Pediatrics. 2022 Jan 1;149(1 Suppl 1):S59-S65. doi: 10.1542/peds.2021-052888I.
Develop evidence-based criteria for individual organ dysfunction.
Evaluate current evidence and develop contemporary consensus criteria for acute liver dysfunction with associated outcomes in critically ill children.
Electronic searches of PubMed and Embase conducted from January 1992 to January 2020, used medical subject heading terms and text words to characterize acute liver dysfunction and outcomes.
Studies evaluating critically ill children with acute liver dysfunction, assessed screening tools, and outcomes were included. Studies evaluating adults, infants ≤36 weeks gestational age, or animals or were reviews/commentaries, case series with sample size ≤10, or non-English language studies were excluded.
Data were abstracted from each eligible study into a data extraction form along with risk of bias assessment by a task force member.
The systematic review supports criteria for acute liver dysfunction, in the absence of known chronic liver disease, as having onset of symptoms <8 weeks, combined with biochemical evidence of acute liver injury, and liver-based coagulopathy, with hepatic encephalopathy required for an international normalized ratio between 1.5 and 2.0.
Unable to assess acute-on-chronic liver dysfunction, subjective nature of hepatic encephalopathy, relevant articles missed by reviewers.
Proposed criteria identify an infant, child, or adolescent who has reached a clinical threshold where any of the 3 outcomes (alive with native liver, death, or liver transplant) are possible and should prompt an urgent liaison with a recognized pediatric liver transplant center if liver failure is the principal driver of multiple organ dysfunction.
制定针对各个器官功能障碍的循证标准。
评估现有证据并制定与危重症儿童相关的急性肝功能障碍及其结局的当代共识标准。
从 1992 年 1 月至 2020 年 1 月,通过电子检索 PubMed 和 Embase,使用医学主题词和文本词来描述急性肝功能障碍和结局。
纳入评估危重症合并急性肝功能障碍儿童的研究,评估筛选工具和结局。排除评估成人、胎龄≤36 周的婴儿、动物或为综述/评论、样本量≤10 的病例系列、或非英语语言的研究。
由一名工作组成员从每项合格研究中提取数据,并进行偏倚风险评估。
系统评价支持急性肝功能障碍的标准,即无已知慢性肝病的情况下,症状发作<8 周,伴有急性肝损伤的生化证据和基于肝脏的凝血功能障碍,国际标准化比值为 1.5 至 2.0 时需要肝性脑病。
无法评估慢性加急性肝功能障碍,肝性脑病的主观性,综述遗漏相关文章。
提出的标准确定了已经达到临床阈值的婴儿、儿童或青少年,这 3 种结局(有原生肝存活、死亡或肝移植)中的任何一种都有可能,并且如果肝功能衰竭是多器官功能障碍的主要驱动因素,应立即与认可的儿科肝移植中心联系。