Pronoun Use among Caregivers of People Living with Dementia: Associations with Dementia Severity Using Text Analysis of a Natural Language Sample.
Autor: | Bernstein Sideman A; 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.; Global Brain Health Institute, University of California, San Francisco, San Francisco, California, USA.; Department of Neurology, University of California, San Francisco, California, USA., Wells JL; Department of Psychology, University of California, Berkeley, California, USA., Merrilees J; Department of Neurology, University of California, San Francisco, California, USA., Shdo SM; Department of Psychology, University of California, Berkeley, California, USA., Yee CI; Department of Psychology, University of California, Berkeley, California, USA., Possin KL; Global Brain Health Institute, University of California, San Francisco, San Francisco, California, USA.; Department of Neurology, University of California, San Francisco, California, USA., Levenson RW; Department of Psychology, University of California, Berkeley, California, USA. |
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Jazyk: | angličtina |
Zdroj: | Dementia and geriatric cognitive disorders extra [Dement Geriatr Cogn Dis Extra] 2022 Apr 21; Vol. 12 (1), pp. 60-68. Date of Electronic Publication: 2022 Apr 21 (Print Publication: 2022). |
DOI: | 10.1159/000522122 |
Abstrakt: | Introduction: 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. Methods: Caregivers of PLWDs ( N = 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. Results: 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. Discussion: 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. Competing Interests: Dr. K.L. Possin reported receiving grants from the Centers for Medicare & Medicaid Services (CMS), National Institute on Aging (NIA), National Institute of Neurological Disorders and Stroke (NINDS), Global Brain Health Institute, Quest Diagnostics, and the Rainwater Foundation during the conduct of the study and personal fees from ClearView Healthcare Partners and Vanguard outside the submitted work. (Copyright © 2022 by S. Karger AG, Basel.) |
Databáze: | MEDLINE |
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