Abstract
This single-center, retrospective review identified 6 patients (n = 6, 100% female) treated by endovascular therapy for May-Thurner syndrome from June
2013 to September 2015. Patients consisted of 3 African American, 2 Caucasian and
1 Asian; mean age was 53.50 ± 8.31 years, range: 39-63 years. Clinical presentations
consisted of left lower extremity deep vein thrombosis in 4, left lower extremity
deep vein thrombosis with pulmonary embolism in 1 and pulmonary embolism with left
common iliac vein thrombosis in 1 patient. All 6 patients were treated with catheter‐directed
thrombolysis and venous stenting to correct the underlying anatomical defect. Hypercoagulability
work up revealed antiphospholipid antibody syndrome in 1 patient. No major periprocedural
complications were observed. Median follow-up period was 22 ± 5.5 months (range: 13-30
months). One patient with pre-exiting antiphospholipid antibody syndrome developed
stent thrombosis with secondary loss of patency. Endovascular therapy for May-Thurner
syndrome in our adult cohort seemed safe and effective. One patient with pre-existing
thrombophilia developed secondary loss of stent patency, suggesting need for further
investigation in this subgroup.
Key Indexing Terms
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Article info
Publication history
Published online: October 17, 2017
Accepted:
September 25,
2017
Received in revised form:
September 19,
2017
Received:
March 17,
2017
Footnotes
☆The authors have no financial or other conflicts of interest to disclose.
Identification
Copyright
© 2017 Southern Society for Clinical Investigation. Published by All rights reserved.