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Life under lockdown and social restrictions - the experiences of people living with dementia and their carers during the COVID-19 pandemic in England

机译:锁定和社会限制下的生活 - 在英格兰的Covid-19大流行病中,生活在痴呆症和他们的照顾者的经历

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The impact of COVID-19 restrictions on people living with dementia and their carers is an emerging focus of recent research determining how we can best support this population. People living with dementia have faced service curtailment, increased risk for COVID-19, as well as potential heightened deterioration. This study reports the experiences of people living with dementia and their family carers during the early months of the COVID-19 pandemic in England and the impact on them. We recruited and remotely interviewed 30 people living with dementia in their own homes and 31 family carers, via video or telephone call in mid-2020. Data were transcribed and analysed using thematic analysis. People living with dementia often had a basic understanding of COVID-19 restrictions but could have difficulty translating this into personalised risk-appraisal of their own actions. Managing COVID-19 risks facing people living with dementia at home was largely done by family carers, exemplified by changes to living arrangements, which could strain or sustain caring relationships. Well-established familial caring relationships contributed to the wellbeing of the person living with dementia and their carer, as well as keeping to simple routines that included leaving the home for exercise and stimulation. People living with dementia reported some negative psychological and cognitive effects due to the imposed restrictions, such as increased apathy, irritability, or anxiety, which were fuelled by lack of social engagement. Structuring routine (remote) social interactions where possible could increase social engagement and improve wellbeing for people living with dementia, especially those with limited familial support in a post-COVID-19 context. As some care relationships had been restructured to manage COVID-19 risks, additional carer strain may emerge as a result of the impact on the independence of the person living with dementia and come to the attention of professionals in health and care services. People living with dementia and their carers highlighted the importance of maintaining or adapting routines which may be useful learning for professionals, although additional support may be necessary for those who are impacted by more severe or worsening symptoms of dementia.
机译:Covid-19限制对生活在痴呆症及其护理人员的人们的影响是最近研究的新兴焦点确定我们如何最好地支持这一人口。生活在痴呆症的人面临服务削减,增加了Covid-19的风险,以及潜在的降低劣化。本研究报告了在英国Covid-19大流行早期的痴呆症和家庭照料中患有痴呆症和家庭照顾者的经验以及对他们的影响。我们在2020年代中期通过视频或电话,我们招募并远程采访了30名患有痴呆症和31家家庭照顾者的人。使用主题分析转录和分析数据。生活在痴呆症的人通常对Covid-19限制的基本了解,但可能难以将其转化为自己行为的个性化风险评估。管理Covid-19面临着家居痴呆症的人的风险基本上由家庭护理人员造成的,而是通过对生活安排的变化来表现出来,这可能会疲劳或维持关怀关系。完善的家族性关怀关系促成了生活在痴呆症及其护理人的人的福祉,以及保持简单的例程,其中包括离开家庭的运动和刺激。患有痴呆症的人们由于施加的限制,例如增加的冷漠,烦躁或焦虑,这是由于缺乏社会参与而导致的。在可能的情况下,在可能会增加社会参与和改善痴呆症的人的社交互动,尤其是在Covid-19后的内容中有限的人来提高社会参与。由于一些关心关系进行了重组来管理Covid-19风险,因此由于对痴呆症患者的独立性的影响,可能会出现额外的护理菌株,并在卫生和护理服务中的专业人员注意力。生活在痴呆症和他们的照顾者身上的人们强调了维持或适应常规的重要性,这对于专业人士来说可能是有用的学习,尽管可能对痴呆症症状更严重或恶化或恶化的人影响的人可能是必要的。

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