Understanding family carer experiences and perceptions of engagement in delirium prevention and care for adults in hospital: Qualitative systematic review

批判性评价 奇纳 心理信息 定性研究 背景(考古学) 护理部 主题分析 医学 谵妄 心理学 梅德林 精神科 心理干预 法学 社会科学 社会学 政治学 古生物学 替代医学 病理 生物
作者
Karen Lee‐Steere,Alison Mudge,Jacki Liddle,Sally Bennett
出处
期刊:Journal of Clinical Nursing [Wiley]
卷期号:33 (4): 1320-1345 被引量:3
标识
DOI:10.1111/jocn.16990
摘要

Abstract Aim To identify, describe and synthesise what is known about family carers' experiences and perspectives of engagement in delirium prevention and care for adults in hospital. Design Systematic review and synthesis of qualitative evidence. Data Sources Comprehensive literature search within PubMed, CINAHL, EMBASE, Scopus, Cochrane Central and PsycInfo databases to August 2022. Peer reviewed original qualitative research published in English. Methods Data were extracted using Covidence systematic review software. Methodological quality was reviewed against the Critical Appraisal Skills Program (CASP) Qualitative Checklist. Thematic synthesis was used to develop analytical themes. Confidence in the Evidence from Reviews of Qualitative Research (GRADE‐CERQual) framework was applied to findings. Results Of 3429 records identified, 29 met criteria for final inclusion. Studies included a range of settings (intensive care, medical and surgical wards) and family carer types (spouse, daughter, parent and friend). Three primary themes Shared Caregiving , Partnership and Support , Communication for Shared Understanding and three cross‐cutting contextual themes Care Transitions , Family Carer Context and Hospital Context were identified. Family carers have mixed experiences of involvement in delirium care and prevention. Family carer engagement in care impacted perceptions of care quality and their own self‐efficacy. Where person‐centred care expectations were not met, some family carers adopted compensatory or care contingency strategies. Information sharing and timely support from hospital staff who understood the carer context supported carer involvement. Supportive physical environments and addressing power imbalances allowed greater engagement. Conclusion Family carers often wish to be involved in delirium prevention and care, but need to be recognised as individuals, listened to, informed and supported to optimise their contribution. Impact The review findings can guide health professional and decision makers to optimise family carer involvement in delirium care programs. Protocol Registration PROSPERO [CRD42020221854]. Reporting ENTREQ. No Patient or Public Contribution.
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