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Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy

Short wavelength automated perimetry (SWAP) is known for detecting the early reduction of retinal sensitivity (RS) in glaucoma. It’s application in retinal diseases have also been discussed previously. We investigated the difference in RS measured between standard white-on-white automated perimetry...

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Autores principales: Zhou, Han Peng, Asaoka, Ryo, Inoue, Tatsuya, Asano, Shotaro, Murata, Hiroshi, Hara, Takumi, Makino, So, Kadonosono, Kazuaki, Obata, Ryo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536216/
https://www.ncbi.nlm.nih.gov/pubmed/33020543
http://dx.doi.org/10.1038/s41598-020-73569-0
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author Zhou, Han Peng
Asaoka, Ryo
Inoue, Tatsuya
Asano, Shotaro
Murata, Hiroshi
Hara, Takumi
Makino, So
Kadonosono, Kazuaki
Obata, Ryo
author_facet Zhou, Han Peng
Asaoka, Ryo
Inoue, Tatsuya
Asano, Shotaro
Murata, Hiroshi
Hara, Takumi
Makino, So
Kadonosono, Kazuaki
Obata, Ryo
author_sort Zhou, Han Peng
collection PubMed
description Short wavelength automated perimetry (SWAP) is known for detecting the early reduction of retinal sensitivity (RS) in glaucoma. It’s application in retinal diseases have also been discussed previously. We investigated the difference in RS measured between standard white-on-white automated perimetry (WW) and blue-on-yellow SWAP in central serous chorioretinopathy (CSC). The overall RS (W-RS, S-RS) as well as the RS inside and outside of the serous retinal detachment (SRD) region were investigated in 26 eyes of 26 CSC patients using WW and SWAP. The central retinal thickness, central choroidal thickness, SRD area (SRDa), and SRD height at the fovea were measured using optic coherence tomography. RS inside the SRD region was lower than that of outside for both perimetries (both p < 0.001). The difference between RS inside and outside of the SRD region was greater in SWAP compared to WW (p < 0.001). Univariate analysis revealed significant correlations between SRDa and both W-RS and S-RS (both p < 0.001); moreover, multivariate analysis indicated that only S-RS was selected as the optimal model for SRDa. Our study demonstrated that SWAP was detected the decrease in RS more accurately than WW in CSC. These results may suggest the usefulness of SWAP for detecting change of retinal function in CSC.
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spelling pubmed-75362162020-10-07 Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy Zhou, Han Peng Asaoka, Ryo Inoue, Tatsuya Asano, Shotaro Murata, Hiroshi Hara, Takumi Makino, So Kadonosono, Kazuaki Obata, Ryo Sci Rep Article Short wavelength automated perimetry (SWAP) is known for detecting the early reduction of retinal sensitivity (RS) in glaucoma. It’s application in retinal diseases have also been discussed previously. We investigated the difference in RS measured between standard white-on-white automated perimetry (WW) and blue-on-yellow SWAP in central serous chorioretinopathy (CSC). The overall RS (W-RS, S-RS) as well as the RS inside and outside of the serous retinal detachment (SRD) region were investigated in 26 eyes of 26 CSC patients using WW and SWAP. The central retinal thickness, central choroidal thickness, SRD area (SRDa), and SRD height at the fovea were measured using optic coherence tomography. RS inside the SRD region was lower than that of outside for both perimetries (both p < 0.001). The difference between RS inside and outside of the SRD region was greater in SWAP compared to WW (p < 0.001). Univariate analysis revealed significant correlations between SRDa and both W-RS and S-RS (both p < 0.001); moreover, multivariate analysis indicated that only S-RS was selected as the optimal model for SRDa. Our study demonstrated that SWAP was detected the decrease in RS more accurately than WW in CSC. These results may suggest the usefulness of SWAP for detecting change of retinal function in CSC. Nature Publishing Group UK 2020-10-05 /pmc/articles/PMC7536216/ /pubmed/33020543 http://dx.doi.org/10.1038/s41598-020-73569-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhou, Han Peng
Asaoka, Ryo
Inoue, Tatsuya
Asano, Shotaro
Murata, Hiroshi
Hara, Takumi
Makino, So
Kadonosono, Kazuaki
Obata, Ryo
Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
title Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
title_full Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
title_fullStr Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
title_full_unstemmed Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
title_short Short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
title_sort short wavelength automated perimetry and standard automated perimetry in central serous chorioretinopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536216/
https://www.ncbi.nlm.nih.gov/pubmed/33020543
http://dx.doi.org/10.1038/s41598-020-73569-0
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