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Immune and metabolic markers for identifying and investigating severe Coronavirus disease and Sepsis in children and young people (pSeP/COVID ChYP study): protocol for a prospective cohort study

Authors :
Richard Skone
Daniel White
Bethan Phillips
Jennifer Evans
Robert Andrews
Benjamin Saunders
Kerry Hood
Mallinath Chakraborty
Sarah Edkins
Barbara Paquete
Sian Foulkes
Anna Barrow
Siske Struik
Valerie O'Donnell
Sara Ali
Patrícia R S Rodrigues
Angela Strang
Summia Zaher
Simran Sharma
Luke C Davies
Linda Moet
James E McLaren
Gareth L Watson
Peter Ghazal
Edward Parkinson
Sivakumar Oruganti
William John Watkins
Selyf Shapey
Rim al Samsam
Malcolm Gajraj
Michelle Jardine
Jong Eun Song
Lloyd Abood
Sarah Joanne Kotecha
Awen Evans
Iona Buchanan
Susan Bowes
Begum Ali
Maya Gore
Rhian Thomas-Turner
Federico Liberatore
Thomas Woolley
Source :
BMJ Open, Vol 13, Iss 3 (2023)
Publication Year :
2023
Publisher :
BMJ Publishing Group, 2023.

Abstract

Introduction 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.Methods and analysis 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.Ethics and dissemination 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.Trial registration number NCT04904523.

Subjects

Subjects :
Medicine

Details

Language :
English
ISSN :
20446055
Volume :
13
Issue :
3
Database :
Directory of Open Access Journals
Journal :
BMJ Open
Publication Type :
Academic Journal
Accession number :
edsdoj.2d1c8f29b48f4539bf38b44ed3678f38
Document Type :
article
Full Text :
https://doi.org/10.1136/bmjopen-2022-067002