Thrombectomy with or without Intravenous Thrombolytics in Basilar Artery Occlusion.


Journal

Annals of neurology
ISSN: 1531-8249
Titre abrégé: Ann Neurol
Pays: United States
ID NLM: 7707449

Informations de publication

Date de publication:
09 2023
Historique:
revised: 01 06 2023
received: 14 02 2023
accepted: 08 06 2023
medline: 5 9 2023
pubmed: 14 6 2023
entrez: 14 6 2023
Statut: ppublish

Résumé

Two randomized trials demonstrated the benefit of endovascular therapy (EVT) in patients suffering from a stroke due to a basilar artery occlusion (BAO). However, intravenous thrombolytic (IVT) use before EVT was low in these trials, questioning the added value of this treatment in this setting. We sought to investigate the efficacy and safety of EVT alone compared to IVT + EVT in stroke patients with a BAO. We analyzed data from the Endovascular Treatment in Ischemic Stroke registry, a prospective, observational, multicenter study of acute ischemic stroke patients treated with EVT in 21 centers in France between 1 January 2015 and 31 December 2021. We included patients with BAO and/or intracranial vertebral artery occlusion and compared patients treated with EVT alone versus IVT + EVT after propensity score (PS) matching. Variables selected for the PS were pre-stroke mRS, dyslipidemia, diabetes, anticoagulation, admission mode, baseline NIHSS and ASPECTS, type of anesthesia, and time from symptom onset to puncture. Efficacy outcomes were good functional outcome (modified Rankin Scale [mRS] 0-3) and functional independence (mRS 0-2) at 90 days. Safety outcomes were symptomatic intracranial hemorrhages and all-cause mortality at 90 days. Among 385 patients, 243 (134 EVT alone and 109 IVT + EVT) were included after PS matching. There was no difference between EVT alone and IVT + EVT regarding good functional outcome (adjusted odd ratio [aOR] labeling = 1.27, 95% confidence interval [CI], 0.68-2.37, p = 0.45) and functional independence (aOR = 1.50, 95% CI, 0.79-2.85, p = 0.21). Symptomatic intracranial hemorrhage and all-cause mortality were also similar between the two groups (aOR = 0.42, 95% CI, 0.10-1.79, p = 0.24 and aOR = 0.56, 95% CI, 0.29-1.10, p = 0.09, respectively). In this PS matching analysis, EVT alone seemed to lead to similar neurological recovery than IVT + EVT, with comparable safety profile. However, given our sample size and the observational nature of this study, further studies are needed to confirm these findings. ANN NEUROL 2023;94:596-604.

Identifiants

pubmed: 37314741
doi: 10.1002/ana.26720
doi:

Substances chimiques

Fibrinolytic Agents 0

Types de publication

Observational Study Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

596-604

Informations de copyright

© 2023 American Neurological Association.

Références

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Auteurs

Benjamin Maïer (B)

Neurology Department, Hôpital Saint-Joseph, Paris, France.
Service de Recherche Clinique, Hôpital Fondation A. de Rothschild, Paris, France.
Université Paris-Cité, Paris, France.
Université Paris-Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.

Stephanos Finitsis (S)

Aristotle University of Thessaloniki, Ahepa Hospital, Thessaoniki, Greece.

Mikael Mazighi (M)

Université Paris-Cité, Paris, France.
Université Paris-Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.
Neurology Department, Hôpital Lariboisière, Paris, France.
Interventional Neuroradiology Department, Hôpital Fondation A. de Rothschild, Paris, France.

Bertrand Lapergue (B)

Department of Neurology, Foch Hospital, Versailles Saint-Quentin en Yvelines University, Suresnes, France.

Gaultier Marnat (G)

Department of Diagnostic and Interventional Neuroradiology, University Hospital of Bordeaux, Bordeaux, France.

Igor Sibon (I)

Neurology Department, University Hospital of Bordeaux, Bordeaux, France.

Sebastien Richard (S)

Department of Neurology, Stroke Unit, CIC-P 1433, INSERM U1116, CHRU-Nancy, Nancy, France.

Christophe Cognard (C)

Department of Neuroradiology, CHU Toulouse, Toulouse, France.

Alain Viguier (A)

Vascular Neurology Department, University Hospital of Toulouse, Toulouse, France.

Jean-Marc Olivot (JM)

Vascular Neurology Department, University Hospital of Toulouse, Toulouse, France.

Benjamin Gory (B)

CHRU-Nancy, Department of Diagnostic and Therapeutic Neuroradiology, Université de Lorraine, Nancy, France.
INSERM 1254, IADI, Université de Lorraine, Nancy, France.

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