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In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography
We present in vivo volumetric images of human retinal micro-circulation using Fourier-domain optical coherence tomography (Fd-OCT) with the phase-variance based motion contrast method. Currently fundus fluorescein angiography (FA) is the standard technique in clinical settings for visualizing blood...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114219/ https://www.ncbi.nlm.nih.gov/pubmed/21698014 http://dx.doi.org/10.1364/BOE.2.001504 |
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author | Kim, Dae Yu Fingler, Jeff Werner, John S. Schwartz, Daniel M. Fraser, Scott E. Zawadzki, Robert J. |
author_facet | Kim, Dae Yu Fingler, Jeff Werner, John S. Schwartz, Daniel M. Fraser, Scott E. Zawadzki, Robert J. |
author_sort | Kim, Dae Yu |
collection | PubMed |
description | We present in vivo volumetric images of human retinal micro-circulation using Fourier-domain optical coherence tomography (Fd-OCT) with the phase-variance based motion contrast method. Currently fundus fluorescein angiography (FA) is the standard technique in clinical settings for visualizing blood circulation of the retina. High contrast imaging of retinal vasculature is achieved by injection of a fluorescein dye into the systemic circulation. We previously reported phase-variance optical coherence tomography (pvOCT) as an alternative and non-invasive technique to image human retinal capillaries. In contrast to FA, pvOCT allows not only noninvasive visualization of a two-dimensional retinal perfusion map but also volumetric morphology of retinal microvasculature with high sensitivity. In this paper we report high-speed acquisition at 125 kHz A-scans with pvOCT to reduce motion artifacts and increase the scanning area when compared with previous reports. Two scanning schemes with different sampling densities and scanning areas are evaluated to find optimal parameters for high acquisition speed in vivo imaging. In order to evaluate this technique, we compare pvOCT capillary imaging at 3x3 mm(2) and 1.5x1.5 mm(2) with fundus FA for a normal human subject. Additionally, a volumetric view of retinal capillaries and a stitched image acquired with ten 3x3 mm(2) pvOCT sub-volumes are presented. Visualization of retinal vasculature with pvOCT has potential for diagnosis of retinal vascular diseases. |
format | Online Article Text |
id | pubmed-3114219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-31142192011-06-22 In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography Kim, Dae Yu Fingler, Jeff Werner, John S. Schwartz, Daniel M. Fraser, Scott E. Zawadzki, Robert J. Biomed Opt Express Optical Coherence Tomography We present in vivo volumetric images of human retinal micro-circulation using Fourier-domain optical coherence tomography (Fd-OCT) with the phase-variance based motion contrast method. Currently fundus fluorescein angiography (FA) is the standard technique in clinical settings for visualizing blood circulation of the retina. High contrast imaging of retinal vasculature is achieved by injection of a fluorescein dye into the systemic circulation. We previously reported phase-variance optical coherence tomography (pvOCT) as an alternative and non-invasive technique to image human retinal capillaries. In contrast to FA, pvOCT allows not only noninvasive visualization of a two-dimensional retinal perfusion map but also volumetric morphology of retinal microvasculature with high sensitivity. In this paper we report high-speed acquisition at 125 kHz A-scans with pvOCT to reduce motion artifacts and increase the scanning area when compared with previous reports. Two scanning schemes with different sampling densities and scanning areas are evaluated to find optimal parameters for high acquisition speed in vivo imaging. In order to evaluate this technique, we compare pvOCT capillary imaging at 3x3 mm(2) and 1.5x1.5 mm(2) with fundus FA for a normal human subject. Additionally, a volumetric view of retinal capillaries and a stitched image acquired with ten 3x3 mm(2) pvOCT sub-volumes are presented. Visualization of retinal vasculature with pvOCT has potential for diagnosis of retinal vascular diseases. Optical Society of America 2011-05-11 /pmc/articles/PMC3114219/ /pubmed/21698014 http://dx.doi.org/10.1364/BOE.2.001504 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially. |
spellingShingle | Optical Coherence Tomography Kim, Dae Yu Fingler, Jeff Werner, John S. Schwartz, Daniel M. Fraser, Scott E. Zawadzki, Robert J. In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
title | In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
title_full | In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
title_fullStr | In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
title_full_unstemmed | In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
title_short | In vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
title_sort | in vivo volumetric imaging of human retinal circulation with phase-variance optical coherence tomography |
topic | Optical Coherence Tomography |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114219/ https://www.ncbi.nlm.nih.gov/pubmed/21698014 http://dx.doi.org/10.1364/BOE.2.001504 |
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