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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Veröffentlicht in:American journal of ophthalmology 2016-12, Vol.172, p.28-38
Hauptverfasser: 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
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container_title American journal of ophthalmology
container_volume 172
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 &lt; 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 &lt; 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. 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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 &lt; 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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