Intravenous Thrombolysis With Tenecteplase in Patients With Large Vessel Occlusions: Systematic Review and Meta-Analysis.


Journal

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

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 5 12 2020
medline: 20 4 2021
entrez: 4 12 2020
Statut: ppublish

Résumé

Accumulating evidence from randomized controlled clinical trials suggests that tenecteplase may represent an effective treatment alternative to alteplase for acute ischemic stroke. In the present systematic review and meta-analysis, we sought to compare the efficacy and safety outcomes of intravenous tenecteplase to intravenous alteplase administration for acute ischemic stroke patients with large vessel occlusions (LVOs). We searched MEDLINE (Medical Literature Analysis and Retrieval System Online) and Scopus for published randomized controlled clinical trials providing outcomes of acute ischemic stroke with confirmed LVO receiving intravenous thrombolysis with either tenecteplase at different doses or alteplase at a standard dose of 0.9 mg/kg. The primary outcome was the odds of modified Rankin Scale score of 0 to 2 at 3 months. We included 4 randomized controlled clinical trials including a total of 433 patients. Patients with confirmed LVO receiving tenecteplase had higher odds of modified Rankin Scale scores of 0 to 2 (odds ratio, 2.06 [95% CI, 1.15-3.69]), successful recanalization (odds ratio, 3.05 [95% CI, 1.73-5.40]), and functional improvement defined as 1-point decrease across all modified Rankin Scale grades (common odds ratio, 1.84 [95% CI, 1.18-2.87]) at 3 months compared with patients with confirmed LVO receiving alteplase. There was little or no heterogeneity between the results provided from included studies regarding the aforementioned outcomes (I Acute ischemic stroke patients with LVO receiving intravenous thrombolysis with tenecteplase have significantly better recanalization and clinical outcomes compared with patients receiving intravenous alteplase.

Sections du résumé

BACKGROUND AND PURPOSE
Accumulating evidence from randomized controlled clinical trials suggests that tenecteplase may represent an effective treatment alternative to alteplase for acute ischemic stroke. In the present systematic review and meta-analysis, we sought to compare the efficacy and safety outcomes of intravenous tenecteplase to intravenous alteplase administration for acute ischemic stroke patients with large vessel occlusions (LVOs).
METHODS
We searched MEDLINE (Medical Literature Analysis and Retrieval System Online) and Scopus for published randomized controlled clinical trials providing outcomes of acute ischemic stroke with confirmed LVO receiving intravenous thrombolysis with either tenecteplase at different doses or alteplase at a standard dose of 0.9 mg/kg. The primary outcome was the odds of modified Rankin Scale score of 0 to 2 at 3 months.
RESULTS
We included 4 randomized controlled clinical trials including a total of 433 patients. Patients with confirmed LVO receiving tenecteplase had higher odds of modified Rankin Scale scores of 0 to 2 (odds ratio, 2.06 [95% CI, 1.15-3.69]), successful recanalization (odds ratio, 3.05 [95% CI, 1.73-5.40]), and functional improvement defined as 1-point decrease across all modified Rankin Scale grades (common odds ratio, 1.84 [95% CI, 1.18-2.87]) at 3 months compared with patients with confirmed LVO receiving alteplase. There was little or no heterogeneity between the results provided from included studies regarding the aforementioned outcomes (I
CONCLUSIONS
Acute ischemic stroke patients with LVO receiving intravenous thrombolysis with tenecteplase have significantly better recanalization and clinical outcomes compared with patients receiving intravenous alteplase.

Identifiants

pubmed: 33272127
doi: 10.1161/STROKEAHA.120.030220
doi:

Substances chimiques

Fibrinolytic Agents 0
Tenecteplase WGD229O42W

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

308-312

Auteurs

Aristeidis H Katsanos (AH)

Division of Neurology, McMaster University/Population Health Research Institute, Hamilton, Canada (A.H.K., A.S.).

Apostolos Safouris (A)

Second Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Attikon University Hospital, Greece (A. Safouris, G.T.).
Stroke Unit, Metropolitan Hospital, Piraeus, Greece (A. Safouris, G.M.).

Amrou Sarraj (A)

Department of Neurology, UT Houston, TX (A. Sarraj).

Georgios Magoufis (G)

Stroke Unit, Metropolitan Hospital, Piraeus, Greece (A. Safouris, G.M.).

Ronen R Leker (RR)

Department of Neurology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel (R.R.L.).

Pooja Khatri (P)

Department of Neurology, University of Cincinnati, OH (P.K.).

Charlotte Cordonnier (C)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience and Cognition, France (C.C., D.L.).

Didier Leys (D)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience and Cognition, France (C.C., D.L.).

Ashkan Shoamanesh (A)

Division of Neurology, McMaster University/Population Health Research Institute, Hamilton, Canada (A.H.K., A.S.).

Niaz Ahmed (N)

Department of Neurology, Karolinska University Hospital, Stockholm, Sweden (N.A.).
Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden (N.A.).

Andrei V Alexandrov (AV)

Department of Neurology, University of Tennessee Health Science Center, Memphis (A.V.A., G.T.).

Georgios Tsivgoulis (G)

Second Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Attikon University Hospital, Greece (A. Safouris, G.T.).
Department of Neurology, University of Tennessee Health Science Center, Memphis (A.V.A., G.T.).

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