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 |
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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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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.</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 & 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 & dementia : diagnosis, assessment & 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. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4763-91b761d25d64be127b53e28cd8d945dd608cd77ab4d93e8a4796059f19beb99a3</citedby><cites>FETCH-LOGICAL-c4763-91b761d25d64be127b53e28cd8d945dd608cd77ab4d93e8a4796059f19beb99a3</cites><orcidid>0000-0001-8120-3229</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219100/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219100/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,4024,11562,27923,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35775022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Griffin, Joan M.</creatorcontrib><creatorcontrib>Kim, Kyungmin</creatorcontrib><creatorcontrib>Gaugler, Joseph E.</creatorcontrib><creatorcontrib>Biggar, Virginia S.</creatorcontrib><creatorcontrib>Frangiosa, Theresa</creatorcontrib><creatorcontrib>Bangerter, Lauren R.</creatorcontrib><creatorcontrib>Batthyany, Alexander</creatorcontrib><creatorcontrib>Finnie, Dawn M.</creatorcontrib><creatorcontrib>Lapid, Maria I.</creatorcontrib><title>Caregiver appraisals of lucid episodes in people with late‐stage Alzheimer's disease or related dementias</title><title>Alzheimer's & dementia : diagnosis, assessment & disease monitoring</title><addtitle>Alzheimers Dement (Amst)</addtitle><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.</description><subject>Alzheimer's disease</subject><subject>Alzheimer's disease and related dementias</subject><subject>appraisal</subject><subject>Appraisals</subject><subject>Caregivers</subject><subject>Communication</subject><subject>Decision making</subject><subject>Dementia</subject><subject>Diversity, Disease Heterogeneity and Symptom Variability</subject><subject>Education</subject><subject>family caregivers</subject><subject>Grief</subject><subject>Living arrangements</subject><subject>Longitudinal studies</subject><subject>lucidity</subject><subject>paradoxical lucidity</subject><subject>Qualitative research</subject><subject>Secondary schools</subject><subject>Short Report</subject><issn>2352-8729</issn><issn>2352-8729</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kc1OGzEURi0EahCw6QMgS12AkEL9MzMebypFobRISGxgbXnGN4lTz3iwZ4jSVR-hz8iT4BBA0EVXvpKPjj_fD6HPlJxTQthXow07p4xTvoP2Gc_ZuBRM7r6bR-goxiUhhGaSZZR8QiOeC5ETxvbRr6kOMLcPELDuuqBt1C5iP8NuqK3B0NnoDURsW9yB7xzgle0X2OkeHv_8jb2eA5643wuwDYSTiI2NoCNgH3CADWWwgQba3up4iPZmyQ5HL-cBurv8fjv9Ob6--XE1nVyP60wUfCxpJQpqWG6KrALKRJVzYGVtSiOz3JiCpFkIXWVGcih1JmRBcjmjsoJKSs0P0LettxuqBkydXg_aqS7YRoe18tqqjzetXai5f1CSUZmWmgSnL4Lg7weIvWpsrME53YIfomJFmfZIOZcJ_fIPuvRDaNP3FBN5yQue4ibqbEvVwccYYPYWhhK1qVFtalTPNSb4-H38N_S1tATQLbCyDtb_UamLyQXbSp8AXcupCQ</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Griffin, Joan M.</creator><creator>Kim, Kyungmin</creator><creator>Gaugler, Joseph E.</creator><creator>Biggar, Virginia S.</creator><creator>Frangiosa, Theresa</creator><creator>Bangerter, Lauren R.</creator><creator>Batthyany, Alexander</creator><creator>Finnie, Dawn M.</creator><creator>Lapid, Maria I.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8120-3229</orcidid></search><sort><creationdate>2022</creationdate><title>Caregiver appraisals of lucid episodes in people with late‐stage Alzheimer's disease or related dementias</title><author>Griffin, Joan M. ; Kim, Kyungmin ; Gaugler, Joseph E. ; Biggar, Virginia S. ; Frangiosa, Theresa ; Bangerter, Lauren R. ; Batthyany, Alexander ; Finnie, Dawn M. ; Lapid, Maria I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4763-91b761d25d64be127b53e28cd8d945dd608cd77ab4d93e8a4796059f19beb99a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alzheimer's disease</topic><topic>Alzheimer's disease and related dementias</topic><topic>appraisal</topic><topic>Appraisals</topic><topic>Caregivers</topic><topic>Communication</topic><topic>Decision making</topic><topic>Dementia</topic><topic>Diversity, Disease Heterogeneity and Symptom Variability</topic><topic>Education</topic><topic>family caregivers</topic><topic>Grief</topic><topic>Living arrangements</topic><topic>Longitudinal studies</topic><topic>lucidity</topic><topic>paradoxical lucidity</topic><topic>Qualitative research</topic><topic>Secondary schools</topic><topic>Short Report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Griffin, Joan M.</creatorcontrib><creatorcontrib>Kim, Kyungmin</creatorcontrib><creatorcontrib>Gaugler, Joseph E.</creatorcontrib><creatorcontrib>Biggar, Virginia S.</creatorcontrib><creatorcontrib>Frangiosa, Theresa</creatorcontrib><creatorcontrib>Bangerter, Lauren R.</creatorcontrib><creatorcontrib>Batthyany, Alexander</creatorcontrib><creatorcontrib>Finnie, Dawn M.</creatorcontrib><creatorcontrib>Lapid, Maria I.</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Alzheimer's & dementia : diagnosis, assessment & disease monitoring</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Griffin, Joan M.</au><au>Kim, Kyungmin</au><au>Gaugler, Joseph E.</au><au>Biggar, Virginia S.</au><au>Frangiosa, Theresa</au><au>Bangerter, Lauren R.</au><au>Batthyany, Alexander</au><au>Finnie, Dawn M.</au><au>Lapid, Maria I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caregiver appraisals of lucid episodes in people with late‐stage Alzheimer's disease or related dementias</atitle><jtitle>Alzheimer's & dementia : diagnosis, assessment & disease monitoring</jtitle><addtitle>Alzheimers Dement (Amst)</addtitle><date>2022</date><risdate>2022</risdate><volume>14</volume><issue>1</issue><spage>e12313</spage><epage>n/a</epage><pages>e12313-n/a</pages><issn>2352-8729</issn><eissn>2352-8729</eissn><abstract>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.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>35775022</pmid><doi>10.1002/dad2.12313</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-8120-3229</orcidid><oa>free_for_read</oa></addata></record> |
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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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