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Published on: January 29, 2011
End-tidal carbon monoxide levels in prematurely born infants developing bronchopulmonary dysplasia
Caroline May1, Sabina Patel, Janet Peacock
1Division of Asthma, Allergy, and Biology, King's College London School of Medicine at Guy's, King's College and St Thomas' Hospitals, London, UK.
Insights
Elevated end-tidal carbon monoxide (ETCO) levels in premature infants may predict bronchopulmonary dysplasia (BPD). Higher ETCO readings on day 14 indicated a significant risk of developing BPD, characterized by oxygen dependency.
Area of Science:
- Neonatal Medicine
- Respiratory Physiology
- Biomarker Discovery
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease in premature infants, linked to early inflammation.
- Inflammatory processes can increase carbon monoxide (CO) production via heme oxygenase-1.
- Elevated end-tidal CO (ETCO) levels are hypothesized to correlate with BPD development.
Purpose of the Study:
- To investigate the association between serial ETCO measurements and the development of BPD in premature infants.
- To determine if ETCO levels can serve as an early predictive biomarker for BPD.
Main Methods:
- Serial ETCO measurements were taken on days 3, 5, 7, 14, 21, and 28 in 50 premature infants.
- Infants were monitored for the development of BPD, defined as oxygen dependency at 36 weeks post-menstrual age (PMA).
- Statistical analysis compared ETCO levels between infants who developed BPD and those who did not.
Main Results:
- Infants who developed BPD exhibited significantly higher ETCO levels on days 7, 14, 21, and 28 compared to non-BPD infants.
- On day 14, mean ETCO levels were 3.19 ppm in the BPD group versus 1.43 ppm in the non-BPD group (p<0.001).
- An ETCO level >2.15 ppm on day 14 demonstrated 80% sensitivity and 92% specificity for predicting oxygen dependency at 36 weeks PMA.
Conclusions:
- Serial ETCO measurements show promise as a non-invasive tool for early BPD prediction in premature infants.
- Elevated ETCO levels may reflect the underlying inflammatory state associated with BPD development.
- Further research could validate ETCO as a routine clinical biomarker for BPD risk stratification.
Abstract:
Bronchopulmonary dysplasia (BPD) is associated with an early inflammatory response that persists after the first week of life. Inflammatory mediators can induce hemoxygenase-1 with a consequent increase in carbon monoxide (CO) production. End-tidal CO (ETCO) levels would be elevated in infants developing BPD. Serial measurements of ETCO levels were attempted on d 3, 5, 7, 14, 21, and 28 in 50 prematurely born infants (median gestational age 29 wk). Fourteen infants developed BPD [oxygen dependent beyond 36 wk post-menstrual age (PMA)] and had higher ETCO levels compared with the rest of the cohort on d 7, 14, 21, and 28. On d 14, the mean (SD) ETCO levels of the BPD group were 3.19 (1.11) ppm and 1.43 (0.61) ppm in the non-BPD group (p<0.001). An ETCO level on d 14>2.15 ppm had a sensitivity of 80% and specificity of 92% in predicting oxygen dependency at 36 wk PMA. Measurement of ETCO levels in prematurely born infants may be useful in the prediction of BPD.
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