Bernstein Sideman Alissa, Wells Jenna L, Merrilees Jennifer, Shdo Suzanne M, Yee Claire I, Possin Katherine L, Levenson Robert W
Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, California, USA.
Department of Humanities & Social Sciences, University of California, San Francisco, California, USA.
Dement Geriatr Cogn Dis Extra. 2022 Apr 21;12(1):60-68. doi: 10.1159/000522122. eCollection 2022 Jan-Apr.
Family caregivers of persons living with dementia (PLWDs) have extensive social, physical, emotional, and financial responsibilities. However, less is known about the relationship and interpersonal connection between caregivers and PLWDs. We examined caregiver pronoun use, as an index of the connection between the caregiver and PLWD and its associations with the caregiver's and PLWD's health and well-being.
Caregivers of PLWDs ( = 320) were asked to describe a recent time they felt connected to the PLWD in their care. Responses were transcribed and coded to quantify pronoun use by category (we-pronouns, I-pronouns, and they-pronouns). Caregivers also reported on their depression, burden, and the PLWD's dementia severity and marital satisfaction. Sixty-eight caregivers repeated the same survey 24 months after the initial survey.
Caregivers used less we-pronouns when the PLWD's dementia was more severe, at both timepoints. Spousal caregivers used more we-pronouns and less I- and they-pronouns than nonspousal caregivers. There was an interaction between spousal relationship and dementia severity, such that spousal caregivers exhibited a stronger negative association between dementia severity and we-pronoun use. There were no associations between pronoun category and caregiver burden or depression.
Caregivers may feel increasingly disconnected from the PLWD as their dementia becomes more severe, as reflected by less we-pronoun usage. This study highlights the opportunity to explore relationship connection through text analysis.
痴呆症患者(PLWD)的家庭照顾者承担着广泛的社会、身体、情感和经济责任。然而,对于照顾者与痴呆症患者之间的关系和人际联系,我们所知甚少。我们研究了照顾者代词的使用情况,以此作为照顾者与痴呆症患者之间联系的指标,以及它与照顾者和痴呆症患者的健康及幸福感之间的关联。
我们要求痴呆症患者的照顾者(n = 320)描述他们最近一次在照顾过程中感到与痴呆症患者有联系的时刻。对回答进行转录和编码,以按类别(“我们”代词、“我”代词和“他们”代词)量化代词的使用情况。照顾者还报告了他们的抑郁程度、负担,以及痴呆症患者的痴呆严重程度和婚姻满意度。68名照顾者在初次调查24个月后重复了相同的调查。
在两个时间点,当痴呆症患者的痴呆程度更严重时,照顾者使用的“我们”代词更少。与非配偶照顾者相比,配偶照顾者使用更多的“我们”代词,更少的“我”和“他们”代词。配偶关系和痴呆严重程度之间存在交互作用,即配偶照顾者在痴呆严重程度和“我们”代词使用之间表现出更强的负相关。代词类别与照顾者负担或抑郁之间没有关联。
随着痴呆症患者的痴呆程度变得更严重,照顾者可能会感到与他们的联系越来越少,这一点通过“我们”代词使用的减少得到反映。本研究强调了通过文本分析探索关系联系的机会。