Implications of culture positivity in acute pancreatitis: does the source matter?

Chalapathi Rao1, Deepak Kumar Bhasin, Surinder Singh Rana

  • 1Department of Gastroenterology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Abstract

Insights

Sepsis from combined pancreatic and extrapancreatic sources in acute pancreatitis (AP) significantly increases persistent organ failure (POF) and length of hospital (LOH) stay. Sepsis from any source worsens outcomes compared to sterile cases.

Area of Science:

  • Gastroenterology
  • Infectious Diseases
  • Critical Care Medicine

Background:

  • Sepsis is a major complication of acute pancreatitis (AP), contributing to significant morbidity and mortality.
  • Sepsis in AP can originate from pancreatic/peripancreatic sources or extrapancreatic sites.

Purpose of the Study:

  • To investigate the impact of sepsis source on patient outcomes in acute pancreatitis.
  • To analyze the relationship between sepsis origin and persistent organ failure (POF), length of hospital (LOH) stay, and mortality.

Main Methods:

  • Retrospective analysis of culture reports from 357 AP patients.
  • Categorization of patients based on sepsis source: pancreatic, extrapancreatic, combined, or sterile.

Main Results:

  • Combined pancreatic and extrapancreatic sepsis sources were associated with the highest rates of POF (90%) and longest LOH stay (47.3 days).
  • Patients with any sepsis source (pancreatic, extrapancreatic, or combined) had significantly higher mortality rates compared to those with sterile cultures.
  • POF occurred in 67.8% of pancreatic, 65% of extrapancreatic, and 90% of combined sepsis cases.

Conclusions:

  • The source of sepsis significantly influences outcomes in acute pancreatitis.
  • Combined pancreatic and extrapancreatic sepsis sources are linked to worse outcomes, including prolonged hospital stays and increased organ failure.
  • Prompt identification and management of sepsis source are crucial for improving survival in AP patients.

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