of EVAR to treat AAA is hindered by several specific anatomic constraints, however, and many patients cannot be treated with commercially available stent-grafts within the device specific instructions for use. Treatment of these complex pararenal aneurysms is increasingly accomplished by extension of EVAR into the visceral segment of the abdominal aorta with branches or fenestrations that allow perfusion of the visceral and renal arteries. Fenestrated endovascular aneurysm repair (FEVAR) was initially developed to treat high-risk patients unfit for open surgery and anatomically ineligible for standard infrarenal EVAR, but this technique has evolved over the past decade into a mature treatment option for complex AAA. High-volume, single-center reports, multicenter series and clinical reviews have demonstrated that FEVAR is a safe and effective technique with favorable results at proficient centers. Generalizability of these outcomes to less advanced centers remains unproven, and reintervention rates following FEVAR in the mid- and long-term, even among the most experienced centers, remain a concern. Several off-the-shelf devices that are undergoing clinical trial seek to broaden the anatomic applicability and overall availability of FEVAR. A significant number of patients are not candidates for off-the-shelf or customized stent-grafts, however, stressing the need for continued refinement of existing devices, development of novel devices with broader indications for use, and maintenance of open surgical skills.
血管腔内主动脉修复术(EVAR)彻底改变了肾下腹主动脉瘤(AAA)的治疗方式,其围手术期发病率和死亡率一直较低。然而,EVAR治疗AAA的普遍适用性受到一些特定解剖学限制的阻碍,许多患者无法在设备特定的使用说明范围内使用市售的覆膜支架进行治疗。对于这些复杂的肾旁动脉瘤,越来越多地通过将EVAR扩展至腹主动脉内脏段来进行治疗,采用带有分支或开窗的方式,以保证内脏动脉和肾动脉的灌注。开窗型血管腔内动脉瘤修复术(FEVAR)最初是为治疗不适合开放手术且解剖结构上不适合标准肾下EVAR的高危患者而开发的,但在过去十年中,这项技术已发展成为治疗复杂AAA的成熟治疗选择。大量的单中心报告、多中心系列研究和临床综述表明,FEVAR是一种安全有效的技术,在专业中心能取得良好的效果。这些结果在不太先进的中心的可推广性仍未得到证实,即使在经验最丰富的中心,FEVAR术后的中长期再干预率仍是一个令人担忧的问题。几种正在进行临床试验的现成设备试图扩大FEVAR的解剖学适用性和总体可用性。然而,相当多的患者不适合使用现成的或定制的覆膜支架,这凸显了持续改进现有设备、开发具有更广泛使用适应症的新型设备以及保持开放手术技能的必要性。