Jj. Schnitzer et al., PRENATAL GLUCOCORTICOID THERAPY REVERSES PULMONARY IMMATURITY IN CONGENITAL DIAPHRAGMATIC-HERNIA IN FETAL SHEEP, Annals of surgery, 224(4), 1996, pp. 430-437
Objective To assess the feasibility of conducting clinical trials of p
renatal steroid therapy for congenital diaphragmatic hernia (CDH) in h
umans, the authors tested whether prenatal glucocorticoid, currently t
he standard treatment to minimize respiratory distress syndrome in pre
mature infants, might improve the pulmonary immaturity in severe CDH i
n a large animal model. Summary Background Data The authors have used
the nitrofen-induced rat model of CDH, which demonstrates immature lun
gs by biochemical, morphometric, and molecular biologic criteria. They
also have shown that the lethally immature lungs of the full-term CDH
rats can be improved by biochemical, morphometric, physiologic, and m
olecular criteria by treating the mothers with parenteral steroids at
doses extrapolated from the current therapy used to accelerate lung de
velopment of premature human babies. Methods During a 3-year period in
88 fetal sheep, 1) left-sided diaphragmatic hernias were created surg
ically at varying gestational ages (day 78-90; term=142-145 days) and
size to maximize severity (n=45), 2) placement and design of indwellin
g fetal intravenous catheters were optimized (n=13), and 3) timing and
dosage of cortisol administration were determined (n=17). As a result
, diaphragmatic hernias were created on day 80, intravenous catheters
were placed on day 120, and twice-daily intravenous cortisol injection
s (n=8) or saline as the control (n=5) were administered (days 133-135
). Lambs were delivered on day 136 via cesarean section to avoid stero
id-induced abortion; vascular access was obtained, and the fetuses wer
e ventilated at standard settings. Physiologic data were collected, an
d lungs were harvested for biochemical and histologic analysis. Result
s Significant improvements were measured in postductal arterial oxygen
pressure ([PaO2] 38+/-6 mmHg after cortisol therapy compared with 20/-3 mmHg for saline controls; p=0.002) and in dynamic compliance (0.42
+/-0.05 mL/cm H2O vs. 0.29+/-0.01 mL/cm H2O; p=0.01). Lung glycogen le
vels in the right lung of the cortisol group were significantly better
than controls (4.6+/-mg/g lung vs. 6.8+/-0.4 mg/g; p=0.002), as were
protein/DNA levels (8.3+/-0.9 mg/mg vs. 14.5+/-2.9 mg/mg; p <0.05). St
riking morphologic maturation of airway architecture was observed in t
he treated lungs. Conclusions Prenatal glucocorticoids correct the pul
monary immaturity of fetal sheep with CDH by physiologic, biochemical,
and histologic criteria. These data, combined with previous small ani
mal studies, have prompted the authors to initiate a prospective phase
I/II clinical trial to examine the efficacy of prenatal glucocorticoi
ds to improve the maturation of hypoplastic lungs associated with CDH.