Agitation in individuals with Alzheimer's disease: An assessment of behaviors using the cohen-mansfield agitation inventory in community-dwellers and impact on caregiver experience.

George Grossberg, Cynthia Willey, Christy Houle, Jeff Schein, Rebecca Bungay, Martin Cloutier, Marjolaine Gauthier-Loiselle, Deborah Chan, Annie Guerin, Zahinoor Ismail, Jyoti Aggarwal
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Abstract

BackgroundAgitation is a common neuropsychiatric symptom of Alzheimer's disease; however, limited information exists on how measurable changes in agitated behaviors relate to overall caregiver experience. We sought to describe agitated behaviors measured by the Cohen-Mansfield Agitation Inventory (CMAI) score among individuals with Alzheimer's disease living in US community-based settings and experience of their caregivers.MethodsAn online survey was conducted (08/26/2021-09/24/2021) among adult caregivers who lived with and provided unpaid care for an individual with Alzheimer's disease. The 3-part survey involved (1) informed consent and screening; (2) CMAI assessment (total and sub-scores for four agitation factors); (3) characteristics and outcomes of caregivers and individuals with Alzheimer's disease. Descriptive statistics are reported. Association between the CMAI total score and caregiver burden (measured using the Zarit Burden Interview), mental health (measured using the Patient Health Questionnaire 4-item), and work/activity impairment (measured using the Work Productivity and Activity Impairment: Caregiver scale) was estimated using regression models.ResultsA total of 250 caregivers (mean age: 44.5 years; 55.2% male; 86.4% White) completed the survey. Based on the CMAI, 99.6% of individuals with Alzheimer's disease (mean age: 68.6 years; 55.2% male; 83.2% White) experienced ≥1 agitated behavior in the past 2 weeks. Caregivers reported providing an average of 39.1 hours of care per week for individuals with Alzheimer's disease (additional non-paid and paid care provided by other caregivers was 58.8% and 38.4%, respectively); 60.8% of caregivers had a high caregiving burden, 35.2% experienced moderate-to-severe distress, and 68.2/64.0% had impairment in work/daily activities. Agitation among individuals with Alzheimer's disease was associated with significantly poorer caregiver outcomes.ConclusionsIndividuals with Alzheimer's disease frequently experience several different agitated behaviors. Effective management of agitated behaviors is important and has the potential to improve the overall caregiver experience.

阿尔茨海默病患者的躁动:使用cohen-mansfield躁动量表对社区居民行为的评估及其对照顾者体验的影响。
躁动是阿尔茨海默病常见的神经精神症状;然而,关于激动行为的可测量变化如何与整体护理经验相关的信息有限。我们试图用科恩-曼斯菲尔德躁动量表(CMAI)来描述生活在美国社区环境中的阿尔茨海默病患者的躁动行为,以及他们的照顾者的经历。方法在2021年8月26日至2021年9月24日期间,对与阿尔茨海默病患者一起生活并为其提供无偿护理的成年护理人员进行在线调查。三部分调查涉及(1)知情同意和筛选;(2) CMAI评估(四个激越因素的总分和分项得分);(3)照顾者和阿尔茨海默病患者的特点和结局。报告了描述性统计数据。使用回归模型估计CMAI总分与照顾者负担(使用Zarit负担访谈测量)、心理健康(使用患者健康问卷4项测量)和工作/活动障碍(使用工作效率和活动障碍:照顾者量表测量)之间的关联。结果共250名护理人员,平均年龄44.5岁;男性55.2%;86.4%(白人)完成了调查。根据CMAI, 99.6%的阿尔茨海默病患者(平均年龄:68.6岁;男性55.2%;83.2%白人)在过去2周内经历过≥1次激动行为。护理人员报告平均每周为阿尔茨海默病患者提供39.1小时的护理(其他护理人员提供的额外无偿和有偿护理分别为58.8%和38.4%);60.8%的照顾者有较高的照顾负担,35.2%的照顾者有中度至重度的痛苦,68.2/64.0%的照顾者有工作/日常活动障碍。阿尔茨海默病患者的躁动与较差的护理结果显著相关。结论阿尔茨海默病患者经常经历几种不同的激动行为。对激动行为的有效管理很重要,并且有可能改善整体护理人员的体验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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