Evidence map›Paper›PMID 41321455›Full record

ArticleFrontiers in pediatrics2025

Causes and risk factors for death in infants with congenital chylothorax.

Yuichi Kubo, Satoshi Ibara, Takuya Tokuhisa, Masaya Kibe, Kazuyoshi Sueyoshi, Masato Kamitomo, Motoi Kato

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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

7 authors.

Yuichi KuboDepartment of Neonatology, Shonan Fujisawa Tokushukai Hospital, Kanagawa, Japan.
Satoshi IbaraDepartment of Neonatology, Shonan Fujisawa Tokushukai Hospital, Kanagawa, Japan.
Takuya TokuhisaDepartment of Neonatology, Kagoshima City Hospital, Kagoshima, Japan.
Masaya KibeDepartment of Neonatology, Imakiire General Hospital, Kagoshima, Japan.
Kazuyoshi SueyoshiDepartment of Pathology, Kagoshima City Hospital, Kagoshima, Japan.
Masato KamitomoDepartment of Obstetrics, Kagoshima City Hospital, Kagoshima, Japan.
Motoi KatoDepartment of Plastic Surgery, Kagoshima University Hospital, Kagoshima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: To identify mortality risk factors in infants with congenital chylothorax (CC) and analyze the causes of death, including pathological examination. Methods: For this single-center retrospective study, we included 27 patients with CC. We divided them into the ALIVE and the DEAD groups, with the DEAD group subdivided into the Early-DEAD group and the Late-DEAD group to compare patient characteristics and risk factors using robust statistical methods. Causes of death were reviewed, including pathological findings from autopsies. Results: The mortality rate was 44% (12 of 27 infants, with 15 survivors). Univariate analysis showed associations between mortality and chromosomal abnormalities and fetal ascites. A longer duration of hydrothorax Conclusion: Poor prognosis in infants with CC is strongly associated with fetal ascites, which we hypothesize serves as a key clinical marker for underlying Generalized Lymphatic Dysplasia (GLD). This systemic lymphatic disorder, identified pathologically as lymphangiectasia in fatal cases, may be the primary driver of mortality. Chromosomal abnormalities appear to be a significant predisposing factor for this severe phenotype.

Indexed as

cause of deathchromosome abnormalitiescongenital chylothoraxinfant mortalitylymphangiectasiarisk factors

Identifiers

PMID41321455
PMCPMC12660280

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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.