Evidence map›Paper›PMID 41704041›Full record

ArticlePediatric pulmonology2026

Peri and Neonatal Risk Factors and Structural Lung Abnormalities Predict Hypoxic Challenge Test Failure in Infants With Severe Bronchopulmonary Dysplasia.

Kishan D Tsang, Daan Caudri, Citta Zaat, Gerdien A Tramper-Stranders, Isme M de Kleer, Pierluigi Ciet, Irwin K M Reiss, Liesbeth Duijts, Mariëlle W Pijnenburg

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Kishan D TsangDepartment of Pediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC Sophia Children's Hospital University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-1546-0638
Daan CaudriDepartment of Pediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC Sophia Children's Hospital University Medical Center, Rotterdam, the Netherlands.
Citta ZaatDepartment of Pediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC Sophia Children's Hospital University Medical Center, Rotterdam, the Netherlands.
Gerdien A Tramper-StrandersDepartment of Pediatrics, Franciscus Gasthuis & Vlietland, Rotterdam, the Netherlands.
Isme M de KleerDepartment of Pediatrics, Franciscus Gasthuis & Vlietland, Rotterdam, the Netherlands.
Pierluigi CietDepartment of Pediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC Sophia Children's Hospital University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0003-4017-8957
Irwin K M ReissDepartment of Neonatology and Pediatric Intensive Care Medicine, University Children's Hospital, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Liesbeth DuijtsDepartment of Pediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC Sophia Children's Hospital University Medical Center, Rotterdam, the Netherlands.
Mariëlle W PijnenburgDepartment of Pediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC Sophia Children's Hospital University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0003-0902-0860

Funding

European Union's Horizon 2020 research and innovation program 101136566European Union's Horizon 2020 research and innovation program 874583rasmus MC Sophia Foundation
6 · The paper itself

Abstract

introductionInfants with severe bronchopulmonary dysplasia (BPD) are at increased risk of hypoxemia and often fail hypoxic challenge testing (HCT). The predictive value of clinical characteristics and structural lung abnormalities on HCT outcomes is unclear.

methodsThis prospective cohort study included preterm-born infants (≤ 32 weeks of gestation) with severe BPD enrolled in a standardized follow-up program. Perinatal and neonatal data were extracted from medical records. At 6 months corrected gestational age, structural lung abnormalities were quantified on chest CT using PRAGMA-BPD scoring. HCT was performed using a sealed body plethysmograph and failure was defined as inability to maintain oxygen saturation ≥ 85% for 20 min. Univariate and multivariable logistic regression analyses identified predictors of HCT failure.

resultsAmong 156 infants, 28.8% failed HCT. Of the perinatal and neonatal factors, patent ductus arteriosus (odds ratio 2.73, 95% confidence interval 1.29-6.14), pulmonary hypertension (2.57, 0.99-6.62), and longer duration of supplemental oxygen therapy (odds ratio per interquartile range increase [OR

conclusionDuration of supplemental oxygen therapy and structural lung abnormalities independently predict HCT failure, highlighting the clinical relevance of both structural and functional impairments in severe BPD.

Indexed as

Bronchopulmonary DysplasiaHypoxiaLungDuctus Arteriosus, PatentFemaleGestational AgeHumansHypertension, PulmonaryInfant, NewbornInfant, PrematureMaleOxygen Inhalation TherapyOxygen SaturationPlethysmographyPredictive Value of TestsProspective Studiesbronchopulmonary dysplasiacomputed tomographyhypoxic challenge testprematurityprematurity associated lung disease

Identifiers

PMID41704041
PMCPMC12914227

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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.