Respiratory distress syndrome (RDS) is associated with prematurity-rel
ated deficiency of surfactant. Surfactant replacement therapy has been
used in premature infants to Prevent RDS or reduce its severity. In t
his study we describe the pathology of the lungs after surfactant repl
acement therapy. All the neonatal autopsies during the years 1989 and
1990 (n = 235) were examined. Infants greater-than-or-equal-to 31 week
s gestation, with congenital anomalies or who lived more than 2 weeks
were excluded from the study. Infants who had received intratracheal S
urvanta, a modified surfactant extracted from cow lung (n = 14), were
compared with infants who did not receive exogenous surfactant (n = 20
). The two groups were statistically comparable in terms of weight, ge
stational and postnatal age, and clinical management. H&E-stained lung
sections were examined independently by two pathologists without know
ledge of surfactant treatment status; any discrepancies in histologica
l evaluation were resolved by joint review. Nine histological features
were evaluated including hyaline membranes, necrosis of the epitheliu
m, hemorrhage, edema, inflammation, metaplasia, arteriolar muscular hy
perplasia interstitial fibrosis, and pulmonary interstitial emphysema
(PIE). Histological changes were graded from 0 to 3+. When it was pres
ent, cerebral periventricular-intraventricular hemorrhage (PVH-IVH) wa
s graded 1-4. The presence or absence of sepsis and necrotizing entero
colitis (AEC) were also determined. Comparisons between patient groups
were performed using the Mann-Whitney U, Student's t and chi2 tests.
The severity of hyaline membrane disease, PIE, and epithelial necrosis
was less severe in the surfactant-treated group than in the untreated
group. There were no differences between the two groups in the degree
of pulmonary hemorrhage or in the incidence of PVH-IVH, sepsis, or NE
C.