Mr. Ashton et al., SURFACTANT PHOSPHATIDYLCHOLINE COMPOSITION DURING DEXAMETHASONE TREATMENT IN CHRONIC LUNG-DISEASE, Archives of Disease in Childhood, 71(2), 1994, pp. 60000114-60000117
Objectives - To determine whether dexamethasone 'matures' the phosphat
idylcholine (PC) composition of broncheoalveolar fluid in infants at h
igh risk of neonatal chronic lung disease (CLD), either by increasing
the proportion of dipalmitoylphosphatidylcholine (DPPC), expressed as
a percentage of total PC (%DPPC), or by increasing the ratio of DPPC t
o palmitoyloleoylphosphatidylcholine (DPPC:POPC ratio). Design - Doubl
e blind, placebo controlled. Setting and patients - Sixteen infants <3
2 weeks' gestation, <1250 g birth weight who were dependent on mechani
cal ventilation and requiring a fractional inspired oxygen of >0.30 at
12 days of chronological age. Intervention - Randomisation to receive
a two week reducing course of dexamethasone base at an initial dose o
f 0.2 mg/kg three times a day, or equivalent volumes of normal saline,
starting at 14 days. Eight infants were randomised into each group. B
roncheoalveolar lavage was performed serially throughout the study per
iod or until extubation. PC composition of the fluid was analysed by h
igh performance liquid chromatography. Outcome measures - The %DPPC an
d the DPPC:POPC ratios were calculated for individual infants for days
-1 and 0 combined, days 1 and 3 combined, and days 5 and 7 combined.
Analysis of covariance was used to analyse the results. Results - The
DPPC:POPC ratio was significantly less in the treated group than the p
lacebo group on days 1 and 3, and not greater as the hypothesis stated
. Three out of five infants treated with dexamethasone and for whom da
ta were available showed a substantial rise in DPPC:POPC ratio on days
5/7, compared with the placebo group, but overall these changes were
not statistically significant. Conclusions - The data do not support t
he hypothesis that dexamethasone's action in producing a clinical impr
ovement within the first 72 hours of treatment for neonatal CLD is by
the 'maturation' of pulmonary surfactant PC.