Clinical Characteristics, Choroidal Neovascularization and Predictors of Visual Outcomes in Acquired Vitelliform Lesions
Abstract Purpose To quantify the temporal properties of the acquired vitelliform lesion (AVL) lifecycle, define the clinical characteristics of choroidal neovascularization (NV) in this setting and determine the predictors of long-term visual outcomes. Design Retrospective cohort study Methods Clini...
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creator | Balaratnasingam, Chandrakumar, MD, PhD Hoang, Quan V., MD, PhD Inoue, Maiko, MD Curcio, Christine A., PhD Dolz-Marco, Rosa, MD, PhD Yannuzzi, Nicolas A., MD Dhrami-Gavazi, Elona, MD Yannuzzi, Lawrence A., MD Freund, K. Bailey, MD |
description | Abstract Purpose To quantify the temporal properties of the acquired vitelliform lesion (AVL) lifecycle, define the clinical characteristics of choroidal neovascularization (NV) in this setting and determine the predictors of long-term visual outcomes. Design Retrospective cohort study Methods Clinical and imaging data from 199 eyes of 124 consecutive patients with AVLs associated with age-related macular degeneration (AMD) and adult-onset foveomacular vitelliform dystrophy (AOFVD) were analyzed. Volumetric calculations of vitelliform material were determined using spectral-domain optical coherence tomography and the temporal properties of the AVL lifecycle were quantified. The clinical characteristics of NV were assessed as were the predictors of final best-corrected visual acuity (BCVA) and change in BCVA. Results Mean age was 79.2±12.1 years. AVLs grew and collapsed at approximately the same rate ( P = 0.275). Fifteen eyes (7.5%) developed NV of which all were type 1. In 13 of these eyes, NV occurred during the collapse phase of the AVL lifecycle, after the peak AVL volume was reached. The risk of NV ( P = 0.006) and the decline in BCVA ( P = 0.001) were both significantly greater among eyes with AMD. Foveal atrophy was the characteristic most significantly associated with final BCVA and change in BCVA from baseline (both P < 0.0005). The development of NV was not predictive of long-term visual outcomes (all P = 0.216). Conclusions Complications associated with AVLs typically occur during the collapse phase of the AVL lifecycle. Visual outcomes and risk of NV are related to the underlying disease associated with AVLs. |
doi_str_mv | 10.1016/j.ajo.2016.09.008 |
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Bailey, MD</creator><creatorcontrib>Balaratnasingam, Chandrakumar, MD, PhD ; Hoang, Quan V., MD, PhD ; Inoue, Maiko, MD ; Curcio, Christine A., PhD ; Dolz-Marco, Rosa, MD, PhD ; Yannuzzi, Nicolas A., MD ; Dhrami-Gavazi, Elona, MD ; Yannuzzi, Lawrence A., MD ; Freund, K. Bailey, MD</creatorcontrib><description>Abstract Purpose To quantify the temporal properties of the acquired vitelliform lesion (AVL) lifecycle, define the clinical characteristics of choroidal neovascularization (NV) in this setting and determine the predictors of long-term visual outcomes. Design Retrospective cohort study Methods Clinical and imaging data from 199 eyes of 124 consecutive patients with AVLs associated with age-related macular degeneration (AMD) and adult-onset foveomacular vitelliform dystrophy (AOFVD) were analyzed. Volumetric calculations of vitelliform material were determined using spectral-domain optical coherence tomography and the temporal properties of the AVL lifecycle were quantified. The clinical characteristics of NV were assessed as were the predictors of final best-corrected visual acuity (BCVA) and change in BCVA. Results Mean age was 79.2±12.1 years. AVLs grew and collapsed at approximately the same rate ( P = 0.275). Fifteen eyes (7.5%) developed NV of which all were type 1. In 13 of these eyes, NV occurred during the collapse phase of the AVL lifecycle, after the peak AVL volume was reached. The risk of NV ( P = 0.006) and the decline in BCVA ( P = 0.001) were both significantly greater among eyes with AMD. Foveal atrophy was the characteristic most significantly associated with final BCVA and change in BCVA from baseline (both P < 0.0005). The development of NV was not predictive of long-term visual outcomes (all P = 0.216). Conclusions Complications associated with AVLs typically occur during the collapse phase of the AVL lifecycle. Visual outcomes and risk of NV are related to the underlying disease associated with AVLs.</description><identifier>ISSN: 0002-9394</identifier><identifier>EISSN: 1879-1891</identifier><identifier>DOI: 10.1016/j.ajo.2016.09.008</identifier><identifier>PMID: 27640006</identifier><identifier>CODEN: AJOPAA</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Age ; Aged ; Cameras ; Choroidal Neovascularization - diagnosis ; Choroidal Neovascularization - etiology ; Disease Progression ; Edema ; Female ; Fluorescein Angiography ; Follow-Up Studies ; Fovea Centralis - pathology ; Fundus Oculi ; Hospitals ; Humans ; Macular degeneration ; Male ; Medical imaging ; Ophthalmology ; Patients ; Prognosis ; Retina ; Retrospective Studies ; Time Factors ; Tomography, Optical Coherence ; Visual Acuity ; Vitelliform Macular Dystrophy - complications ; Vitelliform Macular Dystrophy - diagnosis</subject><ispartof>American journal of ophthalmology, 2016-12, Vol.172, p.28-38</ispartof><rights>Elsevier Inc.</rights><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Dec 01, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-ce876c26b6c997b8b5f7fb3435cfd0dc77fe030d4b7a36bd6f04aabb293173ca3</citedby><cites>FETCH-LOGICAL-c436t-ce876c26b6c997b8b5f7fb3435cfd0dc77fe030d4b7a36bd6f04aabb293173ca3</cites><orcidid>0000-0002-7888-9773</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002939416304469$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27640006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Balaratnasingam, Chandrakumar, MD, PhD</creatorcontrib><creatorcontrib>Hoang, Quan V., MD, PhD</creatorcontrib><creatorcontrib>Inoue, Maiko, MD</creatorcontrib><creatorcontrib>Curcio, Christine A., PhD</creatorcontrib><creatorcontrib>Dolz-Marco, Rosa, MD, PhD</creatorcontrib><creatorcontrib>Yannuzzi, Nicolas A., MD</creatorcontrib><creatorcontrib>Dhrami-Gavazi, Elona, MD</creatorcontrib><creatorcontrib>Yannuzzi, Lawrence A., MD</creatorcontrib><creatorcontrib>Freund, K. Bailey, MD</creatorcontrib><title>Clinical Characteristics, Choroidal Neovascularization and Predictors of Visual Outcomes in Acquired Vitelliform Lesions</title><title>American journal of ophthalmology</title><addtitle>Am J Ophthalmol</addtitle><description>Abstract Purpose To quantify the temporal properties of the acquired vitelliform lesion (AVL) lifecycle, define the clinical characteristics of choroidal neovascularization (NV) in this setting and determine the predictors of long-term visual outcomes. Design Retrospective cohort study Methods Clinical and imaging data from 199 eyes of 124 consecutive patients with AVLs associated with age-related macular degeneration (AMD) and adult-onset foveomacular vitelliform dystrophy (AOFVD) were analyzed. Volumetric calculations of vitelliform material were determined using spectral-domain optical coherence tomography and the temporal properties of the AVL lifecycle were quantified. The clinical characteristics of NV were assessed as were the predictors of final best-corrected visual acuity (BCVA) and change in BCVA. Results Mean age was 79.2±12.1 years. AVLs grew and collapsed at approximately the same rate ( P = 0.275). Fifteen eyes (7.5%) developed NV of which all were type 1. In 13 of these eyes, NV occurred during the collapse phase of the AVL lifecycle, after the peak AVL volume was reached. The risk of NV ( P = 0.006) and the decline in BCVA ( P = 0.001) were both significantly greater among eyes with AMD. Foveal atrophy was the characteristic most significantly associated with final BCVA and change in BCVA from baseline (both P < 0.0005). The development of NV was not predictive of long-term visual outcomes (all P = 0.216). Conclusions Complications associated with AVLs typically occur during the collapse phase of the AVL lifecycle. Visual outcomes and risk of NV are related to the underlying disease associated with AVLs.</description><subject>Age</subject><subject>Aged</subject><subject>Cameras</subject><subject>Choroidal Neovascularization - diagnosis</subject><subject>Choroidal Neovascularization - etiology</subject><subject>Disease Progression</subject><subject>Edema</subject><subject>Female</subject><subject>Fluorescein Angiography</subject><subject>Follow-Up Studies</subject><subject>Fovea Centralis - pathology</subject><subject>Fundus Oculi</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Macular degeneration</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Ophthalmology</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Retina</subject><subject>Retrospective Studies</subject><subject>Time Factors</subject><subject>Tomography, Optical Coherence</subject><subject>Visual Acuity</subject><subject>Vitelliform Macular Dystrophy - complications</subject><subject>Vitelliform Macular Dystrophy - diagnosis</subject><issn>0002-9394</issn><issn>1879-1891</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kl2L1TAQhoMo7nH1B3gjBW-8sDVpcpIGYWE5qCscXMGP25BOU0xtm91Murj-elPOWYW98CqZzDMvk3mHkOeMVowy-Wao7BCqOl8rqitKmwdkwxqlS9Zo9pBsKKV1qbkWJ-QJ4pBDqYR6TE5qJcUabciv3ehnD3Ysdj9stJBc9Jg84Ov8EGLwXU59cuHGIiyjjf63TT7MhZ274nN0nYcUIhahL757XDJ7uSQIk8PCz8U5XC8-QzmX3Dj6PsSp2DvMAviUPOrtiO7Z8Twl396_-7q7KPeXHz7uzvclCC5TCa5REmrZStBatU277VXfcsG30He0A6V6RzntRKssl20neyqsbdtac6Y4WH5KXh10r2K4XhwmM3mE3I2dXVjQsEZwzVhdq4y-vIcOYYlz7m6lpOJbXdNMsQMFMSBG15ur6Ccbbw2jZrXFDCbbYlZbDNUm25JrXhyVl3Zy3d-KOx8y8PYAuDyKG--iQfBuhjzg6CCZLvj_yp_dq4ajqz_drcN_vzBYG2q-rHuxrgWTnAohNf8DxdS0Pg</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Balaratnasingam, Chandrakumar, MD, PhD</creator><creator>Hoang, Quan V., MD, PhD</creator><creator>Inoue, Maiko, MD</creator><creator>Curcio, Christine A., PhD</creator><creator>Dolz-Marco, Rosa, MD, PhD</creator><creator>Yannuzzi, Nicolas A., MD</creator><creator>Dhrami-Gavazi, Elona, MD</creator><creator>Yannuzzi, Lawrence A., MD</creator><creator>Freund, K. Bailey, MD</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7888-9773</orcidid></search><sort><creationdate>20161201</creationdate><title>Clinical Characteristics, Choroidal Neovascularization and Predictors of Visual Outcomes in Acquired Vitelliform Lesions</title><author>Balaratnasingam, Chandrakumar, MD, PhD ; Hoang, Quan V., MD, PhD ; Inoue, Maiko, MD ; Curcio, Christine A., PhD ; Dolz-Marco, Rosa, MD, PhD ; Yannuzzi, Nicolas A., MD ; Dhrami-Gavazi, Elona, MD ; Yannuzzi, Lawrence A., MD ; Freund, K. Bailey, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-ce876c26b6c997b8b5f7fb3435cfd0dc77fe030d4b7a36bd6f04aabb293173ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Age</topic><topic>Aged</topic><topic>Cameras</topic><topic>Choroidal Neovascularization - diagnosis</topic><topic>Choroidal Neovascularization - etiology</topic><topic>Disease Progression</topic><topic>Edema</topic><topic>Female</topic><topic>Fluorescein Angiography</topic><topic>Follow-Up Studies</topic><topic>Fovea Centralis - pathology</topic><topic>Fundus Oculi</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Macular degeneration</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Ophthalmology</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Retina</topic><topic>Retrospective Studies</topic><topic>Time Factors</topic><topic>Tomography, Optical Coherence</topic><topic>Visual Acuity</topic><topic>Vitelliform Macular Dystrophy - complications</topic><topic>Vitelliform Macular Dystrophy - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balaratnasingam, Chandrakumar, MD, PhD</creatorcontrib><creatorcontrib>Hoang, Quan V., MD, PhD</creatorcontrib><creatorcontrib>Inoue, Maiko, MD</creatorcontrib><creatorcontrib>Curcio, Christine A., PhD</creatorcontrib><creatorcontrib>Dolz-Marco, Rosa, MD, PhD</creatorcontrib><creatorcontrib>Yannuzzi, Nicolas A., MD</creatorcontrib><creatorcontrib>Dhrami-Gavazi, Elona, MD</creatorcontrib><creatorcontrib>Yannuzzi, Lawrence A., MD</creatorcontrib><creatorcontrib>Freund, K. Bailey, MD</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 Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balaratnasingam, Chandrakumar, MD, PhD</au><au>Hoang, Quan V., MD, PhD</au><au>Inoue, Maiko, MD</au><au>Curcio, Christine A., PhD</au><au>Dolz-Marco, Rosa, MD, PhD</au><au>Yannuzzi, Nicolas A., MD</au><au>Dhrami-Gavazi, Elona, MD</au><au>Yannuzzi, Lawrence A., MD</au><au>Freund, K. Bailey, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Characteristics, Choroidal Neovascularization and Predictors of Visual Outcomes in Acquired Vitelliform Lesions</atitle><jtitle>American journal of ophthalmology</jtitle><addtitle>Am J Ophthalmol</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>172</volume><spage>28</spage><epage>38</epage><pages>28-38</pages><issn>0002-9394</issn><eissn>1879-1891</eissn><coden>AJOPAA</coden><abstract>Abstract Purpose To quantify the temporal properties of the acquired vitelliform lesion (AVL) lifecycle, define the clinical characteristics of choroidal neovascularization (NV) in this setting and determine the predictors of long-term visual outcomes. Design Retrospective cohort study Methods Clinical and imaging data from 199 eyes of 124 consecutive patients with AVLs associated with age-related macular degeneration (AMD) and adult-onset foveomacular vitelliform dystrophy (AOFVD) were analyzed. Volumetric calculations of vitelliform material were determined using spectral-domain optical coherence tomography and the temporal properties of the AVL lifecycle were quantified. The clinical characteristics of NV were assessed as were the predictors of final best-corrected visual acuity (BCVA) and change in BCVA. Results Mean age was 79.2±12.1 years. AVLs grew and collapsed at approximately the same rate ( P = 0.275). Fifteen eyes (7.5%) developed NV of which all were type 1. In 13 of these eyes, NV occurred during the collapse phase of the AVL lifecycle, after the peak AVL volume was reached. The risk of NV ( P = 0.006) and the decline in BCVA ( P = 0.001) were both significantly greater among eyes with AMD. Foveal atrophy was the characteristic most significantly associated with final BCVA and change in BCVA from baseline (both P < 0.0005). The development of NV was not predictive of long-term visual outcomes (all P = 0.216). Conclusions Complications associated with AVLs typically occur during the collapse phase of the AVL lifecycle. Visual outcomes and risk of NV are related to the underlying disease associated with AVLs.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27640006</pmid><doi>10.1016/j.ajo.2016.09.008</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7888-9773</orcidid></addata></record> |
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subjects | Age Aged Cameras Choroidal Neovascularization - diagnosis Choroidal Neovascularization - etiology Disease Progression Edema Female Fluorescein Angiography Follow-Up Studies Fovea Centralis - pathology Fundus Oculi Hospitals Humans Macular degeneration Male Medical imaging Ophthalmology Patients Prognosis Retina Retrospective Studies Time Factors Tomography, Optical Coherence Visual Acuity Vitelliform Macular Dystrophy - complications Vitelliform Macular Dystrophy - diagnosis |
title | Clinical Characteristics, Choroidal Neovascularization and Predictors of Visual Outcomes in Acquired Vitelliform Lesions |
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