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Multifocal Electroretinograms
16:49

Multifocal Electroretinograms

Published on: December 4, 2011

ERG findings in patients using hydroxychloroquine

Radouil T Tzekov1, Alexandra Serrato, Michael F Marmor

  • 1Department of Ophthalmology, Stanford University Medical Center, Stanford, CA 94305-5308, USA.

Insights

Hydroxychloroquine (HCQ) can cause electroretinography (ERG) abnormalities, even without visible eye damage. Full-field ERG changes were not linked to HCQ dose or duration, but multifocal ERG showed toxicity patterns.

Area of Science:

  • Ophthalmology
  • Pharmacology
  • Neuroscience

Background:

  • Hydroxychloroquine (HCQ) is widely used for autoimmune diseases.
  • HCQ retinopathy is a known complication, typically diagnosed through clinical examination and visual field testing.
  • Early detection of HCQ toxicity is crucial to prevent irreversible vision loss.

Purpose of the Study:

  • To investigate electroretinography (ERG) findings in patients using HCQ.
  • To assess both full-field ERG (ffERG) and multifocal ERG (mfERG) in relation to HCQ exposure duration and dose.
  • To identify subclinical signs of HCQ toxicity using ERG.

Main Methods:

  • Retrospective review of 26 patients (51 eyes) with 1-30 years of HCQ use.
  • Analysis of ffERG and mfERG results in conjunction with clinical evaluations.
  • Classification of patients into groups based on ERG and clinical findings.

Main Results:

  • 13 patients had no abnormalities.
  • 2 patients showed cone b-wave delay.
  • 6 patients had decreased ERG amplitude.
  • 2 patients had borderline toxicity.
  • 3 patients exhibited toxicity (bull's-eye maculopathy).
  • Decreased oscillatory potential (OP) amplitudes were common, even without other abnormalities.
  • mfERGs were normal in asymptomatic patients but showed a bull's-eye pattern in toxic cases.
  • ffERG parameters, including OPs, showed minimal correlation with HCQ duration or cumulative dose.

Conclusions:

  • A significant number of patients displayed diffuse ERG abnormalities without clinical signs of HCQ toxicity.
  • mfERG detected toxicity but its sensitivity for early changes requires further evaluation.
  • Distinguishing between HCQ's pharmacological effects, retinopathy from systemic disease, and toxic effects needs more research.
Abstract

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