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Updated: Sep 8, 2025

Hemodynamic Precision in the Neonatal Intensive Care Unit using Targeted Neonatal Echocardiography
Published on: January 27, 2023
Screening for pulmonary hypertension in preterm infants with bronchopulmonary dysplasia: when, how often and does it
Samuel J Gentle1,2, Waldemar A Carlo3, Namasivayam Ambalavanan3
1Department of Pediatrics, The University of Alabama at Birmingham, Birmingham, Alabama, USA samuel.gentle@yale.edu.
Insights
Serial echocardiography screening for bronchopulmonary dysplasia (BPD) associated pulmonary hypertension (BPD-PH) improves detection, especially after 36 weeks postmenstrual age. Monthly screening offers the highest negative predictive value for identifying BPD-PH in at-risk infants.
Area of Science:
- Neonatal Medicine
- Pediatric Cardiology
- Respiratory Medicine
Background:
- Bronchopulmonary dysplasia (BPD) associated pulmonary hypertension (BPD-PH) represents a severe BPD subtype.
- Optimal screening strategies for BPD-PH in at-risk infants remain undefined.
- Early detection of BPD-PH is crucial for timely intervention and improved outcomes.
Purpose of the Study:
- To evaluate the effectiveness of serial echocardiography for BPD-PH screening in infants.
- To determine the optimal timing and frequency of echocardiographic screening for BPD-PH.
- To assess the negative predictive value (NPV) of echocardiography beyond 36 weeks' postmenstrual age (PMA).
Main Methods:
- A single-center cohort study analyzed 2542 echocardiograms from 394 infants (2017-2023).
- Infants with BPD-PH had prior echocardiograms classified as false negatives; infants with BPD alone had true negatives.
- Four screening strategies were compared for their ability to detect BPD-PH.
Main Results:
- The highest NPVs were achieved with monthly echocardiographic screening starting at 36 weeks' PMA until discharge.
- Detection rates for BPD-PH varied by screening strategy: comprehensive (34.5%), early (20.0%), singular (15.0%), and late (30.7%).
- Diagnostic accuracy of echocardiographic screening improved at and beyond 36 weeks' PMA.
Conclusions:
- Serial echocardiography, particularly from 36 weeks' PMA onwards, enhances BPD-PH detection.
- A singular echocardiogram is insufficient for screening BPD-PH in high-risk infants.
- Monthly screening post-36 weeks' PMA appears to be the most effective strategy for identifying BPD-PH.
Objective:
Bronchopulmonary dysplasia (BPD) associated pulmonary hypertension (BPD-PH) is the most severe endotype of BPD; there is insufficient evidence to support the optimal screening strategy in at-risk infants. We hypothesised that serial echocardiography throughout hospitalisation would improve PH detection with increased negative predictive value (NPV) beyond 36 week's postmenstrual age (PMA).
Study Design:
This was a single centre cohort study conducted between 2017 and 2023. In infants with BPD-PH, all echocardiograms preceding a diagnostic echocardiogram were included and considered false negatives for prediction of later PH. In infants with BPD alone, all echocardiograms were included and were considered true negatives. These indices were then used to estimate the sensitivity and NPV of echocardiographic screening for PH. In addition, we compared the performance of four different potential echocardiographic screening approaches on the ability to identify infants with BPD-PH.
Results:
Data from 394 infants were available for this analysis of whom 258 had BPD alone and 136 had BPD-PH. 2542 echocardiograms were used in estimates of diagnostic accuracy. The highest NPVs occurred with echocardiographic screening starting at 36 weeks' and continuing monthly until discharge. Detection of BPD-PH among infants with BPD differed by screening strategy: 34.5% for comprehensive screening, 20.0% for early screening, 15.0% for singular screening and 30.7% for late screening (p<0.05).
Conclusions:
While the diagnostic accuracy of echocardiographic screening increases at and beyond 36 weeks' PMA, obtaining a singular echocardiogram may be an insufficient screening strategy for the detection of BPD-PH in at-risk infants.
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