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Pathology detection rate of spectral domain optical coherence tomography devices

BACKGROUND: Spectral domain optical coherence tomography (SDOCT) allows for higher resolution scans and higher scanning speeds compared to time domain OCT (TDOCT). The purpose of this study is to compare the pathology detection rates of various SDOCT devices to the Stratus TDOCT. METHODS: Patients w...

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Autores principales: Sharma, Sumit, Sayanagi, Kaori, Kaiser, Peter K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033177/
https://www.ncbi.nlm.nih.gov/pubmed/24568868
http://dx.doi.org/10.1136/bjophthalmol-2013-303846
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author Sharma, Sumit
Sayanagi, Kaori
Kaiser, Peter K
author_facet Sharma, Sumit
Sayanagi, Kaori
Kaiser, Peter K
author_sort Sharma, Sumit
collection PubMed
description BACKGROUND: Spectral domain optical coherence tomography (SDOCT) allows for higher resolution scans and higher scanning speeds compared to time domain OCT (TDOCT). The purpose of this study is to compare the pathology detection rates of various SDOCT devices to the Stratus TDOCT. METHODS: Patients with neovascular age-related macular degeneration were imaged on the Stratus and one of four SDOCT devices. The images were then analysed in a masked manner evaluating for the presence of epiretinal membrane (ERM), pigment epithelial detachment (PED) and subretinal fluid (SRF). After determining that low scan density with one of the devices was likely the cause of missed PED and SRF compared to the other SDOCT devices the study was repeated with a higher scan density. RESULTS: 60 eyes from 60 patients with neovascular macular degeneration were imaged on each SDOCT device, for a total of 240 eyes from 240 patients imaged on Stratus. There were no instances where pathology was visible on Stratus but was missed on SDOCT. The highest incidence of missed pathology was with SRF, followed by ERM and PED. CONCLUSIONS: The increased resolution and image quality of SDOCT devices over TDOCT allows for finer discrimination of retinal structures. The increased speed of SDOCT allows for dense coverage of the macula resulting in the ability to see smaller areas of PED and SRF. There was a critical threshold for the distance between B-scans in the three-dimensional cube scan for detection of pathology.
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spelling pubmed-40331772014-06-05 Pathology detection rate of spectral domain optical coherence tomography devices Sharma, Sumit Sayanagi, Kaori Kaiser, Peter K Br J Ophthalmol Original Article BACKGROUND: Spectral domain optical coherence tomography (SDOCT) allows for higher resolution scans and higher scanning speeds compared to time domain OCT (TDOCT). The purpose of this study is to compare the pathology detection rates of various SDOCT devices to the Stratus TDOCT. METHODS: Patients with neovascular age-related macular degeneration were imaged on the Stratus and one of four SDOCT devices. The images were then analysed in a masked manner evaluating for the presence of epiretinal membrane (ERM), pigment epithelial detachment (PED) and subretinal fluid (SRF). After determining that low scan density with one of the devices was likely the cause of missed PED and SRF compared to the other SDOCT devices the study was repeated with a higher scan density. RESULTS: 60 eyes from 60 patients with neovascular macular degeneration were imaged on each SDOCT device, for a total of 240 eyes from 240 patients imaged on Stratus. There were no instances where pathology was visible on Stratus but was missed on SDOCT. The highest incidence of missed pathology was with SRF, followed by ERM and PED. CONCLUSIONS: The increased resolution and image quality of SDOCT devices over TDOCT allows for finer discrimination of retinal structures. The increased speed of SDOCT allows for dense coverage of the macula resulting in the ability to see smaller areas of PED and SRF. There was a critical threshold for the distance between B-scans in the three-dimensional cube scan for detection of pathology. BMJ Publishing Group 2014-06 2014-02-25 /pmc/articles/PMC4033177/ /pubmed/24568868 http://dx.doi.org/10.1136/bjophthalmol-2013-303846 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Original Article
Sharma, Sumit
Sayanagi, Kaori
Kaiser, Peter K
Pathology detection rate of spectral domain optical coherence tomography devices
title Pathology detection rate of spectral domain optical coherence tomography devices
title_full Pathology detection rate of spectral domain optical coherence tomography devices
title_fullStr Pathology detection rate of spectral domain optical coherence tomography devices
title_full_unstemmed Pathology detection rate of spectral domain optical coherence tomography devices
title_short Pathology detection rate of spectral domain optical coherence tomography devices
title_sort pathology detection rate of spectral domain optical coherence tomography devices
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033177/
https://www.ncbi.nlm.nih.gov/pubmed/24568868
http://dx.doi.org/10.1136/bjophthalmol-2013-303846
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