Evidence map›Paper›PMID 41565004›Full record

ArticleThe Journal of pediatrics2026

Time-Series Machine Learning for Prediction of Bronchopulmonary Dysplasia.

Divya Chhabra, Jingyang Lin, Jinsheng Pan, Irina Prelipcean, Igor Khodak, Colby L Day, Jack Chang, Xing Qiu, Jiebo Luo, Andrew M Dylag

Abstract read
In one paragraph

Article in The Journal of pediatrics, 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

10 authors.

Divya ChhabraDepartment of Pediatrics, University of Rochester, Rochester, NY.
Jingyang LinDepartment of Computer Science, University of Rochester, Rochester, NY.
Jinsheng PanDepartment of Computer Science, University of Rochester, Rochester, NY.
Irina PrelipceanDepartment of Pediatrics, University of Rochester, Rochester, NY.
Igor KhodakDepartment of Pediatrics, University of Rochester, Rochester, NY.
Colby L DayDepartment of Pediatrics, University of Rochester, Rochester, NY.
Jack ChangClinical & Translational Science Institute, University of Rochester, Rochester, NY.
Xing QiuDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY.
Jiebo LuoDepartment of Computer Science, University of Rochester, Rochester, NY.
Andrew M DylagDepartment of Pediatrics, University of Rochester, Rochester, NY. Electronic address: andrew_dylag@urmc.rochester.edu.

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
The Role of Lung Megakaryocytes in Airway Disease after Neonatal HyperoxiaK08HL155491 · NHLBI · UNIVERSITY OF ROCHESTER · PI Andrew Michael Dylag · 2022 to 2026
$811k
NCATS NIH HHS UL1 TR002001NHLBI NIH HHS K08 HL155491
6 · The paper itself

Abstract

objectiveTo build a time-series machine learning (ML) model that improves bronchopulmonary dysplasia (BPD) prediction compared with published online calculators. STUDY

designWe used a single-center, extremely low gestational age newborn cohort (inborn, birth year 2016-2021, n = 438). The primary outcome was a 5-level class outcome for BPD as defined by the Neonatal Research Network (NRN) in 2019. Flowsheet data were extracted from the electronic medical record. Time-series data were generated from birth onward, with 14 static and 35 dynamic input attributes. Iterative static (regression) and dynamic (ML) modeling was performed, comparing model performance with the NRN BPD calculator at several time points (postnatal day 1, 3, 7, 14, and 28) and ranking feature leverage at each time point.

resultsOf the original cohort, 92 infants met all inclusion criteria (gestational age 25.6 ± 1.4 weeks). Static models performed comparably with the NRN BPD calculator (area under the curve = 0.7460), improving to 0.7978 with forward/backward selection. In contrast, dynamic long short-term memory (LSTM) models outperformed static models at all time points, reaching a peak area under the curve of 0.8400 on postnatal day 28. LSTM models performed best for no BPD and severe disease/death. Principal component analysis revealed that respiratory support, ventilator settings, supplemental oxygen requirements, medications, and prenatal/postnatal growth were major factors driving BPD severity.

conclusionsLSTM-based ML time-series analysis substantially outperformed static approaches for predicting BPD and death among extremely low gestational age newborns. Integrating ML methods into clinical applications holds promise for enhancing real-time BPD trajectory mapping.

Indexed as

Bronchopulmonary DysplasiaMachine LearningFemaleGestational AgeHumansInfant, Extremely PrematureInfant, NewbornLong Short Term MemoryMalePrediction AlgorithmsPredictive Learning ModelsTime Factorsartificial intelligencebronchopulmonary dysplasiamachine learning

Identifiers

PMID41565004
PMCPMC12833681

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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.