Assessment of Blood Clot Composition by Spectral Optical Coherence Tomography: An In Vitro Study.
Blood clot
Composition
Optical coherence tomography
Journal
Neurointervention
ISSN: 2093-9043
Titre abrégé: Neurointervention
Pays: Korea (South)
ID NLM: 101561462
Informations de publication
Date de publication:
Mar 2021
Mar 2021
Historique:
received:
12
08
2020
accepted:
12
11
2020
pubmed:
10
12
2020
medline:
10
12
2020
entrez:
9
12
2020
Statut:
ppublish
Résumé
Optical coherence tomography (OCT) has the potential for in vivo clot composition characterization in difficult mechanical embolectomy cases. We performed an in vitro study to determine the OCT characteristics of red blood cells (RBCs) and fibrin rich clots. Analogues of 5 compositions of clots (5% to 95% RBCs from Group A to E) were created from human blood. The blood mixture was injected into the bifurcation of a 3D printed bifurcated silicone tube. The OPTISTM Integrated System (St. Jude Medical Inc.) was used to identify the magnitude of OCT signals from different compositions of clots. Martius Scarlett Blue trichrome (MSB) staining was performed to confirm the composition of RBCs and fibrin in each clot. Group A and B showed less signal attenuation (less than 30%) from its surface to the inside, which indicated high penetration (low-back scattering). Group C indicated intermediate signal attenuation (60%) from its surface to inside the clots, in which signals were found even at the periphery of the clot. Group D and E were superficially signal rich with more signal attenuation (more than 80%) from its surface to the inside indicating low penetration (high-back scattering). Signal-free shadowing was shown in 3 clots in Group E. MSB staining indicated color change (from red in fibrin-rich clots to yellow in RBC-rich clots). Different compositions of clots can be assessed using OCT. Fibrin-rich clots have homogeneous signals with high penetration, while RBC-rich clots can be recognized as superficially signal rich with low penetration.
Identifiants
pubmed: 33296954
pii: neuroint.2020.00297
doi: 10.5469/neuroint.2020.00297
pmc: PMC7946555
doi:
Types de publication
Journal Article
Langues
eng
Pagination
29-33Subventions
Organisme : NINDS NIH HHS
ID : R01 NS105853
Pays : United States
Organisme : NIH HHS
ID : NS105853
Pays : United States
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