Evidence map›Paper›PMID 38898108›Full record

Observational studyPediatric research2025

PDA management strategies and pulmonary hypertension in extreme preterm infants with bronchopulmonary dysplasia.

Audrey Hébert, Patrick J McNamara, Gabriela De Carvalho Nunes, Camille Maltais-Bilodeau, Marie-Ève Leclerc, Punnanee Wutthigate, Jessica Simoneau, Christine Drolet, Gabriel Altit

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Audrey HébertDivision of Neonatology, CHU de Québec, Université Laval, Quebec City, QC, Canada. audrey.hebert.2@ulaval.ca.
Patrick J McNamaraDivision of Neonatology, University of Iowa Children's Hospital, University of Iowa, Iowa city, IA, USA.
Gabriela De Carvalho NunesDivision of Neonatology, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Camille Maltais-BilodeauDivision of Neonatology, CHU de Québec, Université Laval, Quebec City, QC, Canada.
Marie-Ève LeclercDivision of Neonatology, CHU de Québec, Université Laval, Quebec City, QC, Canada.
Punnanee WutthigateDivision of Neonatology, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Jessica SimoneauDivision of Neonatology, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Christine DroletDivision of Neonatology, CHU de Québec, Université Laval, Quebec City, QC, Canada.
Gabriel AltitDivision of Neonatology, McGill University Health Centre, McGill University, Montreal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPremature infants are at risk for developing pulmonary hypertension (PH) in the context of bronchopulmonary dysplasia (BPD). Studies suggest a potential link between prolonged patent ductus arteriosus (PDA) exposure and BPD-PH, though management strategies remain controversial.

methodsRetrospective echocardiographic evaluation of newborns <29 weeks gestational age with BPD at two distinct centers. Primary objective was to evaluate the relationship between center-specific PDA management strategies (interventional or conservative) and the prevalence of BPD-PH. BPD was defined as oxygen or respiratory support at 36 weeks post-menstrual age (PMA). The presence of PH was defined as either an estimated sPAP of ≥40 mmHg or sEI ≥1.3. Center A has a conservative PDA policy. Center B has a targeted interventional policy.

resultsPH rates were similar between sites (21% vs 17%), while rates of PDA treatment was different (7% vs 81). Adjusted models did not demonstrate an association for center or PDA treatment exposure for PH and EI, although infants from Center A had echocardiography evidence of higher systolic eccentricity index (EI; 1.12 ± 0.19 vs 1.06 ± 0.15, p = 0.04). Markers of RV function (TAPSE and RV-FAC) were similar between groups.

conclusionIn preterm infants <29 weeks with BPD, conservative PDA treatment policy was not associated with higher rate of pulmonary hypertension diagnosis. IMPACT: The association between PDA-management approaches and the occurrence of BPD-associated pulmonary vascular disease in premature infants has sparsely been described. We found that a conservative policy, regarding the PDA, was not associated with an increase in pulmonary hypertension diagnosis. We identified that, in patients with BPD, echocardiographic metrics of LV performance were lower.

Indexed as

Bronchopulmonary DysplasiaDuctus Arteriosus, PatentHypertension, PulmonaryInfant, Extremely PrematureEchocardiographyFemaleGestational AgeHumansInfant, NewbornInfant, PrematureMalePrevalenceRetrospective StudiesRisk Factors

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.