T. Saarela et al., Incidence, ultrasonic patterns and resolution of nephrocalcinosis in very low birthweight infants, ACT PAEDIAT, 88(6), 1999, pp. 655-660
This longitudinal study was undertaken in order to elucidate the incidence
and natural course of nephrocalcinosis in preterm infants and to evaluate w
hether the ultrasonic classification for nephrocalcinosis used here is suit
able for predicting subsequent resolution of the condition. A total of 129
very low birthweight infants were screened for nephrocalcinosis by renal ul
trasonography at 2 wk, 6 wk and 3 mo. The pyramidal changes were classified
as peripheral, scattered or extensive. Follow-up renal ultrasonography was
performed on the infants with nephrocalcinosis at 6, 12, 18 and 24 mo, and
thereafter annually up to 6 y of age, or until ultrasonic resolution. The
overall incidence of nephrocalcinosis was 20% (26/129). Nephrocalcinotic ch
anges were peripheral in 14 out of the 26 infants (54%), scattered in 7 (27
%) and extensive in 5 (19%). Ultrasonic resolution had taken place in all t
he cases with peripheral nephrocalcinosis by 12 mo, but 3 of the 7 infants
with the scattered pattern and 3 of the 3 with the extensive pattern (1 die
d) were still affected at 24 mo. In two cases with extensive nephrocalcinos
is the condition still persisted at 5-6 y of age. We conclude that about 20
% of very low birthweight infants develop nephrocalcinosis during the first
3 mo of life. In about half of the affected infants renal changes are rest
ricted and transient, but more extensive forms may last several pears. The
classification of nephrocalcinosis used here is appropriate for predicting
later ultrasonic resolution.