The Superficial Femoral Artery: An Alternative Access for Percutaneous Endovascular Aneurysm Repair

被引:3
|
作者
Aaron, Ashley [1 ,2 ]
el-Hag, Selma [1 ]
de Grandis, Eileen [1 ]
Santilli, Steve [1 ,2 ]
Rosenberg, Michael [2 ,3 ]
Shafii, Susan M. [1 ]
Golzarian, Jafar [2 ,3 ]
Faizer, Rumi [1 ]
机构
[1] Univ Minnesota, Dept Surg, Box 242 UMHC, Minneapolis, MN 55455 USA
[2] Minneapolis Vet Hlth Care Syst, Minneapolis, MN USA
[3] Univ Minnesota, Dept Radiol, Minneapolis, MN 55455 USA
关键词
PRECLOSE TECHNIQUE; EXPERIENCE;
D O I
10.1016/j.avsg.2016.06.018
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: The aim of this study was to report the results of percutaneous endovascular aortic aneurysm repair (PEVAR) using the superficial femoral artery (SFA) for large bore vessel access. Methods: We reviewed all PEVAR procedures at our institution over an 18-month period, identifying all patients who underwent PEVAR with the use of one or both SFAs for endograft delivery with dual ProGlide large bore access closure. Indications for use of the SFA instead of the common femoral artery (CFA) included morbid obesity, CFA vessel wall disease, and scarring from previous CFA surgery. Results: In total, 158 percutaneous access closures were performed in 79 patients. Ten patients had one or both SFAs used. We accessed a total of 13 SFAs: 6 for the endograft main body (size range 18-to 20-French) and 7 for the limb (14-to 16-French). The freedom from open conversion was 84.6%. In comparison, of 145 CFA accesses (in 76 patients) there were 9 conversions (93.7% success). Of the 13 SFAs accessed, there were no major access site complications (pseudoaneurysm, access site bleed, limb ischemia, or need to return to the operating room). All SFAs accessed remained patent at the latest follow-up (range 1e13 months, median 8 months). Conclusions: Our preliminary case series suggests that, in the absence of a healthy or percutaneously accessible CFA, a healthy SFA may be considered for PEVAR access. While likely carrying a higher risk of open conversion, this technique, when combined with intraoperative duplex ultrasound (both before and after the procedure) and with meticulous ultrasoundguided vascular access, appears safe for up to 20-French device diameters.
引用
收藏
页码:339 / 344
页数:6
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