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Minimally invasive intrathecal spinal cord imaging with optical coherence tomography

Significance: Imaging of the spinal cord is challenging due to the surrounding bony anatomy, physiologic motion, and the small diameter of the spinal cord. This precludes the use of non-invasive imaging techniques in assessing structural changes related to trauma and evaluating residual function. Ai...

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Autores principales: Pasarikovski, Christopher R., Ku, Jerry C., Ramjist, Joel, Dobashi, Yuta, Priola, Stefano M., da Costa, Leodante, Kumar, Ashish, Yang, Victor X. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118064/
https://www.ncbi.nlm.nih.gov/pubmed/33988003
http://dx.doi.org/10.1117/1.JBO.26.5.056002
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author Pasarikovski, Christopher R.
Ku, Jerry C.
Ramjist, Joel
Dobashi, Yuta
Priola, Stefano M.
da Costa, Leodante
Kumar, Ashish
Yang, Victor X. D.
author_facet Pasarikovski, Christopher R.
Ku, Jerry C.
Ramjist, Joel
Dobashi, Yuta
Priola, Stefano M.
da Costa, Leodante
Kumar, Ashish
Yang, Victor X. D.
author_sort Pasarikovski, Christopher R.
collection PubMed
description Significance: Imaging of the spinal cord is challenging due to the surrounding bony anatomy, physiologic motion, and the small diameter of the spinal cord. This precludes the use of non-invasive imaging techniques in assessing structural changes related to trauma and evaluating residual function. Aim: The purpose of our research was to apply endovascular technology and techniques and construct a preclinical animal model of intrathecal spinal cord imaging using optical coherence tomography (OCT). Approach: Five animals (2 Yorkshire Swine and 3 New Zealand Rabbits) were utilized. Intrathecal access was gained using a 16-guage Tuohy, and an OCT catheter was advanced under roadmap technique into the cervical canal. The OCT catheter has a motorized pullback, and a total length of 54 mm of the spinal canal is imaged. Results: Image acquisition was successful for all animals. There were no instances of difficult catheter navigation, enabling OCT imaging rostrally to C2. The thecal sac provided excellent thoroughfare for the OCT catheter. The clear cerebrospinal fluid also provided an excellent medium for image acquisition, with no detectable artifact from the contents of the cerebrospinal fluid. The anatomical space of the spinal canal could be readily appreciated including: dural lining of the thecal sac, epidural veins, pial lining of the spinal cord, arachnoid bands, dentate ligaments, and nerve rootlets/roots. Conclusion: Minimally invasive intrathecal imaging using endovascular OCT was feasible in this preclinical animal study. The repurposing of an endovascular device for spinal imaging comes with limitations, and a spine-specific device is necessary.
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spelling pubmed-81180642021-05-14 Minimally invasive intrathecal spinal cord imaging with optical coherence tomography Pasarikovski, Christopher R. Ku, Jerry C. Ramjist, Joel Dobashi, Yuta Priola, Stefano M. da Costa, Leodante Kumar, Ashish Yang, Victor X. D. J Biomed Opt Imaging Significance: Imaging of the spinal cord is challenging due to the surrounding bony anatomy, physiologic motion, and the small diameter of the spinal cord. This precludes the use of non-invasive imaging techniques in assessing structural changes related to trauma and evaluating residual function. Aim: The purpose of our research was to apply endovascular technology and techniques and construct a preclinical animal model of intrathecal spinal cord imaging using optical coherence tomography (OCT). Approach: Five animals (2 Yorkshire Swine and 3 New Zealand Rabbits) were utilized. Intrathecal access was gained using a 16-guage Tuohy, and an OCT catheter was advanced under roadmap technique into the cervical canal. The OCT catheter has a motorized pullback, and a total length of 54 mm of the spinal canal is imaged. Results: Image acquisition was successful for all animals. There were no instances of difficult catheter navigation, enabling OCT imaging rostrally to C2. The thecal sac provided excellent thoroughfare for the OCT catheter. The clear cerebrospinal fluid also provided an excellent medium for image acquisition, with no detectable artifact from the contents of the cerebrospinal fluid. The anatomical space of the spinal canal could be readily appreciated including: dural lining of the thecal sac, epidural veins, pial lining of the spinal cord, arachnoid bands, dentate ligaments, and nerve rootlets/roots. Conclusion: Minimally invasive intrathecal imaging using endovascular OCT was feasible in this preclinical animal study. The repurposing of an endovascular device for spinal imaging comes with limitations, and a spine-specific device is necessary. Society of Photo-Optical Instrumentation Engineers 2021-05-13 2021-05 /pmc/articles/PMC8118064/ /pubmed/33988003 http://dx.doi.org/10.1117/1.JBO.26.5.056002 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Imaging
Pasarikovski, Christopher R.
Ku, Jerry C.
Ramjist, Joel
Dobashi, Yuta
Priola, Stefano M.
da Costa, Leodante
Kumar, Ashish
Yang, Victor X. D.
Minimally invasive intrathecal spinal cord imaging with optical coherence tomography
title Minimally invasive intrathecal spinal cord imaging with optical coherence tomography
title_full Minimally invasive intrathecal spinal cord imaging with optical coherence tomography
title_fullStr Minimally invasive intrathecal spinal cord imaging with optical coherence tomography
title_full_unstemmed Minimally invasive intrathecal spinal cord imaging with optical coherence tomography
title_short Minimally invasive intrathecal spinal cord imaging with optical coherence tomography
title_sort minimally invasive intrathecal spinal cord imaging with optical coherence tomography
topic Imaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118064/
https://www.ncbi.nlm.nih.gov/pubmed/33988003
http://dx.doi.org/10.1117/1.JBO.26.5.056002
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