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Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy

PURPOSE: To improve our understanding of hyperacuity defects measured with preferential hyperacuity perimetry (PHP) by correlating PHP findings with the retinal microstructural changes visible on spectral-domain optical coherence tomography (OCT) in patients with polypoidal choroidal vasculopathy (P...

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Autores principales: Kim, Moosang, Yu, Seung-Young, Kwak, Hyung-Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131323/
https://www.ncbi.nlm.nih.gov/pubmed/24212209
http://dx.doi.org/10.4103/0301-4738.121132
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author Kim, Moosang
Yu, Seung-Young
Kwak, Hyung-Woo
author_facet Kim, Moosang
Yu, Seung-Young
Kwak, Hyung-Woo
author_sort Kim, Moosang
collection PubMed
description PURPOSE: To improve our understanding of hyperacuity defects measured with preferential hyperacuity perimetry (PHP) by correlating PHP findings with the retinal microstructural changes visible on spectral-domain optical coherence tomography (OCT) in patients with polypoidal choroidal vasculopathy (PCV). MATERIALS AND METHODS: Twenty-eight eyes of 28 patients with PCV were retrospectively reviewed. All patients underwent a complete ophthalmologic examination, including best-corrected visual acuity (logMAR) testing, PHP, and OCT. The functional ‘PHP test score’ and ‘total volume of hyperacuity defect zone’ were also analyzed. RESULTS: Patients were classified based on the hyperacuity defect by PHP, as follows: Hyperacuity defect (n = 17 eyes) group and hyperacuity intact (n = 11 eyes) group. The mean best-corrected visual acuity in the hyperacuity intact group (0.46 ± 0.39) was better than that in the hyperacuity defect group (0.82 ± 0.37) (P = 0.014). The presence of serous retinal detachment and retinal pigment epithelial detachment did not differ significantly between groups (P = 0.120 and P = 0.689, respectively). A disrupted photoreceptor layer was more common in the hyperacuity defect group compared with the hyperacuity intact group (P = 0.0001). Among 17 eyes with a hyperacuity defect, 9 eyes showing intra-retinal pathology (intra-retinal cyst or hard exudates) and had a significantly higher PHP test score and larger total volume of the hyperacuity defect zone than 8 eyes without intra-retinal pathology (P = 0.006 and P = 0.021, respectively). CONCLUSION: A hyperacuity defect in PCV was associated with photoreceptor disarrangement. Furthermore, PCV lesions on the inner retina that invaded the photoreceptor layer were associated with a more severe hyperacuity defect.
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spelling pubmed-41313232014-08-14 Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy Kim, Moosang Yu, Seung-Young Kwak, Hyung-Woo Indian J Ophthalmol Original Article PURPOSE: To improve our understanding of hyperacuity defects measured with preferential hyperacuity perimetry (PHP) by correlating PHP findings with the retinal microstructural changes visible on spectral-domain optical coherence tomography (OCT) in patients with polypoidal choroidal vasculopathy (PCV). MATERIALS AND METHODS: Twenty-eight eyes of 28 patients with PCV were retrospectively reviewed. All patients underwent a complete ophthalmologic examination, including best-corrected visual acuity (logMAR) testing, PHP, and OCT. The functional ‘PHP test score’ and ‘total volume of hyperacuity defect zone’ were also analyzed. RESULTS: Patients were classified based on the hyperacuity defect by PHP, as follows: Hyperacuity defect (n = 17 eyes) group and hyperacuity intact (n = 11 eyes) group. The mean best-corrected visual acuity in the hyperacuity intact group (0.46 ± 0.39) was better than that in the hyperacuity defect group (0.82 ± 0.37) (P = 0.014). The presence of serous retinal detachment and retinal pigment epithelial detachment did not differ significantly between groups (P = 0.120 and P = 0.689, respectively). A disrupted photoreceptor layer was more common in the hyperacuity defect group compared with the hyperacuity intact group (P = 0.0001). Among 17 eyes with a hyperacuity defect, 9 eyes showing intra-retinal pathology (intra-retinal cyst or hard exudates) and had a significantly higher PHP test score and larger total volume of the hyperacuity defect zone than 8 eyes without intra-retinal pathology (P = 0.006 and P = 0.021, respectively). CONCLUSION: A hyperacuity defect in PCV was associated with photoreceptor disarrangement. Furthermore, PCV lesions on the inner retina that invaded the photoreceptor layer were associated with a more severe hyperacuity defect. Medknow Publications & Media Pvt Ltd 2014-06 /pmc/articles/PMC4131323/ /pubmed/24212209 http://dx.doi.org/10.4103/0301-4738.121132 Text en Copyright: © Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Moosang
Yu, Seung-Young
Kwak, Hyung-Woo
Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
title Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
title_full Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
title_fullStr Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
title_full_unstemmed Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
title_short Association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
title_sort association between hyperacuity defects and retinal microstructure in polypoidal choroidal vasculopathy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131323/
https://www.ncbi.nlm.nih.gov/pubmed/24212209
http://dx.doi.org/10.4103/0301-4738.121132
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