Fontan-Associated Anatomical Variants and Hepatic Fibrosis

Objective: We hypothesized that a relationship between post-Fontan hepatic fibrosis and anatomical variants might exist. Methods: Attempting to limit confounding variables, we analyzed data from living, stable, post-extracardiac Fontan patients who underwent cardiac catheterization and transvenous hepatic biopsy procedures between March 2012 and June 2020. Results: We identified 120 patients who met the inclusion criteria. Of the 120, 35 (29%) had pulmonary artery stents. For the 35 with pulmonary artery stents, the average total fibrosis score was 3.2 ± 1.9 and the fibrosis progression rate was 0.36 ± 0.33, and for those with no pulmonary artery stents, the total fibrosis score was 2.6 ± 1.8 and the fibrosis progression rate was 0.27 ± 0.33 (P = .13 and P = .11, respectively). Of the 120, 65 had functional univentricles of right ventricular type. Of these 65, 27 had pulmonary artery stents. For the 27 with pulmonary artery stents, the average total fibrosis score was 3.4 ± 1.8 and the average fibrosis progression rate was 0.39 ± 0.30, and for the 38 without pulmonary artery stents, the average fibrosis score was 2.3 ± 1.5 and the average fibrosis progression rate was 0.23 ± 0.21 (P = .01 for comparison of both values). Conclusions: This study’s findings suggest that a post-extracardiac Fontan with a functional univentricle of right ventricular type plus a pulmonary artery stent may have more advanced liver pathology than those without a pulmonary artery stent at similar Fontan duration years and ages at liver biopsy.

[1]  A. Galindo,et al.  The Rate of Hepatic Fibrosis Progression in Patients Post-Fontan , 2020, Pediatric Cardiology.

[2]  Joshua C. Peterson,et al.  Pulmonary ductal coarctation and left pulmonary artery interruption; pathology and role of neural crest and second heart field during development , 2020, bioRxiv.

[3]  A. Yoganathan,et al.  Cardiac Magnetic Resonance Derived Metrics are Predictive of Liver Fibrosis in Fontan Patients. , 2019, The Annals of thoracic surgery.

[4]  T. Willems,et al.  Pulmonary artery size is associated with functional clinical status in the Fontan circulation , 2019, Heart.

[5]  Y. D'udekem,et al.  Evaluation and Management of the Child and Adult With Fontan Circulation: A Scientific Statement From the American Heart Association. , 2019, Circulation.

[6]  J. Dwek,et al.  Evaluation of Fontan liver disease: Correlation of transjugular liver biopsy with magnetic resonance and hemodynamics. , 2019, Congenital heart disease.

[7]  J. Rychik,et al.  Percutaneous liver biopsy in Fontan patients , 2018, Pediatric Radiology.

[8]  S. Serai,et al.  Diagnostic Performance of MR Elastography for Liver Fibrosis in Children and Young Adults with a Spectrum of Liver Diseases. , 2018, Radiology.

[9]  A. Galindo,et al.  A composite noninvasive index correlates with liver fibrosis scores in post‐Fontan patients: Preliminary findings , 2018, Congenital heart disease.

[10]  P. Noonan,et al.  Stenting of the left pulmonary artery after palliation of hypoplastic left heart syndrome , 2016, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

[11]  David Anderson,et al.  Technical and anatomical factors affecting the size of the branch pulmonary arteries following first-stage Norwood palliation for hypoplastic left heart syndrome. , 2015, Interactive cardiovascular and thoracic surgery.

[12]  B. Zikmund‐Fisher,et al.  Fontan-associated protein-losing enteropathy and plastic bronchitis. , 2015, The Journal of pediatrics.

[13]  Sahar Mansour,et al.  The lymphatic phenotype in Turner Syndrome: an evaluation of nineteen patients and literature review , 2015, European Journal of Human Genetics.

[14]  A. Galindo,et al.  Fontan Outcomes and Pulmonary Blood Flow at Birth , 2015, Pediatric Cardiology.

[15]  Z. Kutalik,et al.  Impact of common risk factors of fibrosis progression in chronic hepatitis C , 2014, Gut.

[16]  A. Galindo,et al.  Transvenous Hepatic Biopsy in Stable Fontan Patients Undergoing Cardiac Catheterization , 2014, Pediatric Cardiology.

[17]  J. Galati,et al.  The Australia and New Zealand Fontan Registry: description and initial results from the first population‐based Fontan registry , 2014, Internal medicine journal.

[18]  A. Dohan,et al.  Transjugular liver biopsy: indications, technique and results. , 2014, Diagnostic and interventional imaging.

[19]  C. Backer The functionally univentricular heart: which is better--right or left ventricle? , 2012, Journal of the American College of Cardiology.

[20]  L. Sullivan,et al.  Portal and Sinusoidal Fibrosis are Common on Liver Biopsy After Fontan Surgery , 2012, Pediatric Cardiology.

[21]  Kirk Kanter,et al.  Larger aortic reconstruction corresponds to diminished left pulmonary artery size in patients with single-ventricle physiology. , 2010, The Journal of thoracic and cardiovascular surgery.

[22]  D. Hagler,et al.  Protein-losing enteropathy after the Fontan operation: associations and predictors of clinical outcome. , 2008, Congenital heart disease.

[23]  Joel L. Berry,et al.  Fluid and Solid Mechanical Implications of Vascular Stenting , 2002, Annals of Biomedical Engineering.

[24]  P. Bedossa,et al.  Natural history of liver fibrosis progression in patients with chronic hepatitis C , 1997, The Lancet.

[25]  L. Reid,et al.  Quantitative structural study of pulmonary circulation in the newborn with aortic atresia, stenosis, or coarctation. , 1977, Thorax.

[26]  L. Reid,et al.  Quantitative structural study of pulmonary circulation in the newborn with pulmonary atresia. , 1977, Thorax.