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Safety and efficacy of intravenous thrombolytic therapy in the extended window up to 24 hours: A systematic review and meta‐analysis

Objective About 25% of patients with acute ischemic stroke (AIS) present within the intravenous thrombolytic (IVT) therapeutic window of

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Published in:Annals of clinical and translational neurology 2024-12, Vol.11 (12), p.3310-3319
Main Authors: Al‐Janabi, Omar M., Jazayeri, Seyed Behnam, Toruno, Michelle A., Mahmood, Yamama M., Ghozy, Sherief, Yaghi, Shadi, Rabinstein, Alejandro A., Kallmes, David F.
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container_title Annals of clinical and translational neurology
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creator Al‐Janabi, Omar M.
Jazayeri, Seyed Behnam
Toruno, Michelle A.
Mahmood, Yamama M.
Ghozy, Sherief
Yaghi, Shadi
Rabinstein, Alejandro A.
Kallmes, David F.
description Objective About 25% of patients with acute ischemic stroke (AIS) present within the intravenous thrombolytic (IVT) therapeutic window of
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This study is to elucidate the safety and efficacy of IVT in the extended therapeutic window (ETW) in patients with AIS. Methods Using PRISMA guidelines, a systematic review was conducted using PubMed, Embase, and Scopus. A rigorous risk of bias assessment was conducted using the RoB2 tool. Rates of excellent and good functional outcome (mRS 0–1 and mRS 0–2) at 90 days, symptomatic intracranial hemorrhage (sICH), and mortality at 90 days were pooled using generalized linear mixed model and compared with controls. Meta‐analyses were conducted employing random‐effect models with risk ratio (RR) and 95% confidence intervals (CIs). Subgroup analysis was performed to assess the effect of imaging modalities used for patient selection. Results Eight randomized controlled trials (n = 2221, 59% male) were included. At 90 days IVT showed higher rates of functional recovery: mRS 0–1: RR 1.21 95% CI 1.1–1.34, p &lt; 0.001, and mRS 0–2: RR 1.11 95% CI 1.03–1.18, p = 0.004. Rate of mortality at 90 day was not different between groups: RR 1.17 95% CI 0.93–1.48, p = 0.17. However, the rate of sICH was higher among IVT group: RR 2.93 95% CI 1.53–5.6, p = 0.001. Subgroup analysis showed higher mRS 0–1 among patients who were selected based on perfusion imaging (p &lt; 0.05). Interpretation The use of IVT in AIS in ETW is beneficial especially with the use of perfusion imaging for patients' selection.</description><identifier>ISSN: 2328-9503</identifier><identifier>EISSN: 2328-9503</identifier><identifier>DOI: 10.1002/acn3.52239</identifier><identifier>PMID: 39469780</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Administration, Intravenous ; Age ; Clinical trials ; Fibrinolytic Agents - administration &amp; dosage ; Fibrinolytic Agents - adverse effects ; Humans ; Ischemia ; Ischemic Stroke - drug therapy ; Ischemic Stroke - mortality ; Mortality ; Patients ; Stroke ; Systematic review ; Thrombolytic Therapy - adverse effects ; Thrombolytic Therapy - methods ; Time-to-Treatment ; Tissues</subject><ispartof>Annals of clinical and translational neurology, 2024-12, Vol.11 (12), p.3310-3319</ispartof><rights>2024 The Author(s). published by Wiley Periodicals LLC on behalf of American Neurological Association.</rights><rights>2024 The Author(s). Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4049-3f46bd08b0b824c1c9ed0087baa095463f51126244af117b6bad0d4c788324043</cites><orcidid>0000-0001-5629-3023 ; 0000-0003-0031-1004 ; 0000-0003-2208-4308</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3145668506/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3145668506?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11561,25752,27923,27924,37011,37012,44589,46051,46475,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39469780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Al‐Janabi, Omar M.</creatorcontrib><creatorcontrib>Jazayeri, Seyed Behnam</creatorcontrib><creatorcontrib>Toruno, Michelle A.</creatorcontrib><creatorcontrib>Mahmood, Yamama M.</creatorcontrib><creatorcontrib>Ghozy, Sherief</creatorcontrib><creatorcontrib>Yaghi, Shadi</creatorcontrib><creatorcontrib>Rabinstein, Alejandro A.</creatorcontrib><creatorcontrib>Kallmes, David F.</creatorcontrib><title>Safety and efficacy of intravenous thrombolytic therapy in the extended window up to 24 hours: A systematic review and meta‐analysis</title><title>Annals of clinical and translational neurology</title><addtitle>Ann Clin Transl Neurol</addtitle><description>Objective About 25% of patients with acute ischemic stroke (AIS) present within the intravenous thrombolytic (IVT) therapeutic window of &lt;4.5 h. This study is to elucidate the safety and efficacy of IVT in the extended therapeutic window (ETW) in patients with AIS. Methods Using PRISMA guidelines, a systematic review was conducted using PubMed, Embase, and Scopus. A rigorous risk of bias assessment was conducted using the RoB2 tool. Rates of excellent and good functional outcome (mRS 0–1 and mRS 0–2) at 90 days, symptomatic intracranial hemorrhage (sICH), and mortality at 90 days were pooled using generalized linear mixed model and compared with controls. Meta‐analyses were conducted employing random‐effect models with risk ratio (RR) and 95% confidence intervals (CIs). Subgroup analysis was performed to assess the effect of imaging modalities used for patient selection. Results Eight randomized controlled trials (n = 2221, 59% male) were included. At 90 days IVT showed higher rates of functional recovery: mRS 0–1: RR 1.21 95% CI 1.1–1.34, p &lt; 0.001, and mRS 0–2: RR 1.11 95% CI 1.03–1.18, p = 0.004. 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This study is to elucidate the safety and efficacy of IVT in the extended therapeutic window (ETW) in patients with AIS. Methods Using PRISMA guidelines, a systematic review was conducted using PubMed, Embase, and Scopus. A rigorous risk of bias assessment was conducted using the RoB2 tool. Rates of excellent and good functional outcome (mRS 0–1 and mRS 0–2) at 90 days, symptomatic intracranial hemorrhage (sICH), and mortality at 90 days were pooled using generalized linear mixed model and compared with controls. Meta‐analyses were conducted employing random‐effect models with risk ratio (RR) and 95% confidence intervals (CIs). Subgroup analysis was performed to assess the effect of imaging modalities used for patient selection. Results Eight randomized controlled trials (n = 2221, 59% male) were included. At 90 days IVT showed higher rates of functional recovery: mRS 0–1: RR 1.21 95% CI 1.1–1.34, p &lt; 0.001, and mRS 0–2: RR 1.11 95% CI 1.03–1.18, p = 0.004. 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subjects Administration, Intravenous
Age
Clinical trials
Fibrinolytic Agents - administration & dosage
Fibrinolytic Agents - adverse effects
Humans
Ischemia
Ischemic Stroke - drug therapy
Ischemic Stroke - mortality
Mortality
Patients
Stroke
Systematic review
Thrombolytic Therapy - adverse effects
Thrombolytic Therapy - methods
Time-to-Treatment
Tissues
title Safety and efficacy of intravenous thrombolytic therapy in the extended window up to 24 hours: A systematic review and meta‐analysis
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