Thirty-day Results from the ZEPHYR Registry: Outcomes of EVAR Using the Zenith Alpha™ Abdominal Endovascular Graft for the Treatment of AAA in 347 Patients

•Multicenter registry including patients undergoing EVAR for AAA using the Zenith Alpha™ Abdominal Endovascular Graft.•Reporting 30-day results on 347 patients from 14 sites.•Prospective data collection and core laboratory-controlled follow-up.•Seventy percent of patients had percutaneous arterial a...

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Published inAnnals of vascular surgery Vol. 78; pp. 170 - 179
Main Authors Hatzl, Johannes, Batenburg, Michiel Van Basten, Yeung, Kak K., Fioole, Bram, Verhoeven, Eric, Lauwers, Geert, Kölbel, Tilo, Wever, Jan J., Scheinert, Dierk, Van den Eynde, Wouter, Rouhani, Guido, Mees, Barend M.E., Vermassen, Frank, Schelzig, Hubert, Cuypers, Philippe W.M., Böckler, Dittmar, Katsargyris, Athanasios, Overhagen, Hans Van, Verbist, Jurgen, Schurink, Geert W.H., Statius van Eps, Randolph G., Veger, Hugo T.C., Van Dijk, Lukas C.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.01.2022
Subjects
Online AccessGet full text
ISSN0890-5096
1615-5947
1615-5947
DOI10.1016/j.avsg.2021.06.020

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Abstract •Multicenter registry including patients undergoing EVAR for AAA using the Zenith Alpha™ Abdominal Endovascular Graft.•Reporting 30-day results on 347 patients from 14 sites.•Prospective data collection and core laboratory-controlled follow-up.•Seventy percent of patients had percutaneous arterial access.•One fifths of patients had hostile iliac anatomy. To report technical and clinical 30-day results following treatment with the Zenith Alpha™ abdominal stent graft from the ZEnith alPHa for aneurYsm Repair Registry (ZEPHYR). Multicenter, nonrandomized, single arm, core laboratory-controlled, prospective registry collecting data on the Zenith Alpha Abdominal Endovascular Graft being used in subjects with abdominal aortic aneurysms (AAA) from sites in Germany, Belgium, and The Netherlands between December 2016 and December 2019. Inclusion criteria were non-ruptured AAAs with a maximum diameter ≥50 mm or enlargement >5 mm over 6 months with an AAA neck length ≥10 mm (site reported). Primary outcome measure was treatment success at 30 days. Treatment success was defined as a combined endpoint consisting of technical and clinical success. Technical success was defined as successful stent graft delivery and deployment as well as successful removal of the delivery system. Clinical success at 30 days was defined as freedom from type I and III endoleak, aneurysm rupture, conversion to open surgery and stent graft occlusion. Three hundred forty-seven subjects were included from 14 sites with a median age of 73.0 years (IQR 68.0–79.0). Thirty-four patients were female (9.8%). The median AAA diameter was 58.3 mm (IQR 55.0–63.5). The median proximal neck diameter was 23.6 mm (IQR 22.0–25.2) with a median proximal neck length of 24.4 mm (IQR 15.0–34.8) and a median infrarenal neck angulation of 24.5° (IQR 15.0–35.0). The right and left common iliac diameter were 16.1 mm (IQR 14.1–19.4) and 16.2 mm (IQR 14.1–19.1), respectively. The treatment success rate at 30 days was 94.8% (N = 329). Technical success was achieved in 333 patients (96.0%). The clinical success rate at 30 days was 98.8% (N = 343). Three patients had limb occlusions at 30 day follow up (0.9%). One patient had a type Ib endoleak (0.3%). Seventy percent of vascular access approaches were percutaneous. The reintervention rate was 1.7% (N = 6) within 30 days. Indications for reinterventions were a false aneurysm at puncture site (N = 1), limb complications (N = 2), stentgraft-associated renal artery occlusions (N = 2), and an external iliac artery thrombosis (N = 1). Endovascular aneurysm repair using the Zenith Alpha Abdominal Endovascular Graft is effective in the short term. Long term results will be reported in the future.
AbstractList •Multicenter registry including patients undergoing EVAR for AAA using the Zenith Alpha™ Abdominal Endovascular Graft.•Reporting 30-day results on 347 patients from 14 sites.•Prospective data collection and core laboratory-controlled follow-up.•Seventy percent of patients had percutaneous arterial access.•One fifths of patients had hostile iliac anatomy. To report technical and clinical 30-day results following treatment with the Zenith Alpha™ abdominal stent graft from the ZEnith alPHa for aneurYsm Repair Registry (ZEPHYR). Multicenter, nonrandomized, single arm, core laboratory-controlled, prospective registry collecting data on the Zenith Alpha Abdominal Endovascular Graft being used in subjects with abdominal aortic aneurysms (AAA) from sites in Germany, Belgium, and The Netherlands between December 2016 and December 2019. Inclusion criteria were non-ruptured AAAs with a maximum diameter ≥50 mm or enlargement >5 mm over 6 months with an AAA neck length ≥10 mm (site reported). Primary outcome measure was treatment success at 30 days. Treatment success was defined as a combined endpoint consisting of technical and clinical success. Technical success was defined as successful stent graft delivery and deployment as well as successful removal of the delivery system. Clinical success at 30 days was defined as freedom from type I and III endoleak, aneurysm rupture, conversion to open surgery and stent graft occlusion. Three hundred forty-seven subjects were included from 14 sites with a median age of 73.0 years (IQR 68.0–79.0). Thirty-four patients were female (9.8%). The median AAA diameter was 58.3 mm (IQR 55.0–63.5). The median proximal neck diameter was 23.6 mm (IQR 22.0–25.2) with a median proximal neck length of 24.4 mm (IQR 15.0–34.8) and a median infrarenal neck angulation of 24.5° (IQR 15.0–35.0). The right and left common iliac diameter were 16.1 mm (IQR 14.1–19.4) and 16.2 mm (IQR 14.1–19.1), respectively. The treatment success rate at 30 days was 94.8% (N = 329). Technical success was achieved in 333 patients (96.0%). The clinical success rate at 30 days was 98.8% (N = 343). Three patients had limb occlusions at 30 day follow up (0.9%). One patient had a type Ib endoleak (0.3%). Seventy percent of vascular access approaches were percutaneous. The reintervention rate was 1.7% (N = 6) within 30 days. Indications for reinterventions were a false aneurysm at puncture site (N = 1), limb complications (N = 2), stentgraft-associated renal artery occlusions (N = 2), and an external iliac artery thrombosis (N = 1). Endovascular aneurysm repair using the Zenith Alpha Abdominal Endovascular Graft is effective in the short term. Long term results will be reported in the future.
To report technical and clinical 30-day results following treatment with the Zenith Alpha™ abdominal stent graft from the ZEnith alPHa for aneurYsm Repair Registry (ZEPHYR).BACKGROUNDTo report technical and clinical 30-day results following treatment with the Zenith Alpha™ abdominal stent graft from the ZEnith alPHa for aneurYsm Repair Registry (ZEPHYR).Multicenter, nonrandomized, single arm, core laboratory-controlled, prospective registry collecting data on the Zenith Alpha Abdominal Endovascular Graft being used in subjects with abdominal aortic aneurysms (AAA) from sites in Germany, Belgium, and The Netherlands between December 2016 and December 2019. Inclusion criteria were non-ruptured AAAs with a maximum diameter ≥50 mm or enlargement >5 mm over 6 months with an AAA neck length ≥10 mm (site reported). Primary outcome measure was treatment success at 30 days. Treatment success was defined as a combined endpoint consisting of technical and clinical success. Technical success was defined as successful stent graft delivery and deployment as well as successful removal of the delivery system. Clinical success at 30 days was defined as freedom from type I and III endoleak, aneurysm rupture, conversion to open surgery and stent graft occlusion.METHODSMulticenter, nonrandomized, single arm, core laboratory-controlled, prospective registry collecting data on the Zenith Alpha Abdominal Endovascular Graft being used in subjects with abdominal aortic aneurysms (AAA) from sites in Germany, Belgium, and The Netherlands between December 2016 and December 2019. Inclusion criteria were non-ruptured AAAs with a maximum diameter ≥50 mm or enlargement >5 mm over 6 months with an AAA neck length ≥10 mm (site reported). Primary outcome measure was treatment success at 30 days. Treatment success was defined as a combined endpoint consisting of technical and clinical success. Technical success was defined as successful stent graft delivery and deployment as well as successful removal of the delivery system. Clinical success at 30 days was defined as freedom from type I and III endoleak, aneurysm rupture, conversion to open surgery and stent graft occlusion.Three hundred forty-seven subjects were included from 14 sites with a median age of 73.0 years (IQR 68.0-79.0). Thirty-four patients were female (9.8%). The median AAA diameter was 58.3 mm (IQR 55.0-63.5). The median proximal neck diameter was 23.6 mm (IQR 22.0-25.2) with a median proximal neck length of 24.4 mm (IQR 15.0-34.8) and a median infrarenal neck angulation of 24.5° (IQR 15.0-35.0). The right and left common iliac diameter were 16.1 mm (IQR 14.1-19.4) and 16.2 mm (IQR 14.1-19.1), respectively. The treatment success rate at 30 days was 94.8% (N = 329). Technical success was achieved in 333 patients (96.0%). The clinical success rate at 30 days was 98.8% (N = 343). Three patients had limb occlusions at 30 day follow up (0.9%). One patient had a type Ib endoleak (0.3%). Seventy percent of vascular access approaches were percutaneous. The reintervention rate was 1.7% (N = 6) within 30 days. Indications for reinterventions were a false aneurysm at puncture site (N = 1), limb complications (N = 2), stentgraft-associated renal artery occlusions (N = 2), and an external iliac artery thrombosis (N = 1).RESULTSThree hundred forty-seven subjects were included from 14 sites with a median age of 73.0 years (IQR 68.0-79.0). Thirty-four patients were female (9.8%). The median AAA diameter was 58.3 mm (IQR 55.0-63.5). The median proximal neck diameter was 23.6 mm (IQR 22.0-25.2) with a median proximal neck length of 24.4 mm (IQR 15.0-34.8) and a median infrarenal neck angulation of 24.5° (IQR 15.0-35.0). The right and left common iliac diameter were 16.1 mm (IQR 14.1-19.4) and 16.2 mm (IQR 14.1-19.1), respectively. The treatment success rate at 30 days was 94.8% (N = 329). Technical success was achieved in 333 patients (96.0%). The clinical success rate at 30 days was 98.8% (N = 343). Three patients had limb occlusions at 30 day follow up (0.9%). One patient had a type Ib endoleak (0.3%). Seventy percent of vascular access approaches were percutaneous. The reintervention rate was 1.7% (N = 6) within 30 days. Indications for reinterventions were a false aneurysm at puncture site (N = 1), limb complications (N = 2), stentgraft-associated renal artery occlusions (N = 2), and an external iliac artery thrombosis (N = 1).Endovascular aneurysm repair using the Zenith Alpha Abdominal Endovascular Graft is effective in the short term. Long term results will be reported in the future.CONCLUSIONSEndovascular aneurysm repair using the Zenith Alpha Abdominal Endovascular Graft is effective in the short term. Long term results will be reported in the future.
To report technical and clinical 30-day results following treatment with the Zenith Alpha™ abdominal stent graft from the ZEnith alPHa for aneurYsm Repair Registry (ZEPHYR). Multicenter, nonrandomized, single arm, core laboratory-controlled, prospective registry collecting data on the Zenith Alpha Abdominal Endovascular Graft being used in subjects with abdominal aortic aneurysms (AAA) from sites in Germany, Belgium, and The Netherlands between December 2016 and December 2019. Inclusion criteria were non-ruptured AAAs with a maximum diameter ≥50 mm or enlargement >5 mm over 6 months with an AAA neck length ≥10 mm (site reported). Primary outcome measure was treatment success at 30 days. Treatment success was defined as a combined endpoint consisting of technical and clinical success. Technical success was defined as successful stent graft delivery and deployment as well as successful removal of the delivery system. Clinical success at 30 days was defined as freedom from type I and III endoleak, aneurysm rupture, conversion to open surgery and stent graft occlusion. Three hundred forty-seven subjects were included from 14 sites with a median age of 73.0 years (IQR 68.0-79.0). Thirty-four patients were female (9.8%). The median AAA diameter was 58.3 mm (IQR 55.0-63.5). The median proximal neck diameter was 23.6 mm (IQR 22.0-25.2) with a median proximal neck length of 24.4 mm (IQR 15.0-34.8) and a median infrarenal neck angulation of 24.5° (IQR 15.0-35.0). The right and left common iliac diameter were 16.1 mm (IQR 14.1-19.4) and 16.2 mm (IQR 14.1-19.1), respectively. The treatment success rate at 30 days was 94.8% (N = 329). Technical success was achieved in 333 patients (96.0%). The clinical success rate at 30 days was 98.8% (N = 343). Three patients had limb occlusions at 30 day follow up (0.9%). One patient had a type Ib endoleak (0.3%). Seventy percent of vascular access approaches were percutaneous. The reintervention rate was 1.7% (N = 6) within 30 days. Indications for reinterventions were a false aneurysm at puncture site (N = 1), limb complications (N = 2), stentgraft-associated renal artery occlusions (N = 2), and an external iliac artery thrombosis (N = 1). Endovascular aneurysm repair using the Zenith Alpha Abdominal Endovascular Graft is effective in the short term. Long term results will be reported in the future.
Author Kölbel, Tilo
Schelzig, Hubert
Veger, Hugo T.C.
Cuypers, Philippe W.M.
Schurink, Geert W.H.
Van Dijk, Lukas C.
Batenburg, Michiel Van Basten
Mees, Barend M.E.
Van den Eynde, Wouter
Verbist, Jurgen
Hatzl, Johannes
Wever, Jan J.
Rouhani, Guido
Vermassen, Frank
Verhoeven, Eric
Lauwers, Geert
Scheinert, Dierk
Böckler, Dittmar
Overhagen, Hans Van
Yeung, Kak K.
Fioole, Bram
Statius van Eps, Randolph G.
Katsargyris, Athanasios
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CitedBy_id crossref_primary_10_1016_j_avsg_2025_03_011
crossref_primary_10_1177_15266028241295563
crossref_primary_10_1177_17085381241262575
crossref_primary_10_1016_j_ejvs_2024_03_004
crossref_primary_10_1177_15266028231197151
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ContentType Journal Article
Contributor Veger, Hugo T C
Van Dijk, Lukas C
Overhagen, Hans Van
Statius van Eps, Randolph G
Verbist, Jurgen
Schurink, Geert W H
Katsargyris, Athanasios
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  organization: Departments of Vascular Surgery and Interventional Radiology, Haga Hospital, The Hague, The Netherlands
Copyright 2021 Elsevier Inc.
Copyright © 2021 Elsevier Inc. All rights reserved.
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Zephyr study group collaborators
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Keywords Prospective Studies
Humans
Aneurysm
Aortic Aneurysm
Treatment Outcome
Abdominal
Endovascular aneurysm repair (EVAR)
Zenith
endovascular
Europe/epidemiology
abdominal aortic aneurysm (AAA)
ZEPHYR
Stents
Blood Vessel Prosthesis, Endovascular Procedures/methods
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PublicationTitle Annals of vascular surgery
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Snippet •Multicenter registry including patients undergoing EVAR for AAA using the Zenith Alpha™ Abdominal Endovascular Graft.•Reporting 30-day results on 347 patients...
To report technical and clinical 30-day results following treatment with the Zenith Alpha™ abdominal stent graft from the ZEnith alPHa for aneurYsm Repair...
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SubjectTerms Abdominal
abdominal aortic aneurysm (AAA)
Aged
Aged, 80 and over
Aneurysm
Aneurysm, Ruptured
Aortic Aneurysm
Aortic Aneurysm, Abdominal - surgery
Blood Vessel Prosthesis
Blood Vessel Prosthesis, Endovascular Procedures/methods
Conversion to Open Surgery
Endoleak
endovascular
Endovascular aneurysm repair (EVAR)
Endovascular Procedures - adverse effects
Endovascular Procedures - methods
Europe/epidemiology
Female
Humans
Male
Postoperative Complications - epidemiology
Prospective Studies
Prosthesis Design
Registries
Stents
Treatment Outcome
Zenith
ZEPHYR
Title Thirty-day Results from the ZEPHYR Registry: Outcomes of EVAR Using the Zenith Alpha™ Abdominal Endovascular Graft for the Treatment of AAA in 347 Patients
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0890509621005628
https://dx.doi.org/10.1016/j.avsg.2021.06.020
https://www.ncbi.nlm.nih.gov/pubmed/34474131
https://www.proquest.com/docview/2569377696
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