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社区居住的老年痴呆症患者的照顾者的未满足需求与保护因素、风险因素和结果之间的关联。

The associations between unmet needs with protective factors, risk factors and outcomes among care partners of community-dwelling persons living with dementia.

机构信息

Johns Hopkins School of Nursing, Baltimore, MD, USA.

Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.

出版信息

Aging Ment Health. 2023 Feb;27(2):334-342. doi: 10.1080/13607863.2022.2046698. Epub 2022 Mar 24.

Abstract

OBJECTIVES

Describe the prevalence and types of unmet needs among community-dwelling dementia care partners (CPs) and determine associations between unmet needs with protective factors, risk factors and outcomes.

METHOD

A cross-sectional analysis of 638 racially and cognitively diverse community-dwelling persons living with dementia (PLWD) and their CPs participating in a comprehensive in-home assessment of dementia-related needs. Unmet CP needs (19 items, 6 domains) were rated by a clinician using the Johns Hopkins Dementia Care Needs Assessment (JHDCNA). Multivariate linear regression models were used to examine associations between total percent unmet CP needs with demographic, protective and risk factors.

RESULTS

Nearly all CPs had at least one unmet need (99.53%), with a mean of 5.7 (±2.6). The most common domains with ≥1 unmet need were memory disorder education, care skills and knowledge of resources (98%), legal issues/concerns (73.8%), CP mental health (44.6%) and access to informal support (42.7%). Adjusted multivariate models suggest the strongest consistent predictive factors relate to informal emotional support, CP physical health, use or difficulty getting formal services/supports (both for CPs and PLWD), and CP time spent with PLWD. Greater levels of unmet needs were associated with worse PLWD outcomes and CP outcomes, after adjusting for demographics.

CONCLUSIONS

CPs have high rates of diverse, but modifiable unmet needs. Data suggest optimal approaches to dementia care should take a family-centered home-based approach that includes routine CP needs assessment, offer targeted interventions that include both traditional medical supports as well as strategies to increase and leverage informal social networks, and ones that can bridge and coordinate medical with non-medical supports. These findings can be used to inform new approaches to support CPs, improve PLWD and CP outcomes, and target groups most at risk for inequities.

摘要

目的

描述社区居住的痴呆症照护者(CP)中未满足需求的流行率和类型,并确定未满足需求与保护因素、风险因素和结果之间的关系。

方法

对 638 名不同种族和认知能力的居住在社区中的与痴呆症共存的人(PLWD)及其参与全面家庭评估的认知症相关需求的 CP 进行横断面分析。临床医生使用约翰霍普金斯痴呆症照护需求评估(JHDCNA)对 CP 未满足的需求(19 项,6 个领域)进行评估。使用多元线性回归模型来检验 CP 未满足需求的总百分比与人口统计学、保护和风险因素之间的关系。

结果

几乎所有的 CP 都有至少一项未满足的需求(99.53%),平均为 5.7(±2.6)。≥1 项未满足需求的最常见领域是记忆障碍教育、护理技能和资源知识(98%)、法律问题/关注(73.8%)、CP 心理健康(44.6%)和获得非正式支持(42.7%)。调整后的多元模型表明,最强的一致预测因素与非正式情感支持、CP 身体健康、使用或难以获得正式服务/支持(CP 和 PLWD)以及 CP 与 PLWD 共度的时间有关。在调整人口统计学因素后,更多的未满足需求与 PLWD 和 CP 结果更差相关。

结论

CP 存在各种但可改变的未满足需求的高发生率。数据表明,理想的痴呆症照护方法应该采取以家庭为中心的家庭方法,包括对 CP 进行常规需求评估,提供包括传统医疗支持以及增加和利用非正式社交网络的策略的针对性干预措施,以及可以将医疗与非医疗支持联系起来并协调的方法。这些发现可用于为支持 CP、改善 PLWD 和 CP 结果以及针对最易受不公平待遇的群体提供新方法。

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