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Published on: January 29, 2011
End-tidal carbon monoxide measurements in infant respiratory distress syndrome
Tannette G Krediet1, Geert A Cirkel, Hendrik J Vreman
1Department of Neonatology, Wilhemina Children's Hospital, University Medical Center, Utrecht, the Netherlands. t.krediet@wkz.azu.nl
Insights
Elevated end-tidal carbon monoxide (ETCOc) indicates respiratory distress syndrome (RDS) severity in preterm infants. Early ETCOc measurements can reliably predict the absence of chronic lung disease.
Area of Science:
- Neonatal Medicine
- Respiratory Physiology
- Biomarker Research
Background:
- Respiratory Distress Syndrome (RDS) involves inflammatory and oxidative processes.
- These processes can elevate carbon monoxide (CO) production.
Purpose of the Study:
- To investigate the relationship between end-tidal CO corrected for inhaled CO (ETCOc) and RDS severity in preterm infants.
- To assess the predictive value of early ETCOc measurements for chronic lung disease development.
Main Methods:
- 78 preterm infants were studied, categorized by RDS severity (none, moderate, severe).
- End-tidal CO corrected for inhaled CO (ETCOc) was measured using the CO-Stat End Tidal Breath Analyzer.
Main Results:
- ETCOc levels were significantly higher in infants with RDS compared to those without during the first week of life.
- RDS severity was the most significant independent predictor of ETCOc levels.
- Early ETCOc measurements (<2.5 ppm within 12 hours of birth) demonstrated excellent (100%) negative predictive value for chronic lung disease.
Conclusions:
- Increased ETCOc in severe RDS suggests inflammation and lipid peroxidation contribute to elevated local CO production in the lungs.
- Early ETCOc measurements are valuable for excluding the occurrence of chronic lung disease in preterm infants.
Background:
RDS involving inflammatory and oxidative processes may lead to increased production of carbon monoxide (CO).
Aim:
The relationship between end-tidal CO, corrected for inhaled CO (ETCOc), and RDS severity was investigated in preterm infants as well as the value of early ETCOc measurements to predict chronic lung disease.
Methods:
78 infants (30 no RDS, 32 moderate RDS, 16 severe RDS) were included. ETCOc was measured using the CO-Stat End Tidal Breath Analyzer.
Results:
ETCOc was significantly higher in RDS compared to no RDS during the first week (p<0.05). Severity of RDS was the most significant independent variable in a stepwise regression model related to ETCOc (F-test: 18.17). Negative predictive value of early (within first 12 h of life) ETCOc measurement (<2.5 ppm) for development of chronic lung disease was excellent (100%).
Conclusion:
During severe RDS, inflammation may contribute to increased lipid peroxidation leading to increased local CO production in the lung, indicated by increased ETCOc. Early ETCOc determinations may be helpful to exclude occurrence of chronic lung disease.
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