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Updated: Mar 10, 2026

Author Spotlight: Point-of-Care Ultrasound for Gastric Content Assessment and Risk Stratification in Perioperative Care
Published on: September 22, 2023
Occult upper gastrointestinal mucosal abnormalities in critically ill patients
C Ovenden1, M P Plummer1,2, S Selvanderan1
1Discipline of Acute Care Medicine, University of Adelaide, Adelaide, SA, Australia.
Occult upper gastrointestinal abnormalities were found in one-third of ICU patients. These findings were independent of acid-suppressive therapy and did not impact clinical outcomes like mortality.
Area of Science:
- Gastroenterology
- Critical Care Medicine
- Endoscopy
Background:
- Investigating occult upper gastrointestinal (GI) abnormalities in intensive care unit (ICU) patients.
- Assessing the role of gastric acid secretion in observed GI pathology.
- Determining associations between GI abnormalities and clinical outcomes.
Purpose of the Study:
- To estimate the frequency of occult upper GI abnormalities in ICU patients.
- To evaluate gastric acid as a potential contributing factor to these abnormalities.
- To examine the relationship between GI abnormalities and clinical outcomes such as mortality.
Main Methods:
- Retrospective analysis of endoscopy reports from 74 ICU patients undergoing endoscopy for research.
- Independent adjudication of endoscopic findings by two gastroenterologists.
- Assessment of gastric acid contribution using a 3-point scale.
Main Results:
- Occult abnormalities detected in 34% of patients, including gastritis/erosions and nasogastric tube trauma.
- Gastric acid contribution rated 'probable' in a small subset of patients.
- No association found between acid-suppressive therapy and endoscopic abnormalities (P=0.46).
- Mucosal abnormalities were not linked to hemoglobin levels, transfusion needs, or mortality (P>0.9).
Conclusions:
- One-third of ICU patients exhibit occult upper GI mucosal abnormalities.
- The presence of these abnormalities is not influenced by prior acid-suppressive therapy.
- Observed GI abnormalities did not correlate with adverse clinical outcomes in this cohort.
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