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  3. Evaluation of custom-made Relay® stent-grafts for aortic arch landing zones 0 and I: experience from two high-volume aortic centres.
 

Evaluation of custom-made Relay® stent-grafts for aortic arch landing zones 0 and I: experience from two high-volume aortic centres.

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BORIS DOI
10.48620/84806
Date of Publication
July 1, 2024
Publication Type
Article
Division/Institute

Clinic of Vascular Su...

Clinic of Heart Surge...

Author
Dabravolskaite, Vaiva
Clinic of Vascular Surgery
Makaloski, Vladimir
Clinic of Vascular Surgery
Hakovirta, Harri
Kotelis, Drosos
Clinic of Vascular Surgery
Schoenhoff, Florian S.
Clinic of Heart Surgery
Lescan, Mario
Series
European Journal of Cardio-Thoracic Surgery
ISSN or ISBN (if monograph)
1873-734X
1010-7940
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/ejcts/ezae241
PubMed ID
38991832
Uncontrolled Keywords

Aortic arch

Custom-made platform

Design diversity

Relay®

stent-graft

Description
Objectives
To report experience with a Relay® stent-graft custom-made platform in treating different aortic arch pathology in 2 high-volume aortic centres.Methods
A retrospective analysis of all patients treated between July 2016 and July 2023 with custom-made Relay® stent-graft (custom-made device). Underlying aortic arch pathology was an aneurysm, penetrating aortic ulcer, and dissection. Three custom-made device designs were used: proximal scallop, fenestrations, and inner branches. The endpoints were technical success, perioperative stroke, death, and reintervention rate.Results
Thirty-five patients (89% males) with a mean age of 70 ± 11 years were treated.Indication for treatment was penetrating aortic ulcer in 14 patients (40%), aneurysm in 11 patients (31%) and aortic dissection in 10 patients (29%). The technical success rate was 100%. Twenty-eight patients (80%) had proximal sealing in zone 0, and 7 (20%) had proximal sealing in zone 1. Nine patients (25.6%) had proximal scallops, 9 (25.6%) had 1 big fenestration and 17 (48.8%) had a branched device; 1 with single branch, 15 with double branches and 1 with triple branches. Thirty patients (86%) had previous or simultaneous left subclavian artery revascularization. No patient died during 30 days. Two patients (5.7%) had stroke postoperatively; both recovered without disabling deficits. The mean follow-up was 35 ± 26 months. Six patients (17.1%) died during follow-up. One patient required reinforcement of the bridging stent in the left common carotid artery and one additional vascular plugging of the left subclavian artery. Three patients received distal extension.Conclusions
The Relay® stent-graft custom-made platform showed a good performance in our study with a high technical success rate, low perioperative stroke and mortality, and low reintervention rates during the follow-up.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/194431
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ezae241.pdftextAdobe PDF2.04 MBpublished
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