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Updated: Jul 30, 2025

Author Spotlight: Point-of-Care Ultrasound for Gastric Content Assessment and Risk Stratification in Perioperative Care
Published on: September 22, 2023
Transabdominal gastro-intestinal ultrasonography (TGIU) for predicting feeding intolerance in critically ill
Ge Yu1, Shanshan Jin1, Rui Wang1
1Department of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, No.85 Wujin Road, Shanghai 200080, China.
Background:
This study aimed at verifying the feasibility of transabdominal gastro-intestinal ultrasonography (TGIU) for predicting feeding intolerance (FI).
Methods:
This single-center prospective observational study comprising critically ill patients who were admitted to an intensive care unit (ICU) and received enteral nutrition through a nasogastric tube. TGIU parameters including gastric antral cross-sectional area (CSA) and acute gastrointestinal injury ultrasonography (AGIUS) score, were conducted on days 1, 3, 5, and 7 within the first week of starting enteral nutrition (EN).
Results:
A total of 91 patients were eligible for inclusion and 57 showed FI. The incidence of FI was 28.6%, 41.8%, 29.7%, and 27.5% on days 1, 3, 5, and 7, respectively, and the incidence of FI was 62.6% within the first week of starting EN. Univariate logistic regression analysis showed that SOFA score, CSA, and AGIUS score, were significantly (P < 0.05) associated with the FI on the same day. In the multivariate analysis including two variables, CSA, and AGIUS score were found to remain independent predictors for FI and 28-day mortality. An area under the curve (AUC) for TGIU predicted FI in the first week of starting EN (the cut-off of CSA ≥6.0 cm2 yielded a sensitivity of 86.0% and specificity of 79.4%, and for AGIUS score ≥3.5 yielded a sensitivity of 87.7% and specificity of 82.4%). The predictive value of TGIU for 28-day mortality was higher than the SOFA score [0.827 (0.733-0.921) vs. 0.646 (0.519-0.774), P = 0.001].
Conclusions:
TGIU represented an effective means for predicting FI and 28-day mortality in critically ill patients. These results supported the hypothesis that persistent FI in critically ill patients is an essential determinant for poor prognosis.
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