Thrombolytic therapy for wake-up stroke: A systematic review and meta-analysis.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
06 2021
Historique:
received: 06 03 2021
accepted: 21 03 2021
pubmed: 28 3 2021
medline: 13 8 2021
entrez: 27 3 2021
Statut: ppublish

Résumé

According to evidence-based clinical practice guidelines, patients presenting with disabling stroke symptoms should be treated with intravenous tissue plasminogen activator (IV tPA) within 4.5 h of time last known well. However, 25% of strokes are detected upon awakening (i.e., wake-up stroke [WUS]), which renders patients ineligible for IV tPA administered via time-based treatment algorithms, because it is impossible to establish a reliable time of symptom onset. We performed a systematic review and meta-analysis of the efficacy and safety of IV tPA compared with normal saline, placebo, or no treatment in patients with WUS using imaging-based treatment algorithms. We searched MEDLINE, Web of Science, and Scopus between January 1, 2006 and April 30, 2020. We included controlled trials (randomized or nonrandomized), observational cohort studies (prospective or retrospective), and single-arm studies in which adults with WUS were administered IV tPA after magnetic resonance imaging (MRI)- or computed tomography (CT)-based imaging. Our primary outcome was recovery at 90 days (defined as a modified Rankin Scale [mRS] score of 0-2), and our secondary outcomes were symptomatic intracranial hemorrhage (sICH) within 36 h, mortality, and other adverse effects. We included 16 studies that enrolled a total of 14,017 patients. Most studies were conducted in Europe (37.5%) or North America (37.5%), and 1757 patients (12.5%) received IV tPA. All studies used MRI-based (five studies) or CT-based (10 studies) imaging selection, and one study used a combination of modalities. Sixty-one percent of patients receiving IV tPA achieved an mRS score of 0 to 2 at 90 days (95% confidence interval [CI]: 51%-70%, 12 studies), with a relative risk (RR) of 1.21 compared with patients not receiving IV tPA (95% CI: 1.01-1.46, four studies). Three percent of patients receiving IV tPA experienced sICH within 36 h (95% CI: 2.5%-4.1%; 16 studies), which is an RR of 4.00 compared with patients not receiving IV tPA (95% CI: 2.85-5.61, seven studies). This systematic review and meta-analysis suggests that IV tPA is associated with a better functional outcome at 90 days despite the increased but acceptable risk of sICH. Based on these results, IV tPA should be offered as a treatment for WUS patients with favorable neuroimaging findings.

Sections du résumé

BACKGROUND AND PURPOSE
According to evidence-based clinical practice guidelines, patients presenting with disabling stroke symptoms should be treated with intravenous tissue plasminogen activator (IV tPA) within 4.5 h of time last known well. However, 25% of strokes are detected upon awakening (i.e., wake-up stroke [WUS]), which renders patients ineligible for IV tPA administered via time-based treatment algorithms, because it is impossible to establish a reliable time of symptom onset. We performed a systematic review and meta-analysis of the efficacy and safety of IV tPA compared with normal saline, placebo, or no treatment in patients with WUS using imaging-based treatment algorithms.
METHODS
We searched MEDLINE, Web of Science, and Scopus between January 1, 2006 and April 30, 2020. We included controlled trials (randomized or nonrandomized), observational cohort studies (prospective or retrospective), and single-arm studies in which adults with WUS were administered IV tPA after magnetic resonance imaging (MRI)- or computed tomography (CT)-based imaging. Our primary outcome was recovery at 90 days (defined as a modified Rankin Scale [mRS] score of 0-2), and our secondary outcomes were symptomatic intracranial hemorrhage (sICH) within 36 h, mortality, and other adverse effects.
RESULTS
We included 16 studies that enrolled a total of 14,017 patients. Most studies were conducted in Europe (37.5%) or North America (37.5%), and 1757 patients (12.5%) received IV tPA. All studies used MRI-based (five studies) or CT-based (10 studies) imaging selection, and one study used a combination of modalities. Sixty-one percent of patients receiving IV tPA achieved an mRS score of 0 to 2 at 90 days (95% confidence interval [CI]: 51%-70%, 12 studies), with a relative risk (RR) of 1.21 compared with patients not receiving IV tPA (95% CI: 1.01-1.46, four studies). Three percent of patients receiving IV tPA experienced sICH within 36 h (95% CI: 2.5%-4.1%; 16 studies), which is an RR of 4.00 compared with patients not receiving IV tPA (95% CI: 2.85-5.61, seven studies).
CONCLUSIONS
This systematic review and meta-analysis suggests that IV tPA is associated with a better functional outcome at 90 days despite the increased but acceptable risk of sICH. Based on these results, IV tPA should be offered as a treatment for WUS patients with favorable neuroimaging findings.

Identifiants

pubmed: 33772987
doi: 10.1111/ene.14839
doi:

Substances chimiques

Fibrinolytic Agents 0
Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2006-2016

Informations de copyright

© 2021 European Academy of Neurology.

Références

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Auteurs

Brian Mac Grory (B)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina, USA.

Ian J Saldanha (IJ)

Center for Evidence Synthesis in Health, Department of Health Services, Policy, and Practice, Brown University School of Public Health, Providence, Rhode Island, USA.
Department of Epidemiology, Brown University School of Public Health, Providence, Rhode Island, USA.

Eva A Mistry (EA)

Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Christoph Stretz (C)

Department of Neurology, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.

Sven Poli (S)

Department of Neurology With Focus on Neurovascular Diseases, University Hospital Tübingen, Tübingen, Germany.
Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany.

Marek Sykora (M)

Department of Neurology, St. John's Hospital, Medical Faculty, Sigmund Freud University, Vienna, Austria.

Lars Kellert (L)

Department of Neurology, Ludwig Maximilians University, Munich, Germany.

Katharina Feil (K)

Department of Neurology, Ludwig Maximilians University, Munich, Germany.

Shreyansh Shah (S)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina, USA.

Ryan McTaggart (R)

Department of Neurology, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Department of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Department of Radiology, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.

Derek Riebau (D)

Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Shadi Yaghi (S)

Department of Neurology, New York University School of Medicine, New York, New York, USA.

Kenneth Gaines (K)

Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Ying Xian (Y)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina, USA.

Wuwei Feng (W)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina, USA.

Matthew Schrag (M)

Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

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