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Published on: October 31, 2025
Atypical chronic lung disease in preterm infants
Jayachandran Panickar1, Helen Scholefield, Yadlapalli Kumar
1Neonatal Intensive Care Unit, Liverpool Women's Hospital, Liverpool, UK.
Insights
Atypical chronic lung disease (CLD) is common in preterm infants, affecting larger, more mature babies. This study found no link between intrauterine inflammation and atypical CLD development.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Perinatal Medicine
Background:
- Chronic lung disease (CLD) is a significant complication in preterm infants.
- An atypical pattern of CLD has been observed, with a proposed link to intrauterine inflammation.
- Understanding CLD patterns and associated perinatal factors is crucial for improving infant respiratory outcomes.
Purpose of the Study:
- To describe patterns of CLD in preterm infants.
- To determine the incidence of atypical CLD.
- To compare perinatal factors in infants with classic versus atypical CLD.
Main Methods:
- Retrospective chart review of neonatal admissions with birthweight <1250 g.
- CLD defined as oxygen dependency at 28 days of age.
- Classification of CLD into classic and atypical patterns based on defined criteria.
Main Results:
- CLD developed in 51% of survivors at 28 days; 41% of these were classified as atypical CLD.
- Factors associated with atypical CLD included being inborn, receiving natural surfactant, fewer mechanical ventilation days, and higher birthweight.
- No significant association was found between atypical CLD and chorioamnionitis, postnatal infection, or symptomatic patent ductus arteriosus (PDA).
Conclusions:
- Atypical CLD is a common presentation of prolonged oxygen dependency in preterm survivors.
- Atypical CLD is associated with larger, more mature infants.
- The findings do not support intrauterine inflammation as a primary etiological factor for atypical CLD.
Abstract:
An atypical pattern of chronic lung disease (CLD) has been described in preterm infants and a potential association with intrauterine inflammation has been proposed. We aimed to describe patterns of CLD, to determine the incidence of atypical CLD, and to compare the distribution of various perinatal factors in infants with classic and atypical CLD. Information about demographics, respiratory status and various perinatal variables was collected for all neonatal admissions <1250 g. CLD was defined as oxygen dependency at 28 days of age. Ninety (51%) survivors at 28 days of age developed CLD; of these 37 (41%) were classified as atypical CLD. Factors significantly and independently associated with development of atypical CLD included being inborn, receiving natural surfactant, fewer days of mechanical ventilation within the first 28 days of life and higher birthweight. Chorioamnionitis, postnatal infection and symptomatic PDA were not found to be significantly associated with atypical CLD. Atypical CLD is a common pattern of prolonged oxygen dependency in preterm survivors and is a feature of larger, more mature babies. Our findings do not support the hypothesis that exposure to intrauterine inflammation is an important aetiological factor in the development of atypical CLD.
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