Rapid Successful Reperfusion of Basilar Artery Occlusion Strokes With Pretreatment Diffusion-Weighted Imaging Posterior-Circulation ASPECTS <8 Is Associated With Good Outcome.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
21 05 2019
Historique:
entrez: 10 5 2019
pubmed: 10 5 2019
medline: 25 8 2020
Statut: ppublish

Résumé

Background The association between time to reperfusion and clinical outcome is well known in anterior circulation strokes, whereas the impact of main time metrics remains unknown in posterior circulation strokes. We investigated the clinical effect of different time intervals from symptom onset to reperfusion on the 90-day clinical outcome in acute ischemic stroke patients with basilar artery occlusion, and especially in the subset population presenting a low stroke volume on baseline diffusion-weighted imaging. Methods and Results We studied patients included in the prospective, multicenter, observational ETIS (Endovascular Treatment in Ischemic Stroke) registry who had had basal artery occlusion and had achieved successful reperfusion (modified Thrombolysis In Cerebral Infarction 2b-3). Three time intervals (onset to reperfusion, onset to imaging, and imaging to reperfusion) were considered in all patients and separately in patients with pc- ASPECTS (posterior-circulation Alberta Stroke Program Early Computed Tomography Score) <8 and ≥8 on baseline diffusion-weighted imaging. The primary end point was good outcome defined as 90-day modified Rankin Scale scores of 0 to 2. Among the 95 included patients, 38 (40%) achieved a good outcome. In all patients, no significant association was found between the different time intervals and outcome. In patients evaluated with diffusion-weighted imaging (n=61) at baseline, a significant negative association was found between imaging-to-reperfusion time for patients with pc- ASPECTS <8 (adjusted odds ratio=0.4 per 30-minute increase; 95% CI 0.18-0.85; P=0.02) compared with those with pc- ASPECTS ≥8. Conclusions In patients with basilar artery occlusion and pc- ASPECTS <8 at baseline diffusion-weighted imaging, clinical outcome is highly dependent on the time from imaging to reperfusion, which suggests that rapid endovascular reperfusion should be performed after imaging in these patients.

Identifiants

pubmed: 31070075
doi: 10.1161/JAHA.118.010962
pmc: PMC6585336
doi:

Types de publication

Comparative Study Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e010962

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Auteurs

Morgan Guillaume (M)

1 Stroke Unit Department of Neurology University Hospital of Nancy France.

Bertrand Lapergue (B)

3 Department of Neurology Stroke Center Hôpital Foch Suresnes France.

Benjamin Gory (B)

4 Department of Diagnostic and Therapeutic Neuroradiology University Hospital of Nancy France.
5 IADI, INSERM U1254 University of Lorraine Nancy France.

Julien Labreuche (J)

6 CHU Lille, EA 2694-Santé publique: épidémiologie et qualité des soins University of Lille Lille France.

Arturo Consoli (A)

7 Department of Diagnostic and Therapeutic Neuroradiology Hôpital Foch Suresnes France.

Gioia Mione (G)

1 Stroke Unit Department of Neurology University Hospital of Nancy France.

Lisa Humbertjean (L)

1 Stroke Unit Department of Neurology University Hospital of Nancy France.

Jean-Christophe Lacour (JC)

1 Stroke Unit Department of Neurology University Hospital of Nancy France.

Mikael Mazighi (M)

8 Department of Interventional Neuroradiology Rothschild Foundation Paris France.
9 Laboratory of Vascular Translational Science INSERM U1148 Paris France.
10 DHU NeuroVasc Paris France.

Michel Piotin (M)

8 Department of Interventional Neuroradiology Rothschild Foundation Paris France.

Raphaël Blanc (R)

8 Department of Interventional Neuroradiology Rothschild Foundation Paris France.

Sébastien Richard (S)

1 Stroke Unit Department of Neurology University Hospital of Nancy France.
2 Centre d'Investigation Clinique Plurithématique CIC-P 1433, INSERM U1116 CHRU Nancy France.

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