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May-Thurner Syndrome
Yub Raj Sedhai1, Reshma Golamari1, Aliaksei Salei2
1Department of Internal Medicine, Mercy Catholic Medical Center, Darby, Pennsylvania.
Insights
Endovascular therapy, including thrombolysis and stenting, effectively treated May-Thurner syndrome in this small cohort. While generally safe, one patient with thrombophilia experienced stent thrombosis, indicating a need for further study in this subgroup.
Area of Science:
- Vascular Surgery
- Interventional Radiology
- Cardiovascular Medicine
Background:
- May-Thurner syndrome (MTS) is an anatomical defect leading to venous compression and thrombosis.
- Deep vein thrombosis (DVT) and pulmonary embolism (PE) are common clinical presentations of MTS.
- Endovascular techniques offer a minimally invasive treatment option for MTS.
Purpose of the Study:
- To evaluate the safety and efficacy of endovascular therapy for May-Thurner syndrome.
- To assess outcomes in a cohort of adult patients treated for MTS.
- To identify potential risk factors for treatment failure.
Main Methods:
- Retrospective review of 6 patients treated for MTS between June 2013 and September 2015.
- All patients underwent catheter-directed thrombolysis and venous stenting.
- Clinical presentations, hypercoagulability workup, and follow-up outcomes were analyzed.
Main Results:
- Endovascular therapy was performed in 6 female patients with MTS, presenting with DVT and/or PE.
- No major periprocedural complications were observed.
- One patient with antiphospholipid antibody syndrome developed stent thrombosis and loss of patency during follow-up.
Conclusions:
- Endovascular therapy appears to be a safe and effective treatment for May-Thurner syndrome in adults.
- Patients with underlying thrombophilia may be at higher risk for secondary loss of stent patency.
- Further investigation is warranted for managing MTS in patients with pre-existing hypercoagulable states.
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.
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