Patel Bhavesh, Serper Marina, Ruckdeschel Emily, Partington Sara L, Andrade Lauren, Tobin Lynda, Kim Yuli, Hoteit Maarouf A
Internal Medicine and Pediatrics Residency Program, Hospital of the University of Pennsylvania and Children's Hospital of Philadelphia, 3400 Spruce St, Philadelphia, PA, 19104, USA.
Division of Gastroenterology and Hepatology, Hospital of the University of Pennsylvania, 3400 Spruce St, Philadelphia, PA, 19104, USA.
Int J Cardiol Congenit Heart Dis. 2022 Apr 11;8:100371. doi: 10.1016/j.ijcchd.2022.100371. eCollection 2022 Jun.
The natural history and complications of Fontan-associated liver disease (FALD) are not well-characterized. We aim to describe the incidence and prevalence of and risk factors for adverse liver-related complications in FALD.
This is a single-center, retrospective cohort study of adult Fontan patients followed in an adult congenital heart disease center from 2006 to 2019. The primary outcome was clinical complications of liver disease (CCLD) defined as portal hypertension (pHTN)-related ascites, pHTN-related gastrointestinal bleeding, hepatic encephalopathy, or hepatocellular carcinoma. We also explored the composite outcome of CCLD, transplantation, or death.
Among 182 adult Fontan patients (46% female), median time from Fontan to first liver evaluation was 25.5 years (interquartile range [IQR] 22.3-30.4) with median subsequent follow-up of 4.1 years (IQR 2.5-7.6). There were 14 CCLD, 6 heart-liver and 1 heart transplant, and 16 deaths. The cumulative incidence of CCLD and the composite outcome were 2.6 per 1000-person years and 6.2 per 1000 person-years, respectively. Median time from Fontan to CCLD was 26.8 years (IQR 23.1-31.2), and to the composite outcome 26.6 years (IQR 23.1-30.5). Prior diuretic use was associated with the development of CCLD (hazard ratio [HR] 10.03, 95% confidence interval [CI] 1.25-80.22, P 0.030). Diuretic use (HR 16.47, 95% CI 3.90-69.57, P < 0.001), thrombocytopenia (HR 2.30, 95% CI 1.05-5.01, P 0.036), and cyanosis (HR 5.68, 95% CI 2.47-13.08, P < 0.001) were associated with the composite outcome.
We identified clinical factors associated with adverse outcomes in FALD that may help guide early recognition of complications and clinical management.
Fontan相关肝病(FALD)的自然病史和并发症尚未得到充分描述。我们旨在描述FALD中肝脏相关不良并发症的发生率、患病率及危险因素。
这是一项单中心回顾性队列研究,研究对象为2006年至2019年在一家成人先天性心脏病中心随访的成年Fontan患者。主要结局是肝病临床并发症(CCLD),定义为门静脉高压(pHTN)相关腹水、pHTN相关胃肠道出血、肝性脑病或肝细胞癌。我们还探讨了CCLD、移植或死亡的复合结局。
182例成年Fontan患者中(46%为女性),从Fontan手术到首次肝脏评估的中位时间为25.5年(四分位间距[IQR]22.3 - 30.4),随后中位随访时间为4.1年(IQR 2.5 - 7.6)。发生14例CCLD、6例心肝联合移植和1例心脏移植,以及16例死亡。CCLD的累积发病率和复合结局分别为每1000人年2.6例和每1000人年6.2例。从Fontan手术到CCLD的中位时间为26.8年(IQR 23.1 - 31.2),到复合结局的中位时间为26.6年(IQR 23.1 - 30.5)。既往使用利尿剂与CCLD的发生相关(风险比[HR]10.03,95%置信区间[CI]1.25 - 80.22,P = 0.030)。使用利尿剂(HR 16.47,95%CI 3.90 - 69.57,P < 0.001)、血小板减少(HR 2.30,95%CI 1.05 - 5.01,P = 0.036)和发绀(HR 5.68,95%CI 2.47 - 13.08,P < 0.001)与复合结局相关。
我们确定了与FALD不良结局相关的临床因素,这可能有助于指导并发症的早期识别和临床管理。