Stanski Natalja L, Oh Jun, Basu Rajit K
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH USA.
Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH USA.
Intensive Care Med Paediatr Neonatal. 2025;3(1):35. doi: 10.1007/s44253-025-00086-1. Epub 2025 Sep 24.
Acute kidney injury (AKI) is common in critically ill children and neonates and imparts an increased risk for morbidity and mortality. Despite a growing recognition of the untoward consequences of AKI, its management continues to rely on supportive care alone, after numerous clinical trials have failed to identify effective disease-modifying therapies. This failure to advance the field is likely due in large part to the heterogeneity of AKI, which demands a precision approach to diagnosis and management. Despite the emergence of several novel AKI biomarkers with the ability to refine the AKI diagnosis beyond what is afforded by changes in serum creatinine and/or urine output alone, widespread translation of these biomarkers to practice has been limited. In this review, we outline a roadmap for AKI risk-stratification, diagnosis, management, and follow-up that is rooted in precision medicine principles and feasible with the tools currently available in pediatric ICUs. This roadmap highlights the importance of dynamic (as opposed to static) assessment of the critically ill child with, at-risk for, and recovering from AKI, and introduces the concept of theragnostic biomarkers that are both the target of and change with treatment, thus helping guide the therapeutic approach. Finally, we highlight the need for re-defining appropriate endpoints in AKI clinical trials testing the interventions proposed here (and others) to ensure we are identifying treatments that will meaningfully improve outcomes for critically ill children with AKI.
急性肾损伤(AKI)在危重症儿童和新生儿中很常见,会增加发病和死亡风险。尽管人们越来越认识到AKI的不良后果,但在众多临床试验未能确定有效的疾病改善疗法后,其治疗仍仅依赖支持性治疗。该领域进展停滞很可能在很大程度上是由于AKI的异质性,这需要精准的诊断和管理方法。尽管出现了几种新型AKI生物标志物,能够在仅靠血清肌酐和/或尿量变化所提供的诊断基础上进一步完善AKI诊断,但这些生物标志物在临床实践中的广泛应用仍然有限。在本综述中,我们概述了一个基于精准医学原则、适用于儿科重症监护病房现有工具的AKI风险分层、诊断、管理及随访路线图。该路线图强调了对患有AKI、有AKI风险以及正从AKI中恢复的危重症儿童进行动态(而非静态)评估的重要性,并引入了治疗诊断生物标志物的概念,这类标志物既是治疗的靶点,又会随治疗而变化,从而有助于指导治疗方法。最后,我们强调需要重新定义AKI临床试验中的合适终点,以测试本文(及其他)提出的干预措施,确保我们确定的治疗方法能切实改善患有AKI的危重症儿童的预后。