Non-invasive assessment of liver abnormalities in pediatric Fontan patients
Ruth De Bruyne1, Kristof Vandekerckhove2, Hazel Van Overschelde3
1Department of Pediatric Gastroenterology, Hepatology and Nutrition, Ghent University Hospital, Ghent University, Ghent, Belgium. ruth.debruyne@uzgent.be.
Insights
Pediatric Fontan survivors frequently show liver abnormalities, including abnormal lab results and signs of portal hypertension. Non-invasive tests can detect these issues but struggle to differentiate congestion from fibrosis, necessitating a proposed screening protocol.
Area of Science:
- Pediatric Cardiology
- Hepatology
- Medical Imaging
Background:
- Fontan palliation is crucial for complex congenital heart disease.
- Long-term survivors often develop liver issues, but pediatric data is limited.
- Understanding Fontan-associated liver disease in children is vital for management.
Purpose of the Study:
- To assess the prevalence and degree of liver abnormalities in pediatric Fontan patients.
- To evaluate non-invasive methods for longitudinal follow-up of liver health.
- To propose a screening protocol for early detection of Fontan-associated liver disease.
Main Methods:
- Studied 35 pediatric Fontan patients using blood tests, liver Doppler ultrasound, and transient elastography.
- Compared transient elastography values with healthy children as controls.
- Analyzed laboratory markers, liver/spleen size, portal vein flow, and vena cava collapsibility.
Main Results:
- Elevated liver enzymes (AST, ALT, γGT) and bilirubin were common.
- Portal hypertension and venous congestion were indicated in a significant portion of patients.
- Transient elastography values were significantly higher in Fontan patients, even shortly after surgery.
Conclusions:
- Liver abnormalities are frequent in pediatric Fontan patients.
- Current non-invasive methods face challenges in differentiating hepatic congestion from fibrosis.
- A prospective screening protocol using serial laboratory, Doppler ultrasound, and transient elastography is proposed.
Abstract:
Liver abnormalities are well known among long-term survivors of Fontan palliation, which remains the definite surgery for complex congenital heart disease and single ventricle physiology. Pediatric data however are scarce. We assessed the prevalence and degree of liver abnormalities in pediatric Fontan patients through non-invasive investigations suitable for longitudinal follow-up. Thirty-five patients with a median age of 11.8 years (5.2-16.6) and median time since Fontan of 6 years (1.17-13.83) were studied. Each child underwent a blood test, liver Doppler ultrasound (US), and transient elastography (TE). Healthy children were used as controls for TE measurement. AST, ALT, γGT, and direct bilirubin were abnormal in respectively 12 (34%), 5 (14%), 24 (69%), and 7 (20%) patients, while platelet count was decreased in 7 (20%). Splenomegaly was present in 7 (20%) patients. Portal vein mean flow velocity was < 15 cm/s in 19 (54%) patients indicative of portal hypertension. Twenty-two patients (63%) showed inferior vena cava collapsibility index values below 17%, indicating venous congestion. Hepatic artery and superior mesenteric artery resistance index were inversely correlated with time post Fontan (p < 0.05). TE values in Fontan patients were significantly higher than controls, with a median of 12.6 versus 4.6 kPa (p < 0.001) and were already increased shortly after Fontan completion. Conclusion: Liver abnormalities are frequently observed in pediatric Fontan patients. The non-invasive investigations used were not able to confirm liver fibrosis or differentiate hepatic congestion from fibrosis. Based on our findings, we propose a prospective screening protocol with serial measurements of laboratory, (Doppler) US, and TE parameters. What is Known: • Hepatic dysfunction is a well-known consequence of the Fontan circulation. • The natural history of Fontan-associated liver disease in the pediatric age group remains unclear. What is New: • Liver abnormalities are frequently observed in pediatric Fontan patients; however, differentiating liver fibrosis and hepatic congestion with non-invasive investigations remains challenging. Sonographic Doppler measurements may improve our insight in both Fontan-associated liver disease development and the functioning of the Fontan circulation. • A prospective screening protocol is proposed to improve our ability to detect Fontan-associated liver disease early on and understand its natural history.
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