Patient and public involvement in paediatric intensive care research: Considerations, challenges and facilitating factors

被引:12
作者
Menzies J.C. [1 ]
Morris K.P. [1 ]
Duncan H.P. [1 ]
Marriott J.F. [2 ]
机构
[1] Paediatric Intensive Care Unit, Birmingham Children’s Hospital, Steelhouse Lane, Birmingham
[2] Institute of Clinical Sciences, College of Medical and Dental Sciences, University of Birmingham, Medical School Building, Edgbaston, Birmingham
基金
英国惠康基金;
关键词
Consultation; Consumer involvement; Paediatric intensive care; Patient and public involvement; PPI; Research design;
D O I
10.1186/s40900-016-0046-7
中图分类号
学科分类号
摘要
Introduction Involving the public in health care research is reported to enhance the quality, appropriateness, acceptability and relevance to patients and the public (INVOLVE, Briefing notes for researchers, 2012; Staniszewska et al., Int J Technol Assess Health Care 274:391-9, 2011). Conducting research with children and young people is regarded as challenging and this makes it even more important that the research is well designed and understands the perspective of the child and family. We conducted a narrative literature review of the Patient and Public Involvement (PPI) literature, in the context of Paediatric Intensive Care (PIC). Our aims were to identify what PPI activity has taken place, with whom researchers engaged and what outcomes they reported. Method Electronic databases Medline, CINAHL and Embase (January 2000-June 2016) were searched using the search terms patient and public involvement and consultation. Participants were defined as child, parent, paediatric or pediatric and the context as intensive or critical care. Papers were excluded where activity reflected ‘participants’ as research subjects. Included papers were reviewed using the GRIPP checklist to appraise the quality of reporting. Results The search strategy identified 4717 abstracts. Seventeen papers were reviewed in full and four papers were included, all of which are case studies, describing a consultation approach. None of the papers described PPI as a multi-stage process. Only one study engaged with a former PIC patient and the majority of those consulted did not have any PIC experience. Activity was reported as being of benefit but there was no measurement of the impact of PPI. Conclusion There are numerous challenges associated with the conduct of research in PIC. It is therefore essential that the perspective of children, young people and their parents have been considered in the design of trials. However, there are few published accounts of PPI within the PIC context and the accounts that exist highlight issues about who to approach and when, and a lack of clarity about the best ways to engage with them. Research Ethics Committees and funding bodies expect to see evidence of PPI in research applications and we need to develop our understanding of what contributes towards successful PPI in this context. © The Author(s).
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