Bridging thrombolysis in atrial fibrillation stroke is associated with increased hemorrhagic complications without improved outcomes.


Journal

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

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 06 07 2021
accepted: 27 09 2021
pubmed: 26 11 2021
medline: 17 9 2022
entrez: 25 11 2021
Statut: ppublish

Résumé

Atrial fibrillation (AF) associated ischemic stroke is associated with worse functional outcomes, less effective recanalization, and increased rates of hemorrhagic complications after intravenous thrombolysis (IVT). Conversely, AF is not associated with hemorrhagic complications or functional outcomes in patients undergoing mechanical thrombectomy (MT). This differential effect of MT and IVT in AF associated stroke raises the question of whether bridging thrombolysis increases hemorrhagic complications in AF patients undergoing MT. This international cohort study of 22 comprehensive stroke centers analyzed patients with large vessel occlusion (LVO) undergoing MT between June 1, 2015 and December 31, 2020. Patients were divided into four groups based on comorbid AF and IVT exposure. Baseline patient characteristics, complications, and outcomes were reported and compared. 6461 patients underwent MT for LVO. 2311 (35.8%) patients had comorbid AF. In non-AF patients, bridging therapy improved the odds of good 90 day functional outcomes (adjusted OR (aOR) 1.29, 95% CI 1.03 to 1.60, p=0.025) and did not increase hemorrhagic complications. In AF patients, bridging therapy led to significant increases in symptomatic intracranial hemorrhage and parenchymal hematoma type 2 (aOR 1.66, 1.07 to 2.57, p=0.024) without any benefit in 90 day functional outcomes. Similar findings were noted in a separate propensity score analysis. In this large thrombectomy registry, AF patients exposed to IVT before MT had increased hemorrhagic complications without improved functional outcomes, in contrast with non-AF patients. Prospective trials are warranted to assess whether AF patients represent a subgroup of LVO patients who may benefit from a direct to thrombectomy approach at thrombectomy capable centers.

Sections du résumé

BACKGROUND BACKGROUND
Atrial fibrillation (AF) associated ischemic stroke is associated with worse functional outcomes, less effective recanalization, and increased rates of hemorrhagic complications after intravenous thrombolysis (IVT). Conversely, AF is not associated with hemorrhagic complications or functional outcomes in patients undergoing mechanical thrombectomy (MT). This differential effect of MT and IVT in AF associated stroke raises the question of whether bridging thrombolysis increases hemorrhagic complications in AF patients undergoing MT.
METHODS METHODS
This international cohort study of 22 comprehensive stroke centers analyzed patients with large vessel occlusion (LVO) undergoing MT between June 1, 2015 and December 31, 2020. Patients were divided into four groups based on comorbid AF and IVT exposure. Baseline patient characteristics, complications, and outcomes were reported and compared.
RESULTS RESULTS
6461 patients underwent MT for LVO. 2311 (35.8%) patients had comorbid AF. In non-AF patients, bridging therapy improved the odds of good 90 day functional outcomes (adjusted OR (aOR) 1.29, 95% CI 1.03 to 1.60, p=0.025) and did not increase hemorrhagic complications. In AF patients, bridging therapy led to significant increases in symptomatic intracranial hemorrhage and parenchymal hematoma type 2 (aOR 1.66, 1.07 to 2.57, p=0.024) without any benefit in 90 day functional outcomes. Similar findings were noted in a separate propensity score analysis.
CONCLUSION CONCLUSIONS
In this large thrombectomy registry, AF patients exposed to IVT before MT had increased hemorrhagic complications without improved functional outcomes, in contrast with non-AF patients. Prospective trials are warranted to assess whether AF patients represent a subgroup of LVO patients who may benefit from a direct to thrombectomy approach at thrombectomy capable centers.

Identifiants

pubmed: 34819345
pii: neurintsurg-2021-017954
doi: 10.1136/neurintsurg-2021-017954
doi:

Substances chimiques

Fibrinolytic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

979-984

Investigateurs

Sébastien Richard (S)
Brian Hoh (B)
Adam Polifka (A)
Min Park (M)
Kimberly Kicielinski (K)
Sami Al Kasab (SA)
Eyad Almallouhi (E)
Michelle Allen (M)
Jonathan Lena (J)
Daniel A Hoit (DA)
Lucas Elijovich (L)
Violiza Inoa (V)
Christopher Nickele (C)

Informations de copyright

© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: RMS: consulting and teaching agreements with Penumbra, Abbott, Medtronic, InNeuroCo, and Cerenovus. MNP: travel grants/honoraria from Phenox, Stryker, and Siemens. ASA: consultant for Balt, Johnson and Johnson, Leica, Medtronic, Microvention, Penumbra, Scientia, Siemens, and Stryker; research support for Cerenovus, Microvention, Penumbra, and Siemens; and shareholder of Bendit, Cerebrotech, Endostream, Magneto, Marblehead, Neurogami, Serenity, Synchron, Triad Medical, and Vascular Simulations. LE: consultant for Balt, Cerenovuc, Medtronic, MicroVention, Penumbra, Sequent, and Stryker; and research support for Siemens. PJ: consultant for Medtronics and Microvention. AMS: consultant for Penumbra, Microvention, and Pulsar Vascular; and travel grants/honoraria from Penumbra, Pulsar Vascular, Microvention, and Stryker. KMF, JM, PK, and RDL are on the editorial board of Journal of Neurointerventional Surgery.

Auteurs

Feras Akbik (F)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.
Department of Neurology, Emory University, Atlanta, Georgia, USA.

Ali Alawieh (A)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.
Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.

Laurie Dimisko (L)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.

Brian M Howard (BM)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.

C Michael Cawley (CM)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.

Frank C Tong (FC)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.

Fadi Nahab (F)

Department of Neurology, Emory University, Atlanta, Georgia, USA.

Owen B Samuels (OB)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA.

Ilko Maier (I)

Neurology, University Medicine Goettingen, Goettingen, Germany.

Wuwei Feng (W)

Neurology, Duke University Medical Center, Durham, North Carolina, USA.

Nitin Goyal (N)

Semmes Murphey Clinic, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Robert M Starke (RM)

Neurosurgery and Radiology, University of Miami, Miller School of Medicine, Miami, Florida, USA.

Ansaar Rai (A)

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

Kyle M Fargen (KM)

Neurosurgery, Wake Forest University, Winston-Salem, North Carolina, USA.

Marios N Psychogios (MN)

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

Pascal Jabbour (P)

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

Reade De Leacy (R)

Neurosurgery, The Mount Sinai Health System, New York, New York, USA.

Saleh G Keyrouz (SG)

Department of Neurology, Washington University at St. Louis, St Louis, Missouri, USA.

Travis M Dumont (TM)

Surgery, Division of Neurosurgery, Banner University of Arizona Medical Center, Tucson, Arizona, USA.

Peter Kan (P)

Neurosurgery, The University of Texas Medical Branch at Galveston, Galveston, Texas, USA.

Jan Liman (J)

Neurology, University Medical Center, Göttingen, Germany.

Adam S Arthur (AS)

Semmes Murphey Clinic, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

Stacey Q Wolfe (SQ)

Neurosurgery, Wake Forest University, Winston-Salem, North Carolina, USA.

J Mocco (J)

Neurosurgery, The Mount Sinai Health System, New York, New York, USA.

Roberto Javier Crosa (RJ)

Endovascular Neurosurgery, Médica Uruguaya, Montevideo, Uruguay.

W Christopher Fox (WC)

Neurosurgery, Mayo Clinic Hospital Jacksonville, Jacksonville, Florida, USA.

Benjamin Gory (B)

Department of Diagnostic and Therapeutic Neuroradiology, Université de Lorraine, CHRU-Nancy, Nancy, France.
INSERM, IADI, Université de Lorraine, Nancy, France.

Alejandro M Spiotta (AM)

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

Jonathan A Grossberg (JA)

Department of Neurosurgery, Emory University, Atlanta, Georgia, USA jonathan.a.grossberg@emory.edu.

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