Evidence map›Paper›PMID 41874623›Full record

ArticleEuropean radiology2026

Assessing the feasibility of neonatal chest MRI for bronchopulmonary dysplasia using a standard 1.5-Tesla scanner.

Jantine J Wisse, Bernadette B L J Elders, Merlijn Bonte, Piotr A Wielopolski, André A Kroon, Harm A W M Tiddens, Liesbeth Duijts, Mariëlle W H Pijnenburg, Irwin K M Reiss, Pierluigi Ciet

Abstract read
In one paragraph

Article in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jantine J Wisse *Division of Neonatology, Department of Neonatal and Pediatric Intensive Care, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Bernadette B L J Elders *Division of Respiratory Medicine and Allergology, Department of Pediatrics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Merlijn BonteDivision of Respiratory Medicine and Allergology, Department of Pediatrics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Piotr A WielopolskiDepartment of Radiology and Nuclear Medicine, Erasmus Medical Centre-Sophia Children's Hospital, Rotterdam, The Netherlands.
André A KroonDivision of Neonatology, Department of Neonatal and Pediatric Intensive Care, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Harm A W M TiddensDivision of Respiratory Medicine and Allergology, Department of Pediatrics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Liesbeth DuijtsDivision of Neonatology, Department of Neonatal and Pediatric Intensive Care, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Mariëlle W H PijnenburgDivision of Respiratory Medicine and Allergology, Department of Pediatrics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Irwin K M ReissDivision of Neonatology, Department of Neonatal and Pediatric Intensive Care, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Pierluigi CietDepartment of Radiology and Nuclear Medicine, Erasmus Medical Centre-Sophia Children's Hospital, Rotterdam, The Netherlands. p.ciet@erasmusmc.nl.ORCID http://orcid.org/0000-0003-4017-8957

Funding

Stichting Vrienden van het Sophia B17-02-Step2017
6 · The paper itself

Abstract

objectiveAccurate imaging is essential for assessing structural lung abnormalities in children with bronchopulmonary dysplasia (BPD). Chest MRI offers a radiation-free alternative to CT and enables silent scanning. This study aimed to develop and evaluate a chest MRI protocol for BPD using a standard 1.5-Tesla (T) MRI scanner with a dedicated neonatal chest coil. MATERIALS AND

methodsIn this prospective pilot study, infants underwent feed-and-swaddle chest MRI at ~40 weeks postmenstrual age, and chest CT at six months corrected age. The MRI protocol included free-breathing axial T2-weighted (T2-W) fast spin echo (PROPELLER) and axial proton density-weighted (PD-W) gradient zero echo time (ZTE) sequences. Scans were assessed for image quality, and quantified for normal, hypo-/hyperintense lung tissue and bronchopathy. MRI and CT scores were correlated using Pearson's or Spearman's coefficients, based on data distribution.

resultsEight infants participated (seven preterm < 28 weeks' gestation with severe BPD; one term neonate with asphyxia). T2-w PROPELLER provided superior soft tissue contrast and fewer artefacts than ZTE. ZTE enabled silent scanning and better visualisation of hypointense structures. Quantitative scores were comparable between PROPELLER and ZTE sequences. Significant correlations were found between MRI and CT scores for normal and hyperintense lung tissue (p < 0.05; r = 0.84-0.96), but not for hypointense regions and bronchopathy.

conclusionWe developed a feasible and safe chest MRI protocol for imaging severe BPD-related lung abnormalities in neonates using a standard 1.5-T system. While technically promising, MRI is not yet clinically equivalent to CT. Further validation is needed to define its potential role in BPD assessment. KEY POINTS: Question Can a standard 1.5 T chest MRI protocol performed without anaesthesia reliably image lung abnormalities in neonates with BPD? Findings T2-W PROPELLER sequence provided superior image quality and fewer artefacts compared to the ZTE, especially in depicting fissures and bronchi. Clinical relevance Our BPD-MRI protocol enables safe, radiation-free lung imaging in neonates with severe BPD without requiring anaesthesia. It offers a technically feasible alternative to CT and may support early structural assessment before discharge in routine clinical care.

Indexed as

Bronchopulmonary DysplasiaMagnetic Resonance ImagingFeasibility StudiesFemaleHumansInfant, NewbornMalePilot ProjectsProspective StudiesReproducibility of ResultsSensitivity and SpecificityTomography, X-Ray ComputedBronchopulmonary dysplasiaCTImagingMRINeonatology

Identifiers

PMID41874623
PMCPMC13341914

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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.