TY - JOUR
T1 - Technical aspects and 30-day outcomes of the prospective early feasibility study of the GORE EXCLUDER Thoracoabdominal Branched Endoprosthesis (TAMBE) to treat pararenal and extent IV thoracoabdominal aortic aneurysms
AU - Oderich, Gustavo S.
AU - Farber, Mark A.
AU - Silveira, Pierre Galvagni
AU - Tadros, Rami
AU - Marin, Michael
AU - Fillinger, Mark
AU - Makaroun, Michel
AU - Hemmer, Jason
AU - Madden, Meghan
N1 - Funding Information:
The study is an early feasibility industry-sponsored clinical trial by W. L. Gore & Associates. Data collection was done by clinical trial site investigators. Data analysis was done by a W. L. Gore research team with adjudication of an independent core laboratory and Clinical Events Committee. W. L. Gore had no involvement in the interpretation of data and manuscript writing.Author conflict of interest: G.S.O. has consulting fees and research grants from Cook Medical, W. L. Gore, and GE Healthcare, all paid to Mayo Clinic. M.A.F. has consulting fees and research grants from Cook Medical and W. L. Gore, all paid to University of North Carolina. P.G.S. has received educational grants from W. L. Gore and Medtronic. M.Mar. serves on the scientific advisory board of W. L. Gore and Medtronic. J.H. and M.Mad. are employed by W. L. Gore & Associates and are members of the TAMBE research team.
Funding Information:
The study is an early feasibility industry-sponsored clinical trial by W. L. Gore & Associates. Data collection was done by clinical trial site investigators. Data analysis was done by a W. L. Gore research team with adjudication of an independent core laboratory and Clinical Events Committee. W. L. Gore had no involvement in the interpretation of data and manuscript writing.Author conflict of interest: G.S.O. has consulting fees and research grants from Cook Medical, W. L. Gore, and GE Healthcare, all paid to Mayo Clinic. M.A.F. has consulting fees and research grants from Cook Medical and W. L. Gore, all paid to University of North Carolina. P.G.S. has received educational grants from W. L. Gore and Medtronic. M.Mar. serves on the scientific advisory board of W. L. Gore and Medtronic. J.H. and M.Mad. are employed by W. L. Gore & Associates and are members of the TAMBE research team. The investigators would like to thank the Gore aortic team for their leadership and technical support and Mr David Factor for preparation of illustrations for this manuscript.
Publisher Copyright:
© 2018 Society for Vascular Surgery
PY - 2019/8
Y1 - 2019/8
N2 - Objective: This study reports the technical aspects and 30-day outcomes of the prospective, multicenter early feasibility study designed to evaluate the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis (TAMBE; W. L. Gore & Associates, Flagstaff, Ariz). Methods: Thirteen patients with pararenal or extent IV thoracoabdominal aortic aneurysms were prospectively enrolled at five U.S sites and one non-U.S. site from 2014 to 2016. The TAMBE included four portals with either retrograde or antegrade renal portal configuration and used GORE VIABAHN Balloon-Expandable Endoprosthesis (W. L. Gore & Associates) for stenting of the renal and mesenteric arteries. The primary end point was procedural safety at 30 days, defined by absence of major adverse events, including any-cause mortality, myocardial infarction, stroke, paraplegia, bowel ischemia, respiratory failure, severe acute kidney injury (>50% decline in estimated glomerular filtration rate), dialysis, and procedural blood loss >1000 mL. Results: There were 11 male and two female patients with a mean age of 69 ± 8 years. Mean aneurysm diameter was 61 ± 13 mm. A total of 52 renal and mesenteric arteries were incorporated (4 vessels/patient). Technical success was achieved in 12 patients (92%). One patient had inadvertent occlusion of a right renal artery due to dissection. There was no mortality, aneurysm rupture, conversion to open repair, dialysis, or spinal cord injury. Mean length of hospital stay was 5 ± 3 days. At 30 days, four patients (31%) had major adverse events, all due to procedural blood loss >1000 mL. One patient had a type I endoleak at the distal renal branch, which was successfully treated by placement of an additional renal stent before dismissal. Computed tomography angiography at 30 days showed patent target vessels and no type I or type III endoleak. Conclusions: This study confirms the early feasibility of the TAMBE for treatment of pararenal and extent IV thoracoabdominal aortic aneurysms. The high technical success, no mortality, and low morbidity rate support continuation of clinical investigation in a larger population of patients.
AB - Objective: This study reports the technical aspects and 30-day outcomes of the prospective, multicenter early feasibility study designed to evaluate the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis (TAMBE; W. L. Gore & Associates, Flagstaff, Ariz). Methods: Thirteen patients with pararenal or extent IV thoracoabdominal aortic aneurysms were prospectively enrolled at five U.S sites and one non-U.S. site from 2014 to 2016. The TAMBE included four portals with either retrograde or antegrade renal portal configuration and used GORE VIABAHN Balloon-Expandable Endoprosthesis (W. L. Gore & Associates) for stenting of the renal and mesenteric arteries. The primary end point was procedural safety at 30 days, defined by absence of major adverse events, including any-cause mortality, myocardial infarction, stroke, paraplegia, bowel ischemia, respiratory failure, severe acute kidney injury (>50% decline in estimated glomerular filtration rate), dialysis, and procedural blood loss >1000 mL. Results: There were 11 male and two female patients with a mean age of 69 ± 8 years. Mean aneurysm diameter was 61 ± 13 mm. A total of 52 renal and mesenteric arteries were incorporated (4 vessels/patient). Technical success was achieved in 12 patients (92%). One patient had inadvertent occlusion of a right renal artery due to dissection. There was no mortality, aneurysm rupture, conversion to open repair, dialysis, or spinal cord injury. Mean length of hospital stay was 5 ± 3 days. At 30 days, four patients (31%) had major adverse events, all due to procedural blood loss >1000 mL. One patient had a type I endoleak at the distal renal branch, which was successfully treated by placement of an additional renal stent before dismissal. Computed tomography angiography at 30 days showed patent target vessels and no type I or type III endoleak. Conclusions: This study confirms the early feasibility of the TAMBE for treatment of pararenal and extent IV thoracoabdominal aortic aneurysms. The high technical success, no mortality, and low morbidity rate support continuation of clinical investigation in a larger population of patients.
KW - Feasibility
KW - Thoracoabdominal Branch Endoprosthesis (TAMBE)
KW - Thoracoabdominal aneurysm
UR - http://www.scopus.com/inward/record.url?scp=85059416750&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85059416750&partnerID=8YFLogxK
U2 - 10.1016/j.jvs.2018.10.103
DO - 10.1016/j.jvs.2018.10.103
M3 - Article
C2 - 30612825
AN - SCOPUS:85059416750
SN - 0741-5214
VL - 70
SP - 358-368.e6
JO - Journal of vascular surgery
JF - Journal of vascular surgery
IS - 2
ER -