International survey on immunological diagnostics in children with sepsis.

Nina Schöbi, Philipp K A Agyeman, Vanessa Sancho-Shimizu, Johannes Trück, Julie C Fitzgerald, Luregn J Schlapbach
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Abstract

Background: Sepsis is a leading cause of death and disability in children and it affects in up to 50% previously healthy children who have access to health care. Undiagnosed inborn error of immunity, considered to be rare at population level, may underlie host immune dysregulation and result in exceptionally high risk for life-threatening infections.

Methods: From May 2023 to March 2024, physicians involved in the care of children with sepsis were questioned regarding their follow-up investigation practice in paediatric patients after community-acquired sepsis. This survey was distributed through three international societies.

Results: A total of 168 responses from 50 countries were analysed. The majority (82%), reported to have more than 10 years of experience. More than half (53%) stated to work in Paediatric Infectious Diseases. Major variability across respondents was observed in the approach to different scenarios of patients with sepsis. Severity of presentation, and unusual presentations increased the likelihood of ordering immunological investigations. Only 7% reported to have access to a standardised sepsis specific guideline to immunologically investigate paediatric patients after sepsis.

Conclusion: The results of this survey highlight a broad range of practices surrounding immunological investigations of children with sepsis. A consensus-based algorithm for standardised immunological and genetic testing in paediatric patients after sepsis could guide practice and inform future studies in the field.

Supplementary information: The online version contains supplementary material available at 10.1007/s44253-026-00120-w.

儿童败血症免疫学诊断的国际调查。
背景:败血症是儿童死亡和残疾的主要原因,它影响到多达50%以前健康的儿童,这些儿童可以获得卫生保健。未确诊的先天性免疫错误,在人群水平上被认为是罕见的,可能是宿主免疫失调的基础,并导致危及生命的感染风险异常高。方法:从2023年5月至2024年3月,对参与脓毒症患儿护理的医生进行随访调查,了解他们对社区获得性脓毒症患儿的随访情况。这项调查是通过三个国际学会分发的。结果:共分析了来自50个国家的168份回复。据报道,大多数人(82%)有10年以上的工作经验。超过一半(53%)的人自称在儿科传染病部门工作。在脓毒症患者的不同情况下,观察到应答者的主要差异。严重的表现,和不寻常的表现增加了订购免疫调查的可能性。据报道,只有7%的人可以获得标准化的败血症特异性指南,对败血症后的儿科患者进行免疫调查。结论:本调查的结果突出了脓毒症患儿免疫学调查的广泛实践。一种基于共识的算法用于败血症后儿科患者的标准化免疫和基因检测,可以指导实践并为该领域的未来研究提供信息。补充信息:在线版本包含补充资料,提供地址:10.1007/s44253-026-00120-w。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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