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Published on: October 31, 2025
Lung Function and Relevant Clinical Factors in Very Low Birth Weight Preterm Infants with Chronic Lung Disease: An
I-Ling Chen1, Hsiu-Lin Chen2,3
1School of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Insights
Premature infants with chronic lung disease (CLD) showed comparable lung function at discharge, despite smaller size and longer respiratory support. Functional residual capacity and tidal volume correlated with body size in these infants.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Respiratory Medicine
Background:
- Chronic lung disease (CLD) is a common complication in premature infants requiring mechanical ventilation, leading to long-term respiratory issues.
- This study focuses on very low birth weight (VLBW) preterm infants in Taiwan who needed respiratory support.
- CLD diagnosis was based on oxygen or ventilation support at 36 weeks postmenstrual age (PMA).
Purpose of the Study:
- To evaluate the lung function of premature infants before hospital discharge.
- To identify factors related to lung function in VLBW preterm infants, particularly those with CLD.
Main Methods:
- Enrolled VLBW preterm infants requiring respiratory support.
- Assessed lung function using EXHALYZER® D before discharge.
- Diagnosed CLD based on oxygen or positive-pressure ventilation support at 36 weeks PMA.
Main Results:
- Forty-five VLBW infants underwent lung function testing; 27 had CLD.
- CLD infants had smaller gestational age and birth weight, and required longer respiratory support.
- Despite differences in size and support duration, lung function (functional residual capacity, tidal volume) was comparable between CLD and no-CLD groups.
- Functional residual capacity correlated positively with body length in infants with CLD.
Conclusions:
- Lung function, ventilation, and respiratory mechanics were similar between CLD and no-CLD groups at discharge.
- Functional residual capacity and tidal volume were associated with body size (length, weight) in VLBW preterm infants.
- Body length was a significant factor for functional residual capacity in VLBW infants with CLD.
Background:
Chronic lung disease (CLD), most commonly seen in premature infants who required mechanical ventilation, is associated with functional consequences on lungs and respiratory morbidity. This study aimed to evaluate the lung function of premature infants before discharge and their relevant factors related to the lung function.
Methods:
Very low birth weight (VLBW) preterm infants, who required respiratory support soon after birth and were admitted to a hospital in Taiwan, were enrolled. Infants with a need for supplemental oxygen or positive-pressure ventilation support at the postmenstrual age (PMA) of 36 weeks were diagnosed with CLD. Lung function was examined once using EXHALYZER® D before infants were ready for discharge.
Results:
Forty-five VLBW preterm infants received the lung function test before discharge, 27 of whom were diagnosed with CLD. The gestational age (p=0.001) and birth weight (p < 0.001) were smaller in the CLD group than in the no-CLD group. Furthermore, infants with CLD required a longer duration of respiratory support (p < 0.001). The postnatal age and PMA were higher and body size was bigger in infants with CLD on lung function measurement. However, lung function was comparable between the groups. The functional residual capacity and tidal volume were associated with body size upon measuring lung function among all VLBW premature infants. FRC was positively correlated with the body length on measuring lung function in those with CLD.
Conclusion:
In our study, we showed FRC was positively related to the PMA and body length and tidal volume was positively correlated with the body weight and length on lung function measurement in VLBW preterm infants before discharge. Moreover, FRC was positively correlated with the body length on measuring lung function in those with CLD. The lung volume, ventilation, and respiratory mechanics on discharge were comparable between CLD and no-CLD groups.
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