Developmental delay and magnocellular visual pathway function in very-low-birthweight preterm infants.

This study investigated the effect of very preterm birth (gestation < or =30wks) and very low birth weight (< or =1500g) on the development of magnocellular and parvocellular visual processing streams. Participants were preterm infants (n=55: 31 females, 24 males) born between 24 and 30 weeks'gestation (mean 27.4wks [SD 1.3]), weighing between 720 and 1470g (mean 1015g [SD 215]) and term infants (n=52: 27 females, 25 males) born between 38 and 42 weeks'gestation (mean 39.4wks [SD 0.9]), weighing between 2670 and 4405g (mean 3549g [SD 440]). Visual-evoked potentials to phase-reversing sine-wave gratings, varying in spatial frequency and contrast, were used to elicit magnocellular and parvocellular specific responses. Previous studies found that the N1 component reflects the parvocellular response, while P1 reflects the magnocellular response in adults and infants. Findings from the current study indicate significantly lower P1 amplitudes in preterm compared with term infants under most conditions. No difference was found for the amplitude of the N1 waveform. Results indicate that, for the age-range tested, preterm birth has little effect on the development of parvocellular function, while it appears to disrupt the development of magnocelluar function.

Influence of the state of alertness on the pattern visual evoked potentials (PVEP) in very young infant.

The aim of the study was to evaluate the pattern visual evoked potentials (PVEP) combined with an optimal state of vigilance, called liberated state (LS), in order to improve testing in very young infants. Transient PVEP were recorded in response to a checkerboard pattern of 120, 60 and 30 min of arc. in 56 fullterm newborns and 79 preterm infants from birth to 4 months of age. In the fullterms, 28 infants in each group were tested in LS or spontaneous alertness (SA) while in the preterms, 48 infants in each group were tested in LS or SA. No significant difference was found in the amplitude and/or peak time of the PVEP responses between subjects tested in LS compared to SA groups. However, the LS condition improved by approximately 25% the feasibility of prolonged PVEP testing in preterms aged less than 2 months (corrected age). This suggest that the LS condition enhances the clinical feasibility of PVEP testing in very young infants and should be used to optimize the evaluation of visual development in high risk infants in this age group.