Inner neural retina loss in central retinal artery occlusion
Purpose To report morphologic retinal changes and visual outcomes in acute and chronic central retinal artery occlusion (CRAO). Methods We reviewed ten eyes of ten patients with CRAO (age, 65.3 ± 10.2 years) and measured retinal thicknesses at the central fovea and the perifovea using optical cohere...
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Veröffentlicht in: | Japanese journal of ophthalmology 2010-09, Vol.54 (5), p.423-429 |
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creator | Ikeda, Fumiko Kishi, Shoji |
description | Purpose
To report morphologic retinal changes and visual outcomes in acute and chronic central retinal artery occlusion (CRAO).
Methods
We reviewed ten eyes of ten patients with CRAO (age, 65.3 ± 10.2 years) and measured retinal thicknesses at the central fovea and the perifovea using optical coherence tomography (OCT) over 8 ± 4 months.
Results
During the acute phase (within 10 days), the mean inner retinal thicknesses were 148% and 139% of normal values at 1 mm nasal and temporal to the fovea. They decreased to 22% and 11% of normal inner retinal thickness during the chronic phase (3 months or later). The retinal thickness at the perifovea decreased linearly until 3 months but was stable during the chronic phase. In contrast, the foveal thickness increased slightly in the acute phase but was equivalent to the normal level during the chronic phase. As a result of inner retinal atrophy, the foveal pit was shallow during the chronic phase. The final visual acuity was correlated positively with retinal thickness at the perifovea during the chronic CRAO phase.
Conclusion
OCT showed that inner retinal necrosis with early swelling and late atrophy occurred in CRAO. The fovea and outer retina appeared to be excluded from ischemic change. The residual inner retina at the perifovea determined the final visual outcomes. |
doi_str_mv | 10.1007/s10384-010-0841-x |
format | Article |
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To report morphologic retinal changes and visual outcomes in acute and chronic central retinal artery occlusion (CRAO).
Methods
We reviewed ten eyes of ten patients with CRAO (age, 65.3 ± 10.2 years) and measured retinal thicknesses at the central fovea and the perifovea using optical coherence tomography (OCT) over 8 ± 4 months.
Results
During the acute phase (within 10 days), the mean inner retinal thicknesses were 148% and 139% of normal values at 1 mm nasal and temporal to the fovea. They decreased to 22% and 11% of normal inner retinal thickness during the chronic phase (3 months or later). The retinal thickness at the perifovea decreased linearly until 3 months but was stable during the chronic phase. In contrast, the foveal thickness increased slightly in the acute phase but was equivalent to the normal level during the chronic phase. As a result of inner retinal atrophy, the foveal pit was shallow during the chronic phase. The final visual acuity was correlated positively with retinal thickness at the perifovea during the chronic CRAO phase.
Conclusion
OCT showed that inner retinal necrosis with early swelling and late atrophy occurred in CRAO. The fovea and outer retina appeared to be excluded from ischemic change. The residual inner retina at the perifovea determined the final visual outcomes.</description><identifier>ISSN: 0021-5155</identifier><identifier>EISSN: 1613-2246</identifier><identifier>DOI: 10.1007/s10384-010-0841-x</identifier><identifier>PMID: 21052904</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Acute Disease ; Aged ; Aged, 80 and over ; Atrophy ; Chronic Disease ; Clinical Investigation ; Female ; Humans ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Necrosis ; Ophthalmology ; Retina - pathology ; Retinal Artery Occlusion - complications ; Retinal Artery Occlusion - physiopathology ; Retrospective Studies ; Tomography, Optical Coherence ; Visual Acuity - physiology</subject><ispartof>Japanese journal of ophthalmology, 2010-09, Vol.54 (5), p.423-429</ispartof><rights>Japanese Ophthalmological Society (JOS) 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-3d3c199e7c1a2aa129d71108f2b4610070582a79a57716e169ccc6ea7a548cd73</citedby><cites>FETCH-LOGICAL-c402t-3d3c199e7c1a2aa129d71108f2b4610070582a79a57716e169ccc6ea7a548cd73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10384-010-0841-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10384-010-0841-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21052904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikeda, Fumiko</creatorcontrib><creatorcontrib>Kishi, Shoji</creatorcontrib><title>Inner neural retina loss in central retinal artery occlusion</title><title>Japanese journal of ophthalmology</title><addtitle>Jpn J Ophthalmol</addtitle><addtitle>Jpn J Ophthalmol</addtitle><description>Purpose
To report morphologic retinal changes and visual outcomes in acute and chronic central retinal artery occlusion (CRAO).
Methods
We reviewed ten eyes of ten patients with CRAO (age, 65.3 ± 10.2 years) and measured retinal thicknesses at the central fovea and the perifovea using optical coherence tomography (OCT) over 8 ± 4 months.
Results
During the acute phase (within 10 days), the mean inner retinal thicknesses were 148% and 139% of normal values at 1 mm nasal and temporal to the fovea. They decreased to 22% and 11% of normal inner retinal thickness during the chronic phase (3 months or later). The retinal thickness at the perifovea decreased linearly until 3 months but was stable during the chronic phase. In contrast, the foveal thickness increased slightly in the acute phase but was equivalent to the normal level during the chronic phase. As a result of inner retinal atrophy, the foveal pit was shallow during the chronic phase. The final visual acuity was correlated positively with retinal thickness at the perifovea during the chronic CRAO phase.
Conclusion
OCT showed that inner retinal necrosis with early swelling and late atrophy occurred in CRAO. The fovea and outer retina appeared to be excluded from ischemic change. The residual inner retina at the perifovea determined the final visual outcomes.</description><subject>Acute Disease</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Atrophy</subject><subject>Chronic Disease</subject><subject>Clinical Investigation</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Necrosis</subject><subject>Ophthalmology</subject><subject>Retina - pathology</subject><subject>Retinal Artery Occlusion - complications</subject><subject>Retinal Artery Occlusion - physiopathology</subject><subject>Retrospective Studies</subject><subject>Tomography, Optical Coherence</subject><subject>Visual Acuity - physiology</subject><issn>0021-5155</issn><issn>1613-2246</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkU1Lw0AQhhdRbK3-AC8SvHiKzmz2K-BFih-Fghc9L9vNVlLSTd1NoP33JqRaEMTTwMwz73y8hFwi3CKAvIsImWIpIKSgGKbbIzJGgVlKKRPHZAxAMeXI-YicxbgCAEYzekpGFIHTHNiY3M-8dyHxrg2mSoJrSm-Sqo4xKX1inW8O6SoxoXFhl9TWVm0sa39OTpamiu5iHyfk_enxbfqSzl-fZ9OHeWoZ0CbNisxinjtp0VBjkOaFRAS1pAsm-kOAK2pkbriUKByK3FornJGGM2ULmU3IzaC7CfVn62Kj12W0rqqMd3Ubdc6ZyEAo_i8pBRWKqTzryOtf5KpuQ3dl1AokU1zIfjAOkA3dS4Jb6k0o1ybsNILuN9eDBbqzQPcW6G3Xc7UXbhdrV_x0fP-8A-gAxK7kP1w4TP5b9Qsvuo-D</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Ikeda, Fumiko</creator><creator>Kishi, Shoji</creator><general>Springer Japan</general><general>Springer Nature B.V</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20100901</creationdate><title>Inner neural retina loss in central retinal artery occlusion</title><author>Ikeda, Fumiko ; Kishi, Shoji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-3d3c199e7c1a2aa129d71108f2b4610070582a79a57716e169ccc6ea7a548cd73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acute Disease</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Atrophy</topic><topic>Chronic Disease</topic><topic>Clinical Investigation</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Necrosis</topic><topic>Ophthalmology</topic><topic>Retina - pathology</topic><topic>Retinal Artery Occlusion - complications</topic><topic>Retinal Artery Occlusion - physiopathology</topic><topic>Retrospective Studies</topic><topic>Tomography, Optical Coherence</topic><topic>Visual Acuity - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikeda, Fumiko</creatorcontrib><creatorcontrib>Kishi, Shoji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS 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>Technology Research Database</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>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</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><collection>Neurosciences Abstracts</collection><jtitle>Japanese journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikeda, Fumiko</au><au>Kishi, Shoji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inner neural retina loss in central retinal artery occlusion</atitle><jtitle>Japanese journal of ophthalmology</jtitle><stitle>Jpn J Ophthalmol</stitle><addtitle>Jpn J Ophthalmol</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>54</volume><issue>5</issue><spage>423</spage><epage>429</epage><pages>423-429</pages><issn>0021-5155</issn><eissn>1613-2246</eissn><abstract>Purpose
To report morphologic retinal changes and visual outcomes in acute and chronic central retinal artery occlusion (CRAO).
Methods
We reviewed ten eyes of ten patients with CRAO (age, 65.3 ± 10.2 years) and measured retinal thicknesses at the central fovea and the perifovea using optical coherence tomography (OCT) over 8 ± 4 months.
Results
During the acute phase (within 10 days), the mean inner retinal thicknesses were 148% and 139% of normal values at 1 mm nasal and temporal to the fovea. They decreased to 22% and 11% of normal inner retinal thickness during the chronic phase (3 months or later). The retinal thickness at the perifovea decreased linearly until 3 months but was stable during the chronic phase. In contrast, the foveal thickness increased slightly in the acute phase but was equivalent to the normal level during the chronic phase. As a result of inner retinal atrophy, the foveal pit was shallow during the chronic phase. The final visual acuity was correlated positively with retinal thickness at the perifovea during the chronic CRAO phase.
Conclusion
OCT showed that inner retinal necrosis with early swelling and late atrophy occurred in CRAO. The fovea and outer retina appeared to be excluded from ischemic change. The residual inner retina at the perifovea determined the final visual outcomes.</abstract><cop>Japan</cop><pub>Springer Japan</pub><pmid>21052904</pmid><doi>10.1007/s10384-010-0841-x</doi><tpages>7</tpages></addata></record> |
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subjects | Acute Disease Aged Aged, 80 and over Atrophy Chronic Disease Clinical Investigation Female Humans Male Medicine Medicine & Public Health Middle Aged Necrosis Ophthalmology Retina - pathology Retinal Artery Occlusion - complications Retinal Artery Occlusion - physiopathology Retrospective Studies Tomography, Optical Coherence Visual Acuity - physiology |
title | Inner neural retina loss in central retinal artery occlusion |
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