Evidence map›Paper›PMID 41764195›Full record

ArticleScientific reports2026

Predicting infected pancreatic necrosis in acute pancreatitis using machine learning models and feature selection.

Li Xin, Ding Yixuan, Huang Bohan, Shen Yunheng, Lv Hairong, Cao Feng, Yu Tong, Li Fei, Fei Xiaolu, Li Jia

Abstract read
In one paragraph

Article in Scientific reports, 2026. 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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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

The trial behind it

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3 · Its place in the literature

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4 · The record

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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.

Li Xin *Xuanwu Hospital, Capital Medical University, Beijing, 100053, China.
Ding Yixuan *Xuanwu Hospital, Capital Medical University, Beijing, 100053, China.
Huang BohanXuanwu Hospital, Capital Medical University, Beijing, 100053, China.
Shen YunhengTsinghua University, Beijing, 100084, China.
Lv HairongTsinghua University, Beijing, 100084, China.
Cao FengXuanwu Hospital, Capital Medical University, Beijing, 100053, China.
Yu TongXiongan Xuanwu Hospital, Xiongan New Area, Hebei, 070001, China.
Li FeiXuanwu Hospital, Capital Medical University, Beijing, 100053, China. lifei@xwhospital.com.
Fei XiaoluXuanwu Hospital, Capital Medical University, Beijing, 100053, China. feixiaolu@xwhospital.com.
Li JiaXuanwu Hospital, Capital Medical University, Beijing, 100053, China. lijia@xwh.ccmu.edu.cn.

Funding

Natural Science Foundation of Hebei Province Grant No. H2024112019Program of Xiongan New Area Grant No. XA202401102001K
6 · The paper itself

Abstract

Infected pancreatic necrosis (IPN) is a life-threatening complication of acute pancreatitis (AP), and its early prediction remains challenging. This study aimed to develop and externally validate interpretable machine learning models for individualized IPN risk prediction. A total of 728 patients with AP admitted to Xuanwu Hospital, Capital Medical University, between 2017 and 2023 were retrospectively analyzed. Embedded feature selection was incorporated within model training using regularized linear and tree-based algorithms to enhance interpretability and prevent overfitting. Five machine learning algorithms and one neural network model were evaluated through nested cross-validation and an independent temporal external cohort consisting of 166 AP patients admitted to Xuanwu Hospital, Capital Medical University, between 2022 and 2023. Model discrimination, precision-recall, and probability calibration were assessed, and model explainability was analyzed using Shapley Additive Explanations (SHAP). The Random Forest model achieved the best overall performance, achieving an external AUC of 0.764 (95% CI 0.696-0.830, [Formula: see text]), precision of 0.893, recall of 0.604, and the lowest Brier score, indicating reliable probability calibration. SHAP analysis identified Fibrinogen, APACHE II score, D-dimer, IL-6, and C-reactive protein as key predictors associated with increased IPN risk, while higher Lymphocyte count, and Hematocrit were protective. These findings are consistent clinical pathophysiology. The interpretable Random Forest model demonstrated robust discrimination and calibration for IPN prediction, providing a transparent and data-driven framework for early risk stratification in acute pancreatitis. Prospective multicenter validation is warranted before clinical implementation.

Indexed as

Machine LearningPancreatitisPancreatitis, Acute NecrotizingClassification AlgorithmsFemaleHumansMaleMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRandom ForestRetrospective StudiesAcute pancreatitisDeep learningInfected pancreatic necrosisMachine learningPrognosis prediction

Identifiers

PMID41764195
PMCPMC13048984

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