Kinship And Care: Racial Disparities In Potential Dementia Caregiving In The U.S. From 2000 To 2060

Kai Feng, Xi Song, Hal Caswell
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Abstract

Background Although the family plays a pivotal role in older adults’ care, there is limited research on how evolving demographic trends affect older adults’ support networks and how the trends vary by race. To fill this gap, we examine the influence of shifting family demographics on future care needs for older adults with dementia, emphasizing the unequal health and potential caregiving burdens by race in the U.S. Methods Using demographic models of kinship, we estimate the availability of potential caregivers, and dementia prevalence among one’s kin by race, kin type, and the age of a focal person from 2000 to 2060. We introduce an index called the Dementia Dependency Ratio to assess dementia caregiving demands at the population level, taking into account the age and kinship structure of the population. Results Our findings suggest that Black individuals tend to have more children, grandchildren, and nieces/nephews as they age. However, Black individuals also tend to have more kin with dementia compared to their White counterparts. This elevated prevalence of dementia among Black kinship networks counterbalances the advantage of having more kin as potential caregivers. A further projection analysis suggests that the racial gap in caregiving demand within the kinship network will widen in the next four decades if the racial gap in dementia prevalence remains unchanged. Conclusions These findings emphasize the urgency of reducing racial inequality in dementia prevalence rates and increasing public support for families with extended members affected by dementia. With the shrinkage of nuclear families and population aging in the next few decades, extended family members may undertake more caregiving responsibilities for dementia. We call for a kinship perspective in understanding dementia care in future research.
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亲情与关怀:2000 年至 2060 年美国潜在痴呆症护理中的种族差异
背景 虽然家庭在老年人的护理工作中起着举足轻重的作用,但有关人口发展趋势如何影响老年人的支持网络以及不同种族的趋势有何差异的研究却很有限。为了填补这一空白,我们研究了家庭人口结构的变化对患有痴呆症的老年人未来护理需求的影响,强调了美国不同种族在健康和潜在护理负担方面的不平等。 方法 我们使用亲属关系人口模型,估算了潜在护理人员的可用性,以及从 2000 年到 2060 年按种族、亲属类型和联系人年龄划分的亲属中痴呆症的患病率。考虑到人口的年龄和亲属结构,我们引入了一个名为痴呆症抚养比的指数来评估人口层面的痴呆症护理需求。结果 我们的研究结果表明,随着年龄的增长,黑人往往有更多的子女、孙辈和侄子/侄女。然而,与白人相比,黑人亲属中患痴呆症的人数也更多。黑人亲属网络中痴呆症患病率的升高抵消了拥有更多亲属作为潜在照顾者的优势。进一步的预测分析表明,如果痴呆症发病率的种族差距保持不变,那么亲属网络中护理需求的种族差距将在未来 40 年内扩大。结论 这些研究结果表明,当务之急是减少痴呆症发病率中的种族不平等现象,并为有痴呆症患者的大家庭成员的家庭提供更多的公共支持。随着未来几十年核心家庭的缩小和人口老龄化,大家庭成员可能会承担更多的痴呆症护理责任。我们呼吁在未来的研究中从亲缘关系的角度来理解痴呆症护理。
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