Risk Factors for Post-ERCP Pancreatitis in Pediatric and Young Adult Patients

Ahmad M Hassan1, Tom K Lin2,3, Milton T Smith1

  • 1From the Department of Internal Medicine, University of Cincinnati, Cincinnati, OH.

Insights

Post-ERCP pancreatitis (PEP) is a common complication. In pediatric patients, pancreatic duct stenting and specific procedural factors were associated with PEP, though not in high-risk subgroups. Further trials are needed to clarify interventions.

Area of Science:

  • Gastroenterology
  • Pediatric Endoscopy
  • Clinical Outcomes Research

Background:

  • Post-ERCP pancreatitis (PEP) is the most frequent complication following endoscopic retrograde cholangiopancreatography (ERCP).
  • Existing data on prophylactic pancreatic duct (PD) stenting in pediatric patients suggest a potential increased risk of PEP, but evidence is limited.
  • Identifying factors associated with PEP in pediatric populations is crucial for risk stratification and prevention strategies.

Purpose of the Study:

  • To identify patient and procedure-related factors associated with the development of post-ERCP pancreatitis (PEP) in a pediatric cohort.
  • To analyze the impact of interventions such as rectal indomethacin and pancreatic duct stenting on PEP rates in children.
  • To investigate the association between genetic factors, specifically PRSS1 mutations, and PEP in pediatric patients.

Main Methods:

  • Retrospective review of pediatric patients undergoing ERCP between 2012 and 2020 at a single institution.
  • Collection and analysis of patient demographics, procedural details, and outcomes, including PEP.
  • Statistical analysis using Chi-square or Fisher exact tests and Mann-Whitney-Wilcoxon tests to identify significant associations.

Main Results:

  • Seven hundred thirty-six ERCPs were performed, with a PEP rate of 12.8% (94 cases), predominantly mild.
  • Factors associated with PEP included pancreatic indication, native major papilla, pancreatic duct cannulation/injection, and higher ASGE complexity scores.
  • While rectal indomethacin and PD stenting showed association with PEP in initial analysis, this was not persistent in high-risk subgroups. A lower proportion of PEP patients had PRSS1 mutations.

Conclusions:

  • A significant rate of PEP was observed in this pediatric cohort, potentially linked to higher pancreatic indications and procedural complexity.
  • The association of PD stenting with PEP requires further investigation, particularly in high-risk pediatric patients.
  • Prospective randomized trials are necessary to definitively establish the utility of prophylactic interventions and understand PEP development in pediatric ERCP.
Abstract

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