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Updated: May 24, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
Bronchopulmonary dysplasia: then and now
1Division of Neonatal and Developmental Medicine, Stanford University School of Medicine, Palo Alto, CA 94304, USA. aphilip@stanford.edu
Insights
Bronchopulmonary dysplasia (BPD) has evolved from
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Respiratory Physiology
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease in premature infants.
- Historically, BPD was linked to oxygen toxicity and mechanical ventilation.
- The definition and characteristics of BPD have shifted over time.
Purpose of the Study:
- To describe the evolution of bronchopulmonary dysplasia (BPD) from 'classical' to 'new' BPD.
- To outline the changing etiologies and pathological features of BPD.
- To discuss potential preventative and therapeutic strategies for BPD.
Main Methods:
- Literature review of historical and current BPD research.
- Comparison of pathological and radiographic findings in 'classical' versus 'new' BPD.
- Analysis of factors contributing to BPD development.
Main Results:
- 'Classical' BPD, seen in more mature infants, featured lung cysts and fibrosis.
- 'New' BPD, prevalent in extremely preterm infants, shows arrested lung development.
- The definition of BPD has shifted to oxygen requirement at 36 weeks postmenstrual age.
Conclusions:
- BPD has transformed due to advances in neonatal care and surfactant therapy.
- Understanding the distinct features of 'new' BPD is crucial for management.
- Further research into preventative and therapeutic strategies is warranted.
Abstract:
When bronchopulmonary dysplasia (BPD) was first described in 1967, the use of assisted ventilation in neonates was in its infancy. High concentrations of oxygen were implicated, and BPD was equated with 'pulmonary oxygen toxicity'. The etiologic role of not only oxygen but also peak inspiratory pressures and the duration of exposure to both was emphasized in the 1970s, but BPD remained a dreaded complication of managing respiratory distress syndrome in the 1980s. It was only after exogenous surfactant became commercially available for endotracheal administration that 'classical' BPD began to disappear and was replaced by the 'new' BPD. 'Classical' BPD was seen in more mature preterm infants (>28 weeks' gestational age) and in its severe form was characterized radiographically by micro- and macrocysts of the lung, lung hyperinflation and flattening of the diaphragms. In contrast, 'new' BPD is seen in less mature infants (<28 weeks' gestational age), has comparatively mild radiographic abnormalities and has been defined as continued oxygen requirement at 36 weeks' postmenstrual age. Pathologically, 'classical' BPD frequently revealed obstructive bronchiolitis and fibrosis of lung parenchyma, whereas 'new' BPD demonstrates minimal fibrosis but uniform arrest of development. Herein, factors which may contribute to the etiology of BPD are described, as well as possible preventative and therapeutic strategies.
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Assessment