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Updated: Sep 16, 2025

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Published on: August 1, 2025
Natural progression and prediction markers in non-clinically significant oesophageal varices in children
Cody Chan1, Akshat Goel1, Robert Hegarty1
1Paediatric Liver, GI & Nutrition Centre and MowatLabs, King's College Hospital, London, UK.
Insights
Progression of non-clinically significant varices (nCSV) in children with portal hypertension (PHT) can be predicted using risk scores in chronic liver disease (CLD) and portal vein thrombosis (PVT). Biliary atresia (BA) requires caution with extended endoscopy surveillance.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Clinical Research
Background:
- Limited data exists on non-clinically significant varices (nCSV) and their progression in pediatric portal hypertension (PHT).
- Understanding progression trends is crucial for effective management and surveillance strategies in affected children.
Purpose of the Study:
- To investigate the trends and predictive factors associated with variceal progression in children with nCSV and PHT.
- To evaluate the accuracy of various biomarkers and non-invasive methods in predicting progression across different etiologies of PHT.
Main Methods:
- Retrospective cohort study of 70 children with nCSV undergoing surveillance endoscopy.
- Analysis of laboratory parameters, established prediction scores, and spleen stiffness by fibroscan (SSM).
- Statistical analysis included Mann-Whitney U test, chi-squared test, and receiver operating characteristic (ROC) analysis.
Main Results:
- Variceal progression occurred in 35.7% of children, with median progression times of 3 years in portal vein thrombosis (PVT) and chronic liver disease (CLD), and 2 years in biliary atresia (BA).
- Hemoglobin (Hb), risk score, and SSM showed high accuracy in predicting progression in PVT and CLD.
- Biomarkers like von Willebrand Factor antigen score (vWFAg score) were highly accurate in CLD, while BA biomarkers showed suboptimal predictive accuracy.
Conclusions:
- Risk scores are reliable for monitoring variceal progression in pediatric CLD and PVT.
- Non-invasive scores warrant trial for validation alongside surveillance esophagogastroduodenoscopy (EGD).
- Extended endoscopy periods for children with BA require caution; larger studies are needed to validate SSM and vWFAg score in nCSV.
Objectives:
Limited literature exists on non-clinically significant varices (nCSV) and progression in children with portal hypertension (PHT). This study investigates trends and associations in this cohort.
Methods:
This retrospective cohort study analysed 70 children with nCSV undergoing surveillance endoscopy between January 2012 and 2024. Laboratory parameters, prediction scores and fibroscan results were collected. Statistical analysis include Mann-Whitney U test, chi-squared test and receiver operating characteristic.
Results:
Ten children (14.3%) presented with portal vein thrombosis (PVT), 26 (37.1%) with non-biliary atresia chronic liver disease (CLD) and 34 (48.6%) with biliary atresia (BA). Twenty-five children (35.7%) had variceal progression, with median years until progression of 3 years recorded in PVT and CLD (PVT: 1-6 years, CLD: 2-8 years), and 2 years (1-10 years) in BA. Haemoglobin count (Hb) (area under the curve [AUC] = 0.943), risk score (AUC = 0.748), and spleen stiffness by fibroscan (SSM) (AUC = 1.00) revealed optimal accuracy in predicting progression in PVT, with similar findings in CLD (von Willebrand Factor score [vWFAg score]: AUC = 1.00, risk score: AUC = 0.767, SSM: AUC = 0.882). Suboptimal accuracy was seen in BA biomarkers.
Conclusions:
Risk score is a reliable marker to monitor variceal progression in CLD and PVT. Interim noninvasive scores could be trialled along with surveillance OGD to validate results. Caution is advised extending endoscopy period for children with BA. Due to small subgroup sizes, larger cohort studies are needed to validate SSM and vWFAg score in children with nCSV.
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