The neonatal development of the light flash visual evoked potential

Citation
M. Kraemer et al., The neonatal development of the light flash visual evoked potential, DOC OPHTHAL, 99(1), 1999, pp. 21-39
Citations number
34
Categorie Soggetti
Optalmology
Journal title
DOCUMENTA OPHTHALMOLOGICA
ISSN journal
00124486 → ACNP
Volume
99
Issue
1
Year of publication
1999
Pages
21 - 39
Database
ISI
SICI code
0012-4486(1999)99:1<21:TNDOTL>2.0.ZU;2-H
Abstract
Aims. To follow visual development longitudinally in the normal neonate usi ng the flash visual evoked potential (VEP) and to find indications for a re lationship between potential development and visual development. Methods. T wenty healthy infants, born at term, were included in the study. Flash and patterned flash VEPs were used. The first VEP was recorded the day of birth or just postnatally, and succeeding recordings were performed the followin g weeks and months. Results. The data revealed different types of VEP in th e neonatal period suggesting great variablity in visual function on the day of birth. In the early development a potential of long latency and duratio n preceded the development of a more compound potential of shorter latency. The two types of responses seemed to coalesce during early development; th e first late response was attenuated and was eventually integrated in the m ore mature VEP. At approximately five weeks of age changes in the VEP were simultaneous with the development of responsive smiling and another visual behaviour of the infants. Conclusions. The results showed many similarities between the VEP development in infants and in immature animals. In develop ing animals geniculo-cortical and extra-geniculate visual afferent pathways evoke two types of VEPs similar to those recorded in the present study. Th e early responses were also similar to previous recordings from children wi th lesions in the geniculo-striatal pathway or primary cortex. Our interpre tation of the results was that the human VEP also consists of responses evo ked by afferents running both in geniculo-cortical and extra-geniculate pat hways and that the two types of responses could be separated in the VEP in the neonatal period. These findings are important for our understanding of conditions with a delay in visual maturation, for example intracranial haem orrhages, hydrocephalus, pre/dys-maturity and 'idiopathic' delayed visual m aturation.