Authors
Julien Burel, Mahmoud Elhorany, Giacomo Borsari, Kevin Premat, Julien Allard, Navid Bakhtiari, Stéphanie Lenck, Anne-Laure Boch, Aurélien Nouet, Pierre-Yves Borius, Gaël Nicolas, Maichael Talaat, Nader-Antoine Sourour, Eimad Shotar, Frédéric Clarençon
Published in
Journal of neurointerventional surgery. Sep 15, 2026. Epub Sep 15, 2026.
Abstract
The exclusion treatment of Spetzler-Martin grade (SMG) IV-V brain arteriovenous malformations (bAVMs) remains controversial. This study evaluates the safety and effectiveness of endovascular treatment (EVT) for SMG IV-V bAVMs, either as a standalone strategy or as part of multimodal management.
A retrospective single-center observational cohort study of consecutive adult patients with SMG IV-V bAVMs treated with EVT between 1998 and 2024 was conducted. Baseline characteristics, procedure-related complications, clinical outcomes, and angiographic follow-up were recorded. Independent risk factors for EVT-related complications were analyzed using binary logistic regression.
A total of 73 patients with 73 SMG IV-V bAVMs were included. The median age was 36 (IQR 28-47) years, and 29 (39.7%) bAVMs were ruptured at presentation. Complete angiographic obliteration by EVT alone in intention to cure was achieved in 6/33 patients (18.2%). Overall, complete angiographic obliteration was achieved in 33 patients (45.2%), either by EVT alone or within a multimodal treatment strategy. EVT-related major complications (shift in modified Rankin Scale score of ≥2 or death) occurred in eight patients (11.0%). The presence of a flow-related proximal aneurysm was independently associated with EVT-related complications (OR 4.47; 95% CI 1.18 to 16.98; P=0.028).
In this single-center retrospective series, EVT for SMG IV-V bAVMs was associated with a substantial procedural risk and achieved complete obliteration only in a limited proportion of patients when used as a standalone treatment. Within a multimodal management strategy higher angiographic exclusion rates were observed, although it remained associated with substantial morbidity.
PMID:
42744620
Bibliographic data and abstract were imported from PubMed on 16 Sep 2026.
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