Sakakibara Sakura, Dove Abigail, Guo Jie, Grande Giulia, Akenine Ulrika, Sjölund Britt-Marie, Agerholm Janne, Laukka Erika J, Calderon-Larrañaga Amaia, Xu Weili
Aging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
Stockholm Gerontology Research Centre, Stockholm, Sweden.
J Alzheimers Dis. 2025 Aug;106(3):1010-1020. doi: 10.1177/13872877251350525. Epub 2025 Jun 23.
BackgroundDementia is linked to increased care use, but formal and informal care use throughout the dementia journey remains unclear.ObjectiveTo investigate care use before and after the detection of cognitive impairment, no dementia (CIND) and dementia and to identify care-related factors.MethodsWithin a population-based study, we matched older adults (≥78 years) who developed CIND (n = 244) and dementia (n = 175) with cognitively intact participants to form CIND/intact (n = 732) and dementia/intact (n = 525) samples. Dementia was clinically diagnosed and CIND was determined through a neuropsychological battery. Formal (from public and private providers) and informal (provided by family and friends) care use was interviewed. Care-related factors included age, sex, education, living alone, chronic diseases, and social network. Data was analyzed using logistic regressions and linear mixed-effect models.ResultsCompared to cognitively intact participants, those with CIND had increased care use 3 years after detection (odds ratio [OR] 2.30 and 2.63, 95% confidence interval [95%CI] 1.02-5.18 and 1.25-5.53) and those with dementia had greater care use over time (OR 2.01, 95% CI 1.20-3.38 to OR 13.58, 95% CI 4.46-41.34). People with CIND/dementia showed 6.3 to 32.3 h rapid increase in informal care hours. Older age, female, living alone, and chronic diseases further increased care use.ConclusionsFormal and informal care use during the progression of cognitive impairment begins to increase at the CIND stage, but only informal care hours continue to increase. The findings highlight the complex care needs of people with cognitive impairment and the importance of coordination of care.
背景
痴呆症与护理使用增加有关,但在整个痴呆症病程中正式和非正式护理的使用情况仍不明确。
目的
调查认知障碍、无痴呆(CIND)和痴呆症被检测出之前和之后的护理使用情况,并确定与护理相关的因素。
方法
在一项基于人群的研究中,我们将发展为CIND(n = 244)和痴呆症(n = 175)的老年人(≥78岁)与认知功能正常的参与者进行匹配,以形成CIND/正常(n = 732)和痴呆症/正常(n = 525)样本。痴呆症通过临床诊断确定,CIND通过一套神经心理测试来判定。对正式(来自公共和私人提供者)和非正式(由家人和朋友提供)护理的使用情况进行了访谈。与护理相关的因素包括年龄、性别、教育程度、独居、慢性病和社会网络。使用逻辑回归和线性混合效应模型对数据进行分析。
结果
与认知功能正常的参与者相比,CIND患者在被检测出3年后护理使用增加(优势比[OR]分别为2.30和2.63,95%置信区间[95%CI]为1.02 - 5.18和1.25 - 5.53),痴呆症患者随着时间推移护理使用更多(OR从2.01,95% CI 1.20 - 3.38到OR 13.58,95% CI 4.46 - 41.34)。CIND/痴呆症患者的非正式护理时长迅速增加6.3至32.3小时。年龄较大、女性、独居和患有慢性病会进一步增加护理使用。
结论
在认知障碍进展过程中,正式和非正式护理的使用在CIND阶段开始增加,但只有非正式护理时长持续增加。研究结果突出了认知障碍患者复杂的护理需求以及护理协调的重要性。