Evidence map›Paper›PMID 40709428›Full record

Observational studyThe Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi2025

Late Referral of Biliary Atresia and Poor Clinical Outcomes.

Melinda Masturina, Rendi Aji Prihaningtyas, Bagus Setyoboedi, Sjamsul Arief

Abstract readObservational Study
In one paragraph

Observational study in The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi, 2025. 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

4 authors.

Melinda MasturinaDepartment of Child Health, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.
Rendi Aji PrihaningtyasDepartment of Child Health, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.
Bagus SetyoboediDepartment of Child Health, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.ORCID 0000-0002-3923-6913
Sjamsul AriefDepartment of Child Health, Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Biliary atresia (BA) is a progressive cholangiopathy in infants that often necessitates liver transplantation. This study aimed to evaluate the impact of delayed referral on clinical and histopathological outcomes in BA cases. Methods: This study was a prospective observational study conducted from January to September 2023 at Dr. Soetomo General Academic Hospital, Surabaya, Indonesia. Results: A total of 137 infants with cholestasis were enrolled. Of these, only 85 underwent liver biopsy, with 60 cases (70.6%) confirmed as extrahepatic cholestasis consistent with BA. Among these 60 BA-confirmed patients, 83.3% were referred after 60 days of age. Patients in the late referral group (>60 days) in all cases exhibited higher leukocyte counts, total bilirubin levels, prolonged prothrombin time, and hypoalbuminemia, reflecting a more advanced disease state. Two-phase ultrasonography detected abnormalities in 76.7% of BA-confirmed cases, supporting its potential role as a screening modality in resource-limited settings. Histopathological analysis revealed a significantly higher prevalence of liver fibrosis in patients referred after 60 days (p=0.002), indicating disease progression. Only 9 patients underwent Kasai portoenterostomy, with 8 fatalities due to ascending cholangitis. Conclusions: These findings emphasize the urgent need for earlier detection and referral to improve outcomes in infants with BA.

Indexed as

Biliary AtresiaBilirubinBiopsyCholestasisDisease ProgressionFemaleHumansInfantInfant, NewbornLiverLiver CirrhosisLiver TransplantationMalePortoenterostomy, HepaticProspective StudiesReferral and ConsultationBilirubinBiliary atresiaInfantsLiver fibrosisLiver transplantationMedicine

Identifiers

PMID40709428
PMCPMC12305075

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Registered trials

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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.