Evidence map›Paper›PMID 41657450›Full record

ArticleTranslational pediatrics2026

Proxy-reported health-related quality of life in children with omphalocele: a cross-sectional study in China.

Peng Wang, Hanqi Jin, Lejing Guan, Meiying Gao, Yifei Shao, Abdullah Faizan, Lidan Sun, Tianxin Pan, Jinfa Tou, Guannan Bai

Abstract read
In one paragraph

Article in Translational pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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.

Peng Wang *Department of Neonatal Surgery, Children's Hospital, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Hanqi Jin *Department of Neonatal Surgery, Children's Hospital, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Lejing GuanDepartment of Child Health Care, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Meiying GaoDepartment of Child Health Care, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Yifei ShaoDepartment of Child Health Care, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Abdullah FaizanCollege of Medicine, Xi'an Jiaotong University, Xi'an, China.
Lidan SunDepartment of Child Health Care, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Tianxin PanChild Health Economics Unit, Centre for Health Policy, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Australia.
Jinfa Tou *Department of Neonatal Surgery, Children's Hospital, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.
Guannan Bai *Department of Child Health Care, Zhejiang University School of Medicine, National Children's Regional Medical Center, National Clinical Research Center For Children And Adolescents' Health And Diseases, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Omphalocele is a congenital anomaly requiring complex treatment. Existing evidence on the health-related quality of life (HRQoL) in omphalocele is limited by small sample sizes, inconsistent findings, and a lack of data from Chinese populations. This study aimed to quantify HRQoL in children with omphalocele using the Pediatric Quality of Life Inventory (PedsQL) in a relatively large patient cohort and to identify demographic and clinical factors associated with children's HRQoL. Methods: We conducted a cross-sectional, questionnaire-based study among caregivers of children with omphalocele treated at the Children's Hospital, Zhejiang University School of Medicine in Hangzhou, China. In total, caregivers of 124 children were recruited and completed the questionnaire. HRQoL was assessed using the Chinese version of PedsQL Infants Scales (parent-proxy for infants/toddlers aged 1-24 months) and PedsQL Generic Core Modules (GCM) (parent-proxy for children aged 2-4 years). Additionally, demographic and clinical information were also collected via questionnaires. Differences in HRQoL scores across subgroups were assessed by two-independent-samples t-tests and one-way analysis of variance (ANOVA). Multivariate linear regression analysis was performed to identify the determinants associated with children's HRQoL. Results: Among 124 children, the median age was 2.0 years, and 46.8% were girls. For children aged 1-24 months, the total score and scores of certain scales (i.e., physical functioning, physical symptoms, emotional functioning, cognitive functioning) were significantly lower in patients than scores in the healthy controls (P values <0.05) with the effect sizes ranging from 0.33 to 0.86. For children aged 2 to 4 years, the total score and the scores on three scales (i.e., physical, emotional, and social functioning) were statistically significantly higher in patients than in healthy controls (P values <0.05), with effect sizes ranging from 0.53 to 0.94. Age and the presence of other malformations were significantly associated with the total score of PedsQL GCM (P values <0.05). Conclusions: The HRQoL of children under 2 years of age with omphalocele is lower than that of healthy children. With increasing age, the HRQoL of children with omphalocele improves, whereas the presence of additional malformations has a negative impact on their HRQoL.

Indexed as

childrenhealth profileomphaloceleQuality of life (QoL)

Identifiers

PMID41657450
PMCPMC12877923

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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.