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Published on: August 1, 2025
Ultrasonographic predictors of esophageal varices
Roberta V de Alcantara1, Roberto M Yamada, Sílvia R Cardoso
1*Department of Pediatrics, Hospital de Clínicas, UNICAMP, Campinas †Department of Medicine, Universidade Federal de São Carlos, São Carlos, São Paulo, Brazil.
Insights
Ultrasonography can predict esophageal varices in children with liver disease. Splenorenal shunt and omental thickness indicate varices in chronic liver disease, while gallbladder varices and thickening predict them in extrahepatic portal venous obstruction.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Diagnostic Imaging
Background:
- Esophageal varices (EVs) are a serious complication in children with chronic liver disease (CLD) and extrahepatic portal venous obstruction (EHPVO).
- Early identification of EVs is crucial for timely intervention and management.
- Ultrasonography offers a non-invasive method for assessing liver and portal vein abnormalities.
Purpose of the Study:
- To identify ultrasonographic predictors of esophageal varices (EVs) in pediatric patients with CLD and EHPVO.
- To correlate specific ultrasound findings with the presence and severity of EVs.
Main Methods:
- A cohort of 53 pediatric patients (<20 years) with CLD or EHPVO, without prior bleeding or treatment, was evaluated.
- Ultrasound parameters including splenorenal shunt (SS), gallbladder wall varices, gallbladder wall thickening (GT), and lesser omental thickness (LOT) were assessed.
- Statistical analyses, including univariate and multivariate logistic regression, were performed to determine predictor significance.
Main Results:
- Esophageal varices were present in 48.5% of CLD patients and 83.3% of EHPVO patients.
- In CLD patients, SS and LOT were significant predictors of EVs (P=0.0329 and P=0.0151, respectively). A LOT of 5.3 mm was a key indicator.
- In EHPVO patients, gallbladder varices and GT predicted EVs (P=0.0245 and P=0.0289). SS was an independent predictor of EVs in EHPVO (OR 15).
- Portal hypertensive gastropathy (PHG) was more frequent in CLD patients with SS and greater LOT.
Conclusions:
- Splenorenal shunt and increased lesser omental thickness are valuable ultrasonographic indicators for EVs in pediatric CLD.
- Gallbladder varices and gallbladder wall thickening are significant predictors of EVs in pediatric EHPVO.
- Ultrasonography can effectively identify children at risk for EVs and associated complications like PHG.
Objective:
The aim of this study was to identify ultrasonographic predictors of esophageal varices (EVs) in children and adolescents with chronic liver disease (CLD) and extrahepatic portal venous obstruction (EHPVO).
Methods:
This study evaluates 53 patients younger than 20 years with CLD or EHPVO and no history of bleeding or prophylactic EVs treatment. They were divided into 2 groups: group I (35 with CLD) and group II (18 with EHPVO). Splenorenal shunt (SS), gallbladder wall varices, gallbladder wall thickening (GT), and lesser omental thickness (LOT) were compared with the presence of EVs, gastric varices, and portal hypertensive gastropathy (PHG). Univariate (χ² test, Fisher exact test, and Wilcoxon signed rank test) and multivariate (logistic regression) analyses were performed. The area under the receiver operating curve was calculated.
Results:
EVs were observed in 48.5% of patients with CLD and in 83.3% of patients with EHPVO. SS (P = 0.0329) and LOT (P = 0.0151) predicted EV among patients with CLD. A median of 5.3 mm of LOT was considered a predictor of EVs among these patients. Multivariate analysis showed SS as an independent predictor of EVs in patients with EHPVO (odds ratio 15). Gallbladder varices (P = 0.0245) and GT (P = 0.0289) predicted EVs among patients with EHPVO. PHG occurred more often among patients with CLD who had SS (P = 0.0384) and greater LOT (P = 0.0226).
Conclusions:
SS and a greater LOT were indicative of EV among children and adolescents with CLD. Gallbladder varices and GT were indicative of EVs among patients with EHPVO. SS and a greater LOT were indicative of PHG among patients with CLD.
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