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Delayed transfer from hospital to community settings: the older person's perspective.

机译:从医院到社区的延迟转移:老年人的观点。

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Prevention and management of delayed transfer of older people from hospital to community settings is an enduring issue in industrialised societies and is the subject of many recent policies in the United Kingdom. A deeper, evidence-based understanding of the complex organizational and interprofessional issues which contribute to delays in transfer has emerged in recent years. Despite this, and the relative success of recent policies, two recent reviews of the area highlight the lack of studies on patients' perspectives. We sought to address this deficit by using conversational interviews and a phenomenological approach to explore and interpret participants' perceptions of delayed transfer from hospital into the community. A purposive sampling strategy was employed to incorporate participants from different categories of delay identified on weekly Situation Reports. Participants aged 65 years and over (mean age 82 +/- 5.4 years) and with a mean delay of 32 days (+/- 26) were recruited from three hospitals based in two NHS Trusts in the South of England. This paper focuses on their perceptions of the effects of delayed transfer into the community, their involvement in discharge planning and future community care needs. Our findings show that participants actively or passively relinquished their involvement in the processes of discharge planning because of the perceived expertise of others and also feelings of disempowerment secondary to poor health, low mood, dependency, lack of information and the intricacies of discharge planning processes for complex community care needs. Participants expressed a longing for continuity, emphasised the importance of social contact and sometimes appeared unrealistic about their future care needs. While current policies may have helped reduce overall numbers of delayed patients in the UK, our study suggests that there is scope for improvement in the involvement of delayed patients in planning their discharge into the community.
机译:在工业化社会中,预防和管理老年人从医院到社区的延迟转移是一个长期存在的问题,并且是英国近期许多政策的主题。近年来,人们对导致延误调动的复杂组织和专业间问题有了更深入的,基于证据的理解。尽管如此,并且最近的政策取得了相对的成功,最近对该领域的两次评论强调了缺乏有关患者观点的研究。我们试图通过对话访谈和现象学方法来探讨和解释参与者对从医院到社区的延迟转移的看法,以解决这一不足。采用了有目的的抽样策略,以将每周情况报告中确定的不同类别的延迟纳入参与者。年龄在65岁及以上(平均年龄82 +/- 5.4岁)且平均延迟32天(+/- 26)的参与者是从英格兰南部两个NHS信托基金的三家医院中招募的。本文重点关注他们对延迟转移到社区的影响的看法,他们对出院计划的参与以及未来社区护理的需求。我们的发现表明,由于他人的专业知识,以及由于身体状况差,情绪低落,依赖,缺乏信息以及放电计划过程的复杂性而导致的丧失权能的感觉,参与者主动或被动放弃了对放电计划过程的参与。复杂的社区护理需求。参与者表达了对连续性的渴望,强调了社会接触的重要性,有时对他们未来的护理需求不切实际。尽管当前的政策可能有助于减少英国的延迟患者总数,但我们的研究表明,延迟患者在计划出院时参与的工作还有待改进。

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