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Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes

PURPOSE: To evaluate the clinical validity of the Rabin cone contrast test (RCCT; Innova Systems, Inc.) in patients with normal phakic/pseudophakic eyes and severe dichromatic colour vision deficiency (CVD). METHODS: We evaluated age‐related changes in the RCCT scores in 166 phakic eyes and 34 pseud...

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Autores principales: Fujikawa, Masato, Muraki, Sanae, Niwa, Yuichi, Ohji, Masahito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836892/
https://www.ncbi.nlm.nih.gov/pubmed/28556475
http://dx.doi.org/10.1111/aos.13495
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author Fujikawa, Masato
Muraki, Sanae
Niwa, Yuichi
Ohji, Masahito
author_facet Fujikawa, Masato
Muraki, Sanae
Niwa, Yuichi
Ohji, Masahito
author_sort Fujikawa, Masato
collection PubMed
description PURPOSE: To evaluate the clinical validity of the Rabin cone contrast test (RCCT; Innova Systems, Inc.) in patients with normal phakic/pseudophakic eyes and severe dichromatic colour vision deficiency (CVD). METHODS: We evaluated age‐related changes in the RCCT scores in 166 phakic eyes and 34 pseudophakic eyes and the RCCT sensitivity and specificity in 28 men with severe dichromatic CVD (10 with protanopia, 18 with deutanopia) and nine age‐matched controls. All participants had 20/20 or better Snellen best‐corrected visual acuity (BCVA). The RCCT was used to measure the L, M and S‐CCT scores (range, 0–100). RESULTS: In normal phakic eyes, the mean L, M and S‐CCT scores decreased gradually with ageing, with normal levels in patients in the second to seventh decades of life and some below normal in the eighth and ninth decades of life. In normal pseudophakic eyes, the mean L, M and S‐CCT scores were normal in patients in the seventh to ninth decades of life. In eyes with severe CVD, the mean L, M and S‐CCT scores were, respectively, 31.5 ± 18.3, 86.0 ± 12.6 and 98.0 ± 6.3 in patients with protanopia; 92.8 ± 10.5, 50.8 ± 19.6 and 97.8 ± 5.2 in patients with deutanopia; and 99.4 ± 1.7, 98.3 ± 5.0 and 99.4 ± 1.7 in controls. The RCCT sensitivity and specificity were 100% for diagnosing the CVD type. CONCLUSION: The RCCT can be used in non‐visually impaired patients up to the seventh decade of life and after cataract surgery in elderly patients. The RCCT is available for CVD screening and typing and the score has a wide distribution range even in patients with severe CVD.
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spelling pubmed-58368922018-03-12 Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes Fujikawa, Masato Muraki, Sanae Niwa, Yuichi Ohji, Masahito Acta Ophthalmol Original Articles PURPOSE: To evaluate the clinical validity of the Rabin cone contrast test (RCCT; Innova Systems, Inc.) in patients with normal phakic/pseudophakic eyes and severe dichromatic colour vision deficiency (CVD). METHODS: We evaluated age‐related changes in the RCCT scores in 166 phakic eyes and 34 pseudophakic eyes and the RCCT sensitivity and specificity in 28 men with severe dichromatic CVD (10 with protanopia, 18 with deutanopia) and nine age‐matched controls. All participants had 20/20 or better Snellen best‐corrected visual acuity (BCVA). The RCCT was used to measure the L, M and S‐CCT scores (range, 0–100). RESULTS: In normal phakic eyes, the mean L, M and S‐CCT scores decreased gradually with ageing, with normal levels in patients in the second to seventh decades of life and some below normal in the eighth and ninth decades of life. In normal pseudophakic eyes, the mean L, M and S‐CCT scores were normal in patients in the seventh to ninth decades of life. In eyes with severe CVD, the mean L, M and S‐CCT scores were, respectively, 31.5 ± 18.3, 86.0 ± 12.6 and 98.0 ± 6.3 in patients with protanopia; 92.8 ± 10.5, 50.8 ± 19.6 and 97.8 ± 5.2 in patients with deutanopia; and 99.4 ± 1.7, 98.3 ± 5.0 and 99.4 ± 1.7 in controls. The RCCT sensitivity and specificity were 100% for diagnosing the CVD type. CONCLUSION: The RCCT can be used in non‐visually impaired patients up to the seventh decade of life and after cataract surgery in elderly patients. The RCCT is available for CVD screening and typing and the score has a wide distribution range even in patients with severe CVD. John Wiley and Sons Inc. 2017-05-29 2018-03 /pmc/articles/PMC5836892/ /pubmed/28556475 http://dx.doi.org/10.1111/aos.13495 Text en © 2017 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Fujikawa, Masato
Muraki, Sanae
Niwa, Yuichi
Ohji, Masahito
Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
title Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
title_full Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
title_fullStr Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
title_full_unstemmed Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
title_short Evaluation of clinical validity of the Rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
title_sort evaluation of clinical validity of the rabin cone contrast test in normal phakic or pseudophakic eyes and severely dichromatic eyes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836892/
https://www.ncbi.nlm.nih.gov/pubmed/28556475
http://dx.doi.org/10.1111/aos.13495
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