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Published on: September 13, 2014
Hepatic Fibrosis Is Universal Following Fontan Operation, and Severity is Associated With Time From Surgery: A Liver
David J Goldberg1, Lea F Surrey2, Andrew C Glatz3
1Division of Cardiology, The Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA goldbergda@email.chop.edu.
Insights
Congestive hepatopathy, a complication of Fontan physiology, leads to liver fibrosis in all patients evaluated. The degree of liver fibrosis increases over time after the Fontan operation.
Area of Science:
- Cardiology
- Hepatology
- Pediatric Surgery
Background:
- Congestive hepatopathy is a known complication of Fontan physiology.
- Limited data exist on the incidence and risk factors of hepatopathy post-Fontan.
Purpose of the Study:
- To evaluate the incidence of hepatic fibrosis in patients after Fontan operation.
- To identify risk factors associated with the development of hepatic fibrosis.
Main Methods:
- Liver biopsies and cardiac catheterizations were performed in 67 patients ≥10 years post-Fontan.
- Hepatic fibrosis was quantified using Sirius red staining (%CD).
- Patient characteristics and hemodynamic measures were assessed as potential risk factors.
Main Results:
- All patients exhibited hepatic fibrosis (%CD median 21.6% vs. 2.6% in controls).
- Time from Fontan operation significantly correlated with the degree of hepatic fibrosis (r=0.33, P<0.01).
- No correlation found between fibrosis and serum liver enzymes, platelet count, or inferior vena cava pressure.
Conclusions:
- Hepatic fibrosis is an inherent feature of Fontan physiology.
- The degree of liver fibrosis progresses with time after the Fontan operation.
- Time from Fontan is the primary factor associated with hepatic fibrosis development.
Background:
Congestive hepatopathy is a recognized complication of Fontan physiology. Data regarding the incidence of hepatopathy and risk factors are lacking.
Methods And Results:
Liver biopsies and cardiac catherizations were performed as part of an evaluation offered to all patients ≥10 years after Fontan. Quantitative determination of hepatic fibrosis was performed using Sirius red staining with automated calculation of collagen deposition per slide (%CD). Biopsies from included subjects were compared to stained specimens from controls without known fibrotic liver disease. Patient characteristics, echocardiographic findings, and hemodynamic measures were evaluated as potential risk factors. The cohort consisted of 67 patients (31 female) at mean age of 17.3±4.5 years and mean time from Fontan of 14.9±4.5 years. Right ventricular morphology was present in 37 subjects. Median %CD by Sirius red staining was 21.6% (range 8.7% to 49.4%) compared to 2.6% (range 2.2% to 3.0%) in controls. There was a significant correlation between time from Fontan and degree of Sirius red staining (r=0.33, P<0.01). Serum liver enzymes and platelet count did not correlate with %CD. The median inferior vena cava pressure was 13 mm Hg (range 6-24 mm Hg) and did not correlate with %CD. There was no difference in %CD based on ventricular morphology or severity of atrioventricular valve insufficiency.
Conclusions:
In this cohort of predominantly asymptomatic children and adolescents electively evaluated after a Fontan operation, all exhibited evidence for hepatic fibrosis as measured by collagen deposition in the liver. Time from Fontan was the only factor significantly associated with collagen deposition. These findings demonstrate that liver fibrosis is an inherent feature of Fontan physiology and that the degree of fibrosis increases over time.
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