Rd. Shih et al., ARTIFICIAL SURFACTANT ADMINISTRATION IN AN ANIMAL-MODEL OF HYDROCARBON INDUCED PULMONARY TOXICITY, Journal of toxicology. Clinical toxicology, 34(1), 1996, pp. 139-139
Background: The treatment of severe hydrocarbon (HC) pulmonary aspirat
ion is limited to supportive care. Because the toxicity of HC may be r
elated to surfactant (SFT) depletion, SFT therapy is a possible antido
te for HC pneumonitis. purpose of this study is to assess the effects
of SFT administration in an animal model of severe HC induced pulmonar
y toxicity. Methods: A randomized, placebo-controlled design utilizing
New Zealand white rabbits was employed. After anesthetic induction wi
th xylazine (2 mg/kg IM) and ketamine (50 mg/kg IM), an IV line, an ar
terial line, and a tracheostomy (3.0 cuffed ETT) were performed. The E
XP animals received HC (mineral seal oil, 0.25 cc/kg ETT) followed in
5 minutes by SFT (EXSOURF, 5 cc/kg ETT), and CTL animals received HC a
nd then placebo (sterile water, 5 cc/kg ETT). SEP, HR, pH, pO2, and pC
O2 were measured at 0, 5, 10, 15, 30, 60, and 90 mins post HC administ
ration. Static pulmonary compliance (SPC) was measured at 90 mins afte
r paralysis was induced with pancuronium (0.1 mg/kg IV). All analyses
compared EXP and CTL groups using repeated measures ANOVA. A p-value <
0.05 was considered significant. Results: 14 animals were randomized.
4 animals died for technical reasons prior to the initiation of the p
rotocol and were excluded from analysis leaving 5 animals in each grou
p. All other animals survived to completion of the study. No statistic
al differences were found in SEP, HR, pH, pO2 and pCO2. The SPC curve
was statistically worse for the EXP group as opposed to the CTL group.
Conclusion: Bolus administration of SFT for severe HC induced pulmona
ry toxicity in this animal model was found to be detrimental.