Evidence map›Paper›PMID 39242941›Full record

ArticlePediatric research2025

Health-related quality of life at 5 years of age for children born very preterm with congenital anomalies: a multi-national cohort study.

Sung Wook Kim, Xiaoyu Tian, Lazaros Andronis, Rolf F Maier, Heili Varendi, Anna-Veera Seppänen, Veronica Siljehav, Elizabeth S Draper, Jennifer Zeitlin, Stavros Petrou and 1 more

Abstract readMulticenter 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 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

11 authors.

Sung Wook KimNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK. sungwook.kim@phc.ox.ac.uk.ORCID 0000-0002-1254-5038
Xiaoyu TianKleijnen Systematic Reviews Ltd, York, UK.
Lazaros AndronisWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, UK.
Rolf F MaierChildren's Hospital, Philipps University of Marburg, Marburg, Germany.
Heili VarendiTartu University Hospital, University of Tartu, Tartu, Estonia.
Anna-Veera SeppänenUniversité Paris Cité, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Obstetrical Perinatal and Pediatric Epidemiology Research Team, EPOPé, Paris, France.
Veronica SiljehavDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Elizabeth S DraperDepartment of Population Health Sciences, University of Leicester, Leicester, UK.
Jennifer ZeitlinUniversité Paris Cité, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Obstetrical Perinatal and Pediatric Epidemiology Research Team, EPOPé, Paris, France.
Stavros PetrouNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
SHIPS Research Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to investigate the health-related quality of life (HRQoL) at 5 years of age of European children born very preterm across multi-dimensional outcomes by presence and severity of congenital anomalies.

methodsThe study used data from a European cohort of children born very preterm (<32 weeks of gestation) and followed up to 5 years of age (N = 3493). Multilevel Ordinary Least Squares (OLS) regression were used to explore the associations between the presence and severity of congenital anomalies.

resultsThe mean total PedsQL™ GCS score for children with a mild congenital anomaly was lower than the respective value for children without a congenital anomaly by 3.7 points (p < 0.05), controlling for socioeconomic variables only; this effect was attenuated when accumulatively adjusting for perinatal characteristics (3.3 points (p < 0.05)) and neonatal morbidities (3.1 (p < 0.05)). The mean total PedsQL™ GCS scores for children who had a severe congenital anomaly were lower by 7.1 points (p < 0.001), 6.6 points (p < 0.001) and 6.0 points (p < 0.001) when accumulatively adjusting for socioeconomic, perinatal and neonatal variables, respectively.

conclusionThis study revealed that the presence and severity of congenital anomalies are significant predictors of HRQoL outcomes in children born very preterm. IMPACT: Children born very preterm with congenital anomalies experience poorer health-related quality of life (HRQoL) than their very preterm counterparts born without congenital anomalies. Increased severity of these anomalies compounds the negative impacts on HRQoL. Our findings can be used by stakeholders for clinical and planning purposes.

Indexed as

Congenital AbnormalitiesInfant, Extremely PrematureQuality of LifeChild, PreschoolCohort StudiesEuropeFemaleGestational AgeHumansInfant, NewbornMaleSeverity of Illness IndexSocioeconomic Factors

Identifiers

PMID39242941
PMCPMC12119361

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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.