Early ischemic recurrence in acute spontaneous cervical artery dissection.


Journal

Journal of neuroradiology = Journal de neuroradiologie
ISSN: 0150-9861
Titre abrégé: J Neuroradiol
Pays: France
ID NLM: 7705086

Informations de publication

Date de publication:
Sep 2023
Historique:
received: 30 11 2022
revised: 07 03 2023
accepted: 07 03 2023
medline: 28 8 2023
pubmed: 13 3 2023
entrez: 12 3 2023
Statut: ppublish

Résumé

Early ischemic recurrence (EIR) following the diagnosis of acute spontaneous cervical artery dissection (CeAD) has been little investigated. We aimed to determine the prevalence and determinants on admission of EIR in a large single-center retrospective cohort study of patients with CeAD. EIR was defined as any ipsilateral clinical or radiological cerebral ischemia or intracranial artery occlusion, not present on admission and occurring within 2 weeks. CeAD location, degree of stenosis, circle of Willis support, presence of intraluminal thrombus, intracranial extension, and intracranial embolism were analyzed on initial imaging by 2 independent observers. Uni- and multivariate logistic regression was used to determine their association with EIR. Two hundred thirty-three consecutive patients with 286 CeAD were included. EIR was observed in 21 patients (9%,95%CI=5-13%) with a median time from diagnosis of 1.5 days (range:0.1-14.0 days). No EIR was observed in CeAD without ischemic presentation or with less than 70% stenosis. In the remaining cases, poor circle of Willis (OR=8.5, CI95%=2.0-35.4, p = 0.003), CeAD extending to other intracranial arteries than just V4 (OR=6.8, CI95%=1.4-32.6, p = 0.017), cervical artery occlusion (OR=9.5, CI95%=1.2- 39.0, p = 0.031), and cervical intraluminal thrombus (OR=17.5, CI95%=3.0-101.7, p = 0.001) were independently associated with EIR. Our results suggests that EIR is more frequent than previously reported, and that its risk might be stratified on admission with a standard workup. In particular, the presence of a poor circle of Willis, intracranial extension (other than just V4), cervical occlusion, or cervical intraluminal thrombus are associated with high risk of EIR, for which specific management should be further evaluated.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Early ischemic recurrence (EIR) following the diagnosis of acute spontaneous cervical artery dissection (CeAD) has been little investigated. We aimed to determine the prevalence and determinants on admission of EIR in a large single-center retrospective cohort study of patients with CeAD.
METHODS METHODS
EIR was defined as any ipsilateral clinical or radiological cerebral ischemia or intracranial artery occlusion, not present on admission and occurring within 2 weeks. CeAD location, degree of stenosis, circle of Willis support, presence of intraluminal thrombus, intracranial extension, and intracranial embolism were analyzed on initial imaging by 2 independent observers. Uni- and multivariate logistic regression was used to determine their association with EIR.
RESULTS RESULTS
Two hundred thirty-three consecutive patients with 286 CeAD were included. EIR was observed in 21 patients (9%,95%CI=5-13%) with a median time from diagnosis of 1.5 days (range:0.1-14.0 days). No EIR was observed in CeAD without ischemic presentation or with less than 70% stenosis. In the remaining cases, poor circle of Willis (OR=8.5, CI95%=2.0-35.4, p = 0.003), CeAD extending to other intracranial arteries than just V4 (OR=6.8, CI95%=1.4-32.6, p = 0.017), cervical artery occlusion (OR=9.5, CI95%=1.2- 39.0, p = 0.031), and cervical intraluminal thrombus (OR=17.5, CI95%=3.0-101.7, p = 0.001) were independently associated with EIR.
CONCLUSIONS CONCLUSIONS
Our results suggests that EIR is more frequent than previously reported, and that its risk might be stratified on admission with a standard workup. In particular, the presence of a poor circle of Willis, intracranial extension (other than just V4), cervical occlusion, or cervical intraluminal thrombus are associated with high risk of EIR, for which specific management should be further evaluated.

Identifiants

pubmed: 36907266
pii: S0150-9861(23)00187-6
doi: 10.1016/j.neurad.2023.03.001
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

523-529

Informations de copyright

Copyright © 2023. Published by Elsevier Masson SAS.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no competing interest.

Auteurs

Héloïse Ifergan (H)

Neurointerventional Unit, Tours Hospital, Tours, Paris, France.

Peggy Reiner (P)

Vascular Neurology Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; FHU NeuroVasc, Paris, France.

Davide Simonato (D)

Neurointerventional Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; Université de Paris, Paris, France.

Giulia Frasca Polara (GF)

Vascular Neurology Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; FHU NeuroVasc, Paris, France.

Mikael Mazighi (M)

Vascular Neurology Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; FHU NeuroVasc, Paris, France; Université de Paris, Paris, France.

Emmanuel Houdart (E)

Neurointerventional Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; Université de Paris, Paris, France.

Eric Jouvent (E)

Vascular Neurology Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; FHU NeuroVasc, Paris, France; Université de Paris, Paris, France; INSERM U1141, Paris, France.

Marc-Antoine Labeyrie (MA)

Neurointerventional Unit, Lariboisière Hospital, APHP, F-75475, Paris, France; Université de Paris, Paris, France; INSERM U942, Paris, France. Electronic address: marc-antoine.labeyrie@aphp.fr.

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Classifications MeSH