Paediatric Critical Care Unit, Noah's Ark Children's Hospital for Wales, Cardiff, UK
School of Medicine, Cardiff University, Cardiff, UK.
BMJ Open. 2023 Mar 27;13(3):e067002. doi: 10.1136/bmjopen-2022-067002.
Early recognition and appropriate management of paediatric sepsis are known to improve outcomes. A previous system's biology investigation of the systemic immune response in neonates to sepsis identified immune and metabolic markers that showed high accuracy for detecting bacterial infection. Further gene expression markers have also been reported previously in the paediatric age group for discriminating sepsis from control cases. More recently, specific gene signatures were identified to discriminate between COVID-19 and its associated inflammatory sequelae. Through the current prospective cohort study, we aim to evaluate immune and metabolic blood markers which discriminate between sepses (including COVID-19) from other acute illnesses in critically unwell children and young persons, up to 18 years of age.
We describe a prospective cohort study for comparing the immune and metabolic whole-blood markers in patients with sepsis, COVID-19 and other illnesses. Clinical phenotyping and blood culture test results will provide a reference standard to evaluate the performance of blood markers from the research sample analysis. Serial sampling of whole blood (50 μL each) will be collected from children admitted to intensive care and with an acute illness to follow time dependent changes in biomarkers. An integrated lipidomics and RNASeq transcriptomics analyses will be conducted to evaluate immune-metabolic networks that discriminate sepsis and COVID-19 from other acute illnesses. This study received approval for deferred consent.
The study has received research ethics committee approval from the Yorkshire and Humber Leeds West Research Ethics Committee 2 (reference 20/YH/0214; IRAS reference 250612). Submission of study results for publication will involve making available all anonymised primary and processed data on public repository sites.
NCT04904523.
早期识别和适当处理儿科脓毒症可改善预后。之前对新生儿脓毒症全身免疫反应的系统生物学研究发现了一些免疫和代谢标志物,这些标志物对检测细菌感染具有很高的准确性。此外,之前在儿科年龄组也有报道过用于区分脓毒症与对照病例的基因表达标志物。最近,还确定了特定的基因特征来区分 COVID-19 及其相关炎症后遗症。通过目前的前瞻性队列研究,我们旨在评估免疫和代谢血液标志物,以区分重症患儿和年轻人中脓毒症(包括 COVID-19)与其他急性疾病。
我们描述了一项前瞻性队列研究,用于比较脓毒症、COVID-19 和其他疾病患者的免疫和代谢全血标志物。临床表型和血液培养试验结果将为评估研究样本分析中血液标志物的性能提供参考标准。将从入住重症监护病房的急性疾病患儿中连续采集全血(每次 50 μL),以随时间变化监测生物标志物。将进行整合脂质组学和 RNAseq 转录组学分析,以评估区分脓毒症和 COVID-19 与其他急性疾病的免疫代谢网络。该研究已获得延期同意。
该研究已获得约克郡和亨伯利兹西部研究伦理委员会 2 号(参考号 20/YH/0214;IRAS 参考号 250612)的研究伦理委员会批准。发表研究结果的提交将涉及在公共存储库网站上提供所有匿名的原始和处理后数据。
NCT04904523。