Sutton Harry, Tayler Rachel, Chalmers Iain, Cowieson Jennifer, Fraser Karen, Henderson Paul, Hansen Richard
From the Department of Paediatric Gastroenterology, Royal Hospital for Children, Glasgow, United Kingdom.
Department of Paediatric Gastroenterology, Royal Aberdeen Children's Hospital, Aberdeen, United Kingdom.
JPGN Rep. 2022 Jul 29;3(3):e223. doi: 10.1097/PG9.0000000000000223. eCollection 2022 Aug.
Autoimmune hepatitis (AIH) is a rare, but potentially severe, cause of liver disease in children. We aimed to summarize how children with AIH in Scotland presented, were investigated and managed in addition to producing novel epidemiological data and outcomes.
All prevalent pediatric patients with AIH cared for in pediatric services between January 2013 and September 2018 were included. Individual patient data were obtained from electronic patient records in the 3-main academic pediatric centers in Scotland covering the entire population.
Thirty-eight patients were included (25 female) with median follow-up of 33 months (range, 2-145 mo) and 136 total patient years. The incidence between 2014 and 2017 was 0.49/100 000/y (95% confidence interval, 0.29-0.78) and point prevalence between 2013 and 2018 was 1.75/100 000 (95% confidence interval, 1.42-2.13). Thirty-five (92%) patients were autoantibody positive, most commonly anti-nuclear antibody (63%) and anti-smooth muscle antibody (42%). Thirty-seven (97%) patients had induction therapy with oral corticosteroids, 30 (79%) required maintenance treatment with azathioprine, and 23 (61%) received ursodeoxycholic acid. There were 1.4 disease flares per 10 patient years and 3 patients required liver transplantation with an overall 5-year survival rate without the need for transplantation of 95%.
We calculated a novel incidence and prevalence rate for pediatric AIH in Scotland. Nearly all were invariably treated initially with corticosteroids with most placed-on azathioprine as maintenance therapy. Outcomes were generally favorable with low rates of disease flares and the need for transplantation being rare.
自身免疫性肝炎(AIH)是儿童肝病中一种罕见但可能严重的病因。我们旨在总结苏格兰AIH患儿的临床表现、检查及治疗情况,同时提供新的流行病学数据和预后情况。
纳入2013年1月至2018年9月期间在儿科接受治疗的所有AIH患儿。从苏格兰3个主要学术儿科中心的电子病历中获取个体患者数据,涵盖了全部人群。
共纳入38例患者(25例女性),中位随访时间为33个月(范围2 - 145个月),总计136患者年。2014年至2017年的发病率为0.49/100 000/年(95%置信区间,0.29 - 0.78),2013年至2018年的点患病率为1.75/100 000(95%置信区间,1.42 - 2.13)。35例(92%)患者自身抗体呈阳性,最常见的是抗核抗体(63%)和抗平滑肌抗体(42%)。37例(97%)患者接受口服糖皮质激素诱导治疗,30例(79%)需要硫唑嘌呤维持治疗,23例(61%)接受熊去氧胆酸治疗。每10患者年有1.4次疾病复发,3例患者需要肝移植,无需移植的总体5年生存率为95%。
我们计算出了苏格兰儿童AIH的新发病率和患病率。几乎所有患者最初均接受糖皮质激素治疗,大多数患者使用硫唑嘌呤作为维持治疗。疾病复发率低,肝移植需求罕见,总体预后良好。