Clot composition and recanalization outcomes in mechanical thrombectomy.

Device Stroke Thrombectomy

Journal

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

Informations de publication

Date de publication:
07 Jul 2023
Historique:
received: 06 02 2023
accepted: 24 05 2023
medline: 8 7 2023
pubmed: 8 7 2023
entrez: 7 7 2023
Statut: aheadofprint

Résumé

Mechanical thrombectomy (MT) has become standard for large vessel occlusions, but rates of complete recanalization are suboptimal. Previous reports correlated radiographic signs with clot composition and a better response to specific techniques. Therefore, understanding clot composition may allow improved outcomes. Clinical, imaging, and clot data from patients enrolled in the STRIP Registry from September 2016 to September 2020 were analyzed. Samples were fixed in 10% phosphate-buffered formalin and stained with hematoxylin-eosin and Martius Scarlett Blue. Percent composition, richness, and gross appearance were evaluated. Outcome measures included the rate of first-pass effect (FPE, modified Thrombolysis in Cerebral Infarction 2c/3) and the number of passes. A total of 1430 patients of mean±SD age 68.4±13.5 years (median (IQR) baseline National Institutes of Health Stroke Scale score 17.2 (10.5-23), IV-tPA use 36%, stent-retrievers (SR) 27%, contact aspiration (CA) 27%, combined SR+CA 43%) were included. The median (IQR) number of passes was 1 (1-2). FPE was achieved in 39.3% of the cases. There was no association between percent histological composition or clot richness and FPE in the overall population. However, the combined technique resulted in lower FPE rates for red blood cell (RBC)-rich (P<0.0001), platelet-rich (P=0.003), and mixed (P<0.0001) clots. Fibrin-rich and platelet-rich clots required a higher number of passes than RBC-rich and mixed clots (median 2 and 1.5 vs 1, respectively; P=0.02). CA showed a trend towards a higher number of passes with fibrin-rich clots (2 vs 1; P=0.12). By gross appearance, mixed/heterogeneous clots had lower FPE rates than red and white clots. Despite the lack of correlation between clot histology and FPE, our study adds to the growing evidence supporting the notion that clot composition influences recanalization treatment strategy outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Mechanical thrombectomy (MT) has become standard for large vessel occlusions, but rates of complete recanalization are suboptimal. Previous reports correlated radiographic signs with clot composition and a better response to specific techniques. Therefore, understanding clot composition may allow improved outcomes.
METHODS METHODS
Clinical, imaging, and clot data from patients enrolled in the STRIP Registry from September 2016 to September 2020 were analyzed. Samples were fixed in 10% phosphate-buffered formalin and stained with hematoxylin-eosin and Martius Scarlett Blue. Percent composition, richness, and gross appearance were evaluated. Outcome measures included the rate of first-pass effect (FPE, modified Thrombolysis in Cerebral Infarction 2c/3) and the number of passes.
RESULTS RESULTS
A total of 1430 patients of mean±SD age 68.4±13.5 years (median (IQR) baseline National Institutes of Health Stroke Scale score 17.2 (10.5-23), IV-tPA use 36%, stent-retrievers (SR) 27%, contact aspiration (CA) 27%, combined SR+CA 43%) were included. The median (IQR) number of passes was 1 (1-2). FPE was achieved in 39.3% of the cases. There was no association between percent histological composition or clot richness and FPE in the overall population. However, the combined technique resulted in lower FPE rates for red blood cell (RBC)-rich (P<0.0001), platelet-rich (P=0.003), and mixed (P<0.0001) clots. Fibrin-rich and platelet-rich clots required a higher number of passes than RBC-rich and mixed clots (median 2 and 1.5 vs 1, respectively; P=0.02). CA showed a trend towards a higher number of passes with fibrin-rich clots (2 vs 1; P=0.12). By gross appearance, mixed/heterogeneous clots had lower FPE rates than red and white clots.
CONCLUSIONS CONCLUSIONS
Despite the lack of correlation between clot histology and FPE, our study adds to the growing evidence supporting the notion that clot composition influences recanalization treatment strategy outcomes.

Identifiants

pubmed: 37419694
pii: jnis-2023-020117
doi: 10.1136/jnis-2023-020117
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: RGN reported consulting fees for advisory roles with Anaconda, Biogen, Cerenovus, Genentech, Hybernia, Imperative Care, Medtronic, Phenox, Philips, Prolong Pharmaceuticals, Stryker Neurovascular, Shanghai Wallaby, and Synchron and stock options for advisory roles with Astrocyte, Brainomix, Cerebrotech, Ceretrieve, Corindus Vascular Robotics, Vesalio, Viz-AI, RapidPulse, and Perfuze, and investments in Viz-AI, Perfuze, Cerebrotech, Reist/Q’Apel Medical, Truvic, and Viseon. WB is a consulting medical director for MIVI Neurovascular, consultant for Cerenovus, Microvention, Stryker, Medtronic, Imperative Care and receives research funding from Cerenovus, Brainomix, NIH. ARA-B is a consultant for Stryker Neurovascular. RAH is a consultant for Stryker, Medtronic, Cerenovous, Microvention, Balt, Phenox, Rapid Medical, and Q’Apel. He is on the advisory board for MiVI, eLum, Three Rivers, Shape Medical, and Corindus. AJY receives grants from Medtronic, Cerenovus, Penumbra, Stryker, and Penumbra. He is a consultant for Cerenovus, Penumbra, Vesalio, Zoll, Philips, Rapid Medical, and StrokeNet (MOST trial). AJY also has equity interest in Insera Therapeutics and Nicolab. MJG has been a consultant on a fee-per-hour basis for Alembic LLC, Astrocyte Pharmaceuticals, BendIt Technologies, Cerenovus, Imperative Care, the Jacob’s Institute, Medtronic Neurovascular, Mentice, Mivi Neurosciences, phenox GmbH, Q’Apel, Route 92 Medical, Scientia, Stryker, Wallaby Medical; holds stock in Imperative Care, InNeuroCo, Galaxy Therapeutics and Neurogami; and has received research support from the National Institutes of Health (NIH), the United States – Israel Binational Science Foundation, Anaconda, ApicBio, Arsenal Medical, Axovant, Balt, Cerenovus, Ceretrieve, CereVasc LLC, Cook Medical, Galaxy Therapeutics, Gentuity, Gilbert Foundation, Imperative Care, InNeuroCo, Insera, Jacob’s Institute, Magneto, Microvention, Medtronic Neurovascular, MIVI Neurosciences, Naglreiter MDDO, Neurogami, Philips Healthcare, Progressive Medical, Pulse Medical, Rapid Medical, Route 92 Medical, Scientia, Stryker Neurovascular, Syntheon, ThrombX Medical, Wallaby Medical, the Wyss Institute and Xtract Medical. KD is supported by a grant from Science Foundation Ireland (SFI) and the European Regional Development Fund (ERDF) under grant number 13/RC/2073_P2. ASP is a consultant for Medtronic Neurovascular, Stryker Neurovascular, Balt, Q’Apel Medical, Cerenovus, Microvention, Imperative Care, Agile, Merit, CereVasc and Arsenal Medical and receives research grants from NIH, Microvention. DCH is a consultant for Stryker,Cerenovus and is a member of the Data and Safety Monitoring Board for Vesalio and Jacobs Institute. He also holds stock options of VizAI. The other authors have no competing interests to disclose.

Auteurs

Raul G Nogueira (RG)

UPMC Stroke Institute, Pittsburgh, Pennsylvania, USA raul.g.nogueira@icloud.com.

Agostinho Pinheiro (A)

Neurology, UPMC Stroke Institute, Pittsburgh, Pennsylvania, USA.

Waleed Brinjikji (W)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Mehdi Abbasi (M)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Alhamza R Al-Bayati (AR)

Neurology, UPMC Stroke Institute, Pittsburgh, Pennsylvania, USA.

Mahmoud H Mohammaden (MH)

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

Lorena Souza Viana (L)

Neurology, Emory University, Atlanta, Georgia, USA.

Felipe Ferreira (F)

Neurology, Emory University, Atlanta, Georgia, USA.

Hend Abdelhamid (H)

Neurology, Emory University, Atlanta, Georgia, USA.

Nirav R Bhatt (NR)

UPMC Stroke Institute, Pittsburgh, Pennsylvania, USA.

Peter Kvamme (P)

Radiology, University of Tennessee Medical Center, Knoxville, Tennessee, USA.

Kennith F Layton (KF)

NeuroInterventional Radiology, Baylor University Medical Center, Dallas, Texas, USA.

Josser E Delgado Almandoz (JE)

Interventional Neuroradiology, Abbot Northwestern Hospital, 55435, Minnesota, USA.

Ricardo A Hanel (RA)

Neurosurgery, Baptist Medical Center Jacksonville, Jacksonville, Florida, USA.

Vitor Mendes Pereira (V)

Division of Neuroradiology, Department of Medical Imaging and Division of Neurosurgery, Department of Surgery, University Health Network - Toronto Western Hospital, Toronto, Ontario, Canada.

Mohammed A Almekhlafi (MA)

Clinical Neurosciences, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.

Albert J Yoo (AJ)

Neurointervention, Texas Stroke Institute, Plano, Texas, USA.

Babak S Jahromi (BS)

Neurosurgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

Matthew J Gounis (MJ)

New England Center for Stroke Research, Department of Radiology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.

Biraj Patel (B)

Radiology, Virginia Tech Carilion School of Medicine, Roanoke, Virginia, USA.
Radiology, Neurosurgery, Carilion Clinic, Roanoke, Virginia, USA.

Jorge L Arturo Larco (JL)

Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.

Sean Fitzgerald (S)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Oana Madalina Mereuta (OM)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.
CÚRAM-SFI Research Centre for Medical Devices and Physiology Department, National University of Ireland Galway, Galway, Ireland.

Karen Doyle (K)

Physiology, CURAM, National University of Ireland Galway, Galway, Ireland.

Luis E Savastano (LE)

Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.

Harry J Cloft (HJ)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Ike C Thacker (IC)

NeuroInterventional Radiology, Baylor University Medical Center, Dallas, Texas, USA.

Yasha Kayan (Y)

Interventional Neuroradiology, Abbot Northwestern Hospital, 55435, Minnesota, USA.

Alexander Copelan (A)

NeuroInterventional Radiology, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Amin Aghaebrahim (A)

Lyerly Neurosurgery, Baptist Health System, Jacksonville, Florida, USA.

Eric Sauvageau (E)

Lyerly Neurosurgery, Baptist Neurological Institute, Jacksonville, Florida, USA.

Andrew M Demchuk (AM)

Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
University of Calgary, Calgary, Alberta, Canada.

Parita Bhuva (P)

Neuroendovascular Surgery, Texas Stroke Institute, Plano, Texas, USA.

Jazba Soomro (J)

Neurointervention, Texas Stroke Institute, Plano, Texas, USA.

Pouya Nazari (P)

Neurosurgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Neurosurgery and Radiology, Northwestern University, Chicago, Illinois, USA.

Donald Robert Cantrell (DR)

Radiology, Northwestern University, Chicago, Illinois, USA.

Ajit S Puri (AS)

Radiology, University of Massachusetts, Worcester, Massachusetts, USA.

John Entwistle (J)

Radiology, Neurosurgery, Carilion Clinic, Roanoke, Virginia, USA.

Eric C Polley (EC)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Michael R Frankel (MR)

Department of Neurology, Emory University Atlanta, Atlanta, Georgia, USA.
Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, Georgia, USA.

David F Kallmes (DF)

Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Diogo C Haussen (DC)

Neurology and Radiology, Emory University School of Medicine, Atlanta, Georgia, USA.

Classifications MeSH