Subretinal Fibrosis Detection Using Polarization Sensitive Optical Coherence Tomography
Subretinal fibrosis (SRFib) is an important cause of permanent loss-of-vision diseases with submacular neovascularization, but a reliable diagnostic method is currently missing. This study uses polarization-sensitive optical coherence tomography (PS-OCT) to detect SRFib within retinal lesions by mea...
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Veröffentlicht in: | Translational vision science & technology 2020-03, Vol.9 (4), p.13-13 |
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creator | Gräfe, Maximilian G O van de Kreeke, Jacoba A Willemse, Joy Braaf, Boy de Jong, Yvonne Tan, H Stevie Verbraak, Frank D de Boer, Johannes F |
description | Subretinal fibrosis (SRFib) is an important cause of permanent loss-of-vision diseases with submacular neovascularization, but a reliable diagnostic method is currently missing. This study uses polarization-sensitive optical coherence tomography (PS-OCT) to detect SRFib within retinal lesions by measurement of its birefringent collagen fibers.
Twenty-five patients were enrolled with retinal pathology in one or both eyes containing (1) suspected SRFib, (2) lesions suspected not to be fibrotic, or (3) lesions with doubtful presence of SRFib. All eyes were evaluated for SRFIb using conventional diagnostics by three retinal specialists. PS-OCT images were visually evaluated for SRFib based on cumulative phase retardation, local birefringence, and optic axis uniformity.
Twenty-nine eyes from 22 patients were scanned successfully. In 13 eyes, SRFib was diagnosed by all retinal specialists; of these, 12 were confirmed by PS-OCT and one was inconclusive. In nine eyes, the retinal specialists expected no SRFib, which was confirmed by PS-OCT in all cases. In seven eyes, the retinal specialists' evaluations were inconsistent with regard to the presence of SRFib. PS-OCT confirmed the presence of SRFib in four of these eyes and the absence of SRFib in two eyes and was inconclusive in one eye.
In 21 out of 22 eyes, PS-OCT confirmed the evaluation of retinal specialists regarding the presence of SRFib. PS-OCT provided additional information to distinguish SRFib from other tissues within subretinal neovascular lesions in 6 out of 7 eyes.
PS-OCT can identify and quantify SRFib in doubtful cases for which a reliable diagnosis is currently lacking. |
doi_str_mv | 10.1167/tvst.9.4.13 |
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Twenty-five patients were enrolled with retinal pathology in one or both eyes containing (1) suspected SRFib, (2) lesions suspected not to be fibrotic, or (3) lesions with doubtful presence of SRFib. All eyes were evaluated for SRFIb using conventional diagnostics by three retinal specialists. PS-OCT images were visually evaluated for SRFib based on cumulative phase retardation, local birefringence, and optic axis uniformity.
Twenty-nine eyes from 22 patients were scanned successfully. In 13 eyes, SRFib was diagnosed by all retinal specialists; of these, 12 were confirmed by PS-OCT and one was inconclusive. In nine eyes, the retinal specialists expected no SRFib, which was confirmed by PS-OCT in all cases. In seven eyes, the retinal specialists' evaluations were inconsistent with regard to the presence of SRFib. PS-OCT confirmed the presence of SRFib in four of these eyes and the absence of SRFib in two eyes and was inconclusive in one eye.
In 21 out of 22 eyes, PS-OCT confirmed the evaluation of retinal specialists regarding the presence of SRFib. PS-OCT provided additional information to distinguish SRFib from other tissues within subretinal neovascular lesions in 6 out of 7 eyes.
PS-OCT can identify and quantify SRFib in doubtful cases for which a reliable diagnosis is currently lacking.</description><identifier>ISSN: 2164-2591</identifier><identifier>EISSN: 2164-2591</identifier><identifier>DOI: 10.1167/tvst.9.4.13</identifier><identifier>PMID: 32818100</identifier><language>eng</language><publisher>United States: The Association for Research in Vision and Ophthalmology</publisher><subject>Birefringence ; Fibrosis ; Fluorescein Angiography ; Humans ; Retina - diagnostic imaging ; Tomography, Optical Coherence</subject><ispartof>Translational vision science & technology, 2020-03, Vol.9 (4), p.13-13</ispartof><rights>Copyright 2020 The Authors.</rights><rights>Copyright 2020 The Authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-285c7656b3fdb85dba1befc743f9d45aec552eed67b37b805695fe2ae350508d3</citedby><cites>FETCH-LOGICAL-c381t-285c7656b3fdb85dba1befc743f9d45aec552eed67b37b805695fe2ae350508d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396173/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396173/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32818100$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gräfe, Maximilian G O</creatorcontrib><creatorcontrib>van de Kreeke, Jacoba A</creatorcontrib><creatorcontrib>Willemse, Joy</creatorcontrib><creatorcontrib>Braaf, Boy</creatorcontrib><creatorcontrib>de Jong, Yvonne</creatorcontrib><creatorcontrib>Tan, H Stevie</creatorcontrib><creatorcontrib>Verbraak, Frank D</creatorcontrib><creatorcontrib>de Boer, Johannes F</creatorcontrib><title>Subretinal Fibrosis Detection Using Polarization Sensitive Optical Coherence Tomography</title><title>Translational vision science & technology</title><addtitle>Transl Vis Sci Technol</addtitle><description>Subretinal fibrosis (SRFib) is an important cause of permanent loss-of-vision diseases with submacular neovascularization, but a reliable diagnostic method is currently missing. This study uses polarization-sensitive optical coherence tomography (PS-OCT) to detect SRFib within retinal lesions by measurement of its birefringent collagen fibers.
Twenty-five patients were enrolled with retinal pathology in one or both eyes containing (1) suspected SRFib, (2) lesions suspected not to be fibrotic, or (3) lesions with doubtful presence of SRFib. All eyes were evaluated for SRFIb using conventional diagnostics by three retinal specialists. PS-OCT images were visually evaluated for SRFib based on cumulative phase retardation, local birefringence, and optic axis uniformity.
Twenty-nine eyes from 22 patients were scanned successfully. In 13 eyes, SRFib was diagnosed by all retinal specialists; of these, 12 were confirmed by PS-OCT and one was inconclusive. In nine eyes, the retinal specialists expected no SRFib, which was confirmed by PS-OCT in all cases. In seven eyes, the retinal specialists' evaluations were inconsistent with regard to the presence of SRFib. PS-OCT confirmed the presence of SRFib in four of these eyes and the absence of SRFib in two eyes and was inconclusive in one eye.
In 21 out of 22 eyes, PS-OCT confirmed the evaluation of retinal specialists regarding the presence of SRFib. PS-OCT provided additional information to distinguish SRFib from other tissues within subretinal neovascular lesions in 6 out of 7 eyes.
PS-OCT can identify and quantify SRFib in doubtful cases for which a reliable diagnosis is currently lacking.</description><subject>Birefringence</subject><subject>Fibrosis</subject><subject>Fluorescein Angiography</subject><subject>Humans</subject><subject>Retina - diagnostic imaging</subject><subject>Tomography, Optical Coherence</subject><issn>2164-2591</issn><issn>2164-2591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1LAzEQDaJoqZ68yx4FaU02H7t7EaRaFQoVVDyGJDvbRnY3NckW6q936xd1LjPMvHkzvIfQKcFjQkR2GdchjosxGxO6hwYpEWyU8oLs79RH6CSEN9yHyDlj4hAd0TQnOcF4gF6fOu0h2lbVydRq74INyQ1EMNG6NnkJtl0kj65W3n6or9YTtMFGu4ZkvorW9HsTtwQPrYHk2TVu4dVquTlGB5WqA5z85CF6md4-T-5Hs_ndw-R6NjI0J3GU5txkggtNq1LnvNSKaKhMxmhVlIwrMJynAKXINM10jrkoeAWpAsoxx3lJh-jqm3fV6QZKA230qpYrbxvlN9IpK_9PWruUC7eWGS0EyWhPcP5D4N17ByHKxgYDda1acF2QKaOC4bTARQ-9-IaaXqbgofo7Q7DcuiG3bshCMkm2xGe7n_1hf7Wnn_ImiRs</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Gräfe, Maximilian G O</creator><creator>van de Kreeke, Jacoba A</creator><creator>Willemse, Joy</creator><creator>Braaf, Boy</creator><creator>de Jong, Yvonne</creator><creator>Tan, H Stevie</creator><creator>Verbraak, Frank D</creator><creator>de Boer, Johannes F</creator><general>The Association for Research in Vision and Ophthalmology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200301</creationdate><title>Subretinal Fibrosis Detection Using Polarization Sensitive Optical Coherence Tomography</title><author>Gräfe, Maximilian G O ; van de Kreeke, Jacoba A ; Willemse, Joy ; Braaf, Boy ; de Jong, Yvonne ; Tan, H Stevie ; Verbraak, Frank D ; de Boer, Johannes F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-285c7656b3fdb85dba1befc743f9d45aec552eed67b37b805695fe2ae350508d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Birefringence</topic><topic>Fibrosis</topic><topic>Fluorescein Angiography</topic><topic>Humans</topic><topic>Retina - diagnostic imaging</topic><topic>Tomography, Optical Coherence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gräfe, Maximilian G O</creatorcontrib><creatorcontrib>van de Kreeke, Jacoba A</creatorcontrib><creatorcontrib>Willemse, Joy</creatorcontrib><creatorcontrib>Braaf, Boy</creatorcontrib><creatorcontrib>de Jong, Yvonne</creatorcontrib><creatorcontrib>Tan, H Stevie</creatorcontrib><creatorcontrib>Verbraak, Frank D</creatorcontrib><creatorcontrib>de Boer, Johannes F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Translational vision science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gräfe, Maximilian G O</au><au>van de Kreeke, Jacoba A</au><au>Willemse, Joy</au><au>Braaf, Boy</au><au>de Jong, Yvonne</au><au>Tan, H Stevie</au><au>Verbraak, Frank D</au><au>de Boer, Johannes F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subretinal Fibrosis Detection Using Polarization Sensitive Optical Coherence Tomography</atitle><jtitle>Translational vision science & technology</jtitle><addtitle>Transl Vis Sci Technol</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>9</volume><issue>4</issue><spage>13</spage><epage>13</epage><pages>13-13</pages><issn>2164-2591</issn><eissn>2164-2591</eissn><abstract>Subretinal fibrosis (SRFib) is an important cause of permanent loss-of-vision diseases with submacular neovascularization, but a reliable diagnostic method is currently missing. This study uses polarization-sensitive optical coherence tomography (PS-OCT) to detect SRFib within retinal lesions by measurement of its birefringent collagen fibers.
Twenty-five patients were enrolled with retinal pathology in one or both eyes containing (1) suspected SRFib, (2) lesions suspected not to be fibrotic, or (3) lesions with doubtful presence of SRFib. All eyes were evaluated for SRFIb using conventional diagnostics by three retinal specialists. PS-OCT images were visually evaluated for SRFib based on cumulative phase retardation, local birefringence, and optic axis uniformity.
Twenty-nine eyes from 22 patients were scanned successfully. In 13 eyes, SRFib was diagnosed by all retinal specialists; of these, 12 were confirmed by PS-OCT and one was inconclusive. In nine eyes, the retinal specialists expected no SRFib, which was confirmed by PS-OCT in all cases. In seven eyes, the retinal specialists' evaluations were inconsistent with regard to the presence of SRFib. PS-OCT confirmed the presence of SRFib in four of these eyes and the absence of SRFib in two eyes and was inconclusive in one eye.
In 21 out of 22 eyes, PS-OCT confirmed the evaluation of retinal specialists regarding the presence of SRFib. PS-OCT provided additional information to distinguish SRFib from other tissues within subretinal neovascular lesions in 6 out of 7 eyes.
PS-OCT can identify and quantify SRFib in doubtful cases for which a reliable diagnosis is currently lacking.</abstract><cop>United States</cop><pub>The Association for Research in Vision and Ophthalmology</pub><pmid>32818100</pmid><doi>10.1167/tvst.9.4.13</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Birefringence Fibrosis Fluorescein Angiography Humans Retina - diagnostic imaging Tomography, Optical Coherence |
title | Subretinal Fibrosis Detection Using Polarization Sensitive Optical Coherence Tomography |
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