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采用系统诊断方法对儿童急性肝衰竭进行病因学分析的高收益率:一项全国性队列研究

High yield on aetiology using a systematic diagnostic approach to paediatric acute liver failure, analysis of a nationwide cohort.

作者信息

Nordmann Winther Thilde, Nielsen Alex Yde, Lund Allan, Larsen Fin Stolze, Jørgensen Marianne Hørby

机构信息

Department of Paediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Department of Clinical Microbiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

出版信息

Acta Paediatr. 2023 May;112(5):1082-1090. doi: 10.1111/apa.16746. Epub 2023 Mar 24.

Abstract

AIM

Paediatric acute liver failure (P-ALF) is a rare and devastating condition that leads to death or liver transplantation (LTx) in 40%-60% of cases. Determining the aetiology can enable disease-specific treatment, aid in prognostication for hepatic recovery and guide the decision-making for liver transplantation. This study aimed to retrospectively evaluate a systematic diagnostic approach to P-ALF in Denmark and to collect epidemiological nationwide data.

METHODS

All Danish children aged 0-16 years with P-ALF diagnosed between 2005 and 2018, and who were evaluated using a standardised diagnostic assessment programme, were eligible for retrospective analysis of clinical data.

RESULTS

A total of 102 children with P-ALF were included (presentation at 0 days to 16.6 years of age, 57 females). Aetiological diagnosis was established in 82% of cases, the remainder were indeterminate. Fifty percent of children with P-ALF of indeterminate aetiology died or underwent LTx within 6 months after their P-ALF diagnosis, compared to 24% of children with an aetiological diagnosis, p = 0.04.

CONCLUSION

Following a systematic diagnostic evaluation programme, made it possible to identify the aetiology of P-ALF in 82% of cases which is associated with improved outcomes. The diagnostic workup should never be considered complete but rather adapt to ongoing diagnostic advances.

摘要

目的

小儿急性肝衰竭(P-ALF)是一种罕见且严重的疾病,40%-60%的病例会导致死亡或肝移植(LTx)。确定病因可实现针对性治疗,有助于预测肝脏恢复情况并指导肝移植决策。本研究旨在回顾性评估丹麦针对P-ALF的系统诊断方法,并收集全国范围内的流行病学数据。

方法

所有在2005年至2018年间被诊断为P-ALF、年龄在0-16岁之间且使用标准化诊断评估程序进行评估的丹麦儿童,均符合对临床数据进行回顾性分析的条件。

结果

共纳入102例P-ALF患儿(年龄从0天至16.6岁,57例为女性)。82%的病例确定了病因诊断,其余病例病因不明。病因不明的P-ALF患儿中有50%在P-ALF诊断后6个月内死亡或接受了肝移植,而病因明确的患儿这一比例为24%,p = 0.04。

结论

遵循系统的诊断评估程序,82%的病例能够确定P-ALF的病因,这与改善的预后相关。诊断检查不应被视为已完成,而应适应不断发展的诊断进展。

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