Preliminary experience of the isolate left subclavian artery in-situ fenestration during "zone 2" thoracic endovascular aortic repair.

TEVAR adjustable needle in-situ fenestration left subclavian artery fenestration “zone 2”

Journal

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
ISSN: 1873-734X
Titre abrégé: Eur J Cardiothorac Surg
Pays: Germany
ID NLM: 8804069

Informations de publication

Date de publication:
10 Sep 2024
Historique:
received: 31 05 2024
revised: 31 07 2024
accepted: 06 09 2024
medline: 10 9 2024
pubmed: 10 9 2024
entrez: 10 9 2024
Statut: aheadofprint

Résumé

To evaluate the results of isolate left subclavian artery (LSA) in-situ fenestration (ISF) during "zone 2" thoracic endovascular aortic repair (TEVAR) using a new adjustable needle puncturing device system. It is a multicentre, retrospective, physician-initiated cohort study of patients treated from July 28th 2021 to April 3rd 2024. Inclusion criteria were isolate LSA revascularization for elective or urgent/emergent "zone 2" TEVAR. The primary outcome was technical success and freedom from ISF TEVAR-related reintervention or endoleak. We treated 50 patients: 28 (56.0%) atherosclerotic thoracic aneurysms, 12 (24.0%) type B aortic dissection, and 10 (20.0%) penetrating aortic ulcers. Elective intervention was carried out in 46 (92.0%) cases. ISF was successful in all cases, with a procedural primary technical success in 47 (94.0%) cases. Median time of intervention was 184 min (IQR, 135-220) with a median fenestration time of 20 min (IQR, 13-35). Operative mortality did not occur. We observed 1 case of spinal cord ischaemia, and 2 cases of bilateral posterior non-disabling stroke. Mortality at 30 days occurred in 1 (2.0%) patient (not aorta-related). The median follow-up median follow-up of 4 months (IQR, 1-12.25). Bridging stent graft patency was 100% with no ISF-related endoleak. In-situ fenestration-related reintervention was never required. ISF TEVAR using the Ankura™-II device with the self-centering adjustable needle system showed high technical success, promising stability, and stable aortic-related outcomes. Owing to these results, it represents a safe and effective alternative for standard "zone 2" TEVAR.

Identifiants

pubmed: 39254638
pii: 7754490
doi: 10.1093/ejcts/ezae332
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Auteurs

Gabriele Piffaretti (G)

Vascular Surgery-Department of Medicine and Surgery, University of Insubria School of Medicine and °ASST Settelaghi University Teaching Hospital, (Varese, -Italy).

Andrea Gaggiano (A)

Vascular and Endovascular Surgery Unit, Mauriziano Umberto I Hospital, (Turin, -Italy).

Giovanni Pratesi (G)

Vascular Surgery-Department of Surgical Sciences and Integrated Diagnostics, University of Genoa School of Medicine, (Genoa, -Italy).

Valerio Tolva (V)

Vascular Surgery-Grande Ospedale Metropolitano Niguarda, (Milan, -Italy).

Davide Pacini (D)

Cardiac Surgery-Department of Medical and Surgical Sciences, University of Bologna School of Medicine, (Bologna, -Italy).

Raffaele Pulli (R)

Vascular Surgery-Department of Cardiothoracic and Vascular Surgery, University of Florence School of Medicine, (Florence, -Italy).

Santi Trimarchi (S)

Vascular Surgery-Department of Clinical Sciences and Community Health, University of Milan School of Medicine, (Milan, -Italy).

Luca Bertoglio (L)

Vascular Surgery, Department of Clinical and Experimental Sciences, University of Brescia School of Medicine, (Brescia, -Italy).

Domenico Angiletta (D)

Vascular Surgery-Department of Department of Emergency and Organs Transplantation, University of Bari School of Medicine, (Bari, -Italy).

Classifications MeSH