Size and Composition of Caregiver Networks Who Manage Medications for Persons Living With Dementia: Cross-Sectional Analysis of the 2011-2022 National Health and Aging Trends Study.
Reed Wr Bratches, Frank Puga, Paul J Barr, Amanda N Leggett, Meredith Masel, James Nicholas Odom, Rita Jablonski
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引用次数: 0
Abstract
Background: Family caregivers commonly help manage medications taken by persons living with dementia. Recent work has highlighted the importance of caregiver networks, which are multiple caregivers managing care for a single person, on managing care for persons living with dementia, especially medication management. However, less is known about the composition of caregiver networks.
Objective: The objective of this analysis was to describe the composition of caregiver networks that manage medications, the factors associated with helping with medications within caregiver networks, and whether racial or ethnic differences exist in caregiver network composition.
Methods: This cross-sectional secondary analysis used data from the National Health and Aging Trends Study (NHATS) "other person" files from 2011 to 2022. Descriptive statistics were calculated for caregivers who were identified as helping manage medications for a person with dementia. Mixed-effect logistic regression was used to determine factors associated with helping with medications among caregiver networks, with odds ratios converted to predicted probabilities using marginal standardization. A P value of .05 or less was considered statistically significant. Secondary analysis was stratified by race and ethnicity due to identified cultural differences in living situation and overall caregiver network composition.
Results: A total of 15,809 caregivers were analyzed. Of those, 3048 (19.2%) managed medications for persons living with dementia. Caregiver networks that manage medications tend to include a spouse or partner and child, at least one of whom has a college degree. Every person with dementia reported at least 1 person who managed their medications. White persons with dementia had an average of 2.4 (range 1-9) people who managed medications, while Black or African American persons with dementia had an average of 2.8 (range 1-9) and Hispanic or Latino persons with dementia had an average of 2.9 (range 1-8) people who managed medications. Spouses were most likely to manage medications across all racial and ethnic groups. In regression modeling, female gender (predicted probability [PP] 15%, 95% CI 13%-17%; P<.001), Black or African American race (PP 7%, 95% CI 4%-10%; P<.001), and Hispanic ethnicity (PP 4%, 95% CI 1%-9%; P=.04) were associated with an increased probability of helping with medications.
Conclusions: The size and composition of caregiver networks that manage medications for persons living with dementia differ by race and ethnicity but typically includes at least 2 people, one of whom has a college degree. Helping with medications was more likely among non-White family caregivers, while White patients with dementia were more likely to use paid help to manage medications.
背景:家庭照顾者通常帮助管理痴呆症患者服用的药物。最近的工作强调了照顾者网络(由多个照顾者管理对一个人的照顾)在管理对痴呆症患者的照顾,特别是药物管理方面的重要性。然而,人们对照顾者网络的构成知之甚少。目的:本分析的目的是描述管理药物的护理人员网络的组成,在护理人员网络中帮助使用药物的相关因素,以及在护理人员网络组成中是否存在种族或民族差异。方法:本横断面二次分析使用了国家健康与老龄化趋势研究(NHATS)的数据。“其他人”文件从2011年到2022年。描述性统计计算了被确定为帮助管理痴呆症患者药物治疗的护理人员。混合效应逻辑回归用于确定护理人员网络中与帮助用药相关的因素,并使用边际标准化将优势比转换为预测概率。P值小于等于0.05被认为具有统计学意义。由于生活状况和整体护理网络构成的文化差异,二级分析按种族和民族分层。结果:共对15809名护理人员进行分析。其中,3048家(19.2%)管理痴呆症患者的药物治疗。管理药物的护理人员网络往往包括配偶或伴侣和孩子,其中至少有一人拥有大学学位。每个痴呆症患者报告至少有一个人管理他们的药物。白人痴呆症患者平均有2.4人(范围1-9)管理药物,而黑人或非裔美国人痴呆症患者平均有2.8人(范围1-9),西班牙裔或拉丁裔痴呆症患者平均有2.9人(范围1-8)管理药物。在所有种族和族裔群体中,配偶最有可能管理药物。在回归模型中,女性(预测概率[PP] 15%, 95% CI 13%-17%;结论:管理痴呆症患者药物治疗的护理人员网络的规模和组成因种族和民族而异,但通常包括至少2人,其中一人拥有大学学位。非白人家庭护理人员更有可能帮助治疗,而患有痴呆症的白人患者更有可能使用有偿帮助来管理药物。