PCO2 and room air saturation values in premature infants at risk for bronchopulmonary dysplasia

Objective:To determine the capillary partial pressure of carbon dioxide (PCO2) and room air transcutaneous hemoglobin saturation (RA SAT) at 36 weeks’ postmenstrual age (PMA) in infants born with weight between 501 and 1250 g.Study Design:Multicenter, prospective investigation with primary data collection within 72 h of 36 weeks PMA or discharge, whichever first. PCO2 and RA SAT determinations were done at rest on infants not requiring mechanical ventilation or nasal continuous positive airway pressure (NCPAP).Result:A total of 220 infants were enrolled (mean gestational age 27.7 weeks, mean birthweight 951 g). In infants with traditionally defined chronic lung disease (CLD) compared to those without CLD, the mean PCO2 was significantly higher (54 versus 45 mm Hg) and the median RA SAT significantly lower (<80 versus 97%). In infants with the new classification of bronchopulmonary dysplasia (BPD), there was a significant linear trend toward increasing PCO2 with increasing severity of BPD (45, 47, 54 and 62 mm Hg in No, Mild, Moderate and Severe BPD). There was a significant linear trend toward decreasing RA SAT with increasing severity of BPD (97, 95 <80, <80% in No, Mild, Moderate and Severe BPD).Conclusion:Defining CLD as BPD based upon a RA SAT test is a more discriminate, objective method to categorize lung injury. PCO2 is an objective measure of lung function that inversely correlates with RA SAT. These determinations done together at 36 weeks PMA may provide more precise and accurate estimates of lung injury that might allow for better understanding of pulmonary therapies and clearer comparison of BPD rates and severities among NICUs.

[1]  S. Hurd,et al.  Is chronic lung disease in low birth weight infants preventable? A survey of eight centers. , 1987, Pediatrics.

[2]  J. Widness,et al.  Neonatal Laboratory Blood Sampling: Comparison of Results from Arterial Catheters with Those from an Automated Capillary Device , 2000, Neonatal Network.

[3]  M. Moore,et al.  Do clinical markers of barotrauma and oxygen toxicity explain interhospital variation in rates of chronic lung disease? The Neonatology Committee for the Developmental Network. , 2000, Pediatrics.

[4]  E. Bancalari,et al.  Bronchopulmonary dysplasia. , 1986, Pediatric clinics of North America.

[5]  J. Klein,et al.  Variability in the use of supplemental oxygen for bronchopulmonary dysplasia. , 2002, The Journal of pediatrics.

[6]  Lily C Chow,et al.  Can changes in clinical practice decrease the incidence of severe retinopathy of prematurity in very low birth weight infants? , 2003, Pediatrics.

[7]  J. Kaempf,et al.  Implementing potentially better practices to improve neonatal outcomes after reducing postnatal dexamethasone use in infants born between 501 and 1250 grams. , 2003, Pediatrics.

[8]  R. E. Hoekstra,et al.  Survival and long-term neurodevelopmental outcome of extremely premature infants born at 23-26 weeks' gestational age at a tertiary center. , 2004, Pediatrics.

[9]  M. Walsh,et al.  Impact of a Physiologic Definition on Bronchopulmonary Dysplasia Rates , 2004, Pediatrics.

[10]  V. Baum Oxygen-Saturation Targets and Outcomes in Extremely Preterm Infants , 2004 .

[11]  R. Polin,et al.  Is the New Definition of Bronchopulmonary Dysplasia More Useful? , 2005, Journal of Perinatology.

[12]  M. Walsh,et al.  Validation of the National Institutes of Health Consensus Definition of Bronchopulmonary Dysplasia , 2005, Pediatrics.

[13]  M. Blayney,et al.  Elevated Carbon Dioxide Tension as a Predictor of Subsequent Adverse Events in Infants with Bronchopulmonary Dysplasia , 2005, Lung.

[14]  D. Phelps,et al.  A Pulmonary Score for Assessing the Severity of Neonatal Chronic Lung Disease , 2005, Pediatrics.

[15]  J. Goldsmith,et al.  Reduction of Bronchopulmonary Dysplasia After Participation in the Breathsavers Group of the Vermont Oxford Network Neonatal Intensive Care Quality Improvement Collaborative , 2006, Pediatrics.

[16]  R. Ryan A new look at bronchopulmonary dysplasia classification , 2006, Journal of Perinatology.

[17]  S. Kazzi,et al.  A Cluster-Randomized Trial of Benchmarking and Multimodal Quality Improvement to Improve Rates of Survival Free of Bronchopulmonary Dysplasia for Infants With Birth Weights of Less Than 1250 Grams , 2007, Pediatrics.