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Psychosocial Effects of Corona Measures on Patients With Dementia, Mild Cognitive Impairment and Subjective Cognitive Decline

Background: The recent COVID-19 pandemic is not only a major healthcare problem in itself, but also poses enormous social challenges. Though nursing homes increasingly receive attention, the majority of people with cognitive decline and dementia live at home. We aimed to explore the psychosocial eff...

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Published in:Frontiers in psychiatry 2020-10, Vol.11, p.585686-585686
Main Authors: van Maurik, Ingrid S., Bakker, Els D., van den Buuse, Susanne, Gillissen, Freek, van de Beek, Marleen, Lemstra, Evelien, Mank, Arenda, van den Bosch, Karlijn A., van Leeuwenstijn, Mardou, Bouwman, Femke H., Scheltens, Philip, van der Flier, Wiesje M.
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container_title Frontiers in psychiatry
container_volume 11
creator van Maurik, Ingrid S.
Bakker, Els D.
van den Buuse, Susanne
Gillissen, Freek
van de Beek, Marleen
Lemstra, Evelien
Mank, Arenda
van den Bosch, Karlijn A.
van Leeuwenstijn, Mardou
Bouwman, Femke H.
Scheltens, Philip
van der Flier, Wiesje M.
description Background: The recent COVID-19 pandemic is not only a major healthcare problem in itself, but also poses enormous social challenges. Though nursing homes increasingly receive attention, the majority of people with cognitive decline and dementia live at home. We aimed to explore the psychosocial effects of corona measures in memory clinic (pre-)dementia patients and their caregivers. Methods: Between April 28th and July 13th 2020, n = 389 patients of Alzheimer center Amsterdam [ n = 121 symptomatic (age = 69 ± 6, 33%F, MMSE = 23 ± 5), n = 268 cognitively normal (age = 66 ± 8, 40% F, MMSE = 29 ± 1)] completed a survey on psychosocial effects of the corona measures. Questions related to social isolation, worries for faster cognitive decline, behavioral problems and discontinuation of care. In addition, n = 147 caregivers of symptomatic patients completed a similar survey with additional questions on caregiver burden. Results: Social isolation was experienced by n = 42 (35%) symptomatic and n = 67 (25%) cognitively normal patients and two third of patients [ n = 129 (66%); n = 58 (75%) symptomatic, n = 71 (61%) cognitively normal] reported that care was discontinued. Worries for faster cognitive decline were existed in symptomatic patients [ n = 44 (44%)] and caregivers [ n = 73 (53%)], but were also reported by a subgroup of cognitively normal patients [ n = 27 (14%)]. Both patients [ n = 56 (46%) symptomatic, n = 102 (38%) cognitively normal] and caregivers [ n = 72 (48%)] reported an increase in psychological symptoms. More than three quarter of caregivers [ n = 111(76%)] reported an increase in patients' behavioral problems. A higher caregiver burden was experienced by n = 69 (56%) of caregivers and n = 43 (29%) of them reported that a need for more support. Discontinuation of care (OR = 3.3 [1.3–7.9]), psychological (OR = 4.0 [1.6–9.9]) and behavioral problems (OR = 3.0 [1.0–9.0]) strongly related to experiencing a higher caregiver burden. Lastly, social isolation (OR = 3.2 [1.2–8.1]) and psychological symptoms (OR = 8.1 [2.8–23.7]) were red flags for worries for faster cognitive decline. Conclusion: Not only symptomatic patients, but also cognitively normal patients express worries for faster cognitive decline and psychological symptoms. Moreover, we identified patients who are at risk of adverse outcomes of the corona measures, i.e., discontinued care, social isolation, psychological and behavioral problems. This underlines the need for health care pro
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Though nursing homes increasingly receive attention, the majority of people with cognitive decline and dementia live at home. We aimed to explore the psychosocial effects of corona measures in memory clinic (pre-)dementia patients and their caregivers. Methods: Between April 28th and July 13th 2020, n = 389 patients of Alzheimer center Amsterdam [ n = 121 symptomatic (age = 69 ± 6, 33%F, MMSE = 23 ± 5), n = 268 cognitively normal (age = 66 ± 8, 40% F, MMSE = 29 ± 1)] completed a survey on psychosocial effects of the corona measures. Questions related to social isolation, worries for faster cognitive decline, behavioral problems and discontinuation of care. In addition, n = 147 caregivers of symptomatic patients completed a similar survey with additional questions on caregiver burden. Results: Social isolation was experienced by n = 42 (35%) symptomatic and n = 67 (25%) cognitively normal patients and two third of patients [ n = 129 (66%); n = 58 (75%) symptomatic, n = 71 (61%) cognitively normal] reported that care was discontinued. Worries for faster cognitive decline were existed in symptomatic patients [ n = 44 (44%)] and caregivers [ n = 73 (53%)], but were also reported by a subgroup of cognitively normal patients [ n = 27 (14%)]. Both patients [ n = 56 (46%) symptomatic, n = 102 (38%) cognitively normal] and caregivers [ n = 72 (48%)] reported an increase in psychological symptoms. More than three quarter of caregivers [ n = 111(76%)] reported an increase in patients' behavioral problems. A higher caregiver burden was experienced by n = 69 (56%) of caregivers and n = 43 (29%) of them reported that a need for more support. Discontinuation of care (OR = 3.3 [1.3–7.9]), psychological (OR = 4.0 [1.6–9.9]) and behavioral problems (OR = 3.0 [1.0–9.0]) strongly related to experiencing a higher caregiver burden. Lastly, social isolation (OR = 3.2 [1.2–8.1]) and psychological symptoms (OR = 8.1 [2.8–23.7]) were red flags for worries for faster cognitive decline. Conclusion: Not only symptomatic patients, but also cognitively normal patients express worries for faster cognitive decline and psychological symptoms. Moreover, we identified patients who are at risk of adverse outcomes of the corona measures, i.e., discontinued care, social isolation, psychological and behavioral problems. This underlines the need for health care professionals to provide ways to warrant the continuation of care and support (informal) networks surrounding patients and caregivers to mitigate the higher risk of negative psychosocial effects.</description><identifier>ISSN: 1664-0640</identifier><identifier>EISSN: 1664-0640</identifier><identifier>DOI: 10.3389/fpsyt.2020.585686</identifier><identifier>PMID: 33192733</identifier><language>eng</language><publisher>Frontiers Media S.A</publisher><subject>behavioral problems ; COVID-19 ; dementia ; MCI ; Psychiatry ; psychosocial effects ; SCD</subject><ispartof>Frontiers in psychiatry, 2020-10, Vol.11, p.585686-585686</ispartof><rights>Copyright © 2020 van Maurik, Bakker, van den Buuse, Gillissen, van de Beek, Lemstra, Mank, van den Bosch, van Leeuwenstijn, Bouwman, Scheltens and van der Flier. 2020 van Maurik, Bakker, van den Buuse, Gillissen, van de Beek, Lemstra, Mank, van den Bosch, van Leeuwenstijn, Bouwman, Scheltens and van der Flier</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-a2b7e84758dd0c5c60abe90c8a59fca31e2a0461164f7a781e7e89ab12641eac3</citedby><cites>FETCH-LOGICAL-c442t-a2b7e84758dd0c5c60abe90c8a59fca31e2a0461164f7a781e7e89ab12641eac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649118/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649118/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids></links><search><creatorcontrib>van Maurik, Ingrid S.</creatorcontrib><creatorcontrib>Bakker, Els D.</creatorcontrib><creatorcontrib>van den Buuse, Susanne</creatorcontrib><creatorcontrib>Gillissen, Freek</creatorcontrib><creatorcontrib>van de Beek, Marleen</creatorcontrib><creatorcontrib>Lemstra, Evelien</creatorcontrib><creatorcontrib>Mank, Arenda</creatorcontrib><creatorcontrib>van den Bosch, Karlijn A.</creatorcontrib><creatorcontrib>van Leeuwenstijn, Mardou</creatorcontrib><creatorcontrib>Bouwman, Femke H.</creatorcontrib><creatorcontrib>Scheltens, Philip</creatorcontrib><creatorcontrib>van der Flier, Wiesje M.</creatorcontrib><title>Psychosocial Effects of Corona Measures on Patients With Dementia, Mild Cognitive Impairment and Subjective Cognitive Decline</title><title>Frontiers in psychiatry</title><description>Background: The recent COVID-19 pandemic is not only a major healthcare problem in itself, but also poses enormous social challenges. Though nursing homes increasingly receive attention, the majority of people with cognitive decline and dementia live at home. We aimed to explore the psychosocial effects of corona measures in memory clinic (pre-)dementia patients and their caregivers. Methods: Between April 28th and July 13th 2020, n = 389 patients of Alzheimer center Amsterdam [ n = 121 symptomatic (age = 69 ± 6, 33%F, MMSE = 23 ± 5), n = 268 cognitively normal (age = 66 ± 8, 40% F, MMSE = 29 ± 1)] completed a survey on psychosocial effects of the corona measures. Questions related to social isolation, worries for faster cognitive decline, behavioral problems and discontinuation of care. In addition, n = 147 caregivers of symptomatic patients completed a similar survey with additional questions on caregiver burden. Results: Social isolation was experienced by n = 42 (35%) symptomatic and n = 67 (25%) cognitively normal patients and two third of patients [ n = 129 (66%); n = 58 (75%) symptomatic, n = 71 (61%) cognitively normal] reported that care was discontinued. Worries for faster cognitive decline were existed in symptomatic patients [ n = 44 (44%)] and caregivers [ n = 73 (53%)], but were also reported by a subgroup of cognitively normal patients [ n = 27 (14%)]. Both patients [ n = 56 (46%) symptomatic, n = 102 (38%) cognitively normal] and caregivers [ n = 72 (48%)] reported an increase in psychological symptoms. More than three quarter of caregivers [ n = 111(76%)] reported an increase in patients' behavioral problems. A higher caregiver burden was experienced by n = 69 (56%) of caregivers and n = 43 (29%) of them reported that a need for more support. Discontinuation of care (OR = 3.3 [1.3–7.9]), psychological (OR = 4.0 [1.6–9.9]) and behavioral problems (OR = 3.0 [1.0–9.0]) strongly related to experiencing a higher caregiver burden. Lastly, social isolation (OR = 3.2 [1.2–8.1]) and psychological symptoms (OR = 8.1 [2.8–23.7]) were red flags for worries for faster cognitive decline. Conclusion: Not only symptomatic patients, but also cognitively normal patients express worries for faster cognitive decline and psychological symptoms. Moreover, we identified patients who are at risk of adverse outcomes of the corona measures, i.e., discontinued care, social isolation, psychological and behavioral problems. This underlines the need for health care professionals to provide ways to warrant the continuation of care and support (informal) networks surrounding patients and caregivers to mitigate the higher risk of negative psychosocial effects.</description><subject>behavioral problems</subject><subject>COVID-19</subject><subject>dementia</subject><subject>MCI</subject><subject>Psychiatry</subject><subject>psychosocial effects</subject><subject>SCD</subject><issn>1664-0640</issn><issn>1664-0640</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkk9r3DAQxU1pSEKSD5Cbjj10t_pv-VIom6RdSGigLT2KsTze1WJbW8kO7KHfvXI2tM1cNJr3-A0DryiuGV0KYaoP7T4dxiWnnC6VUdroN8U501ouqJb07X_9WXGV0o7mElUltDotzoRgFS-FOC9-P6aD24YUnIeO3LYtujGR0JJViGEA8oCQpoh5NJBHGD0OWf7pxy25wT5_PLwnD75rsn8z-NE_IVn3e_BxFgkMDfk21bsMnZV_nht0nR_wsjhpoUt49fJeFD_ubr-vvizuv35erz7dL5yUfFwAr0s0slSmaahTTlOosaLOgKpaB4IhByo1Y1q2JZSGYbZXUDOuJUNw4qJYH7lNgJ3dR99DPNgA3j4PQtxYiKN3HVrW8NrVXHPFammUAFNrITnjFVWNom1mfTyy9lPdY-PynRG6V9DXyuC3dhOebKllxZjJgHcvgBh-TZhG2_vksOtgwDAly_MllDLBZys7Wl0MKUVs_65h1M4psM8psHMK7DEF4g8Kg6bb</recordid><startdate>20201026</startdate><enddate>20201026</enddate><creator>van Maurik, Ingrid S.</creator><creator>Bakker, Els D.</creator><creator>van den Buuse, Susanne</creator><creator>Gillissen, Freek</creator><creator>van de Beek, Marleen</creator><creator>Lemstra, Evelien</creator><creator>Mank, Arenda</creator><creator>van den Bosch, Karlijn A.</creator><creator>van Leeuwenstijn, Mardou</creator><creator>Bouwman, Femke H.</creator><creator>Scheltens, Philip</creator><creator>van der Flier, Wiesje M.</creator><general>Frontiers Media S.A</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20201026</creationdate><title>Psychosocial Effects of Corona Measures on Patients With Dementia, Mild Cognitive Impairment and Subjective Cognitive Decline</title><author>van Maurik, Ingrid S. ; Bakker, Els D. ; van den Buuse, Susanne ; Gillissen, Freek ; van de Beek, Marleen ; Lemstra, Evelien ; Mank, Arenda ; van den Bosch, Karlijn A. ; van Leeuwenstijn, Mardou ; Bouwman, Femke H. ; Scheltens, Philip ; van der Flier, Wiesje M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-a2b7e84758dd0c5c60abe90c8a59fca31e2a0461164f7a781e7e89ab12641eac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>behavioral problems</topic><topic>COVID-19</topic><topic>dementia</topic><topic>MCI</topic><topic>Psychiatry</topic><topic>psychosocial effects</topic><topic>SCD</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Maurik, Ingrid S.</creatorcontrib><creatorcontrib>Bakker, Els D.</creatorcontrib><creatorcontrib>van den Buuse, Susanne</creatorcontrib><creatorcontrib>Gillissen, Freek</creatorcontrib><creatorcontrib>van de Beek, Marleen</creatorcontrib><creatorcontrib>Lemstra, Evelien</creatorcontrib><creatorcontrib>Mank, Arenda</creatorcontrib><creatorcontrib>van den Bosch, Karlijn A.</creatorcontrib><creatorcontrib>van Leeuwenstijn, Mardou</creatorcontrib><creatorcontrib>Bouwman, Femke H.</creatorcontrib><creatorcontrib>Scheltens, Philip</creatorcontrib><creatorcontrib>van der Flier, Wiesje M.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Maurik, Ingrid S.</au><au>Bakker, Els D.</au><au>van den Buuse, Susanne</au><au>Gillissen, Freek</au><au>van de Beek, Marleen</au><au>Lemstra, Evelien</au><au>Mank, Arenda</au><au>van den Bosch, Karlijn A.</au><au>van Leeuwenstijn, Mardou</au><au>Bouwman, Femke H.</au><au>Scheltens, Philip</au><au>van der Flier, Wiesje M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Psychosocial Effects of Corona Measures on Patients With Dementia, Mild Cognitive Impairment and Subjective Cognitive Decline</atitle><jtitle>Frontiers in psychiatry</jtitle><date>2020-10-26</date><risdate>2020</risdate><volume>11</volume><spage>585686</spage><epage>585686</epage><pages>585686-585686</pages><issn>1664-0640</issn><eissn>1664-0640</eissn><abstract>Background: The recent COVID-19 pandemic is not only a major healthcare problem in itself, but also poses enormous social challenges. Though nursing homes increasingly receive attention, the majority of people with cognitive decline and dementia live at home. We aimed to explore the psychosocial effects of corona measures in memory clinic (pre-)dementia patients and their caregivers. Methods: Between April 28th and July 13th 2020, n = 389 patients of Alzheimer center Amsterdam [ n = 121 symptomatic (age = 69 ± 6, 33%F, MMSE = 23 ± 5), n = 268 cognitively normal (age = 66 ± 8, 40% F, MMSE = 29 ± 1)] completed a survey on psychosocial effects of the corona measures. Questions related to social isolation, worries for faster cognitive decline, behavioral problems and discontinuation of care. In addition, n = 147 caregivers of symptomatic patients completed a similar survey with additional questions on caregiver burden. Results: Social isolation was experienced by n = 42 (35%) symptomatic and n = 67 (25%) cognitively normal patients and two third of patients [ n = 129 (66%); n = 58 (75%) symptomatic, n = 71 (61%) cognitively normal] reported that care was discontinued. Worries for faster cognitive decline were existed in symptomatic patients [ n = 44 (44%)] and caregivers [ n = 73 (53%)], but were also reported by a subgroup of cognitively normal patients [ n = 27 (14%)]. Both patients [ n = 56 (46%) symptomatic, n = 102 (38%) cognitively normal] and caregivers [ n = 72 (48%)] reported an increase in psychological symptoms. More than three quarter of caregivers [ n = 111(76%)] reported an increase in patients' behavioral problems. A higher caregiver burden was experienced by n = 69 (56%) of caregivers and n = 43 (29%) of them reported that a need for more support. Discontinuation of care (OR = 3.3 [1.3–7.9]), psychological (OR = 4.0 [1.6–9.9]) and behavioral problems (OR = 3.0 [1.0–9.0]) strongly related to experiencing a higher caregiver burden. Lastly, social isolation (OR = 3.2 [1.2–8.1]) and psychological symptoms (OR = 8.1 [2.8–23.7]) were red flags for worries for faster cognitive decline. Conclusion: Not only symptomatic patients, but also cognitively normal patients express worries for faster cognitive decline and psychological symptoms. Moreover, we identified patients who are at risk of adverse outcomes of the corona measures, i.e., discontinued care, social isolation, psychological and behavioral problems. This underlines the need for health care professionals to provide ways to warrant the continuation of care and support (informal) networks surrounding patients and caregivers to mitigate the higher risk of negative psychosocial effects.</abstract><pub>Frontiers Media S.A</pub><pmid>33192733</pmid><doi>10.3389/fpsyt.2020.585686</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects behavioral problems
COVID-19
dementia
MCI
Psychiatry
psychosocial effects
SCD
title Psychosocial Effects of Corona Measures on Patients With Dementia, Mild Cognitive Impairment and Subjective Cognitive Decline
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