Evidence map›Paper›PMID 42012682›Full record

ArticlePediatric surgery international2026

International disparities in biliary atresia outcomes.

Rani Kassir, Grégoire Schneider, Rémi Dubois, Guillaume Rossignol

Abstract read
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In one paragraph

Article in Pediatric surgery international, 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

4 authors.

Rani KassirDepartment of Pediatric Visceral, Urological and Transplant Surgery, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France. rani.kassir@outlook.com.
Grégoire SchneiderDepartment of Pediatric Visceral, Urological and Transplant Surgery, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France.
Rémi DuboisDepartment of Pediatric Visceral, Urological and Transplant Surgery, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France.
Guillaume RossignolDepartment of Pediatric Visceral, Urological and Transplant Surgery, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Japanese Biliary Atresia Registry, reported by Okubo et al., provides a comprehensive long-term perspective on biliary atresia (BA) across 3951 patients (1989–2023). With jaundice clearance rates exceeding 60% and 10-year native liver survival of 50.5%, outcomes in Japan remain consistently superior to those reported in Western cohorts. These disparities are likely multifactorial. BA represents a heterogeneous phenotype shaped by genetic, immunological, environmental, and developmental factors that may differ across populations. The lower prevalence of biliary atresia splenic malformation syndrome in Japan (2.2% vs. 8–15%) may partly contribute but does not fully explain the gap. Differences in management strategies, including earlier surgery, greater use of revision Kasai portoenterostomy, and adjuvant therapies, may also play a key role.

Indexed as

Biliary AtresiaHumansJapanPortoenterostomy, HepaticTreatment Outcome

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.