Effect of intravenous thrombolysis before endovascular therapy on outcomes in patients with large core infarct.

CT Stroke Thrombectomy Thrombolysis

Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
29 Mar 2023
Historique:
received: 16 08 2022
accepted: 17 02 2023
entrez: 29 3 2023
pubmed: 30 3 2023
medline: 30 3 2023
Statut: aheadofprint

Résumé

The safety and efficacy of bridging therapy with intravenous thrombolysis (IVT) and mechanical thrombectomy (MT) in patients with large core infarct has not been sufficiently studied. In this study, we compared the efficacy and safety outcomes between patients who received IVT+MT and those treated with MT alone. This is a retrospective analysis of the Stroke Thrombectomy Aneurysm Registry (STAR). Patients with Alberta Stroke Program Early CT Score (ASPECTS) ≤5 treated with MT were included in this study. Patients were divided into two groups based on pre-treatment IVT (IVT, no IVT). Propensity score matched analysis were used to compare outcomes between groups. A total of 398 patients were included; 113 pairs were generated using propensity score matching analyses. Baseline characteristics were well balanced in the matched cohort. The rate of any intracerebral hemorrhage (ICH) was similar between groups in both the full cohort (41.4% vs 42.3%, P=0.85) and matched cohort (38.55% vs 42.1%, P=0.593). Similarly, the rate of significant ICH was similar between the groups (full cohort: 13.1% vs 16.9%, P=0.306; matched cohort: 15.6% vs 18.95, P=0.52). There was no difference in favorable outcome (90-day modified Rankin Scale 0-2) or successful reperfusion between groups. In an adjusted analysis, IVT was not associated with any of the outcomes. Pretreatment IVT was not associated with an increased risk of hemorrhage in patients with large core infarct treated with MT. Future studies are needed to assess the safety and efficacy of bridging therapy in patients with large core infarct.

Sections du résumé

BACKGROUND BACKGROUND
The safety and efficacy of bridging therapy with intravenous thrombolysis (IVT) and mechanical thrombectomy (MT) in patients with large core infarct has not been sufficiently studied. In this study, we compared the efficacy and safety outcomes between patients who received IVT+MT and those treated with MT alone.
METHODS METHODS
This is a retrospective analysis of the Stroke Thrombectomy Aneurysm Registry (STAR). Patients with Alberta Stroke Program Early CT Score (ASPECTS) ≤5 treated with MT were included in this study. Patients were divided into two groups based on pre-treatment IVT (IVT, no IVT). Propensity score matched analysis were used to compare outcomes between groups.
RESULTS RESULTS
A total of 398 patients were included; 113 pairs were generated using propensity score matching analyses. Baseline characteristics were well balanced in the matched cohort. The rate of any intracerebral hemorrhage (ICH) was similar between groups in both the full cohort (41.4% vs 42.3%, P=0.85) and matched cohort (38.55% vs 42.1%, P=0.593). Similarly, the rate of significant ICH was similar between the groups (full cohort: 13.1% vs 16.9%, P=0.306; matched cohort: 15.6% vs 18.95, P=0.52). There was no difference in favorable outcome (90-day modified Rankin Scale 0-2) or successful reperfusion between groups. In an adjusted analysis, IVT was not associated with any of the outcomes.
CONCLUSION CONCLUSIONS
Pretreatment IVT was not associated with an increased risk of hemorrhage in patients with large core infarct treated with MT. Future studies are needed to assess the safety and efficacy of bridging therapy in patients with large core infarct.

Identifiants

pubmed: 36990690
pii: jnis-2022-019537
doi: 10.1136/jnis-2022-019537
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MRL: Grants from the NIH (R01NS105692, R01NS088072, U24NS100654, UL1TR002319, R25NS079200) and the American Heart Association (18CDA34110295). Unrestricted educational grants from Medtronic, Stryker and Philips Volcano. Consultant for Medtronic. Minor equity/ownership interest in Proprio, Cerebrotech, Synchron. Adviser to Metis Innovative. AMS: Research support from Penumbra, Stryker, Medtronic, and Siemens. Consultant for Penumbra, Stryker, Terumo, and Arsenal. RMS: Grants from the NREF, Joe Niekro Foundation, Brain Aneurysm Foundation, Bee Foundation, the NIH (R01NS111119-01A1, UL1TR002736, KL2TR002737), the National Center for Advancing Translational Sciences, the National Institute on Minority Health and Health Disparities, and Medtronic. Consultant for Penumbra, Abbott, Medtronic, InNeuroCo and Cerenovus. JRM is on the editorial board of JNIS.

Auteurs

Mohammad Anadani (M)

Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA spiotta@musc.edu anadani@musc.edu.

Eyad Almallouhi (E)

Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.

Ilko Maier (I)

Neurology, University Medicine Goettingen, Goettingen, Germany.

Sami Al Kasab (S)

Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.

Pascal Jabbour (P)

Neurological Surgery, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Joon-Tae Kim (JT)

Neurology, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, South Korea.

Stacey Q Wolfe (SQ)

Neurosurgery, Wake Forest School of Medicine, Winston Salem, North Carolina, USA.

Ansaar Rai (A)

Radiology, West Virginia University Hospitals, Morgantown, West Virginia, USA.

Robert M Starke (RM)

Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.

Marios-Nikos Psychogios (MN)

Department of Neuroradiology, Clinic of Radiology and Nuclear Medicine, University Hospital Basel, Basel, Switzerland.

Edgar A Samaniego (EA)

Neurology, Radiology and Neurosurgery, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Adam S Arthur (AS)

Semmes-Murphey Neurologic and Spine Institute, Memphis, Tennessee, USA.
Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Shinichi Yoshimura (S)

Department of Neurosurgery, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.

Hugo Cuellar (H)

Neurosurgery, LSUHSC, Shreveport, Louisiana, USA.

Brian M Howard (BM)

Neurosurgery, Emory University School of Medicine, Atlanta, Georgia, USA.
Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, Georgia, USA.

Ali Alawieh (A)

Neurosurgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Isabel Fragata (I)

Neuroradiology, Centro Hospitalar de Lisboa Central, Lisboa, Portugal.

Adam J Polifka (AJ)

Department of Neurosurgery, University of Florida, Gainesville, Florida, USA.

Justin R Mascitelli (JR)

Department of Neurosurgery, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.

Joshua W Osbun (JW)

Neurosurgery, Washington University in Saint Louis School of Medicine, Saint Louis, Missouri, USA.

Charles Matouk (C)

Neurosurgery, Yale University, New Haven, Connecticut, USA.

Min S Park (MS)

Neurosurgery, Barrow Neurological Institute, Phoenix, Arizona, USA.

Michael R Levitt (MR)

Neurological Surgery, University of Washington, Seattle, Washington, USA.

Travis M Dumont (TM)

Department of Surgery, Division of Neurosurgery, University of Arizona/Arizona Health Science Center, Tucson, Arizona, USA.

Richard Williamson (R)

Neurology, Allegheny Health Network, Pittsburgh, Pennsylvania, USA.

Alejandro M Spiotta (AM)

Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA spiotta@musc.edu anadani@musc.edu.

Classifications MeSH