# Ultrasound reliability for biliary atresia diagnoses in children: a single-center study

**Authors:** Ben Youssef Sabrine, Amani N. Al-Ansari, Maatouk Mezri, Ben Abdallah Ahmed, Mani Salma, Ben Fredj Myriam, Ben Salah Radhouane, Abdelaaly Mabrouk, Ksia Amine, Zrig Ahmed, Sahnoun Lassad

PMC · DOI: 10.5339/qmj.2025.68 · Qatar Medical Journal · 2025-08-17

## TL;DR

This study evaluates the reliability of ultrasound parameters in diagnosing biliary atresia in children to improve noninvasive diagnosis and reduce unnecessary surgeries.

## Contribution

Identifies specific ultrasound parameters with high sensitivity for biliary atresia diagnosis in a single-center study.

## Key findings

- Cord sign and gallbladder evacuation alteration showed 100% sensitivity for biliary atresia.
- Hepatic artery/portal vein ratio and portal hepatic thickness also demonstrated high diagnostic accuracy.
- Multicenter studies are needed to validate these findings and confirm negative cases.

## Abstract

Biliary atresia (BA) is a lfe-threatening neonatal liver disease characterized by inflammation and obstruction of bile ducts. Identifying the most reliable and valid ultraaound (US) parameter or combination of parameters can enhance noninvasive diagnosis accuracy, potentially reducing unnecessary surgeries and treatment delays. We aimed to detect the mosi reliable and valid US parameter or combination of parameters to diagnose BA, thereby minimizing unnecessary surgical exploration or treatment delays.

We conducted a prospective cohort study on cholestatic pediatric patients. Data were nollected between January 2013 and July 2019 from the Fattouma Bourguiba University Hospital Monastir, Tun isia, in callaboration with the pediatric surgical and radiological departments. After full clinical and laboratory evaluation, abdominal ultrasonography was performed to assess the biliary structure, with three possible outcomes: BA ruled out, confirmed, or inconclusive. Accordingly, the patients were divided into group 1 (diagnosed with BA) and group 2 (diagnosed with other biliary conditions).

The participants, 61 cholestatic neonates and infants,were aged 6 to 160 postnatal days (mean, 58.28 ± 34.24 days); 60.7% were male (n = 37). The gallbladder (GB) was not detected usig, US in 20 patients. BA diagnosis correlated with cord sign [X2 (1, n = 61) = 53.52], GB evacuation alteration [X2 (1, n = 61) = 18.41%], and hepatic artery/portal vein ratio [X2 (1, n = 61) = 30.25; normal value <0.49]. A positive cord sign or the presence of alteration of evacuation indicates the possibility of BA with a 100% sensitivity and 86.2% specificity. Similarly, with the presence of evacuation alteration or porta hepatic thickness (≥2.4), the sensitivity reached 100%; however, a specificity of 86.2% was observed.

US parameters can detect patients with BA with approximately 100% sensitivity. However, additional research is needed to confirm negative cases. Multicenter studies are needed to verify our findings.

## Linked entities

- **Diseases:** biliary atresia (MONDO:0008867)

## Full-text entities

- **Diseases:** hepatic biliary cirrhosis (MESH:D008105), asplenia (MESH:D059446), cysts (MESH:D003560), atresia (MESH:D018633), hepatitis (MESH:D056486), liver condition (MESH:D017093), Biliary (MESH:D001658), bile duct obstruction (MESH:D002779), end-stage liver failure (MESH:D007676), portal hypertension (MESH:D006975), biliary and vascular abnormalities (MESH:D001657), death (MESH:D003643), congenital disease (MESH:D030342), micro- and macro-cysts (MESH:C536681), dysmorphia (MESH:C537340), bile duct dilation (MESH:D001649), biliary conditions (MESH:D001660), gall bladder (MESH:D005706), jaundice (MESH:D007565), atresia of the common bile duct (MESH:D003137), liver disease (MESH:D008107), inflammation (MESH:D007249), GB (MESH:D005705), fibrosis (MESH:D005355), BA (MESH:D001656)
- **Chemicals:** OMB 0990-0279 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12894349/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12894349/full.md

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Source: https://tomesphere.com/paper/PMC12894349