Thrombolysis for Wake-Up Stroke Versus Non-Wake-Up Unwitnessed Stroke: EOS Individual Patient Data Meta-Analysis.

intravenous alteplase intravenous thrombolysis ischemic stroke unknown-onset stroke wake-up stroke

Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
08 Mar 2024
Historique:
medline: 8 3 2024
pubmed: 8 3 2024
entrez: 8 3 2024
Statut: aheadofprint

Résumé

Stroke with unknown time of onset can be categorized into 2 groups; wake-up stroke (WUS) and unwitnessed stroke with an onset time unavailable for reasons other than wake-up (non-wake-up unwitnessed stroke, non-WUS). We aimed to assess potential differences in the efficacy and safety of intravenous thrombolysis (IVT) between these subgroups. Patients with an unknown-onset stroke were evaluated using individual patient-level data of 2 randomized controlled trials (WAKE-UP [Efficacy and Safety of MRI-Based Thrombolysis in Wake-Up Stroke], THAWS [Thrombolysis for Acute Wake-Up and Unclear-Onset Strokes With Alteplase at 0.6 mg/kg]) comparing IVT with placebo or standard treatment from the EOS (Evaluation of Unknown-Onset Stroke Thrombolysis trial) data set. A favorable outcome was prespecified as a modified Rankin Scale score of 0 to 1 at 90 days. Safety outcomes included symptomatic intracranial hemorrhage at 22 to 36 hours and 90-day mortality. The IVT effect was compared between the treatment groups in the WUS and non-WUS with multivariable logistic regression analysis. Six hundred thirty-four patients from 2 trials were analyzed; 542 had WUS (191 women, 272 receiving alteplase), and 92 had non-WUS (42 women, 43 receiving alteplase). Overall, no significant interaction was noted between the mode of onset and treatment effect ( There was no difference in the effect of IVT between patients with WUS and non-WUS. IVT showed a significant benefit in patients with WUS, while there was insufficient statistical power to detect a substantial benefit in the non-WUS subgroup. URL: https://www.clinicaltrials.gov; Unique identifier: CRD42020166903.

Sections du résumé

BACKGROUND UNASSIGNED
Stroke with unknown time of onset can be categorized into 2 groups; wake-up stroke (WUS) and unwitnessed stroke with an onset time unavailable for reasons other than wake-up (non-wake-up unwitnessed stroke, non-WUS). We aimed to assess potential differences in the efficacy and safety of intravenous thrombolysis (IVT) between these subgroups.
METHODS UNASSIGNED
Patients with an unknown-onset stroke were evaluated using individual patient-level data of 2 randomized controlled trials (WAKE-UP [Efficacy and Safety of MRI-Based Thrombolysis in Wake-Up Stroke], THAWS [Thrombolysis for Acute Wake-Up and Unclear-Onset Strokes With Alteplase at 0.6 mg/kg]) comparing IVT with placebo or standard treatment from the EOS (Evaluation of Unknown-Onset Stroke Thrombolysis trial) data set. A favorable outcome was prespecified as a modified Rankin Scale score of 0 to 1 at 90 days. Safety outcomes included symptomatic intracranial hemorrhage at 22 to 36 hours and 90-day mortality. The IVT effect was compared between the treatment groups in the WUS and non-WUS with multivariable logistic regression analysis.
RESULTS UNASSIGNED
Six hundred thirty-four patients from 2 trials were analyzed; 542 had WUS (191 women, 272 receiving alteplase), and 92 had non-WUS (42 women, 43 receiving alteplase). Overall, no significant interaction was noted between the mode of onset and treatment effect (
CONCLUSIONS UNASSIGNED
There was no difference in the effect of IVT between patients with WUS and non-WUS. IVT showed a significant benefit in patients with WUS, while there was insufficient statistical power to detect a substantial benefit in the non-WUS subgroup.
REGISTRATION UNASSIGNED
URL: https://www.clinicaltrials.gov; Unique identifier: CRD42020166903.

Identifiants

pubmed: 38456303
doi: 10.1161/STROKEAHA.123.043358
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Bastian Cheng (B)
Martin Bendszus (M)
Christopher Bladin (C)
Leonid Churilov (L)
Brunce Campbell (B)
Mark Parsons (M)
Nawaf Yassi (N)
Martin Ebinger (M)
Matthias Endres (M)
Jochen B Fiebach (JB)
Timothy Kleinig (T)
Lawrence Latour (L)
Robin Lemmens (R)
Christopher Levi (C)
Didier Leys (D)
Carlos Molina (C)
Keith Muir (K)
Norbert Nighoghossian (N)
Salvador Pedraza (S)
Peter D Schellinger (PD)
Stefan Schwab (S)
Claus Z Simonsen (CZ)
Shlee S Song (SS)
Vincent Thijs (V)
Danilo Toni (D)
Chung Y Hsu (CY)
Nils Wahlgren (N)

Auteurs

Naruhiko Kamogawa (N)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan (N.K., K.M., K.T., M.I., S.Y., M.K.).

Kaori Miwa (K)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan (N.K., K.M., K.T., M.I., S.Y., M.K.).

Kazunori Toyoda (K)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan (N.K., K.M., K.T., M.I., S.Y., M.K.).

Märit Jensen (M)

Klinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, Universitätsklinikum Hamburg-Eppendorf, Germany (M.J., C.G., G.T.).

Manabu Inoue (M)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan (N.K., K.M., K.T., M.I., S.Y., M.K.).

Sohei Yoshimura (S)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan (N.K., K.M., K.T., M.I., S.Y., M.K.).

Mayumi Fukuda-Doi (M)

Center for Advancing Clinical and Translational Sciences, National Cerebral, and Cardiovascular Center, Suita, Japan (M.F.-D.).

Takanari Kitazono (T)

Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan (T.K.).

Florent Boutitie (F)

Hospices Civils de Lyon, Service de Biostatistique, France (F.B.).
Villeurbanne, France; Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, France (F.B.).

Henry Ma (H)

Department of Medicine, School of Clinical Sciences, Monash University, Melbourne, VIC, Australia (H.M.).

Peter Ringleb (P)

Department of Neurology, University of Heidelberg, Germany (P.R., W.H.).

Ona Wu (O)

Athinoula A Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown (O.W.).

Lee H Schwamm (LH)

Department of Neurology, Massachusetts General Hospital, Boston (L.H.S.).

Steven Warach (S)

Dell Medical School, University of Texas at Austin (S.W.).

Werner Hacke (W)

Department of Neurology, University of Heidelberg, Germany (P.R., W.H.).

Stephen M Davis (SM)

Departments of Medicine and Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, the University of Melbourne, VIC, Australia (S.M.D., G.A.D.).

Geoffrey A Donnan (GA)

Departments of Medicine and Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, the University of Melbourne, VIC, Australia (S.M.D., G.A.D.).

Christian Gerloff (C)

Klinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, Universitätsklinikum Hamburg-Eppendorf, Germany (M.J., C.G., G.T.).

Götz Thomalla (G)

Klinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, Universitätsklinikum Hamburg-Eppendorf, Germany (M.J., C.G., G.T.).

Masatoshi Koga (M)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan (N.K., K.M., K.T., M.I., S.Y., M.K.).

Classifications MeSH