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Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study

PURPOSE: To assess the visual, ocular, extraocular, and multifocal electroretinography (mfERG) outcomes of computer vision syndrome (CVS) among medical students. METHODS: This study was designed as a cross-sectional case-control study that included 733 medical students. All students completed a spec...

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Autores principales: Iqbal, Mohammed, Said, Omar, Ibrahim, Ola, Soliman, Ashraf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035040/
https://www.ncbi.nlm.nih.gov/pubmed/33868724
http://dx.doi.org/10.1155/2021/6630286
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author Iqbal, Mohammed
Said, Omar
Ibrahim, Ola
Soliman, Ashraf
author_facet Iqbal, Mohammed
Said, Omar
Ibrahim, Ola
Soliman, Ashraf
author_sort Iqbal, Mohammed
collection PubMed
description PURPOSE: To assess the visual, ocular, extraocular, and multifocal electroretinography (mfERG) outcomes of computer vision syndrome (CVS) among medical students. METHODS: This study was designed as a cross-sectional case-control study that included 733 medical students. All students completed a specially designed and validated CVS questionnaire survey (CVS-F3). Students from the control (No-CVS) and CVS groups underwent comprehensive ophthalmic examinations including the mfERG examinations. Our main outcome measures included uncorrected and corrected distance visual acuity (UDVA and CDVA, resp.) measurements, subjective and cycloplegic refractions, slit-lamp examination, intraocular pressure measurement, pupillary reflexes tests, ocular movements' tests, dry eye disease tests, and fundus and mfERG examinations. RESULTS: The CVS-F3 identified that 87.9% of students had complaints that might be related to CVS. We documented a 76% prevalence rate in students undergoing an ophthalmologic exam. The most common ocular and extraocular complaints included visual blur and headache (40.9% and 46.8%, resp.). Statistical logistic and linear regression analyses showed that refractive errors, prolonged screen-hours, close eye-screen distance, improper gaze angle, poor screen-resolution, and screen-glare were risk factors for developing CVS and influencing its severity. In the mfERG subgroup, 42.5% demonstrated reduced amplitudes of mfERG rings and quadrants, indicating reduced foveal responses. CONCLUSION: Surveys cannot yield an accurate CVS prevalence. However, they help to identify subjects at risk who should be comprehensively assessed to confirm or exclude CVS diagnosis. Smartphone misuse primarily caused CVS among users. Our mfERG findings might be a sign of potential CVS visual sequelae; however, future studies are warranted. Clinicians need to understand these sequelae to appropriately identify and treat CVS.
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spelling pubmed-80350402021-04-15 Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study Iqbal, Mohammed Said, Omar Ibrahim, Ola Soliman, Ashraf J Ophthalmol Research Article PURPOSE: To assess the visual, ocular, extraocular, and multifocal electroretinography (mfERG) outcomes of computer vision syndrome (CVS) among medical students. METHODS: This study was designed as a cross-sectional case-control study that included 733 medical students. All students completed a specially designed and validated CVS questionnaire survey (CVS-F3). Students from the control (No-CVS) and CVS groups underwent comprehensive ophthalmic examinations including the mfERG examinations. Our main outcome measures included uncorrected and corrected distance visual acuity (UDVA and CDVA, resp.) measurements, subjective and cycloplegic refractions, slit-lamp examination, intraocular pressure measurement, pupillary reflexes tests, ocular movements' tests, dry eye disease tests, and fundus and mfERG examinations. RESULTS: The CVS-F3 identified that 87.9% of students had complaints that might be related to CVS. We documented a 76% prevalence rate in students undergoing an ophthalmologic exam. The most common ocular and extraocular complaints included visual blur and headache (40.9% and 46.8%, resp.). Statistical logistic and linear regression analyses showed that refractive errors, prolonged screen-hours, close eye-screen distance, improper gaze angle, poor screen-resolution, and screen-glare were risk factors for developing CVS and influencing its severity. In the mfERG subgroup, 42.5% demonstrated reduced amplitudes of mfERG rings and quadrants, indicating reduced foveal responses. CONCLUSION: Surveys cannot yield an accurate CVS prevalence. However, they help to identify subjects at risk who should be comprehensively assessed to confirm or exclude CVS diagnosis. Smartphone misuse primarily caused CVS among users. Our mfERG findings might be a sign of potential CVS visual sequelae; however, future studies are warranted. Clinicians need to understand these sequelae to appropriately identify and treat CVS. Hindawi 2021-04-02 /pmc/articles/PMC8035040/ /pubmed/33868724 http://dx.doi.org/10.1155/2021/6630286 Text en Copyright © 2021 Mohammed Iqbal et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Iqbal, Mohammed
Said, Omar
Ibrahim, Ola
Soliman, Ashraf
Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study
title Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study
title_full Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study
title_fullStr Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study
title_full_unstemmed Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study
title_short Visual Sequelae of Computer Vision Syndrome: A Cross-Sectional Case-Control Study
title_sort visual sequelae of computer vision syndrome: a cross-sectional case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035040/
https://www.ncbi.nlm.nih.gov/pubmed/33868724
http://dx.doi.org/10.1155/2021/6630286
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