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Updated: Aug 18, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
Does sustained lung inflation at resuscitation reduce lung injury in the preterm infant?
A E Harling1, M W Beresford, G S Vince
1NICU, Liverpool Women's Hospital, Liverpool L8 7SS, UK. Elizabeth.Harling@lwh-tr.nwest.nhs.uk
Insights
Sustained lung inflation during resuscitation did not reduce lung injury in preterm infants. This method did not significantly alter inflammatory markers or improve survival without bronchopulmonary dysplasia (BPD).
Area of Science:
- Neonatal Resuscitation
- Pulmonary Medicine
- Pediatric Critical Care
Background:
- Bronchopulmonary dysplasia (BPD) is a frequent complication in preterm infants, often linked to initial lung injury from ventilation strategies.
- Sustained lung inflation (SLI) at birth may aid lung fluid clearance and functional residual capacity (FRC) establishment.
- Previous studies suggest SLI could enable gentler ventilation, reducing inflammation and BPD.
Purpose of the Study:
- To evaluate if SLI at initial resuscitation reduces lung fluid, establishes FRC, and improves alveolar distribution in preterm neonates.
- To determine if SLI leads to less aggressive ventilation, reduced pulmonary inflammation, and decreased BPD incidence.
- To assess the impact of SLI on inflammatory markers and clinical outcomes in very preterm infants.
Main Methods:
- A study involving 52 preterm infants (<31 weeks gestation) compared SLI (5 seconds) versus conventional lung inflation (2 seconds) at birth.
- Pulmonary inflammation was assessed by quantifying interleukins (IL-6, IL-10, IL-1β) and tumor necrosis factor-alpha (TNF-α) in bronchoalveolar lavage fluid.
- Enzyme-linked immunosorbent assay (ELISA) was used for cytokine quantification.
Main Results:
- No significant differences were observed in the measured cytokine levels between the SLI and conventional groups.
- Mortality rates were 3/26 in the conventional group and 6/26 in the SLI group.
- Survival without BPD occurred in 13/26 infants in the conventional group and 14/26 in the SLI group.
Conclusions:
- Sustained lung inflation at resuscitation did not significantly reduce lung injury, as indicated by inflammatory markers.
- The study did not find evidence that SLI improves inflammatory status or reduces BPD in this cohort.
- SLI did not demonstrate a benefit in reducing lung injury markers in preterm infants.
Background:
Bronchopulmonary dysplasia (BPD) is a common outcome of preterm birth. Experimental animal work has shown that initial ventilation strategies injure the immature lung and may lead to BPD. Studies with asphyxiated babies have shown that, if tidal ventilation at birth is preceded by sustained lung inflation, larger inflation volumes can be achieved, which is thought to lead to clearance of lung fluid and formation of the functional residual capacity (FRC).
Objective:
To see if sustained lung inflation at initial resuscitation of preterm babies would facilitate the removal of lung fluid, establish the FRC, and allow an even distribution of alveolar opening, permitting less aggressive ventilation, leading to a reduction in pulmonary inflammation and subsequent BPD.
Method:
The outcomes of 52 babies of less than 31 weeks gestation, resuscitated at birth using either a sustained lung inflation of five seconds or a conventional lung inflation of two seconds for the first assisted breath of resuscitation, were examined. Evidence of pulmonary inflammation was determined by quantification of interleukins 6, 10, and 1beta and tumour necrosis factor alpha in bronchoalveolar lavage fluid by enzyme linked immunosorbent assay.
Results:
There were no significant differences in any of the cytokines. Death occurred in 3/26 babies in the conventional group and 6/26 babies in the sustained lung inflation group. Survival without BPD occurred in 13/26 and 14/26 respectively.
Conclusion:
The use of sustained lung inflation at resuscitation did not reduce lung injury, as measured by inflammatory markers.
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