Department of Pediatric Hepatology, Institute of Liver and Biliary Sciences, New Delhi, 110070, India.
Indian J Pediatr. 2024 Apr;91(4):374-382. doi: 10.1007/s12098-023-04717-3. Epub 2023 Jun 22.
Acute-on-chronic liver failure (ACLF) is characterized by an acute hepatic insult happening in a patient with underlying cirrhosis with compromised hepatic reserve leading to development of systemic inflammation, sepsis, and organ failure resulting in poor outcome in majority. While Asia Pacific Association for Study of Liver Diseases (APASL) emphasizes on early diagnosis before development of organ failure, European Association for Study of Liver Diseases (EASL) mandates the presence of organ failures to define ACLF. There is a lack of consensus definition of pediatric ACLF although recent APASL guidelines have tried to address the issue. While Wilson disease (WD) and autoimmune hepatitis (AIH) are the most common cause of underlying cirrhosis in children, acute viral hepatitis and flares of WD and AIH are the commonest acute precipitating events. Poor outcomes [death and liver transplantation (LT)] ranging from 19 to 59% have been reported. Prognosis in pediatric ACLF is usually better than that in adults due to greater proportion of treatable etiologies, lesser organ failures, comorbidities and better hepatic reserves. APASL ACLF Research Consortium (AARC) score more than or equal to 11 is predictive of poor 28-90 d mortality. Treatment of pediatric ACLF relies mainly on prompt diagnosis and medical management of a potentially treatable etiology of underlying cirrhosis. Bridging therapies, especially high volume plasma exchange can be initiated early as a bridge to LT or native liver recovery. Those with no improvement in 4-7 d should undergo LT before development of sepsis or multi-organ failure.
慢加急性肝衰竭(ACLF)的特点是在基础肝硬化患者中发生急性肝损伤,导致肝脏储备功能受损,进而引发全身炎症、脓毒症和器官衰竭,多数患者预后不良。亚太肝脏研究学会(APASL)强调在器官衰竭发生之前进行早期诊断,而欧洲肝脏研究学会(EASL)则要求存在器官衰竭来定义 ACLF。虽然最近的 APASL 指南试图解决这个问题,但对于儿科 ACLF 缺乏共识性定义。虽然威尔逊病(WD)和自身免疫性肝炎(AIH)是儿童基础肝硬化的最常见原因,但急性病毒性肝炎和 WD 及 AIH 的发作是最常见的急性诱发事件。不良结局(死亡和肝移植(LT))的报告率为 19%至 59%。由于可治疗病因的比例较高、器官衰竭较少、合并症较少和肝脏储备功能较好,儿科 ACLF 的预后通常比成人好。APASL ACLF 研究联盟(AARC)评分大于或等于 11 预测 28-90 天死亡率较高。儿科 ACLF 的治疗主要依赖于潜在肝硬化病因的及时诊断和药物治疗。桥接治疗,特别是大体积血浆置换,可以在 LT 或原生肝脏恢复的桥梁作用下尽早开始。对于那些在 4-7 天内没有改善的患者,应在发生脓毒症或多器官衰竭之前进行 LT。