Neurological and cognitive impairment in COVID‐19: clinical characterization andepidemiological

Background COVID‐19 neurological manifestations were demonstrated during the pandemic, including cognitive impairment. Objectives: To determine the prevalence of cognitive and behavioral complaints (such as dementia, MCI or SCD) in a outpatient sample with recent SARS‐COV2 infection. Specific: Evalu...

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Veröffentlicht in:Alzheimer's & dementia 2023-06, Vol.19 (S4), p.n/a
Hauptverfasser: Júnior, José Wagner Leonel Tavares, Neto, Pedro Braga, Neto, Manoel Alves Sobreira, MONTENEGRO, RAQUEL CARVALHO, MOREIRA, CAROLINE DE FÁTIMA AQUINO, de Oliveira, Lais Lacerda Brasil, da Silva, Jean Breno Silveira, Gomes, Carmem Meyve Pereira, Gaspar, Safira de Brito, Cunha, Letícia Chaves Vieira, Sousa, Artur Victor Menezes, Feitosa, Werbety Lucas Queiroz, Oliveira, Danilo Nunes
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container_end_page n/a
container_issue S4
container_start_page
container_title Alzheimer's & dementia
container_volume 19
creator Júnior, José Wagner Leonel Tavares
Neto, Pedro Braga
Neto, Manoel Alves Sobreira
MONTENEGRO, RAQUEL CARVALHO
MOREIRA, CAROLINE DE FÁTIMA AQUINO
de Oliveira, Lais Lacerda Brasil
da Silva, Jean Breno Silveira
Gomes, Carmem Meyve Pereira
Gaspar, Safira de Brito
Cunha, Letícia Chaves Vieira
Sousa, Artur Victor Menezes
Feitosa, Werbety Lucas Queiroz
Oliveira, Danilo Nunes
description Background COVID‐19 neurological manifestations were demonstrated during the pandemic, including cognitive impairment. Objectives: To determine the prevalence of cognitive and behavioral complaints (such as dementia, MCI or SCD) in a outpatient sample with recent SARS‐COV2 infection. Specific: Evaluate the association of cognitive impairment with the presence of the polymorphism found in the APOE gene and with respiratory disease Method Observational, longitudinal, prospective clinical study. Inclusion criteria: patients with confirmed Covid‐19. Patients are evaluated in an outpatient clinic. They are evaluated through a standardized attendance record, with somatic and cognitive neurological assessment. Cognitive assessment involves the application of cognitive (ACER, MMSE and CDR), functional (Pfeffer) and psychiatric (GDS or Beck) screening instruments, in addition to subsequent extensive neuropsychological assessment. In addition, APOE polymorphism is analysed. Results To date, 200 patients were evaluated. The average age is 46.5 years, with 65.4% female, 79.16% with 8 or more years of schooling, in addition to 57.5% of the sample with cognitive complaints. Conclusions The results so far in our study demonstrate that cognitive complaints are frequent in patients even in the chronic phase of the disease.
doi_str_mv 10.1002/alz.059664
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Objectives: To determine the prevalence of cognitive and behavioral complaints (such as dementia, MCI or SCD) in a outpatient sample with recent SARS‐COV2 infection. Specific: Evaluate the association of cognitive impairment with the presence of the polymorphism found in the APOE gene and with respiratory disease Method Observational, longitudinal, prospective clinical study. Inclusion criteria: patients with confirmed Covid‐19. Patients are evaluated in an outpatient clinic. They are evaluated through a standardized attendance record, with somatic and cognitive neurological assessment. Cognitive assessment involves the application of cognitive (ACER, MMSE and CDR), functional (Pfeffer) and psychiatric (GDS or Beck) screening instruments, in addition to subsequent extensive neuropsychological assessment. In addition, APOE polymorphism is analysed. Results To date, 200 patients were evaluated. The average age is 46.5 years, with 65.4% female, 79.16% with 8 or more years of schooling, in addition to 57.5% of the sample with cognitive complaints. Conclusions The results so far in our study demonstrate that cognitive complaints are frequent in patients even in the chronic phase of the disease.</description><identifier>ISSN: 1552-5260</identifier><identifier>EISSN: 1552-5279</identifier><identifier>DOI: 10.1002/alz.059664</identifier><language>eng</language><ispartof>Alzheimer's &amp; dementia, 2023-06, Vol.19 (S4), p.n/a</ispartof><rights>2023 the Alzheimer's Association.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Falz.059664$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Falz.059664$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Júnior, José Wagner Leonel Tavares</creatorcontrib><creatorcontrib>Neto, Pedro Braga</creatorcontrib><creatorcontrib>Neto, Manoel Alves Sobreira</creatorcontrib><creatorcontrib>MONTENEGRO, RAQUEL CARVALHO</creatorcontrib><creatorcontrib>MOREIRA, CAROLINE DE FÁTIMA AQUINO</creatorcontrib><creatorcontrib>de Oliveira, Lais Lacerda Brasil</creatorcontrib><creatorcontrib>da Silva, Jean Breno Silveira</creatorcontrib><creatorcontrib>Gomes, Carmem Meyve Pereira</creatorcontrib><creatorcontrib>Gaspar, Safira de Brito</creatorcontrib><creatorcontrib>Cunha, Letícia Chaves Vieira</creatorcontrib><creatorcontrib>Sousa, Artur Victor Menezes</creatorcontrib><creatorcontrib>Feitosa, Werbety Lucas Queiroz</creatorcontrib><creatorcontrib>Oliveira, Danilo Nunes</creatorcontrib><title>Neurological and cognitive impairment in COVID‐19: clinical characterization andepidemiological</title><title>Alzheimer's &amp; dementia</title><description>Background COVID‐19 neurological manifestations were demonstrated during the pandemic, including cognitive impairment. Objectives: To determine the prevalence of cognitive and behavioral complaints (such as dementia, MCI or SCD) in a outpatient sample with recent SARS‐COV2 infection. Specific: Evaluate the association of cognitive impairment with the presence of the polymorphism found in the APOE gene and with respiratory disease Method Observational, longitudinal, prospective clinical study. Inclusion criteria: patients with confirmed Covid‐19. Patients are evaluated in an outpatient clinic. They are evaluated through a standardized attendance record, with somatic and cognitive neurological assessment. Cognitive assessment involves the application of cognitive (ACER, MMSE and CDR), functional (Pfeffer) and psychiatric (GDS or Beck) screening instruments, in addition to subsequent extensive neuropsychological assessment. In addition, APOE polymorphism is analysed. Results To date, 200 patients were evaluated. The average age is 46.5 years, with 65.4% female, 79.16% with 8 or more years of schooling, in addition to 57.5% of the sample with cognitive complaints. 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Objectives: To determine the prevalence of cognitive and behavioral complaints (such as dementia, MCI or SCD) in a outpatient sample with recent SARS‐COV2 infection. Specific: Evaluate the association of cognitive impairment with the presence of the polymorphism found in the APOE gene and with respiratory disease Method Observational, longitudinal, prospective clinical study. Inclusion criteria: patients with confirmed Covid‐19. Patients are evaluated in an outpatient clinic. They are evaluated through a standardized attendance record, with somatic and cognitive neurological assessment. Cognitive assessment involves the application of cognitive (ACER, MMSE and CDR), functional (Pfeffer) and psychiatric (GDS or Beck) screening instruments, in addition to subsequent extensive neuropsychological assessment. In addition, APOE polymorphism is analysed. Results To date, 200 patients were evaluated. The average age is 46.5 years, with 65.4% female, 79.16% with 8 or more years of schooling, in addition to 57.5% of the sample with cognitive complaints. Conclusions The results so far in our study demonstrate that cognitive complaints are frequent in patients even in the chronic phase of the disease.</abstract><doi>10.1002/alz.059664</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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