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Addressing the Needs of Persons Living With Dementia Across Care Settings (A Collaborative Symposium between the Assisted Living and Research in Quality Care Interest Groups)

机译:解决患有护理环境中痴呆症的人的需求(在辅助生活与质量保健兴趣集团的辅助生活和研究之间的合作研讨会)

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摘要

Understanding the needs of persons living with dementia is critical to promoting quality of life and care. Co-sponsored by the Assisted Living (AL) and Research in Quality Care Interest Groups, this symposium includes four papers that present new ways to use claims data, qualitative data, benchmarking data, and intervention data to promote well-being for persons living with dementia. First, Degenholtz and Van Cleve use Pennsylvania Medicaid data from 2014-2016 to examine the provision of personal care to persons with and without dementia. They find that those living with dementia received more personal care per day across levels of physical disability and discuss implications for home and community based services policy. Next, Kemp et al. investigate meaningful engagement among assisted living residents with dementia using qualitative data collected over a one-year period in four diverse care communities. Findings show a range of engagement experiences and point to the influence of key resident, care partner, and care community influences. Third, Morgan et al. use data from a statewide probability sample of nursing home staff (n=438) to identify barriers and facilitators to person-centered care. Findings show key barriers to delivering person-centered care, including a lack of staff empowerment practices and low use of consistent assignment. Last, Zimmerman et al. present an evidence-based program, “Mouth Care Without a Battle” developed in nursing homes. Using data from over 2,000 assisted living stakeholders, they situate their findings within implementation science and the NIH Stage Model and make their findings transferable regardless of focus or setting.
机译:了解痴呆症的人的需求对于促进生活质量和关怀至关重要。此次专题讨论会的研究包括四篇论文,包括四篇论文,这些论文呈现了使用索赔数据,定性数据,基准数据和干预数据的新方法,以促进与生活人员促进福祉痴呆。首先,Degenholtz和Van Cleve使用2014 - 2016年的宾夕法尼亚医疗补助数据来检查为有和没有痴呆症的人提供个人护理。他们发现,痴呆症的人每天患上物理残疾水平获得更多个人护理,并讨论为家庭和社区的服务政策的影响。接下来,Kemp等人。使用在四个不同护理社区中的一年内收集的定性数据,调查患有痴呆症的辅助生活居民之间的有意义的参与。调查结果显示了一系列参与体验和关键居民,护理合作伙伴和护理社区影响的影响。第三,Morgan等。使用来自护理家庭工作人员(n = 438)的州各种概率样本的数据,以确定以人为本的护理障碍和促进者。调查结果显示提供以人为本的护理,包括缺乏员工赋予权力实践和低使用一致的任务。最后,Zimmerman等。在护理家庭中提出了一种以证据为基础的计划,“没有战斗”。使用来自超过2,000个辅助的生活利益相关者的数据,它们在实施科学和NIH阶段模型中占据了他们的调查结果,并使他们的发现可以转移,而不管焦点或设置。

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