Evidence map›Paper›PMID 40215128›Full record

ArticleUnited European gastroenterology journal2025

Pediatric Autoimmune Pancreatitis: Clinical Findings and Outcomes in Sweden.

Miroslav Vujasinovic, Fredrik Lindgren, Nikolaos Kartalis, Raffaella Pozzi Mucelli, Dawid Rutkowski, Alexander Waldthaler, Poya Ghorbani, Carlos Fernández Moro, Thomas Casswall, J-Matthias Löhr

Abstract read
In one paragraph

Article in United European gastroenterology journal, 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. Review
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.

Miroslav VujasinovicDepartment of Upper Abdominal Diseases, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-6496-295X
Fredrik LindgrenDepartment of Clinical Science, Intervention, and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-7984-7754
Nikolaos KartalisDepartment of Clinical Science, Intervention, and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-8003-1787
Raffaella Pozzi MucelliDepartment of Clinical Science, Intervention, and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-7668-0394
Dawid RutkowskiDepartment of Clinical Science, Intervention, and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-7680-2275
Alexander WaldthalerDepartment of Upper Abdominal Diseases, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0003-3299-1729
Poya GhorbaniDepartment of Upper Abdominal Diseases, Karolinska University Hospital, Stockholm, Sweden.
Carlos Fernández MoroDepartment of Clinical Pathology and Cancer Diagnostics, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0001-6863-5959
Thomas CasswallDepartment of Clinical Science, Intervention, and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-4546-826X
J-Matthias LöhrDepartment of Upper Abdominal Diseases, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-7647-198X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPediatric autoimmune pancreatitis (AIP) is a rare form of pancreatitis in children with poorly understood pathophysiology. It is a recognized risk factor for chronic pancreatitis in approximately 4% of pediatric cases. This study aims to describe the demographics, clinical characteristics, and outcomes of a large Swedish cohort of pediatric AIP patients. PATIENTS AND

methodsA retrospective analysis of medical records was conducted for patients diagnosed with pediatric AIP between January 2006 and December 2022.

resultsThirty-seven patients were included (20 males, 17 females; mean age 13.5 ± 2.8 years). None had a family history of pancreatic diseases. Most patients (62.2%) presented with acute pancreatitis, followed by weight loss (45.9%), abdominal pain (43.2%), jaundice (21.6%), and fatigue (16.2%). Acute pancreatitis was mild in all cases according to the Atlanta criteria. Multi-organ involvement was observed in 81.1% of patients, and inflammatory bowel disease (IBD) was present in 62.2%. A total of 75.7% of patients received treatment, mainly glucocorticoids, while 24.3% had spontaneous regression. Complete clinical and radiological remission was achieved in 83.8% of treated patients. Pancreatic exocrine insufficiency was present in 43.2% of patients at diagnosis, reducing to 24.3% at the final follow-up. No patients developed diabetes mellitus, except for one who underwent total pancreatectomy due to suspected pancreatic tumor.

conclusionsPediatric AIP is a rare condition often associated with multi-organ involvement particularly IBD. Most patients respond well to glucocorticoid treatment and achieve remission. Managing IBD may improve the outcomes for both conditions.

Indexed as

Autoimmune PancreatitisGlucocorticoidsInflammatory Bowel DiseasesAbdominal PainAcute DiseaseAdolescentChildExocrine Pancreatic InsufficiencyFemaleHumansMaleRetrospective StudiesSwedenTreatment OutcomeGlucocorticoidsautoimmune pancreatitischronic pancreatic inflammationdiabetes mellitusglucocorticoid treatmentinflammatory bowel diseasemulti‐organ involvementpancreatic exocrine insufficiencypediatric pancreatitis

Identifiers

PMID40215128
PMCPMC12188370

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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.