April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
ERG Results and Correlations With Psychophysical Measures in Patients With Non-Syndromic Retinitis Pigmentosa
Author Affiliations & Notes
  • J. Nilsson
    Dept of Clinical Neurophysiology, University of Gothenburg, Goteborg, Sweden
    Visual Electrophysiology Unit, The Hospital for Sick Children, Toronto, Ontario, Canada
  • T. Wright
    Dept of Clinical Neurophysiology, University of Gothenburg, Goteborg, Sweden
    Visual Electrophysiology Unit, The Hospital for Sick Children, Toronto, Ontario, Canada
  • C. A. Westall
    Visual Electrophysiology Unit, The Hospital for Sick Children, Toronto, Ontario, Canada
    Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ontario, Canada
  • Footnotes
    Commercial Relationships  J. Nilsson, None; T. Wright, None; C.A. Westall, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 5309. doi:
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      J. Nilsson, T. Wright, C. A. Westall; ERG Results and Correlations With Psychophysical Measures in Patients With Non-Syndromic Retinitis Pigmentosa. Invest. Ophthalmol. Vis. Sci. 2009;50(13):5309.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Evaluation of Retinitis Pigmentosa is one of the most common reasons for performing an ERG (Electroretinogram). This study aims to compare ERG results with psychophysical measures of visual function.

Methods: : 408 patients with non-syndromic Retinitis Pigmentosa and results from both ERG and psychophysical testing (visual acuity, contrast sensitivity and colour vision) were included in a retrospective study.

Results: : ERG results were divided into four categories. There was a very wide distribution of results for all psychophysical measures and ERG results could not be predicted by psychophysical results. For visual acuity and colour vision, patients with non-recordable ERGs performed significantly worse than those with recordable ERGs. However, there was no difference in performance between patients in the three categories with abnormal, but recordable, ERGs. For contrast sensitivity, there was a gradual decline in performance with increasing ERG abnormality.

Conclusions: : These findings are consistent with visual acuity and colour vision representing central cone functions, likely present until late stages of disease. Contrast sensitivity has been reported to accompany the decrease in visual fields in RP, consistent with a more gradual loss of function. Patients with RP should be referred for an initial, diagnostic ERG regardless of psychophysical results.

Keywords: electroretinography: clinical • retinal degenerations: hereditary • visual acuity 
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