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J. Heart Lung Transplant. · Jul 2015
Portal and centrilobular hepatic fibrosis in Fontan circulation and clinical outcomes.
- Fred M Wu, Maureen M Jonas, Alexander R Opotowsky, Amy Harmon, Roshan Raza, Chinweike Ukomadu, Michael J Landzberg, Michael N Singh, Anne Marie Valente, Egidy AssenzaGabrieleGDepartment of Cardiology, Boston Children's Hospital, Harvard Medical School; Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School., and Antonio R Perez-Atayde.
- Department of Cardiology, Boston Children's Hospital, Harvard Medical School; Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School. Electronic address: fred.wu@cardio.chboston.org.
- J. Heart Lung Transplant. 2015 Jul 1; 34 (7): 883-91.
BackgroundThe Fontan operation redirects venous blood flow directly to the pulmonary circulation in subjects with single ventricle anatomy. Congestive hepatopathy and cirrhosis have been described in subjects with Fontan circulation, but the prevalence of and predictors for liver disease remain unknown.MethodsWe performed a retrospective study of liver histopathology in Fontan subjects who had liver biopsy or autopsy. All specimens were graded using a pre-determined protocol. Additional data were collected through chart review. Among 68 subjects, specimens were obtained at a median age of 23.2 years (range 5.0 to 52.7 years). Median time since Fontan was 18.1 years (range 1.2 to 32.7 years).ResultsCentrilobular fibrosis was seen in every specimen, with 41.2% showing Grade 4 centrilobular fibrosis. Portal fibrosis was seen in 82.3% of specimens, with 14.7% showing cirrhosis. Megamitochondria were seen in 58.8% of specimens. Centrilobular fibrosis grade was greater in those with a dominant left or right ventricle than in those with a combined right and left systemic ventricle (p = 0.008). Portal fibrosis grade correlated with alkaline phosphatase (p = 0.04) and mode of biopsy (p = 0.02). Neither centrilobular fibrosis nor portal fibrosis grade was predictive of transplant-free survival or overall survival.ConclusionsIndividuals with Fontan physiology have a high prevalence of hepatic fibrosis. Signs and symptoms of liver disease did not predict histopathologic findings. Few risk factors for advanced disease were identified. Histopathology findings did not predict transplant-free survival. The role of liver biopsy in this population remains uncertain.Copyright © 2015 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.
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