Caregiver appraisals of lucid episodes in people with late‐stage Alzheimer's disease or related dementias

Introduction Little is known about how family caregivers who witness unexpected and spontaneous communication among people in late stages of Alzheimer's disease and related dementias (ADRD) appraise these episodes of lucidity (EL). Methods In an electronic, cross‐sectional survey for former and...

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Veröffentlicht in:Alzheimer's & dementia : diagnosis, assessment & disease monitoring assessment & disease monitoring, 2022, Vol.14 (1), p.e12313-n/a
Hauptverfasser: Griffin, Joan M., Kim, Kyungmin, Gaugler, Joseph E., Biggar, Virginia S., Frangiosa, Theresa, Bangerter, Lauren R., Batthyany, Alexander, Finnie, Dawn M., Lapid, Maria I.
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container_issue 1
container_start_page e12313
container_title Alzheimer's & dementia : diagnosis, assessment & disease monitoring
container_volume 14
creator Griffin, Joan M.
Kim, Kyungmin
Gaugler, Joseph E.
Biggar, Virginia S.
Frangiosa, Theresa
Bangerter, Lauren R.
Batthyany, Alexander
Finnie, Dawn M.
Lapid, Maria I.
description Introduction Little is known about how family caregivers who witness unexpected and spontaneous communication among people in late stages of Alzheimer's disease and related dementias (ADRD) appraise these episodes of lucidity (EL). Methods In an electronic, cross‐sectional survey for former and current caregivers who participate in UsAgainstAlzheimer's A‐LIST®, participants who reported witnessing an EL were asked how positive and stressful ELs were, if they made or changed decisions based on an EL, and what resources they sought out to explain ELs. Results Caregivers reported 72% of ELs to be quite a bit or very positive, 17% to be stressful, and 10% to be both stressful and positive. Twelve percent of caregivers changed care plans because of ELs and 13% sought out information about ELs. Discussion These exploratory data suggest caregiver reactions to EL vary. Caregivers may change or postpone care decisions due to EL, and few resources exist to address caregiver queries about EL.
doi_str_mv 10.1002/dad2.12313
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Methods In an electronic, cross‐sectional survey for former and current caregivers who participate in UsAgainstAlzheimer's A‐LIST®, participants who reported witnessing an EL were asked how positive and stressful ELs were, if they made or changed decisions based on an EL, and what resources they sought out to explain ELs. Results Caregivers reported 72% of ELs to be quite a bit or very positive, 17% to be stressful, and 10% to be both stressful and positive. Twelve percent of caregivers changed care plans because of ELs and 13% sought out information about ELs. Discussion These exploratory data suggest caregiver reactions to EL vary. Caregivers may change or postpone care decisions due to EL, and few resources exist to address caregiver queries about EL.</description><identifier>ISSN: 2352-8729</identifier><identifier>EISSN: 2352-8729</identifier><identifier>DOI: 10.1002/dad2.12313</identifier><identifier>PMID: 35775022</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Alzheimer's disease ; Alzheimer's disease and related dementias ; appraisal ; Appraisals ; Caregivers ; Communication ; Decision making ; Dementia ; Diversity, Disease Heterogeneity and Symptom Variability ; Education ; family caregivers ; Grief ; Living arrangements ; Longitudinal studies ; lucidity ; paradoxical lucidity ; Qualitative research ; Secondary schools ; Short Report</subject><ispartof>Alzheimer's &amp; dementia : diagnosis, assessment &amp; disease monitoring, 2022, Vol.14 (1), p.e12313-n/a</ispartof><rights>2022 The Authors. published by Wiley Periodicals, LLC on behalf of Alzheimer's Association</rights><rights>2022 The Authors. 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Methods In an electronic, cross‐sectional survey for former and current caregivers who participate in UsAgainstAlzheimer's A‐LIST®, participants who reported witnessing an EL were asked how positive and stressful ELs were, if they made or changed decisions based on an EL, and what resources they sought out to explain ELs. Results Caregivers reported 72% of ELs to be quite a bit or very positive, 17% to be stressful, and 10% to be both stressful and positive. Twelve percent of caregivers changed care plans because of ELs and 13% sought out information about ELs. Discussion These exploratory data suggest caregiver reactions to EL vary. 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source Wiley Journals; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; Wiley Online Library (Open Access Collection); PubMed Central
subjects Alzheimer's disease
Alzheimer's disease and related dementias
appraisal
Appraisals
Caregivers
Communication
Decision making
Dementia
Diversity, Disease Heterogeneity and Symptom Variability
Education
family caregivers
Grief
Living arrangements
Longitudinal studies
lucidity
paradoxical lucidity
Qualitative research
Secondary schools
Short Report
title Caregiver appraisals of lucid episodes in people with late‐stage Alzheimer's disease or related dementias
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