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Consensus statement of the international summit on intellectual disability and Dementia related to post-diagnostic support(*)

机译:与诊断后支援有关的智力残疾和痴呆症的国际峰会的共识声明(*)

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Objectives: Post diagnostic support (PDS) has varied definitions within mainstream dementia services and different health and social care organizations, encompassing a range of supports that are offered to adults once diagnosed with dementia until death. Method: An international summit on intellectual disability and dementia held in Glasgow, Scotland in 2016 identified how PDS applies to adults with an intellectual disability and dementia. The Summit proposed a model that encompassed seven focal areas: post-diagnostic counseling; psychological and medical surveillance; periodic reviews and adjustments to the dementia care plan; early identification of behaviour and psychological symptoms; reviews of care practices and supports for advanced dementia and end of life; supports to carers/ support staff; and evaluation of quality of life. It also explored current practices in providing PDS in intellectual disability services. Results: The Summit concluded that although there is limited research evidence for pharmacological or non-pharmacological interventions for people with intellectual disability and dementia, viable resources and guidelines describe practical approaches drawn from clinical practice. Post diagnostic support is essential, and the model components in place for the general population, and proposed here for use within the intellectual disability field, need to be individualized and adapted to the person's needs as dementia progresses. Conclusions: Recommendations for future research include examining the prevalence and nature of behavioral and psychological symptoms (BPSD) in adults with an intellectual disability who develop dementia, the effectiveness of different non-pharmacological interventions, the interaction between pharmacological and non-pharmacological interventions, and the utility of different models of support.
机译:目标:诊断后支持(PDS)在主流痴呆服务和不同的健康和社会护理组织内具有各种定义,包括一系列向成年人提供的一系列支持,曾经诊断患有痴呆症直至死亡。方法:2016年苏格兰苏格兰格拉斯哥举行的智力残疾和痴呆症国际首脑会议确定了如何对具有智力残疾和痴呆症的成年人适用于成年人。首脑会议提出了一种包含七个焦点领域的模型:诊断后咨询;心理和医疗监测;定期审查和调整对痴呆症护理计划;早期识别行为和心理症状;审查护理实践和高级痴呆和终生结束的支持;支持照顾者/支持人员;评估生活质量。它还探讨了在智力残疾服务中提供PDS的现行做法。结果:峰会得出结论,尽管对具有智力残疾和痴呆症的人的药理学或非药理干预有限的研究证据,但是可行的资源和指导方针描述了从临床实践中汲取的实用方法。后诊断支持是必不可少的,并且普通人口的模型组件,并提出在智力残疾领域的使用,需要进行个性化,适应该人的需求,因为痴呆症进展。结论:未来研究的建议包括检查成人的行为和心理症状(BPSD)的患病率和性质,具有发展痴呆,不同非药理学干预的有效性,药理学和非药理学干预之间的相互作用,以及不同型号的支持效用。

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