Teschke Rolf, Eickhoff Axel
Department of Internal Medicine II, Division of Gastroenterology and Hepatology, Klinikum Hanau, D-63450 Hanau, Academic Teaching Hospital of the Medical Faculty, Goethe University Frankfurt/Main, Frankfurt/Main, Germany.
J Clin Transl Hepatol. 2025 Aug 28;13(8):693-700. doi: 10.14218/JCTH.2025.00203. Epub 2025 Aug 7.
Acute liver failure (ALF) is a disorder with various etiologies. Although the causes leading to this disruptive condition are well documented in published ALF cohorts, there is significant concern among patients who experience ALF with indeterminate causes, an issue requiring thorough analysis. This review aimed to analyze cohort studies on ALF with a focus on unknown causes leading to classification as indeterminate ALF. The analysis revealed that, among 67 worldwide adult and pediatric ALF cohorts, indeterminate causes of ALF ranged from 2% to 100%, with an average of 30%. Among the 13 pediatric ALF cohorts, the corresponding range was 22% to 100%, with an average of 47%, while among the 55 adult ALF cohorts, the range was 2% to 78%, with an average of 26%. The percentage values were higher in pediatric cohorts due to the higher incidence of rare genetic causes compared to adult patients. Notably, higher rates of indeterminate causes were found in cohorts studied before the availability of diagnostic serologic screening parameters and polymerase chain reaction techniques for various hepatitis virus infections. Patients with indeterminate ALF may not have received a specific treatment that, if effective, could have helped prevent liver transplantation. It is concluded that, in future cases, all efforts must be undertaken to clearly establish the cause of severe liver injury, enabling effective therapy when available and helping reduce the risk of progression to ALF and the need for liver transplantation.
急性肝衰竭(ALF)是一种病因多样的病症。尽管导致这种破坏性状况的病因在已发表的ALF队列研究中有充分记载,但病因不明的ALF患者仍存在重大担忧,这一问题需要深入分析。本综述旨在分析关于ALF的队列研究,重点关注导致被归类为不明原因ALF的未知病因。分析显示,在全球67个成人和儿童ALF队列中,ALF的不明原因比例从2%到100%不等,平均为30%。在13个儿童ALF队列中,相应比例为22%到100%,平均为47%,而在55个成人ALF队列中,比例为2%到78%,平均为26%。由于与成年患者相比,罕见遗传病因的发生率较高,儿童队列中的百分比值更高。值得注意的是,在各种肝炎病毒感染的诊断血清学筛查参数和聚合酶链反应技术可用之前进行研究的队列中,不明原因发生率更高。病因不明的ALF患者可能未接受过特定治疗,而这种治疗若有效,本可有助于预防肝移植。结论是,在未来的病例中,必须尽一切努力明确严重肝损伤的病因,以便在有有效治疗方法时进行有效治疗,并有助于降低进展为ALF的风险以及肝移植的需求。