The Assessment of Visual Fields in Infants Using Saccadic Vector Optokinetic Perimetry (SVOP): A Feasibility Study

Antonios Perperidis1,2, Alice D McTrusty1,2,3, Lorraine A Cameron1,3

  • 1Department of Child Life and Health, University of Edinburgh, Edinburgh, UK.

Insights

Saccadic vector optokinetic perimetry (SVOP) shows promise for infant visual field (VF) testing. Modified SVOP successfully assessed VFs in most healthy infants, suggesting its potential for early detection of visual impairments.

Area of Science:

  • Ophthalmology
  • Pediatric Optometry
  • Vision Science

Background:

  • Assessing visual fields (VF) in infants is crucial for early detection of visual impairments.
  • Traditional methods can be challenging due to infants' limited cooperation and attention spans.
  • Automated eye-tracking perimetry offers a potential solution for objective VF assessment.

Purpose of the Study:

  • To evaluate the feasibility of saccadic vector optokinetic perimetry (SVOP) for infant visual field assessment.
  • To determine if an adapted SVOP protocol can be successfully implemented in healthy infants.

Main Methods:

  • Thirteen healthy infants (3.5-12.0 months) underwent testing with an adapted SVOP protocol.
  • Modifications included animated fixation targets, larger stimuli, and a tiered test pattern.
  • Binocular confrontation VF testing and visual acuity tests were also performed for comparison.

Main Results:

  • 92.3% of infants completed a 4-point screening test, with higher completion rates for more complex tests.
  • Performance metrics like completion rate and accuracy were analyzed.
  • The adapted SVOP protocol was feasible for assessing binocular visual fields in this cohort.

Conclusions:

  • Modified saccadic vector optokinetic perimetry (SVOP) is a feasible method for assessing infant visual fields.
  • Further research with larger cohorts is needed to establish normative data and diagnostic accuracy.
  • Eye-tracking perimetry holds potential for automated visual field assessment in infants.
Abstract

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