A. Spinillo et al., OBSTETRIC RISK-FACTORS FOR PERIVENTRICULAR LEUKOMALACIA AMONG PRETERMINFANTS, British journal of obstetrics and gynaecology, 105(8), 1998, pp. 865-871
Objective To evaluate the obstetric antecedents of cystic periventricu
lar leukomalacia and transient echodense periventricular lesions among
preterm infants. Design A cohort study of preterm singleton infants b
orn between 25 and 33 weeks gestation. Setting Pavia, Italy. Populatio
n Three hundred and forty-nine infants admitted to a Division of Neona
tal Intensive Care who were screened for periventricular leukomalacia.
Method The obstetric factors in infants with either cystic periventri
cular leukomalacia or transient echodense periventricular lesions were
compared to those in infants with negative cranial ultrasonographic f
indings. Stepwise multiple logistic regression analysis was used to ev
aluate the association between risk factors and outcomes adjusting for
confounders. Results The prevalence of cystic periventricular leukoma
lacia and transient echodense lesions was 5.7% (20/349) and 14% (49/34
9), respectively. The main risk factors for cystic leukomalacia were f
irst trimester haemorrhage (OR 4.49; 95% CI 1.63-12.39), maternal urin
ary tract infection on admission (OR 5.71; 95% CI 1.91-17.07), and neo
natal acidosis (pH < 7.2) at birth (OR 5.97; 95% CI 1.93-18.52). Mecon
ium-stained amniotic fluid (OR 3.95; 95% CI 1.42-10.98) and long term
(> 72 hours) ritodrine tocolysis (OR 2.54; 95% CI 1.28-5.05) were asso
ciated with an increased risk of echodense lesions. The likelihood of
overall leukomalacia (cystic plus echodense periventricular lesions) w
as increased among cases with meconium-stained amniotic fluid (OR 4.06
; 95% CI 1.65-10.0), long-term ritodrine tocolysis (OR 2.56; 95% CI 1.
38-4.72), maternal infection (OR 1.73; 95% CI 1.0-3.0), and acidosis a
t birth (OR 1.98; 95% CI 1.0-3.98). Conclusions This study confirms th
at maternal infection, acidosis at birth, and meconium-stained amnioti
c fluid increase the risk of periventricular leukomalacia in preterm i
nfants. Long-term ritodrine use seems to increase the risk for transie
nt echodense lesions.