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Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency

CONTEXT: Visual evoked potentials are useful in investigating the physiology and pathophysiology of the human visual system. Flash visual evoked potential (FVEP), though technically easier, has less clinical utility because it shows great variations in both latency and amplitude for normal subjects....

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Autores principales: Subramanian, Senthil Kumar, Gaur, Giriwar Singh, Narayan, Sunil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841612/
https://www.ncbi.nlm.nih.gov/pubmed/24339591
http://dx.doi.org/10.4103/0972-2327.120492
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author Subramanian, Senthil Kumar
Gaur, Giriwar Singh
Narayan, Sunil K.
author_facet Subramanian, Senthil Kumar
Gaur, Giriwar Singh
Narayan, Sunil K.
author_sort Subramanian, Senthil Kumar
collection PubMed
description CONTEXT: Visual evoked potentials are useful in investigating the physiology and pathophysiology of the human visual system. Flash visual evoked potential (FVEP), though technically easier, has less clinical utility because it shows great variations in both latency and amplitude for normal subjects. AIM: To study the effect of eye closure, low luminance, and monochromatic stimulation on the variability of FVEPs. SUBJECTS AND METHODS: Subjects in self-reported good health in the age group of 18-30 years were divided into three groups. All participants underwent FVEP recording with eyes open and with white light at 0.6 J luminance (standard technique). Next recording was done in group 1 with closed eyes, group 2 with 1.2 and 20 J luminance, and group 3 with red and blue lights, while keeping all the other parameters constant. Two trials were given for each eye, for each technique. The same procedure was repeated at the same clock time on the following day. STATISTICAL ANALYSIS: Variation in FVEP latencies between the individuals (interindividual variability) and the variations within the same individual for four trials (intraindividual variability) were assessed using coefficient of variance (COV). The technique with lower COV was considered the better method. RESULTS: Recording done with closed eyes, 0.6 J luminance, and monochromatic light (blue > red) showed lower interindividual and intraindividual variability in P2 and N2 as compared to standard techniques. CONCLUSIONS: Low luminance flash stimulations and monochromatic light will reduce FVEP latency variability and may be clinically useful modifications of FVEP recording technique.
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spelling pubmed-38416122013-12-11 Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency Subramanian, Senthil Kumar Gaur, Giriwar Singh Narayan, Sunil K. Ann Indian Acad Neurol Original Article CONTEXT: Visual evoked potentials are useful in investigating the physiology and pathophysiology of the human visual system. Flash visual evoked potential (FVEP), though technically easier, has less clinical utility because it shows great variations in both latency and amplitude for normal subjects. AIM: To study the effect of eye closure, low luminance, and monochromatic stimulation on the variability of FVEPs. SUBJECTS AND METHODS: Subjects in self-reported good health in the age group of 18-30 years were divided into three groups. All participants underwent FVEP recording with eyes open and with white light at 0.6 J luminance (standard technique). Next recording was done in group 1 with closed eyes, group 2 with 1.2 and 20 J luminance, and group 3 with red and blue lights, while keeping all the other parameters constant. Two trials were given for each eye, for each technique. The same procedure was repeated at the same clock time on the following day. STATISTICAL ANALYSIS: Variation in FVEP latencies between the individuals (interindividual variability) and the variations within the same individual for four trials (intraindividual variability) were assessed using coefficient of variance (COV). The technique with lower COV was considered the better method. RESULTS: Recording done with closed eyes, 0.6 J luminance, and monochromatic light (blue > red) showed lower interindividual and intraindividual variability in P2 and N2 as compared to standard techniques. CONCLUSIONS: Low luminance flash stimulations and monochromatic light will reduce FVEP latency variability and may be clinically useful modifications of FVEP recording technique. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3841612/ /pubmed/24339591 http://dx.doi.org/10.4103/0972-2327.120492 Text en Copyright: © Annals of Indian Academy of Neurology 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
Subramanian, Senthil Kumar
Gaur, Giriwar Singh
Narayan, Sunil K.
Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
title Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
title_full Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
title_fullStr Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
title_full_unstemmed Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
title_short Low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
title_sort low luminance/eyes closed and monochromatic stimulations reduce variability of flash visual evoked potential latency
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841612/
https://www.ncbi.nlm.nih.gov/pubmed/24339591
http://dx.doi.org/10.4103/0972-2327.120492
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