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Published on: October 31, 2025
Bronchopulmonary dysplasia associated pulmonary hypertension: implications across the lifespan
Taylor P Saley1, Natalie Villafranco2, Megan Griffiths3
1The University of Texas at Austin Dell Medical School, 4910 Mueller Blvd. Suite 100A, Austin, TX 78723, USA.
Insights
Bronchopulmonary dysplasia with pulmonary hypertension (BPD-PH) can resolve in infancy but may persist lifelong. Early intervention optimizes vascular growth, but lifelong monitoring is crucial for survivors of preterm birth.
Area of Science:
- Neonatology
- Pulmonology
- Pediatric Cardiology
Background:
- Bronchopulmonary dysplasia (BPD) is a common complication of preterm birth, frequently leading to pulmonary hypertension (BPD-PH).
- BPD-PH presents with underdeveloped pulmonary vasculature and altered microvascular function, contributing to significant infant morbidity and mortality.
- Improved neonatal care increases survival rates, with a trend towards BPD-PH resolution through respiratory support and growth.
Purpose of the Study:
- To review the lifelong care of patients with BPD-PH.
- To highlight critical windows of opportunity for intervention across the lifespan.
- To emphasize strategies for reducing lifetime pulmonary hypertension exposure.
Main Methods:
- Literature review of BPD-PH natural history and management.
- Analysis of hemodynamic phenotypes and vascular development.
- Examination of long-term outcomes in preterm survivors.
Main Results:
- While BPD-PH may resolve in infancy, long-term follow-up reveals persistent or recurrent pulmonary hypertension into adulthood.
- The pulmonary vasculature undergoes development, growth, and aging, with each stage presenting unique risks for BPD-PH.
- Early recognition and intervention are key to optimizing vascular growth potential.
Conclusions:
- The concept of BPD-PH "resolution" requires reevaluation due to lifelong vascular risks.
- Lifespan care strategies are essential to manage BPD-PH and mitigate long-term pulmonary hypertension burden.
- Targeting developmental windows can reduce lifetime pulmonary hypertension exposure in BPD survivors.
Abstract:
Bronchopulmonary dysplasia is a frequent complication of preterm birth and is often associated with the development of pulmonary hypertension (BPD-PH). BPD-PH is a multifactorial disease with variable hemodynamic phenotypes typically characterized by underdeveloped pulmonary vascular networks with altered microvascular function, carrying significant morbidity and mortality in infancy. Advances in neonatal care have improved the survival of preterm infants. Amongst survivors, there is a trend toward resolution of BPD-PH with adequate respiratory support and somatic growth, highlighting the importance of early recognition and intervention to optimize vascular growth potential. However, as this population ages the idea of "resolution" has been brought into question. There is increasing awareness of subclinical or recurrent pulmonary hypertension as survivors of prematurity from childhood through early adulthood suggesting that the vasculature remains at risk throughout life. The natural history of pulmonary vasculature is one of development, growth and aging. Each window presents unique opportunities and potential insults that impact overall BPD-PHseverity and progression. Here we review care of the BPD-PH patient across the lifespan highlighting windows of opportunity to reduce lifetime exposure to pulmonary hypertension.
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