Affiliations 

  • 1 Division of Gastroenterology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA
  • 2 Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA
  • 3 Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, Netherlands
  • 4 Division of Gastroenterology and Hepatology, Medical University of South Carolina, Charleston, South Carolina, USA
  • 5 Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, China
  • 6 Division of Gastroenterology, University of Southern California, Los Angeles, California, USA
  • 7 Section of Gastroenterology and Hepatology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire
  • 8 Moffitt Cancer Center, Department of Gastrointestinal Oncology, Division of Gastroenterology, Tampa, Florida
  • 9 Division of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana
  • 10 Klinik und Poliklinik für Innere Medizin II, Klinikum rechts der Isar, Technische Universität München, München, Germany
  • 11 Department of Internal Medicine, Dankook University College of Medicine, Dankook University Hospital, Cheonan, Korea
  • 12 Ministry of Health, Kota Kinabalu, Malaysia
  • 13 Division of Gastroenterology, Department of Internal Medicine, Mackay Memorial Hospital, Taipei, Taiwan
  • 14 Department of Gastroenterology, Asian Institute of Gastroenterology, Hyderabad, India
  • 15 Department of Gastroenterology, Apollo Gleneagles Hospital, Kolkata, India
  • 16 Department of Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
  • 17 Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA; Division of Biostatistics and Bioinformatics, Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, USA
  • 18 Division of Gastroenterology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA. Electronic address: vakshin1@jhmi.edu
Gastrointest Endosc, 2025 Jan;101(1):129-138.e0.
PMID: 39147103 DOI: 10.1016/j.gie.2024.08.009

Abstract

BACKGROUND AND AIMS: A robust model of post-ERCP pancreatitis (PEP) risk is not currently available. We aimed to develop a machine learning-based tool for PEP risk prediction to aid in clinical decision making related to periprocedural prophylaxis selection and postprocedural monitoring.

METHODS: Feature selection, model training, and validation were performed using patient-level data from 12 randomized controlled trials. A gradient-boosted machine (GBM) model was trained to estimate PEP risk, and the performance of the resulting model was evaluated using the area under the receiver operating curve (AUC) with 5-fold cross-validation. A web-based clinical decision-making tool was created, and a prospective pilot study was performed using data from ERCPs performed at the Johns Hopkins Hospital over a 1-month period.

RESULTS: A total of 7389 patients were included in the GBM with an 8.6% rate of PEP. The model was trained on 20 PEP risk factors and 5 prophylactic interventions (rectal nonsteroidal anti-inflammatory drugs [NSAIDs], aggressive hydration, combined rectal NSAIDs and aggressive hydration, pancreatic duct stenting, and combined rectal NSAIDs and pancreatic duct stenting). The resulting GBM model had an AUC of 0.70 (65% specificity, 65% sensitivity, 95% negative predictive value, and 15% positive predictive value). A total of 135 patients were included in the prospective pilot study, resulting in an AUC of 0.74.

CONCLUSIONS: This study demonstrates the feasibility and utility of a novel machine learning-based PEP risk estimation tool with high negative predictive value to aid in prophylaxis selection and identify patients at low risk who may not require extended postprocedure monitoring.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.