Evidence map›Paper›PMID 39900835›Full record

ArticlePediatric research2025

Development and validation of a prediction model for bronchopulmonary dysplasia using respiratory severity score.

Takahiro Kanzawa, Fumie Kinoshita, Fumihiko Namba, Taihei Tanaka, Makoto Oshiro, Takahiro Sugiura, Yuichi Kato, Masafumi Miyata, Yasumasa Yamada, Osuke Iwata and 4 more

Abstract readValidation Study
In one paragraph

Article in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Toward precision for bronchopulmonary dysplasia: Moving past current definitions.Journal of perinatology : official journal of the California Perinatal Association · 2026
    Review
  4. Article
  5. 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

14 authors.

Takahiro KanzawaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Fumie KinoshitaStatistical Analysis Section, Department of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.
Fumihiko NambaDepartment of Pediatrics, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Taihei TanakaDepartment of Neonatology, Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital, Nagoya, Japan.
Makoto OshiroDepartment of Pediatrics, Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital, Nagoya, Japan.
Takahiro SugiuraDepartment of Pediatrics and Neonatology, Toyohashi Municipal Hospital, Toyohashi, Aichi, Japan.
Yuichi KatoDepartment of Pediatrics, Anjo Kosei hospital, Anjo, Aichi, Japan.
Masafumi MiyataDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Yasumasa YamadaDepartment of Perinatal and Neonatal Medicine, Aichi Medical University, Nagakute, Aichi, Japan.
Osuke IwataDepartment of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Masahiro HayakawaMedical Corporation Kishokai, Nagoya, Japan.
Yoshiaki SatoDivision of Neonatology, Center for Maternal-Neonatal Care, Nagoya University Hospital, Nagoya, Japan. y.sato@nagoya-u.jp.ORCID http://orcid.org/0000-0001-6320-9176
BPD Prediction Model Collaborative Clinical Research Team
Neonatal Research Network of Japan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo develop and validate a prediction model for severe bronchopulmonary dysplasia (BPD) that integrates the respiratory severity (RS) score with early postnatal risk factors.

methodsThis retrospective cohort study included preterm infants born at less than 32 weeks gestation or with a birth weight of less than 1500 g, from Aichi Prefecture (training dataset) and Saitama Medical University (validation dataset) from April 1, 2016, to March 31, 2020. The primary outcome was severe BPD, defined as the use of home oxygen therapy or death due to BPD. We used classification and regression tree (CART) analysis to explore the relationship between outcomes and BPD risk factors in the training dataset.

resultsThe incidence of severe BPD was 149 out of 2026 (7.3%) in the training dataset and 35 out of 387 (8.9%) in the validation dataset. CART analysis identified gestational age and the RS score as significant predictors of outcome in the day 7 and day 14 models, with C-statistics of 0.789 and 0.779, respectively. When applied to the validation dataset, these models achieved C-statistics of 0.753 and 0.827, respectively.

conclusionOur prediction models demonstrated the ability to predict severe BPD, with the RS score being a crucial predictor. IMPACT: Many existing prediction models for bronchopulmonary dysplasia (BPD) use multiple predictors, and do not provide specific cutoff values, which complicates their clinical application. To address this issue, we developed a prediction model for severe BPD based on a score derived from mean airway pressure and inhaled oxygen concentration at 1-2 weeks of age. This user-friendly model can be easily integrated into clinical practice, facilitating treatment decisions based on predicted probabilities.

Indexed as

Bronchopulmonary DysplasiaFemaleGestational AgeHumansIncidenceInfant, NewbornInfant, PrematureJapanMaleOxygen Inhalation TherapyReproducibility of ResultsRetrospective StudiesRisk FactorsSeverity of Illness Index

Identifiers

PMID39900835
PMCPMC12454154

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