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Aortic endograft technology has evolved significantly since the initial U.S. commercial release in late 1999. Second- and third-generation endografts have come to market, providing improvements in fixation, sizing, versatility, tractability, and delivery profile. These device improvements have made it possible to treat challenging anatomy that would not have been feasible in the early days of endovascular aneurysm repair (EVAR). However, anatomic limitations continue to persist despite the improvements that have been incorporated among currently available endografts. Thus the ability to safely “push” the anatomic envelope is predicated on the ability of the experienced operator to make wise decisions with regards to patient and device selection.
Detailed examination of computed tomography (CT) angiography imaging is critical to evaluate concerns regarding the aortic neck, iliac access, or maintenance of hypogastric perfusion.
All measurements related to selection of the size of the endograft should be made by the operator.
The presence of anatomic constraints should anticipate the potential need for adjunctive techniques.
A stock of ancillary devices (stents, wires, catheters, and sheaths) that could be required should be available.
Persistent type IA endoleak may occur from poor patient selection, inaccurate endograft placement, or both.
Iliac perforation and hemorrhage can occur from overly aggressive attempts at treating challenging iliac anatomy.
Iliac limb occlusion from kinking, external compression, or excessive oversizing may be observed, particularly if endografts extend into the external iliac arteries.
Colonic ischemia can result from atheroemboli or simultaneous bilateral hypogastric occlusion.
Severe iliac occlusive disease, calcification, and tortuosity can combine to make access for EVAR difficult. Although these challenges can frequently be overcome with adjunctive techniques when only a single anatomic problem is present, the combination of multiple anatomic access issues may make EVAR difficult or impossible to perform. Commercially available endografts are 14 to 20 Fr and thus require a minimum 5- to 7-mm iliac diameter for passage. Although focal areas of iliac occlusive disease can be readily treated to gain access to the aorta, a diffusely diseased iliac artery can be more problematic. Use of longer angioplasty balloons or hydrophilic Coons dilators (over a stiff wire) can sometimes be helpful in these situations. The placement of uncovered stents in the iliac vessel should be avoided before EVAR. Finally, a surgically placed iliofemoral conduit can be considered if the patient is anatomically suitable. Placement of the proximal iliac artery anastomosis typically is performed at the iliac bifurcation, allowing deployment of the ipsilateral endograft limb in the common iliac artery.
An alternate method of obtaining access in a patient with extensive iliac occlusive disease is to create an “internal endoconduit” by placing a covered stent in the external iliac vessel, which is then aggressively angioplastied to the required diameter. The covered stent protects against extensive dissection, free rupture of the native vessel caused by the aggressive angioplasty, or both. There must be a sufficient proximal and distal seal zone for the covered stent for this approach to be safe. Although these techniques have been anecdotally reported with successful outcomes, larger series are needed to establish the safety of this approach.
Significant iliac tortuosity can often be straightened with use of a very stiff guidewire, such as the Lunderquist or Amplatz (Cook Medical, Bloomington, Ind.) guidewires. Severe circumferential calcification in association with tortuosity must be approached cautiously, because even the stiffest guidewire may not straighten the vessel. Rarely, a second “buddy wire” may be helpful in this situation. Superstiff wires should be exchanged for a soft J wire before completion arteriography. Otherwise, an apparent high-grade stenosis may be seen in the external iliac artery that is caused by the vessel “accordioning” on the wire. These pseudolesions disappear with replacement of the stiff wire for a more flexible wire and thus do not require intervention.
“Through and through” access or brachial-femoral access was commonly used in the early period of EVAR to manage tortuous and challenging access vessel anatomy. It is rarely needed today given the development of smaller hydrophilic delivery systems.
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