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Registration of retinal sequences from new video-ophthalmoscopic camera

BACKGROUND: Analysis of fast temporal changes on retinas has become an important part of diagnostic video-ophthalmology. It enables investigation of the hemodynamic processes in retinal tissue, e.g. blood-vessel diameter changes as a result of blood-pressure variation, spontaneous venous pulsation i...

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Autores principales: Kolar, Radim, Tornow, Ralf. P., Odstrcilik, Jan, Liberdova, Ivana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875736/
https://www.ncbi.nlm.nih.gov/pubmed/27206477
http://dx.doi.org/10.1186/s12938-016-0191-0
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author Kolar, Radim
Tornow, Ralf. P.
Odstrcilik, Jan
Liberdova, Ivana
author_facet Kolar, Radim
Tornow, Ralf. P.
Odstrcilik, Jan
Liberdova, Ivana
author_sort Kolar, Radim
collection PubMed
description BACKGROUND: Analysis of fast temporal changes on retinas has become an important part of diagnostic video-ophthalmology. It enables investigation of the hemodynamic processes in retinal tissue, e.g. blood-vessel diameter changes as a result of blood-pressure variation, spontaneous venous pulsation influenced by intracranial-intraocular pressure difference, blood-volume changes as a result of changes in light reflection from retinal tissue, and blood flow using laser speckle contrast imaging. For such applications, image registration of the recorded sequence must be performed. METHODS: Here we use a new non-mydriatic video-ophthalmoscope for simple and fast acquisition of low SNR retinal sequences. We introduce a novel, two-step approach for fast image registration. The phase correlation in the first stage removes large eye movements. Lucas-Kanade tracking in the second stage removes small eye movements. We propose robust adaptive selection of the tracking points, which is the most important part of tracking-based approaches. We also describe a method for quantitative evaluation of the registration results, based on vascular tree intensity profiles. RESULTS: The achieved registration error evaluated on 23 sequences (5840 frames) is 0.78 ± 0.67 pixels inside the optic disc and 1.39 ± 0.63 pixels outside the optic disc. We compared the results with the commonly used approaches based on Lucas-Kanade tracking and scale-invariant feature transform, which achieved worse results. CONCLUSION: The proposed method can efficiently correct particular frames of retinal sequences for shift and rotation. The registration results for each frame (shift in X and Y direction and eye rotation) can also be used for eye-movement evaluation during single-spot fixation tasks.
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spelling pubmed-48757362016-05-22 Registration of retinal sequences from new video-ophthalmoscopic camera Kolar, Radim Tornow, Ralf. P. Odstrcilik, Jan Liberdova, Ivana Biomed Eng Online Research BACKGROUND: Analysis of fast temporal changes on retinas has become an important part of diagnostic video-ophthalmology. It enables investigation of the hemodynamic processes in retinal tissue, e.g. blood-vessel diameter changes as a result of blood-pressure variation, spontaneous venous pulsation influenced by intracranial-intraocular pressure difference, blood-volume changes as a result of changes in light reflection from retinal tissue, and blood flow using laser speckle contrast imaging. For such applications, image registration of the recorded sequence must be performed. METHODS: Here we use a new non-mydriatic video-ophthalmoscope for simple and fast acquisition of low SNR retinal sequences. We introduce a novel, two-step approach for fast image registration. The phase correlation in the first stage removes large eye movements. Lucas-Kanade tracking in the second stage removes small eye movements. We propose robust adaptive selection of the tracking points, which is the most important part of tracking-based approaches. We also describe a method for quantitative evaluation of the registration results, based on vascular tree intensity profiles. RESULTS: The achieved registration error evaluated on 23 sequences (5840 frames) is 0.78 ± 0.67 pixels inside the optic disc and 1.39 ± 0.63 pixels outside the optic disc. We compared the results with the commonly used approaches based on Lucas-Kanade tracking and scale-invariant feature transform, which achieved worse results. CONCLUSION: The proposed method can efficiently correct particular frames of retinal sequences for shift and rotation. The registration results for each frame (shift in X and Y direction and eye rotation) can also be used for eye-movement evaluation during single-spot fixation tasks. BioMed Central 2016-05-20 /pmc/articles/PMC4875736/ /pubmed/27206477 http://dx.doi.org/10.1186/s12938-016-0191-0 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kolar, Radim
Tornow, Ralf. P.
Odstrcilik, Jan
Liberdova, Ivana
Registration of retinal sequences from new video-ophthalmoscopic camera
title Registration of retinal sequences from new video-ophthalmoscopic camera
title_full Registration of retinal sequences from new video-ophthalmoscopic camera
title_fullStr Registration of retinal sequences from new video-ophthalmoscopic camera
title_full_unstemmed Registration of retinal sequences from new video-ophthalmoscopic camera
title_short Registration of retinal sequences from new video-ophthalmoscopic camera
title_sort registration of retinal sequences from new video-ophthalmoscopic camera
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875736/
https://www.ncbi.nlm.nih.gov/pubmed/27206477
http://dx.doi.org/10.1186/s12938-016-0191-0
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