Strokes Averted by Intravenous Thrombolysis: A Secondary Analysis of a Prospective, Multicenter, Controlled Trial of Mobile Stroke Units.


Journal

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

Informations de publication

Date de publication:
06 Oct 2023
Historique:
revised: 29 09 2023
received: 20 02 2023
accepted: 30 09 2023
pubmed: 6 10 2023
medline: 6 10 2023
entrez: 6 10 2023
Statut: aheadofprint

Résumé

This study was undertaken to examine averted stroke in optimized stroke systems. This secondary analysis of a multicenter trial from 2014 to 2020 compared patients treated by mobile stroke unit (MSU) versus standard management. The analytical cohort consisted of participants with suspected stroke treated with intravenous thrombolysis. The main outcome was a tissue-defined averted stroke, defined as a final diagnosis of stroke with resolution of presenting symptoms/signs by 24 hours attributed to thrombolysis and no acute infarction/hemorrhage on imaging. An additional outcome was stroke with early symptom resolution, defined as a final diagnosis of stroke with resolution of presenting symptoms/signs by 24 hours attributed to thrombolysis. Among 1,009 patients with a median last known well to thrombolysis time of 87 minutes, 159 (16%) had tissue-defined averted stroke and 276 (27%) had stroke with early symptom resolution. Compared with standard management, MSU care was associated with more tissue-defined averted stroke (18% vs 11%, adjusted odds ratio [aOR] = 1.82, 95% confidence interval [CI] = 1.13-2.98) and stroke with early symptom resolution (31% vs 21%, aOR = 1.74, 95% CI = 1.12-2.61). The relationships between thrombolysis treatment time and averted/early recovered stroke appeared nonlinear. Most models indicated increased odds for stroke with early symptom resolution but not tissue-defined averted stroke with earlier treatment. Additionally, younger age, female gender, hyperlipidemia, lower National Institutes of Health Stroke Scale, lower blood pressure, and no large vessel occlusion were associated with both tissue-defined averted stroke and stroke with early symptom resolution. In optimized stroke systems, 1 in 4 patients treated with thrombolysis recovered within 24 hours and 1 in 6 had no demonstrable brain injury on imaging. ANN NEUROL 2023.

Identifiants

pubmed: 37801480
doi: 10.1002/ana.26816
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Patient-Centered Outcomes Research Institute
ID : R-1511-33024
Pays : United States

Informations de copyright

© 2023 American Neurological Association.

Références

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Auteurs

Babak B Navi (BB)

Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute and Department of Neurology, Weill Cornell Medicine, New York, NY.

Ivo Bach (I)

Department of Neurology, UTHealth McGovern Medical School, Houston, TX.

Alexandra L Czap (AL)

Department of Neurology, UTHealth McGovern Medical School, Houston, TX.

Mengxi Wang (M)

Department of Biostatistics and Data Science, UTHealth School of Public Health, Houston, TX.

Jose-Miguel Yamal (JM)

Department of Biostatistics and Data Science, UTHealth School of Public Health, Houston, TX.

Asha P Jacob (AP)

Department of Neurology, UTHealth McGovern Medical School, Houston, TX.

Stephanie A Parker (SA)

Department of Neurology, UTHealth McGovern Medical School, Houston, TX.

Suja S Rajan (SS)

Department of Biostatistics and Data Science, UTHealth School of Public Health, Houston, TX.

Saad Mir (S)

Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute and Department of Neurology, Weill Cornell Medicine, New York, NY.

Carla Sherman (C)

Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute and Department of Neurology, Weill Cornell Medicine, New York, NY.

Joshua Z Willey (JZ)

Department of Neurology, Columbia University Irving Medical Center, New York, NY.

Jeffrey L Saver (JL)

Department of Neurology, Ronald Reagan UCLA Medical Center, Los Angeles, CA.

Michael O Gonzalez (MO)

Department of Biostatistics and Data Science, UTHealth School of Public Health, Houston, TX.

Noopur Singh (N)

Department of Biostatistics and Data Science, UTHealth School of Public Health, Houston, TX.

William J Jones (WJ)

Department of Neurology, University of Colorado, Aurora, CO.

David Ornelas (D)

Department of Neurology, University of Colorado, Aurora, CO.

Nicole R Gonzales (NR)

Department of Neurology, University of Colorado, Aurora, CO.

Anne W Alexandrov (AW)

Department of Neurology, College of Nursing and College of Medicine, University of Tennessee Health Science Center, Memphis, TN.

Andrei V Alexandrov (AV)

Department of Neurology, University of Arizona, Banner University Medical Center, Phoenix, AZ.

May Nour (M)

Department of Neurology, Ronald Reagan UCLA Medical Center, Los Angeles, CA.

Ilana Spokoyny (I)

Department of Neurology, Mills Peninsula Medical Center, Burlingame, CA.

Jason Mackey (J)

Department of Neurology, Indiana University School of Medicine, Indianapolis, IN.

Sarah Q Collins (SQ)

Department of Neurology, Indiana University School of Medicine, Indianapolis, IN.

Kelly Silnes (K)

University of Buckingham Medical School, Buckingham, UK.

Mathew E Fink (ME)

Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute and Department of Neurology, Weill Cornell Medicine, New York, NY.

Joey English (J)

Department of Neurology, Mills Peninsula Medical Center, Burlingame, CA.

Nobl Barazangi (N)

Department of Neurology, Mills Peninsula Medical Center, Burlingame, CA.

Patti L Bratina (PL)

Department of Neurology, UTHealth McGovern Medical School, Houston, TX.

Jay Volpi (J)

Department of Neurology, Houston Methodist Hospital, Houston, TX.

Chethan P V Rao (CPV)

Department of Neurology, Baylor College of Medicine, Houston, TX.

Laura Griffin (L)

HCA Houston Healthcare, Houston, TX.

David Persse (D)

Department of Emergency Medicine, Baylor College of Medicine, Houston, TX.

James C Grotta (JC)

Clinical Innovation and Research Institute, Memorial Hermann Hospital-Texas Medical Center, Houston, TX.

Classifications MeSH