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Fully Endoscopic Mitral Valve Repair with Percutaneous Cannulation of Groin Vessels
Published on: May 26, 2023
An Initial Single-Center European Experience with the Gore Thoracic Branch Endoprosthesis
Mark Dirven1, Guillaume S C Geuzebroek2, Foeke J H Nauta2
1Department of Vascular Surgery, Radboud University Medical Center, 6525 GA Nijmegen, Netherlands.
This study shows the GORE Thoracic Branched Endoprosthesis (TBE) is a promising off-the-shelf device for treating complex aortic arch and descending thoracic aorta pathologies, with successful initial implantation in 20 patients. Further research is needed to confirm long-term outcomes.
Area of Science:
- Vascular Surgery
- Interventional Cardiology
- Medical Device Technology
Background:
- Complex pathologies of the aortic arch and descending thoracic aorta present significant treatment challenges.
- Traditional open surgical repair carries high morbidity and mortality.
- Endovascular solutions are evolving to address these complex anatomies.
Purpose of the Study:
- To evaluate the initial clinical experience with a novel off-the-shelf single branched thoracic aortic stent graft.
- To assess the feasibility and safety of the GORE Thoracic Branched Endoprosthesis (TBE) in preserving aortic arch vessels.
- To report outcomes in patients with diverse aortic arch and descending thoracic pathologies.
Main Methods:
- Retrospective cohort analysis of 20 patients treated between 2024 and 2025.
- Utilized the GORE Thoracic Branched Endoprosthesis (TBE) for aortic arch and descending thoracic aorta repair.
- Median follow-up of six months, with imaging via computed tomography angiography (CT-A).
Main Results:
- Successful implantation of the TBE in all 20 patients.
- Sidebranch preservation of the left subclavian artery (17), innominate artery (2), and left carotid artery (1).
- No in-hospital or 30-day mortality; two late deaths of unknown causes at 7-8 weeks post-procedure.
Conclusions:
- The GORE TBE demonstrates satisfying technical results for various aortic arch and descending pathologies.
- The device was successfully implanted with patent branches on postoperative CT-A.
- Longer follow-up and larger patient series are required to validate these findings.
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