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Published on: May 4, 2020
Long-term outcomes of infants with severe BPD
Joseph M Collaco1, Sharon A McGrath-Morrow2
1Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University, Baltimore, MD, United States.
Insights
Bronchopulmonary dysplasia (BPD) affects preterm infants due to disrupted lung development and respiratory support. This review examines BPD phenotypes and long-term health outcomes in children.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Developmental Biology
Background:
- Preterm birth significantly alters normal lung development, increasing the risk of bronchopulmonary dysplasia (BPD).
- Interventions like positive pressure ventilation and supplemental oxygen, while necessary, can worsen lung injury in preterm infants.
- Bronchopulmonary dysplasia affects approximately 50,000 US infants annually, presenting with diverse and age-dependent respiratory pathologies.
Approach:
- This review examines common respiratory endotypes in infants and children with severe BPD.
- It analyzes the heterogeneity of BPD phenotypes, including alveolar, airway, and vascular components.
- The influence of gestational age and respiratory support on BPD endotype development is discussed.
Key Points:
- BPD phenotypes are varied and can evolve throughout childhood, impacting different respiratory tract regions.
- Small airway disease is a prevalent phenotype in school-aged children and adolescents with BPD.
- Gestational age and the type/duration of respiratory support are critical factors influencing BPD development.
Conclusions:
- Understanding diverse BPD endotypes is crucial for predicting long-term pulmonary outcomes.
- This review highlights the variability in long-term prognoses for cardiovascular, neurological, and gastrointestinal systems in children with severe BPD.
- Persistent small airway disease is a significant factor in the chronic respiratory health of individuals with a history of severe BPD.
Abstract:
Preterm birth disrupts the normal sequence of lung development. Additionally, interventions that support gas exchange, including positive pressure ventilation and supplemental oxygen can further exacerbate lung injury, increasing the risk of developing bronchopulmonary dysplasia (BPD) in infants born preterm. Approximately 50,000 preterm infants each year in the United States develop BPD. Heterogeneous lung pathology involving the upper and lower respiratory tract can contribute to the BPD phenotype and can be age-dependent. These phenotypes include alveolar, upper airway, large airways, small airways, and vascular. Each of these phenotypes may improve, resolve, or persist at different ages, throughout childhood. The development of BPD endotypes can be influenced by gestational age and length and type of respiratory support. Although, long-term pulmonary outcomes of infants with severe BPD are variable, the presence of small airway disease is a common phenotype in school age and adolescent children. In this review we examine the more common respiratory endotypes found in infants and children with severe BPD and discuss the long-term prognosis for cardiovascular, neurological, and gastrointestinal morbidities in this patient population.
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