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Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome

PURPOSE: To evaluate the long-term outcome of autologous graft of retinal pigment epithelium (RPE) in patients with geographic atrophy. METHODS: Ten patients with progressive geographic atrophy underwent translocation of an autologous graft of RPE, Bruch membrane and choroid. The visual acuity (VA),...

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Autores principales: Caramoy, Albert, Liakopoulos, Sandra, Menrath, Erica, Kirchhof, Bernd
Formato: Texto
Lenguaje:English
Publicado: BMJ Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976216/
https://www.ncbi.nlm.nih.gov/pubmed/19692368
http://dx.doi.org/10.1136/bjo.2009.161299
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author Caramoy, Albert
Liakopoulos, Sandra
Menrath, Erica
Kirchhof, Bernd
author_facet Caramoy, Albert
Liakopoulos, Sandra
Menrath, Erica
Kirchhof, Bernd
author_sort Caramoy, Albert
collection PubMed
description PURPOSE: To evaluate the long-term outcome of autologous graft of retinal pigment epithelium (RPE) in patients with geographic atrophy. METHODS: Ten patients with progressive geographic atrophy underwent translocation of an autologous graft of RPE, Bruch membrane and choroid. The visual acuity (VA), reading performance, microperimetry, optical coherence tomography (OCT), fundus autofluorescence, fluorescein angiography and indocyanine green angiography were assessed. RESULTS: No recurrence of RPE atrophy was seen. All but one transplant were revascularised. Vascularisation persisted throughout the 3 years' follow-up. Spectral-domain OCT in some cases showed intact photoreceptors or intact outer nuclear and outer plexiform layer overlying the graft. In three cases, the grafts were positioned eccentrically; these patients did not benefit from surgery. The mean VA decreased from 20/80 (range: 20/800 to 20/40) at baseline to 20/200 (range: perception of hand movements to 20/32) at last follow-up. In two patients, VA were stable from 20/50 to 20/32 and 20/40 at the last follow-up, respectively. Postoperative complications included retinal detachment due to proliferative vitreoretinopathy, macular pucker, iritis, branch retinal vein occlusion and secondary ocular hypertension. CONCLUSIONS: Some patients benefit for at least 3 years from a functioning RPE-choroid graft. Functional outcome in most patients, however, was limited due to complications and unfavourable patient selection.
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spelling pubmed-29762162010-11-26 Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome Caramoy, Albert Liakopoulos, Sandra Menrath, Erica Kirchhof, Bernd Br J Ophthalmol Clinical Science PURPOSE: To evaluate the long-term outcome of autologous graft of retinal pigment epithelium (RPE) in patients with geographic atrophy. METHODS: Ten patients with progressive geographic atrophy underwent translocation of an autologous graft of RPE, Bruch membrane and choroid. The visual acuity (VA), reading performance, microperimetry, optical coherence tomography (OCT), fundus autofluorescence, fluorescein angiography and indocyanine green angiography were assessed. RESULTS: No recurrence of RPE atrophy was seen. All but one transplant were revascularised. Vascularisation persisted throughout the 3 years' follow-up. Spectral-domain OCT in some cases showed intact photoreceptors or intact outer nuclear and outer plexiform layer overlying the graft. In three cases, the grafts were positioned eccentrically; these patients did not benefit from surgery. The mean VA decreased from 20/80 (range: 20/800 to 20/40) at baseline to 20/200 (range: perception of hand movements to 20/32) at last follow-up. In two patients, VA were stable from 20/50 to 20/32 and 20/40 at the last follow-up, respectively. Postoperative complications included retinal detachment due to proliferative vitreoretinopathy, macular pucker, iritis, branch retinal vein occlusion and secondary ocular hypertension. CONCLUSIONS: Some patients benefit for at least 3 years from a functioning RPE-choroid graft. Functional outcome in most patients, however, was limited due to complications and unfavourable patient selection. BMJ Group 2009-08-18 2010-08 /pmc/articles/PMC2976216/ /pubmed/19692368 http://dx.doi.org/10.1136/bjo.2009.161299 Text en © 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Clinical Science
Caramoy, Albert
Liakopoulos, Sandra
Menrath, Erica
Kirchhof, Bernd
Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
title Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
title_full Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
title_fullStr Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
title_full_unstemmed Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
title_short Autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
title_sort autologous translocation of choroid and retinal pigment epithelium in geographic atrophy: long-term functional and anatomical outcome
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976216/
https://www.ncbi.nlm.nih.gov/pubmed/19692368
http://dx.doi.org/10.1136/bjo.2009.161299
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