December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Multifocal Visual Evoked Potentials to Cone Specific Stimuli in Patients with Retinitis Pigmentosa (RP)
Author Affiliations & Notes
  • SM Shuwairi
    Department of Psychology Columbia University New York NY
  • K Holopigian
    School of Medicine New York University New York NY
  • VC Greenstein
    School of Medicine New York University New York NY
  • X Zhang
    Department of Psychology Columbia University New York NY
  • DC Hood
    Department of Psychology Columbia University New York NY
  • Footnotes
    Commercial Relationships   S.M. Shuwairi, None; K. Holopigian, None; V.C. Greenstein, None; X. Zhang, None; D.C. Hood, None. Grant Identification: NIH/NEI Grant EY02115; The Foundation Fighting Blindness
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 1172. doi:
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    • Get Citation

      SM Shuwairi, K Holopigian, VC Greenstein, X Zhang, DC Hood; Multifocal Visual Evoked Potentials to Cone Specific Stimuli in Patients with Retinitis Pigmentosa (RP) . Invest. Ophthalmol. Vis. Sci. 2002;43(13):1172.

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

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Abstract

Abstract: : Purpose: To examine whether the multifocal visual evoked potential (mfVEP) to cone specific stimuli in patients with RP supplies additional information not available in the multifocal electroretinogram (mfERG) or visual fields. Methods: RP patients were enrolled based on the following criteria: visual acuity of 20/25 or better and central visual fields of at least 10 degrees. Monocular mfVEPs were obtained to a pattern reversing display that modulated only the L- or M-cones. The mfVEP display was a scaled, 60 sector, dartboard array 44 degrees in diameter. Electrodes were placed at the inion, 4 cm above, and at 1 cm above and 4 cm lateral to the inion on both sides. The cone contrasts were 47% for both the L and M-stimuli. In addition, mfVEPS were recorded to a standard black and white dartboard array. Humphrey visual fields (24-2), color vision tests, and mfERGs were obtained on all patients. The mfERGs were measured using a 46 degree display with 103 scaled black and white hexagons. Results: The correspondence between the mfVEPs and visual field sensitivity was better than the correspondence between mfVEPS and mfERGs. This was true for both chromatic and achromatic mfVEPs. For example, mfVEP responses could not be detected in regions with large mfERG responses and poor visual field sensitivity and there were examples of mfVEP responses in regions with non-detectable mfERGs. However, for a few patients, neither mfERG nor mfVEP responses were detectable in regions with relatively good visual field sensitivity. There was no evidence of color-specific latency or amplitude differences in the mfVEP as has been reported for the mfERG [1]. Conclusion: The mfVEP supplies information about visual function not necessarily seen in the visual field or mfERG. 1. Scholl & Kremers. (2000). IOVS, 41(10).

Keywords: 562 retinal degenerations: hereditary • 395 electroretinography: clinical • 393 electrophysiology: clinical 
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