Premium
Early postnatal dexamethasone therapy may lessen lung inflammation in premature infants with respiratory distress syndrome on mechanical ventilation
Author(s) -
Wang J. Y.,
Yeh T. F.,
Lin Y. J.,
Chen W. Y.,
Lin C. H.
Publication year - 1997
Publication title -
pediatric pulmonology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.866
H-Index - 106
eISSN - 1099-0496
pISSN - 8755-6863
DOI - 10.1002/(sici)1099-0496(199703)23:3<193::aid-ppul4>3.0.co;2-p
Subject(s) - medicine , dexamethasone , respiratory distress , ventilation (architecture) , lung , mechanical ventilation , pulmonary function testing , anesthesia , respiratory disease , mechanical engineering , engineering
Early postnatal use of dexamethasone has recently been shown to be effective in improving the pulmonary status in premature infants with respiratory distress syndrome (RDS). To study the effect of dexamethasone on pulmonary inflammatory responses, we studied ten infants treated with dexamethasone and ten infants without this treatment. Serial tracheal aspirates were obtained for cell counts, neutrophil counts, total protein concentrations, and leukotriene B 4 (LTB 4 ) and 6‐keto prostaglandin (PG)F 1α levels before and after starting the study. Infants in the dexamethasone‐treated group required significantly lower mean airway pressures for ventilation and had lower P a CO 2 values from day 3 to day 14 than infants in the control group, suggesting better pulmonary function. For infants in the dexamethasone group, the tracheal aspirates showed significantly lower cell and neutrophil counts, protein concentrations, and 6‐keto‐PGF 1α and LTB 4 levels than in the control group. We conclude that early postnatal dexamethasone therapy may lessen lung inflammation and improve pulmonary function in infants with RDS. Pediatr Pulmonol. 1997; 23:193–197. © 1997 Wiley‐Liss, Inc.