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dc.contributor.authorCuevas-Asturias, Sofia
dc.contributor.authorRafferty, Claire
dc.contributor.authorMitchell, Hannah
dc.contributor.authorTremlett, William
dc.contributor.authorRamnarayan, Padmanabhan
dc.contributor.authorPattison, Natalie
dc.date.accessioned2025-02-07T12:15:02Z
dc.date.available2025-02-07T12:15:02Z
dc.date.issued2025-02-06
dc.identifier.citationCuevas-Asturias , S , Rafferty , C , Mitchell , H , Tremlett , W , Ramnarayan , P & Pattison , N 2025 , ' Protocol on a systematic review of nomenclature and outcomes in children with complex critical illness in Paediatric Critical Care: The basis for consensus definition ' , PLoS ONE , vol. 20 , no. 2 , e0318312 , pp. 1-8 . https://doi.org/10.1371/journal.pone.0318312
dc.identifier.issn1932-6203
dc.identifier.otherJisc: 2663341
dc.identifier.otherpublisher-id: pone-d-24-25160
dc.identifier.urihttp://hdl.handle.net/2299/28787
dc.description© 2025 The Author(s). This is an open access article distributed under the Creative Commons Attribution License (CC BY), https://creativecommons.org/licenses/by/4.0/
dc.description.abstractIntroduction: Paediatric Critical Care (PCC) supports the recovery of children with severe illness. In the UK, there are 30 PCC units with a total of approximately 400 beds. There is constant demand for these beds with a mean five-day length of stay and admissions increasing at a greater rate than age-specific population growth. Prolonged stay patients account for approximately half of all PCC patient bed days. Children with complex critical illness (CCI) need input from multiple different teams alongside support for their family. CCI often become prolonged PCC-stay patients too. Internationally, there is variation in the definition of CCI, this creates service variation and tensions around what resources can be provided including discharge planning, provision, and support. Objective: The face of Paediatric Critical Care, in the UK and internationally has changed over the last ten years with a growing cohort of complex critically ill patients. This systematic review aims to look at current nomenclature, criteria, and outcome measures of priority in this undefined patient population. Methods and materials: Inclusion criteria: All types of studies examining children with complex critical illness (age 18 years old. The final search strategy was developed in Medline and peer-reviewed by a health research librarian not involved in the study. This was translated to other databases as appropriate. Four independent reviewers will screen citations for eligible studies and perform data extraction. Discussion: A systematic review methodology has been used to develop a broad understanding of the literature which will be used to develop further work in this area. Using a rigorous and stepwise approach, the whole spectrum of scientific publications on children with complex critical illness in paediatric intensive care will be reviewed, ensuring this study is as comprehensive as possible. This includes quantitative, qualitative, theoretical, and grey literature. A limitation of this systematic review is the use of many terms to describe children with complex critical illness in the literature resulting in a high number of publications on this topic.en
dc.format.extent8
dc.format.extent280141
dc.language.isoeng
dc.relation.ispartofPLoS ONE
dc.titleProtocol on a systematic review of nomenclature and outcomes in children with complex critical illness in Paediatric Critical Care: The basis for consensus definitionen
dc.contributor.institutionCentre for Applied Clinical, Health and Care Research (CACHE)
dc.contributor.institutionCentre for Future Societies Research
dc.contributor.institutionDepartment of Adult Nursing and Primary Care
dc.contributor.institutionSchool of Health and Social Work
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1371/journal.pone.0318312
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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