The Role of Hyperdense Basilar Artery Sign in Predicting Outcome of Acute Basilar Artery Occlusion within 12 Hours of Onset.
ATTENTION trial
Acute basilar artery occlusion
function outcome
hyperdense basilar artery sign
thrombectomy
Journal
World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275
Informations de publication
Date de publication:
28 Dec 2023
28 Dec 2023
Historique:
received:
14
11
2023
revised:
20
12
2023
accepted:
21
12
2023
medline:
2
1
2024
pubmed:
2
1
2024
entrez:
30
12
2023
Statut:
aheadofprint
Résumé
The correlation between hyperdense basilar artery sign (HDBAS) and outcome after acute basilar artery occlusion (ABAO) is debated. Our objective was to determine the usefulness of HDBAS in predicting the outcomes of patients with ABAO after endovascular treatment (EVT), intravenous thrombolysis (IVT), and best medical treatment (BMT). The study's participants were selected from the ATTENTION trial. The study's primary outcome was a 90-day modified Rankin Scale (mRS) score, and the secondary outcome was the recanalization rate, any intracranial hemorrhage, and 90-day mortality. The study comprised 276 participants, with cohorts for EVT (N=188), IVT (N=82), and BMT (N=88). In EVT cohort, the HDBAS was not associated with 90-day mRS (adjusted OR, 0.87; 95% CI, 0.51-1.48; P=0.6029), the recanalization after 24 hours of onset (adjusted OR, 0.76; 95% CI, 0.30-3.61; P=0.9422), and 90-day mortality (adjusted OR, 0.77; 95% CI, 0.41-1.46; P=0.4238). In IVT cohort, the HDBAS was not associated with 90-day mRS (adjusted OR, 0.69; 95% CI, 0.31-1.56; P=0.3742), the recanalization after 24 hours of onset (adjusted OR, 2.24; 95% CI, 0.47-10.78; P=0.3132), and 90-day mortality (adjusted OR, 0.64; 95% CI, 0.26-1.57; P=0.3264). Similarly, in BMT cohort, the HDBAS was not associated with 90-day mRS (adjusted OR, 1.11; 95% CI, 0.47-2.63; P=0.8152), the recanalization after 24 hours of onset (adjusted OR, 1.27; 95% CI, 0.40-4.02; P=0.6874), and 90-day mortality (adjusted OR, 1.17; 95% CI, 0.46-2.96; P=0.748). The HDBAS may not be a reliable predictor of outcomes for patients with ABAO, regardless of whether they received EVT, IVT, or BMT.
Sections du résumé
BACKGROUND
BACKGROUND
The correlation between hyperdense basilar artery sign (HDBAS) and outcome after acute basilar artery occlusion (ABAO) is debated. Our objective was to determine the usefulness of HDBAS in predicting the outcomes of patients with ABAO after endovascular treatment (EVT), intravenous thrombolysis (IVT), and best medical treatment (BMT).
METHODS
METHODS
The study's participants were selected from the ATTENTION trial. The study's primary outcome was a 90-day modified Rankin Scale (mRS) score, and the secondary outcome was the recanalization rate, any intracranial hemorrhage, and 90-day mortality.
RESULTS
RESULTS
The study comprised 276 participants, with cohorts for EVT (N=188), IVT (N=82), and BMT (N=88). In EVT cohort, the HDBAS was not associated with 90-day mRS (adjusted OR, 0.87; 95% CI, 0.51-1.48; P=0.6029), the recanalization after 24 hours of onset (adjusted OR, 0.76; 95% CI, 0.30-3.61; P=0.9422), and 90-day mortality (adjusted OR, 0.77; 95% CI, 0.41-1.46; P=0.4238). In IVT cohort, the HDBAS was not associated with 90-day mRS (adjusted OR, 0.69; 95% CI, 0.31-1.56; P=0.3742), the recanalization after 24 hours of onset (adjusted OR, 2.24; 95% CI, 0.47-10.78; P=0.3132), and 90-day mortality (adjusted OR, 0.64; 95% CI, 0.26-1.57; P=0.3264). Similarly, in BMT cohort, the HDBAS was not associated with 90-day mRS (adjusted OR, 1.11; 95% CI, 0.47-2.63; P=0.8152), the recanalization after 24 hours of onset (adjusted OR, 1.27; 95% CI, 0.40-4.02; P=0.6874), and 90-day mortality (adjusted OR, 1.17; 95% CI, 0.46-2.96; P=0.748).
CONCLUSION
CONCLUSIONS
The HDBAS may not be a reliable predictor of outcomes for patients with ABAO, regardless of whether they received EVT, IVT, or BMT.
Identifiants
pubmed: 38159602
pii: S1878-8750(23)01855-7
doi: 10.1016/j.wneu.2023.12.122
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2023 Elsevier Inc. All rights reserved.