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Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe
Significance: The current gold standard for monitoring small intestinal transplant (IT) rejection is endoscopic visual assessment and biopsy of suspicious lesions; however, these lesions are only superficially visualized by endoscopy. Invasive biopsies provide a coarse sampling of tissue health with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461564/ https://www.ncbi.nlm.nih.gov/pubmed/34561973 http://dx.doi.org/10.1117/1.JBO.26.9.096008 |
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author | Jelly, Evan T. Kwun, Jean Schmitz, Robin Farris, Alton B. Steelman, Zachary A. Sudan, Debra L. Knechtle, Stuart J. Wax, Adam |
author_facet | Jelly, Evan T. Kwun, Jean Schmitz, Robin Farris, Alton B. Steelman, Zachary A. Sudan, Debra L. Knechtle, Stuart J. Wax, Adam |
author_sort | Jelly, Evan T. |
collection | PubMed |
description | Significance: The current gold standard for monitoring small intestinal transplant (IT) rejection is endoscopic visual assessment and biopsy of suspicious lesions; however, these lesions are only superficially visualized by endoscopy. Invasive biopsies provide a coarse sampling of tissue health without depicting the true presence and extent of any pathology. Optical coherence tomography (OCT) presents a potential alternative approach with significant advantages over traditional white-light endoscopy. Aim: The aim of our investigation was to evaluate OCT performance in distinguishing clinically relevant morphological features associated with IT graft failure. Approach: OCT was applied to evaluate the small bowel tissues of two rhesus macaques that had undergone IT of the ileum. The traditional assessment from routine histological observation was compared with OCT captured using a handheld surgical probe during the days post-transplant and subsequently was compared with histophaology. Results: The reported OCT system was capable of identifying major biological landmarks in healthy intestinal tissue. Following IT, one nonhuman primate (NHP) model suffered a severe graft ischemia, and the second NHP graft failed due to acute cellular rejection. OCT images show visual evidence of correspondence with histological signs of IT rejection. Conclusions: Results suggest that OCT imaging has significant potential to reveal morphological changes associated with IT rejection and to improve patient outcomes overall. |
format | Online Article Text |
id | pubmed-8461564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-84615642021-09-27 Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe Jelly, Evan T. Kwun, Jean Schmitz, Robin Farris, Alton B. Steelman, Zachary A. Sudan, Debra L. Knechtle, Stuart J. Wax, Adam J Biomed Opt Imaging Significance: The current gold standard for monitoring small intestinal transplant (IT) rejection is endoscopic visual assessment and biopsy of suspicious lesions; however, these lesions are only superficially visualized by endoscopy. Invasive biopsies provide a coarse sampling of tissue health without depicting the true presence and extent of any pathology. Optical coherence tomography (OCT) presents a potential alternative approach with significant advantages over traditional white-light endoscopy. Aim: The aim of our investigation was to evaluate OCT performance in distinguishing clinically relevant morphological features associated with IT graft failure. Approach: OCT was applied to evaluate the small bowel tissues of two rhesus macaques that had undergone IT of the ileum. The traditional assessment from routine histological observation was compared with OCT captured using a handheld surgical probe during the days post-transplant and subsequently was compared with histophaology. Results: The reported OCT system was capable of identifying major biological landmarks in healthy intestinal tissue. Following IT, one nonhuman primate (NHP) model suffered a severe graft ischemia, and the second NHP graft failed due to acute cellular rejection. OCT images show visual evidence of correspondence with histological signs of IT rejection. Conclusions: Results suggest that OCT imaging has significant potential to reveal morphological changes associated with IT rejection and to improve patient outcomes overall. Society of Photo-Optical Instrumentation Engineers 2021-09-24 2021-09 /pmc/articles/PMC8461564/ /pubmed/34561973 http://dx.doi.org/10.1117/1.JBO.26.9.096008 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Imaging Jelly, Evan T. Kwun, Jean Schmitz, Robin Farris, Alton B. Steelman, Zachary A. Sudan, Debra L. Knechtle, Stuart J. Wax, Adam Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
title | Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
title_full | Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
title_fullStr | Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
title_full_unstemmed | Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
title_short | Optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
title_sort | optical coherence tomography of small intestine allograft biopsies using a handheld surgical probe |
topic | Imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461564/ https://www.ncbi.nlm.nih.gov/pubmed/34561973 http://dx.doi.org/10.1117/1.JBO.26.9.096008 |
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