Evidence map›Paper›PMID 40783427›Full record

ArticleScientific reports2025

Combining bedside index of severity in acute pancreatitis (BISAP) and Charlson comorbidity index improves early risk stratification in biliary acute pancreatitis.

Julian Prosenz, Tobias Hadrigan, Larissa Brandl, Anna Wittmann, Moira Birkl, Florian Koutny, Andreas Maieron

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

7 authors.

Julian ProsenzKarl Landsteiner University of Health Sciences, Krems, Austria. julian.prosenz@kl.ac.at.ORCID http://orcid.org/0000-0001-5918-6987
Tobias HadriganKarl Landsteiner University of Health Sciences, Krems, Austria.
Larissa BrandlKarl Landsteiner University of Health Sciences, Krems, Austria.
Anna WittmannKarl Landsteiner University of Health Sciences, Krems, Austria.
Moira BirklKarl Landsteiner University of Health Sciences, Krems, Austria.
Florian KoutnyKarl Landsteiner University of Health Sciences, Krems, Austria.
Andreas MaieronKarl Landsteiner University of Health Sciences, Krems, Austria.ORCID http://orcid.org/0000-0003-4525-3549

Funding

Karl Landsteiner Privatuniversität für Gesundheitswissenschaften SF_0046
6 · The paper itself

Abstract

Risk stratification in acute pancreatitis (AP) remains a clinical challenge. Because AP populations are diverse, focusing on one etiology might reveal interesting insights concerning predictors of outcomes. In this retrospective multicenter cohort study, all patients with biliary AP admitted between 2018 and 2021 were included. Predictors of clinical outcomes - including severity, ICU-admission, complications, and 90-day mortality - were assessed. In total, 217 biliary AP patients, mean age 65.9 years (SD 17.4), 49.3% female, were included, with a median length of stay 7 days (IQR 4;11). BISAP scores were 0 in 30.0%, 1-2 in 63.5%, and 3-5 in 6.4% of patients. Higher BISAP and Charlson comorbidity index (CCI) were significantly associated with worse outcomes, including ICU admission, persistent organ dysfunction, and mortality (p < 0.001). When combined, BISAP and CCI identified five risk groups with progressively increasing rates of complications and mortality. Notably, 41.1% of patients fell into the lowest risk group, with only 2 ICU admissions, and with an uncomplicated course in 97.6% of cases, supporting potential early discharge. Mortality in the very-high risk group (BISAP 3-5, CCI ≥ 6) was 50%. The combination (BISAP-C) enhances early prognostication in biliary AP and may guide individualized management and healthcare resource utilization.

Indexed as

PancreatitisSeverity of Illness IndexAcute DiseaseAgedComorbidityFemaleHumansIntensive Care UnitsLength of StayMaleMiddle AgedPrognosisRetrospective StudiesRisk AssessmentRisk Factors

Identifiers

PMID40783427
PMCPMC12335518

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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.