Evidence map›Paper›PMID 42723840›Full record

ArticleFrontiers in pediatrics2026

Gestational age-dependent risk patterns in small for gestational age preterm infants: a large multivariable cohort study.

Josep Figueras-Aloy, Xavier Carbonell-Estrany, Francesc Botet-Mussons, Óscar García-Algar, Martí Iriondo-Sanz, Giorgia Sebastiani

Abstract read
In one paragraph

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

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

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

6 authors.

Josep Figueras-AloyNeonatology Department, Center for Maternal-Fetal and Neonatal Medicine (BCNatal), Hospital Clínic and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Xavier Carbonell-EstranyNeonatology Department, Center for Maternal-Fetal and Neonatal Medicine (BCNatal), Hospital Clínic and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Francesc Botet-MussonsNeonatology Department, Center for Maternal-Fetal and Neonatal Medicine (BCNatal), Hospital Clínic and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Óscar García-AlgarNeonatology Department, Center for Maternal-Fetal and Neonatal Medicine (BCNatal), Hospital Clínic and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Martí Iriondo-SanzNeonatology Department, Center for Maternal-Fetal and Neonatal Medicine (BCNatal), Hospital Clínic and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Giorgia SebastianiNeonatology Department, Center for Maternal-Fetal and Neonatal Medicine (BCNatal), Hospital Clínic and Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Small for gestational age (SGA) preterm infants remain at high risk for morbidity and mortality, yet the influence of gestational age (GA) on these outcomes is not fully understood. Methods: The influence of gestational age on morbidity and mortality in SGA preterm infants (23-34 weeks) was analyzed in a cohort of 11,208 preterm infants. Infants were divided into three groups according to gestational age (23-27 weeks, 28-31 weeks, and 32-34 weeks). Results: Compared with non-SGA infants of the same gestational age group, SGA infants showed higher rates of fetal distress and Apgar score ≤5 at any gestational age. Hyaline membrane disease increased between 23 and 27 weeks but decreased between 32 and 34 weeks, whereas intraventricular hemorrhage showed the opposite trend. Pneumothorax and periventricular leukomalacia increased mainly between 23 and 27 weeks, while necrotizing enterocolitis, sepsis, and gastrointestinal perforation increased between 28 and 31 weeks. Mortality was higher between 23 and 31 weeks. In survivors, moderate-severe bronchopulmonary dysplasia increased between 23 and 31 weeks, and retinopathy of prematurity increased after 28 weeks. Gestational age appeared to modify the associations between SGA status and selected neonatal outcomes, including hyaline membrane disease, intraventricular hemorrhage, and mortality. Conclusions: Gestational age may influence the pattern of associated morbidities among SGA preterm infants born at 23 to 34 weeks of gestation. In these newborns, the risk of mortality was increased 3.13-fold.

Indexed as

fetal growth restrictionneonatal morbidityneonatal mortalityprematuritysmall for gestational age

Identifiers

PMID42723840
PMCPMC13558139

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.