Evidence map›Paper›PMID 41217383›Full record

ArticlePediatric pulmonology2025

Lower Respiratory Tract Bacterial Profiles Are Associated With Respiratory Severity and Bronchopulmonary Dysplasia in Neonates.

Jelte Kelchtermans, Pelton Phinizy, Joseph Piccione, Sharon A McGrath-Morrow

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2025. 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

4 authors.

Jelte KelchtermansChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0001-9186-7547
Pelton PhinizyChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Joseph PiccioneChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Sharon A McGrath-MorrowChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-1576-5394

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Clinical and Biochemical Features of Metabolic Dysregulation in Formerly Preterm ChildrenR01HL169859 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Eric Douglas Austin, Joseph Michael Collaco · 2024 to 2026
$2.2M
Critical Life Event supplement to 'Air pollution sensitivity in pediatric asthma'K08HL173625 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Jelte Kelchtermans · 2025 to 2026
$317k
NHLBI NIH HHS K08 HL173625NHLBI NIH HHS R01 HL169859NIEHS NIH HHS P30 ES013508This study was supported by the Parker B. Francis Fellowship Program. The study was funded by an Institute Development Fund and a K-readiness pilot grant from The Children's Hospital of Philadelphia. Research reported in this publication was supported by the National Institute of Environmental Health Sciences of the National Institutes of Health under grant number P30ES013508 and by the National Heart, Lung, and Blood Institute under grant number R01HL169859 and K08HL173625. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
6 · The paper itself

Abstract

introductionBronchopulmonary dysplasia (BPD) is a major complication of prematurity, marked by heterogeneous pulmonary phenotypes and variable clinical outcomes. The airway microbiome may influence disease severity and progression, yet quantitative associations between airway pathogens and clinically relevant outcomes remain poorly understood.

methodsWe conducted a retrospective analysis of 204 neonates who underwent flexible bronchoscopy with quantitative bronchoalveolar lavage (BAL) cultures in the NICU at the Children's Hospital of Philadelphia. Cultures yielding ≥ 10,000 colony-forming units per milliliter for a single bacterial species were classified as positive. Respiratory severity score (RSS), calculated as the product of mean airway pressure and fraction of inspired oxygen, served as the primary indicator of respiratory status. Linear, logistic, and negative binomial regression models were used to assess associations between bacterial species and clinical outcomes, adjusted for sex and race, with standard errors clustered at the patient level.

resultsNo bacterial species were significantly associated with RSS after correction for multiple testing. Klebsiella pneumoniae was associated with a diagnosis of BPD (adjusted p = 0.026), but no organisms were significantly associated with prolonged time to extubation. In secondary analyses, the presence of several organisms was significantly associated with higher MAP, including K. pneumoniae (β = 2.66, FDR-adjusted p = 0.014).

conclusionsMultiple bacterial species identified on quantitative BAL culture were associated with higher mean airway pressure, and K. pneumoniae was additionally associated with BPD diagnosis. These findings support the potential utility of quantitative microbiologic data in risk stratification and management of neonatal respiratory disease.

Indexed as

Bronchopulmonary DysplasiaBronchoalveolar Lavage FluidBronchoscopyFemaleHumansInfant, NewbornInfant, PrematureIntensive Care Units, NeonatalKlebsiella pneumoniaeMaleMicrobiotaRetrospective StudiesSeverity of Illness IndexbronchoscopyKlebsiella pneumoniaemicrobiologyprematurity

Identifiers

PMID41217383
PMCPMC12617032

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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.