PEDIATRICS Vol. 117 No. 2 February 2006, pp. 448-454 (doi:10.1542/peds.2005-0123)
Onset of Mechanical Ventilation Is Associated With Rapid Activation of Circulating Phagocytes in Preterm Infants
a Hospital for Children and Adolescents
b Department of Bacteriology and Immunology, Haartman Institute
d Department of Medicine, Division of Infectious Diseases, University of Helsinki, Helsinki, Finland
c Department of Clinical Chemistry, Helsinki University Central Hospital, Helsinki, Finland
OBJECTIVE. In preterm infants with respiratory distress syndrome (RDS), circulating neutrophils are activated. Kinetics and effects of surfactant therapy on this activation are unknown. Therefore, we studied activation of circulating neutrophils and monocytes in newborn preterm infants with and without RDS.
PATIENTS AND METHODS. Preterm infants with RDS who were mechanically ventilated and received surfactant ("ventilated infants": n = 38; mean gestational age ± SD: 28.3 ± 2.2 weeks; mean birth weight ± SD: 1086 ± 353 g) and preterm infants who received nasal continuous positive airway pressure (n = 8) or no ventilatory support (n = 17) ("control infants": mean gestational age ± SD: 32.1 ± 1.2 weeks; mean birth weight ± SD: 1787 ± 457 g) were recruited. Blood samples were taken from ventilated infants at birth, before surfactant treatment, at 1 and 2 hours after surfactant, and at 12 to 24 hours of age. Blood samples were taken from control infants at birth, at 2 to 6 hours, and at 12 to 24 hours of age. Phagocyte CD11b expression was analyzed by flow cytometry.
RESULTS. In ventilated infants, phagocyte CD11b expression increased from birth to the first postnatal samples. It increased further by 12 to 24 hours of age. Control infants with or without nasal continuous positive airway pressure showed no significant increase after birth. At 12 to 24 hours of age, phagocyte CD11b expression was higher in ventilated infants than in control infants. In ventilated infants, neutrophil CD11b expression at 1 and 2 hours after surfactant correlated positively with gestational age.
CONCLUSIONS. In preterm infants with RDS, significant activation of circulating phagocytes occurs within 1 to 3 hours of the onset of mechanical ventilation, independent of surfactant administration, which indicates that mechanical ventilation may be the inducer of this systemic inflammatory response.
Key Words: CD11b mechanical ventilation monocyte neutrophil respiratory distress syndrome systemic inflammation
Abbreviations: RDSrespiratory distress syndrome FIO2fraction of inspired oxygen nCPAPnasal continuous positive airway pressure RFUrelative fluorescence unit BPDbronchopulmonary dysplasia
Accepted Jun 16, 2005.
![]()
CiteULike
Connotea
Del.icio.us
Digg
Facebook
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
H. J. Birenbaum, A. Dentry, J. Cirelli, S. Helou, M. A. Pane, K. Starr, C. F. Melick, L. Updegraff, C. Arnold, A. Tamayo, et al. Reduction in the Incidence of Chronic Lung Disease in Very Low Birth Weight Infants: Results of a Quality Improvement Process in a Tertiary Level Neonatal Intensive Care Unit Pediatrics, January 1, 2009; 123(1): 44 - 50. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Soni and P. Williams Positive pressure ventilation: what is the real cost? Br. J. Anaesth., October 1, 2008; 101(4): 446 - 457. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Janer, S. Andersson, C. Haglund, R. Karikoski, and P. Lassus Placental Growth Factor and Vascular Endothelial Growth Factor Receptor-2 in Human Lung Development Pediatrics, August 1, 2008; 122(2): 340 - 346. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Geary, M. Caskey, R. Fonseca, and M. Malloy Decreased Incidence of Bronchopulmonary Dysplasia After Early Management Changes, Including Surfactant and Nasal Continuous Positive Airway Pressure Treatment at Delivery, Lowered Oxygen Saturation Goals, and Early Amino Acid Administration: A Historical Cohort Study Pediatrics, January 1, 2008; 121(1): 89 - 96. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Janer, S. Andersson, C. Haglund, and P. Lassus Pulmonary Endostatin Perinatally and in Lung Injury of the Newborn Infant Pediatrics, January 1, 2007; 119(1): e241 - e246. [Abstract] [Full Text] [PDF] |
||||






