Flash visual evoked potentials in patients with periventricular leucomalacia in children less than 1 year of age

Jitendra Jethani1, Monika Jethani

  • 1Pediatric Ophthalmology and Squint Clinic, Dr. Thakorbhai V Patel Eye Institute, Vadodara, Gujarat, India.

Insights

Flash visual evoked potentials (fVEPs) in infants with periventricular leucomalacia (PVL) show delayed latency at 8 Hz but not 1.4 Hz. Amplitudes may appear normal, making them unreliable for assessing PVL-related visual changes.

Area of Science:

  • Pediatric Neurology
  • Ophthalmology
  • Neurophysiology

Background:

  • Periventricular leucomalacia (PVL) is a common cause of visual impairment in infants.
  • Existing literature on visual evoked potentials (VEPs) in young children with PVL is limited.
  • Visual impairments associated with PVL include reduced vision, visual field defects, and coordination issues.

Purpose of the Study:

  • To evaluate flash visual evoked potentials (fVEPs) in children under one year of age diagnosed with PVL.
  • To investigate the impact of different flash frequencies on fVEPs in this population.
  • To determine the reliability of fVEPs in detecting visual pathway abnormalities in infants with PVL.

Main Methods:

  • Nine infants diagnosed with PVL via MRI were included.
  • The mean age of the participants was 9.7 months.
  • Handheld fVEPs were performed under sedation at 1.4 Hz and 8 Hz flash frequencies.

Main Results:

  • Mean N1 and P1 latencies at 1.4 Hz were 47.9 ms and 77.7 ms, respectively.
  • Mean N1 and P1 latencies significantly increased to 189.8 ms and 238.4 ms at 8 Hz.
  • Mean amplitudes were similar at both frequencies (5.6 μV at 1.4 Hz and 5.59 μV at 8 Hz), suggesting potential normality despite latency changes.

Conclusions:

  • For the first time, a change in latency, specifically a delay at 8 Hz stimulation, was observed in infants with PVL.
  • fVEP amplitudes may appear normal in the presence of PVL-related brain changes.
  • fVEP amplitudes are not reliable indicators of visual pathway integrity in infants with PVL; latency changes are more indicative.
Abstract

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