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Published on: October 31, 2025
Bronchopulmonary dysplasia and extremely preterm birth: time for a broader perspective on long-term outcomes
Luca Bonadies1,2,3, Lorenzo Zanetto1,2,3, Valentina Agnese Ferraro2,4
1Neonatal Intensive Care Unit, Department of Women's and Children's Health, University Hospital of Padova, Padova, Italy.
Insights
Bronchopulmonary dysplasia, a complication of prematurity, impacts multiple organ systems long after birth. Early airflow limitation and cardiovascular issues are common, requiring integrated, multidisciplinary follow-up for preterm survivors.
Area of Science:
- Pulmonary Medicine
- Neonatology
- Developmental Pediatrics
Background:
- Bronchopulmonary dysplasia (BPD) is a primary respiratory complication in very preterm infants.
- Its effects extend beyond the neonatal period, influencing long-term health trajectories.
- Preterm survivors often exhibit airflow limitation, cardiovascular vulnerability, and multisystemic issues.
Purpose of the Study:
- To highlight the multisystemic impact of bronchopulmonary dysplasia beyond the neonatal period.
- To emphasize the need for integrated, multidisciplinary follow-up for preterm survivors.
- To underscore the distinct pathobiology of BPD compared to common respiratory conditions like asthma.
Main Methods:
- Review of existing literature on the long-term outcomes of prematurity and BPD.
- Analysis of pathobiological mechanisms including arrested alveolar/vascular growth, inflammation, and oxidative stress.
- Examination of extrapulmonary involvement in cardiovascular, neurodevelopmental, renal, and metabolic domains.
Main Results:
- Preterm individuals show divergent developmental trajectories with early airflow limitation and increased cardiovascular risk.
- Distinct pathobiological mechanisms, not typical asthma, underlie BPD's respiratory impact.
- Extrapulmonary involvement significantly shapes long-term outcomes and necessitates systematic monitoring.
Conclusions:
- Current follow-up programs are insufficient for the diverse needs of preterm survivors.
- Increased healthcare professional awareness of long-term prematurity implications is crucial.
- Future research and integrated clinical pathways are needed to optimize outcomes for survivors of prematurity.
Abstract:
Bronchopulmonary dysplasia is a hallmark respiratory complication of prematurity and remains a major health determinant of individuals born very preterm. Its impact, however, extends far beyond the neonatal period and far beyond the lungs. Children, adolescents and adults born very preterm often follow diverse developmental trajectories that diverge from typical postnatal growth. These trajectories often display early airflow limitation, as well as features of increased cardiovascular vulnerability and altered multisystemic profiles. Although common respiratory labels such as asthma are often applied to these patients, evidence highlights distinct pathobiological mechanisms rooted in arrested alveolar and vascular growth, with a possible contribution from persistent airway inflammation and oxidative stress. Extrapulmonary involvement, including cardiovascular, neurodevelopmental, neurosensory, renal and metabolic domains, further shapes long-term outcomes and should be systematically integrated into long-term monitoring. Yet, despite improving survival and growing recognition of this multisystemic burden, current evidence remains insufficient to design a dedicated, holistic, multidisciplinary follow-up programme tailored to the diverse subgroups of preterm-born individuals. Increasing awareness among healthcare professionals of the long-term implications of prematurity is essential to ensure that these patients receive appropriate and coordinated attention. Emerging lines of research, spanning new preventive and therapeutic options, advanced imaging, mechanistic studies, and long-term cohort designs, hold promise in elucidating the biological determinants of disease. Integrating these insights into clinical pathways, together with sustained implementation of family-centred care models, will be crucial to optimise organ function trajectories, delay deterioration and ultimately improve the quality of life of the growing population of survivors of prematurity.
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