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Published on: March 6, 2019
Bronchopulmonary Dysplasia in the First Year: Insights Into Severity, Medication Use, and Healthcare Utilization
Eliaz Brumer1,2, Veronika Shabanova2,3, Haley Urbach2
1Department of Pediatrics, Section of Pulmonary, Allergy-Immunology, and Sleep Medicine, Yale University, New Haven, Connecticut, USA.
Insights
Infants with bronchopulmonary dysplasia (BPD) face significant respiratory issues and healthcare needs post-discharge, increasing with disease severity. Structured follow-up is crucial for all BPD patients, regardless of severity, to manage respiratory morbidity.
Area of Science:
- Neonatal Medicine
- Pediatric Pulmonology
- Respiratory Medicine
Background:
- Bronchopulmonary dysplasia (BPD) is a prevalent chronic lung disease in premature infants.
- Understanding BPD severity's impact on respiratory outcomes and healthcare use is critical for optimizing care.
- The role of NICU interventions like dexamethasone and post-NICU follow-up requires further characterization.
Purpose of the Study:
- To examine the association between BPD severity and post-NICU respiratory outcomes and healthcare utilization.
- To evaluate the impact of outpatient pediatric pulmonology follow-up on respiratory morbidity.
- To assess the influence of dexamethasone administration during NICU stay on postdischarge respiratory health.
Main Methods:
- Retrospective cohort study of 161 infants diagnosed with BPD (2021-2023) using the 2019 severity classification.
- Key outcomes assessed: medication prescriptions (albuterol, inhaled/systemic steroids), ED visits, and hospital admissions within one year post-NICU discharge.
- Analysis of dexamethasone use, pulmonology follow-up, and respiratory morbidity associations.
Main Results:
- BPD severity distribution: 32.9% grade-1, 59.0% grade-2, 8.1% grade-3.
- Dexamethasone use and pulmonology follow-up rates increased with BPD severity (p<0.001).
- Nearly half (47.2%) experienced postdischarge respiratory hospital visits; 22.3% were hospitalized.
Conclusions:
- Respiratory morbidity and healthcare utilization in infants with BPD increase with disease severity.
- A significant burden of respiratory hospital visits exists across all BPD severity levels, including milder cases.
- Structured longitudinal follow-up is essential for all infants with BPD to mitigate respiratory morbidity.
Background And Objectives:
Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting premature infants. This study aimed to (1) examine associations between BPD severity and respiratory outcomes and healthcare utilization; (2) evaluate the impact of outpatient pediatric pulmonology follow-up; and (3) assess whether dexamethasone administration during NICU stay influences postdischarge respiratory morbidity.
Methods:
This retrospective cohort study included 161 infants diagnosed with BPD (2021-2023) using the 2019 BPD severity classification. Key outcomes included the prevalence of prescriptions for albuterol, inhaled corticosteroid, and systemic steroids, as well as ED visits and admission within the first-year postdischarge. The study analyzed associations between dexamethasone use during NICU admission, outpatient pulmonology follow-ups, and respiratory morbidity.
Results:
Of 161 infants, 32.9% had grade-1, 59.0% grade-2, and 8.1% grade-3 BPD. Dexamethasone administration during NICU admission increased with BPD severity (p < 0.001). Pediatric pulmonology follow-up was common in grade-2 (77.9%) and grade-3 (84.6%) but lower in grade-1 (47.2%, p < 0.001). Use of inhaled medications and systemic steroids varied significantly by severity. Nearly half of the cohort (47.2%) had a hospital visit for respiratory issues postdischarge, and 22.3% required hospitalization.
Conclusion:
This study characterizes respiratory outcomes and healthcare utilization in infants with BPD during the first-year post-NICU discharge. While morbidity and healthcare utilization increased with BPD severity, nearly half of the entire cohort required hospital visits, underscoring a significant disease burden even among infants with milder disease. These findings highlight the importance of structured longitudinal follow-up across all BPD severity levels.
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