Fontan-Associated Liver Disease and the Double Organ Transplant: Addressing the Heart of the Argument

被引:0
|
作者
Ravanbakhsh N. [1 ]
Emamaullee J. [2 ,3 ]
机构
[1] Division of Gastroenterology and Hepatology, Department of Pediatrics, Lurie Children’s Hospital, 30 E Huron Street #2706, Chicago, 60611, IL
[2] Department of Surgery, University of Southern California, Los Angeles, CA
[3] Liver Transplant Program, Children’s Hospital-Los Angeles, Los Angeles, CA
关键词
Cirrhosis; Combined heart liver transplant; Congenital heart disease; FALD; HCC; Hepatic fibrosis;
D O I
10.1007/s40746-024-00295-4
中图分类号
学科分类号
摘要
Purpose of Review: Describe the history, background, histopathology, and current practices of Fontan-associated liver disease (FALD), a universal sequelae of Fontan physiology. Build awareness and insight into the risk factors for disease progression, its impact on long-term mortality, and implications for heart transplant (HT) alone versus combined heart liver transplant (CHLT). Highlight an era in which > 90% of patients with single ventricle physiology are reaching adulthood, manifesting the sequelae of multi-organ dysfunction including FALD and highlighting the urgent need to create evidence-based practices to help support this patient population. Recent Findings: Patients with advanced FALD are at higher risk of adverse events and even suboptimal outcomes. Multiple centers are now reporting comparable, if not superior, outcomes for patients post-Fontan with compensated FALD who undergo CHLT compared to HT. Summary: In the setting of organ scarcity, it is especially important to identify high risk patients with FALD who may benefit from CHLT, as the dual organ transplant may optimize long-term survival, quality of life, and reduce sequelae of allograft rejection for patients with single ventricle physiology CHD. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2024.
引用
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页码:25 / 38
页数:13
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