Platelet-rich clots as identified by Martius Scarlet Blue staining are isodense on NCCT.


Journal

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

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 06 12 2018
revised: 28 02 2019
accepted: 03 03 2019
pubmed: 7 4 2019
medline: 1 1 2020
entrez: 7 4 2019
Statut: ppublish

Résumé

Current studies on clot characterization in acute ischemic stroke focus on fibrin and red blood cell composition. Few studies have examined platelet composition in acute ischemic stroke clots. We characterize clot composition using the Martius Scarlet Blue stain and assess associations between platelet density and CT density. Histopathological analysis of the clots collected as part of the multi-institutional STRIP registry was performed using Martius Scarlet Blue stain and the composition of the clots was quantified using Orbit Image Analysis (www.orbit.bio) machine learning software. Prior to endovascular treatment, each patient underwent non-contrast CT (NCCT) and the CT density of each clot was measured. Correlations between clot components and clinical information were assessed using the χ Eighty-five patients were included in the study. The mean platelet density of the clots was 15.7% (2.5-72.5%). There was a significant correlation between platelet-rich clots and the absence of hyperdensity on NCCT, (ρ=0.321, p=0.003*, n=85). Similarly, there was a significant inverse correlation between the percentage of platelets and the mean Hounsfield Units on NCCT (ρ=-0.243, p=0.025*, n=85). Martius Scarlet Blue stain can identify patients who have platelet-rich clots. Platelet-rich clots are isodense on NCCT.

Sections du résumé

BACKGROUND BACKGROUND
Current studies on clot characterization in acute ischemic stroke focus on fibrin and red blood cell composition. Few studies have examined platelet composition in acute ischemic stroke clots. We characterize clot composition using the Martius Scarlet Blue stain and assess associations between platelet density and CT density.
MATERIALS AND METHOD METHODS
Histopathological analysis of the clots collected as part of the multi-institutional STRIP registry was performed using Martius Scarlet Blue stain and the composition of the clots was quantified using Orbit Image Analysis (www.orbit.bio) machine learning software. Prior to endovascular treatment, each patient underwent non-contrast CT (NCCT) and the CT density of each clot was measured. Correlations between clot components and clinical information were assessed using the χ
RESULTS RESULTS
Eighty-five patients were included in the study. The mean platelet density of the clots was 15.7% (2.5-72.5%). There was a significant correlation between platelet-rich clots and the absence of hyperdensity on NCCT, (ρ=0.321, p=0.003*, n=85). Similarly, there was a significant inverse correlation between the percentage of platelets and the mean Hounsfield Units on NCCT (ρ=-0.243, p=0.025*, n=85).
CONCLUSION CONCLUSIONS
Martius Scarlet Blue stain can identify patients who have platelet-rich clots. Platelet-rich clots are isodense on NCCT.

Identifiants

pubmed: 30952688
pii: neurintsurg-2018-014637
doi: 10.1136/neurintsurg-2018-014637
pmc: PMC7754082
mid: NIHMS1046800
doi:

Substances chimiques

Fibrin 9001-31-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1145-1149

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS105853
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Sean T Fitzgerald (ST)

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

Shunli Wang (S)

Department of Pathology, Shanghai East Hospital, Tongji University, Shanghai, China.

Daying Dai (D)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Andrew Douglas (A)

CÚRAM - Centre for Research in Medical Devices, National University of Ireland Galway, Galway, Ireland.
Department of Physiology, National University of Ireland Galway, Galway, Ireland.

Ramanathan Kadirvel (R)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Matthew J Gounis (MJ)

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

Juyu Chueh (J)

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

Ajit S Puri (AS)

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

Kennith F Layton (KF)

Department of Radiology, Baylor University Medical Center, Dallas, Texas, USA.

Ike C Thacker (IC)

Department of Radiology, Baylor University Medical Center, Dallas, Texas, USA.

Ricardo A Hanel (RA)

Stroke & Cerebrovascular Center, Lyerly Neurosurgery/Baptist Neurological Center, Jacksonville, Florida, USA.

Eric Sauvageau (E)

Stroke & Cerebrovascular Center, Lyerly Neurosurgery/Baptist Neurological Center, Jacksonville, Florida, USA.

Amin Aghaebrahim (A)

Stroke & Cerebrovascular Center, Lyerly Neurosurgery/Baptist Neurological Center, Jacksonville, Florida, USA.

Mohammed A Almekhlafi (MA)

Department of Radiology, Hotchkiss Brain Institute, Calgary, Alberta, Canada.

Andrew M Demchuk (AM)

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

Raul G Nogueira (RG)

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

Vitor M Pereira (VM)

Joint Department of Medical Imaging, Neuroradiology, Toronto Western Hospital, Toronto, Ontario, Canada.

Peter Kvamme (P)

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

Yasha Kayan (Y)

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

Josser E Delgado Almandoz (JE)

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

Albert J Yoo (AJ)

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

David F Kallmes (DF)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Karen M Doyle (KM)

CÚRAM - Centre for Research in Medical Devices, National University of Ireland Galway, Galway, Ireland.
Department of Physiology, National University of Ireland Galway, Galway, Ireland.

Waleed Brinjikji (W)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

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