Longitudinal vasculature changes in branch retinal vein occlusion with projection-resolved optical coherence tomography angiography
Purpose To analyze vascular changes in branch retinal vein occlusion (BRVO) using projection-resolved optical coherence tomography angiography (PR-OCTA). Methods We reviewed 30 consecutive eyes of 30 cases with BRVO retrospectively. PR-OCTA was performed during the acute, intermediate, and remission...
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creator | Tsuboi, Kotaro Kamei, Motohiro |
description | Purpose
To analyze vascular changes in branch retinal vein occlusion (BRVO) using projection-resolved optical coherence tomography angiography (PR-OCTA).
Methods
We reviewed 30 consecutive eyes of 30 cases with BRVO retrospectively. PR-OCTA was performed during the acute, intermediate, and remission phases when anti-vascular endothelial growth factor drugs suppress cystic changes. The main outcome measures were vessel density (VD) and retinal thickness changes in the superficial capillary plexus (SCP), intermediate capillary plexus (ICP), and deep capillary plexus (DCP).
Results
The VDs did not change longitudinally in the SCP and DCP during the follow-up period. The VD was significantly (
p
= 0.0105) greater in the ICP during remission than the acute phase. The full retinal thickness (internal limiting membrane [ILM] to retinal pigment epithelium [RPE]) and inner retinal thickness (ILM to inner plexiform layer [IPL]) decreased significantly (
p
= 0.0002 and
p
= 0.0014, respectively) during the follow-up period. When the inner retina was thinner than 117 μm, the VD in the ICP increased significantly (
p
= 0.045) during the follow-up period. When the inner retinal layer did not become thinner, the VD in the ICP remained unchanged.
Conclusion
PR-OCTA showed the three distinct vascular plexuses in BRVO. The VDs remained unchanged during the follow-up period in the SCP and DCP but increased significantly in the ICP during remission. Inner retinal thinning might cause increases in the VD in the ICP because of projection artifacts and segmentation errors despite using PR-OCTA. |
doi_str_mv | 10.1007/s00417-019-04371-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2275272376</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2235403016</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-e1c5d50a605584b3f4b87a25b3c15bdd1b9c0f913784d8d5445630dd91fe35423</originalsourceid><addsrcrecordid>eNp9kUtv1DAURi1ERYfCH2CBLLFhY_AzTpao4lFpJDZU6s5y7JuJR5l4sJ2irvvH8ZABJBas_Dr38706CL1i9B2jVL_PlEqmCWUdoVJoRponaMOkUERTfvcUbajmjLSC312i5znvaeWFYs_QpWCsUZ3gG_S4jfMulMWH2U743ma3TLYsCbAb7byDjMOM-2RnN-IEZaWg3kXnpiWHOOMfoYz4mOIeXKlnkiDH6R48jscSXOVdHCHB7ACXeIi7ZI_jA67h4bx_gS4GO2V4eV6v0O2nj9-uv5Dt18831x-2xAmtCgHmlFfUNlSpVvZikH2rLVe9cEz13rO-c3TomNCt9K1XUqpGUO87NoBQkosr9HbNrc1-XyAXcwjZwTTZGeKSDedacc2Fbir65h90H5dUhz9RNYwKyk4UXymXYs4JBnNM4WDTg2HUnBSZVZGpiswvReZU9PocvfQH8H9KfjupgFiBXJ-qgvT37__E_gTUwZ7m</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2235403016</pqid></control><display><type>article</type><title>Longitudinal vasculature changes in branch retinal vein occlusion with projection-resolved optical coherence tomography angiography</title><source>SpringerLink Journals - AutoHoldings</source><creator>Tsuboi, Kotaro ; Kamei, Motohiro</creator><creatorcontrib>Tsuboi, Kotaro ; Kamei, Motohiro</creatorcontrib><description>Purpose
To analyze vascular changes in branch retinal vein occlusion (BRVO) using projection-resolved optical coherence tomography angiography (PR-OCTA).
Methods
We reviewed 30 consecutive eyes of 30 cases with BRVO retrospectively. PR-OCTA was performed during the acute, intermediate, and remission phases when anti-vascular endothelial growth factor drugs suppress cystic changes. The main outcome measures were vessel density (VD) and retinal thickness changes in the superficial capillary plexus (SCP), intermediate capillary plexus (ICP), and deep capillary plexus (DCP).
Results
The VDs did not change longitudinally in the SCP and DCP during the follow-up period. The VD was significantly (
p
= 0.0105) greater in the ICP during remission than the acute phase. The full retinal thickness (internal limiting membrane [ILM] to retinal pigment epithelium [RPE]) and inner retinal thickness (ILM to inner plexiform layer [IPL]) decreased significantly (
p
= 0.0002 and
p
= 0.0014, respectively) during the follow-up period. When the inner retina was thinner than 117 μm, the VD in the ICP increased significantly (
p
= 0.045) during the follow-up period. When the inner retinal layer did not become thinner, the VD in the ICP remained unchanged.
Conclusion
PR-OCTA showed the three distinct vascular plexuses in BRVO. The VDs remained unchanged during the follow-up period in the SCP and DCP but increased significantly in the ICP during remission. Inner retinal thinning might cause increases in the VD in the ICP because of projection artifacts and segmentation errors despite using PR-OCTA.</description><identifier>ISSN: 0721-832X</identifier><identifier>EISSN: 1435-702X</identifier><identifier>DOI: 10.1007/s00417-019-04371-6</identifier><identifier>PMID: 31165932</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Angiography ; Epithelium ; Medical imaging ; Medicine ; Medicine & Public Health ; Occlusion ; Ophthalmology ; Remission ; Retina ; Retinal Disorders ; Retinal pigment epithelium ; Segmentation ; Tomography ; Vascular endothelial growth factor</subject><ispartof>Graefe's archive for clinical and experimental ophthalmology, 2019-09, Vol.257 (9), p.1831-1840</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2019</rights><rights>Graefe's Archive for Clinical and Experimental Ophthalmology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-e1c5d50a605584b3f4b87a25b3c15bdd1b9c0f913784d8d5445630dd91fe35423</citedby><cites>FETCH-LOGICAL-c375t-e1c5d50a605584b3f4b87a25b3c15bdd1b9c0f913784d8d5445630dd91fe35423</cites><orcidid>0000-0001-5119-8414</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00417-019-04371-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00417-019-04371-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31165932$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsuboi, Kotaro</creatorcontrib><creatorcontrib>Kamei, Motohiro</creatorcontrib><title>Longitudinal vasculature changes in branch retinal vein occlusion with projection-resolved optical coherence tomography angiography</title><title>Graefe's archive for clinical and experimental ophthalmology</title><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><description>Purpose
To analyze vascular changes in branch retinal vein occlusion (BRVO) using projection-resolved optical coherence tomography angiography (PR-OCTA).
Methods
We reviewed 30 consecutive eyes of 30 cases with BRVO retrospectively. PR-OCTA was performed during the acute, intermediate, and remission phases when anti-vascular endothelial growth factor drugs suppress cystic changes. The main outcome measures were vessel density (VD) and retinal thickness changes in the superficial capillary plexus (SCP), intermediate capillary plexus (ICP), and deep capillary plexus (DCP).
Results
The VDs did not change longitudinally in the SCP and DCP during the follow-up period. The VD was significantly (
p
= 0.0105) greater in the ICP during remission than the acute phase. The full retinal thickness (internal limiting membrane [ILM] to retinal pigment epithelium [RPE]) and inner retinal thickness (ILM to inner plexiform layer [IPL]) decreased significantly (
p
= 0.0002 and
p
= 0.0014, respectively) during the follow-up period. When the inner retina was thinner than 117 μm, the VD in the ICP increased significantly (
p
= 0.045) during the follow-up period. When the inner retinal layer did not become thinner, the VD in the ICP remained unchanged.
Conclusion
PR-OCTA showed the three distinct vascular plexuses in BRVO. The VDs remained unchanged during the follow-up period in the SCP and DCP but increased significantly in the ICP during remission. Inner retinal thinning might cause increases in the VD in the ICP because of projection artifacts and segmentation errors despite using PR-OCTA.</description><subject>Angiography</subject><subject>Epithelium</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Occlusion</subject><subject>Ophthalmology</subject><subject>Remission</subject><subject>Retina</subject><subject>Retinal Disorders</subject><subject>Retinal pigment epithelium</subject><subject>Segmentation</subject><subject>Tomography</subject><subject>Vascular endothelial growth factor</subject><issn>0721-832X</issn><issn>1435-702X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtv1DAURi1ERYfCH2CBLLFhY_AzTpao4lFpJDZU6s5y7JuJR5l4sJ2irvvH8ZABJBas_Dr38706CL1i9B2jVL_PlEqmCWUdoVJoRponaMOkUERTfvcUbajmjLSC312i5znvaeWFYs_QpWCsUZ3gG_S4jfMulMWH2U743ma3TLYsCbAb7byDjMOM-2RnN-IEZaWg3kXnpiWHOOMfoYz4mOIeXKlnkiDH6R48jscSXOVdHCHB7ACXeIi7ZI_jA67h4bx_gS4GO2V4eV6v0O2nj9-uv5Dt18831x-2xAmtCgHmlFfUNlSpVvZikH2rLVe9cEz13rO-c3TomNCt9K1XUqpGUO87NoBQkosr9HbNrc1-XyAXcwjZwTTZGeKSDedacc2Fbir65h90H5dUhz9RNYwKyk4UXymXYs4JBnNM4WDTg2HUnBSZVZGpiswvReZU9PocvfQH8H9KfjupgFiBXJ-qgvT37__E_gTUwZ7m</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Tsuboi, Kotaro</creator><creator>Kamei, Motohiro</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5119-8414</orcidid></search><sort><creationdate>20190901</creationdate><title>Longitudinal vasculature changes in branch retinal vein occlusion with projection-resolved optical coherence tomography angiography</title><author>Tsuboi, Kotaro ; Kamei, Motohiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-e1c5d50a605584b3f4b87a25b3c15bdd1b9c0f913784d8d5445630dd91fe35423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Angiography</topic><topic>Epithelium</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Occlusion</topic><topic>Ophthalmology</topic><topic>Remission</topic><topic>Retina</topic><topic>Retinal Disorders</topic><topic>Retinal pigment epithelium</topic><topic>Segmentation</topic><topic>Tomography</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsuboi, Kotaro</creatorcontrib><creatorcontrib>Kamei, Motohiro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsuboi, Kotaro</au><au>Kamei, Motohiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal vasculature changes in branch retinal vein occlusion with projection-resolved optical coherence tomography angiography</atitle><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle><stitle>Graefes Arch Clin Exp Ophthalmol</stitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>257</volume><issue>9</issue><spage>1831</spage><epage>1840</epage><pages>1831-1840</pages><issn>0721-832X</issn><eissn>1435-702X</eissn><abstract>Purpose
To analyze vascular changes in branch retinal vein occlusion (BRVO) using projection-resolved optical coherence tomography angiography (PR-OCTA).
Methods
We reviewed 30 consecutive eyes of 30 cases with BRVO retrospectively. PR-OCTA was performed during the acute, intermediate, and remission phases when anti-vascular endothelial growth factor drugs suppress cystic changes. The main outcome measures were vessel density (VD) and retinal thickness changes in the superficial capillary plexus (SCP), intermediate capillary plexus (ICP), and deep capillary plexus (DCP).
Results
The VDs did not change longitudinally in the SCP and DCP during the follow-up period. The VD was significantly (
p
= 0.0105) greater in the ICP during remission than the acute phase. The full retinal thickness (internal limiting membrane [ILM] to retinal pigment epithelium [RPE]) and inner retinal thickness (ILM to inner plexiform layer [IPL]) decreased significantly (
p
= 0.0002 and
p
= 0.0014, respectively) during the follow-up period. When the inner retina was thinner than 117 μm, the VD in the ICP increased significantly (
p
= 0.045) during the follow-up period. When the inner retinal layer did not become thinner, the VD in the ICP remained unchanged.
Conclusion
PR-OCTA showed the three distinct vascular plexuses in BRVO. The VDs remained unchanged during the follow-up period in the SCP and DCP but increased significantly in the ICP during remission. Inner retinal thinning might cause increases in the VD in the ICP because of projection artifacts and segmentation errors despite using PR-OCTA.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>31165932</pmid><doi>10.1007/s00417-019-04371-6</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5119-8414</orcidid></addata></record> |
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subjects | Angiography Epithelium Medical imaging Medicine Medicine & Public Health Occlusion Ophthalmology Remission Retina Retinal Disorders Retinal pigment epithelium Segmentation Tomography Vascular endothelial growth factor |
title | Longitudinal vasculature changes in branch retinal vein occlusion with projection-resolved optical coherence tomography angiography |
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