Lenz Dominic, Abdulaziz Muhammad, Peters Bianca, Wagner Matias, Schlieben Lea D, Corman Victor M, Baumann Ulrich, Bufler Philip, Dattner Tal, Ganschow Rainer, Genzel Kristin, Hammann Nicole, Hartleif Steffen, Hegen Bianca, Henning Stephan, Hoerning André, Jankofsky Martin, Junge Norman, Kathemann Simone, Knoppke Birgit, Kohl-Sobania Martina, Laass Martin, Lainka Elke, Lurz Eberhard, Melter Michael, Müller Hanna, Pilic Denisa, Ries Markus, Schiefele Lisa, Schwerd Tobias, Sturm Ekkehard, Wegner Mechtild, Urschitz Michael S, Garbade Sven F, Wenning Daniel, Drosten Christian, Fichtner Alexander, Kölker Stefan, Hoffmann Georg F, Prokisch Holger, Staufner Christian
Department I, Medical Faculty Heidelberg, Center for Pediatric and Adolescent Medicine, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
Clinic for Pediatrics I, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany.
J Pediatr Gastroenterol Nutr. 2025 Sep;81(3):653-662. doi: 10.1002/jpn3.70149. Epub 2025 Jul 7.
Paediatric acute liver failure (PALF) is a rare but life-threatening condition, yet comprehensive epidemiological data in Germany are lacking. Our study aimed to systematically analyse incidence, aetiology, and outcome of PALF in Germany.
In a nationwide, population-based surveillance study, cases of PALF (defined following the PALF study group inclusion criteria) were queried from 2016 to 2018 through the German Paediatric Surveillance Unit (ESPED). Demographic, clinical, laboratory, therapeutic, and outcome data were collected and analysed. In case of unexplained aetiology, whole exome and virus sequencing was offered as a complementary diagnostic.
Over the 3-year period, 148 cases were reported, yielding an estimated incidence of 3.7 per 1 million children per year. Neonates and infants were predominantly affected (45% of the cases); median age at PALF was 1.2 years (range: 0-17.9 years). Metabolic/genetic diseases were the most common cause (23%), followed by infectious causes (17%). The overall diagnostic yield was 73%, diagnosis remained unknown in 40 cases. Clinical outcome was age-dependent: new-borns showed a significant higher lethality (42%), followed by infants (29%), toddlers (15%), and school children (12%). Liver transplantation was reported in 22% of cases.
This study provides comprehensive insights into PALF epidemiology in Germany. Metabolic/genetic causes and infectious diseases were most common. Advances in standardised diagnostic work-up and genetic analysis have enhanced diagnostic yield, yet mortality remains substantial, particularly among neonates. Further research is warranted to improve diagnostic accuracy, therapeutic outcomes, and overall management of PALF.
儿童急性肝衰竭(PALF)是一种罕见但危及生命的疾病,然而德国缺乏全面的流行病学数据。我们的研究旨在系统分析德国PALF的发病率、病因及转归。
在一项全国性的基于人群的监测研究中,通过德国儿科监测单位(ESPED)查询2016年至2018年符合PALF研究组纳入标准的PALF病例。收集并分析人口统计学、临床、实验室、治疗及转归数据。对于病因不明的病例,提供全外显子组和病毒测序作为补充诊断。
在这3年期间,共报告148例病例,估计每年每百万儿童中的发病率为3.7例。新生儿和婴儿受影响最为显著(占病例的45%);PALF的中位年龄为1.2岁(范围:0 - 17.9岁)。代谢/遗传疾病是最常见的病因(23%),其次是感染性病因(17%)。总体诊断率为73%,40例病例诊断仍不明确。临床转归与年龄相关:新生儿的致死率显著更高(42%),其次是婴儿(29%)、幼儿(15%)和学龄儿童(12%)。22%的病例接受了肝移植。
本研究为德国PALF的流行病学提供了全面的见解。代谢/遗传病因和感染性疾病最为常见。标准化诊断检查和基因分析的进展提高了诊断率,但死亡率仍然很高,尤其是在新生儿中。有必要进一步开展研究以提高PALF的诊断准确性、治疗效果及整体管理水平。