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Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis

BACKGROUND: Acute Systemic Diseases (ASD) impact on extended leukoaraiosis (ExL-A) have been seldom described. We study the deterioration in daily life activities (DLA) and cognition associated with ASD events compared with the well-described impacts of stroke in patients with leu-koaraiosis (L-A)....

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Autores principales: Domínguez, Raúl O., Marschoff, Enrique R., Oudkerk, Liliana M., Neira, Luis J., Serra, Jorge A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388423/
https://www.ncbi.nlm.nih.gov/pubmed/30338749
http://dx.doi.org/10.2174/1874609811666181019103642
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author Domínguez, Raúl O.
Marschoff, Enrique R.
Oudkerk, Liliana M.
Neira, Luis J.
Serra, Jorge A.
author_facet Domínguez, Raúl O.
Marschoff, Enrique R.
Oudkerk, Liliana M.
Neira, Luis J.
Serra, Jorge A.
author_sort Domínguez, Raúl O.
collection PubMed
description BACKGROUND: Acute Systemic Diseases (ASD) impact on extended leukoaraiosis (ExL-A) have been seldom described. We study the deterioration in daily life activities (DLA) and cognition associated with ASD events compared with the well-described impacts of stroke in patients with leu-koaraiosis (L-A). METHODS: Cross-sectional surveys of aged adults from the emergency room after an acute event of ASD or stroke, hospitalized or receiving home care, were followed for one year. From 268 initial pa-tients 206 were included in the study, all with moderate to severe L-A (Fazekas 2 and 3). The Clinical Deterioration Rating (CDR) and the modified Rankin scale with structured interview were obtained one week previous to admission and after 3 and 12 months of evolution. Comparisons were conduct-ed within and between groups with nonparametric techniques. RESULTS: We formed three groups of similar age, A: Inpatients with one Stroke, B: Inpatients with one ASD, and C: Outpatients with one ASD. A sudden deterioration in Rankin was evident in Group A, while in B and C impairment was progressive. Impairment in CDR was smooth in all groups while in Rankin it was always greater than in cognition (CDR). No differences were found in the associations between groups and risk factors, hypertension being the most frequent one. CONCLUSION: ASD in ExL-A causes a worsening of DLA and cognition similar to that observed in ExL-A with concomitant stroke indicating the need, in ageing patients, of differential diagnosis in or-der to achieve the best possible treatment.
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spelling pubmed-63884232019-03-26 Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis Domínguez, Raúl O. Marschoff, Enrique R. Oudkerk, Liliana M. Neira, Luis J. Serra, Jorge A. Curr Aging Sci Article BACKGROUND: Acute Systemic Diseases (ASD) impact on extended leukoaraiosis (ExL-A) have been seldom described. We study the deterioration in daily life activities (DLA) and cognition associated with ASD events compared with the well-described impacts of stroke in patients with leu-koaraiosis (L-A). METHODS: Cross-sectional surveys of aged adults from the emergency room after an acute event of ASD or stroke, hospitalized or receiving home care, were followed for one year. From 268 initial pa-tients 206 were included in the study, all with moderate to severe L-A (Fazekas 2 and 3). The Clinical Deterioration Rating (CDR) and the modified Rankin scale with structured interview were obtained one week previous to admission and after 3 and 12 months of evolution. Comparisons were conduct-ed within and between groups with nonparametric techniques. RESULTS: We formed three groups of similar age, A: Inpatients with one Stroke, B: Inpatients with one ASD, and C: Outpatients with one ASD. A sudden deterioration in Rankin was evident in Group A, while in B and C impairment was progressive. Impairment in CDR was smooth in all groups while in Rankin it was always greater than in cognition (CDR). No differences were found in the associations between groups and risk factors, hypertension being the most frequent one. CONCLUSION: ASD in ExL-A causes a worsening of DLA and cognition similar to that observed in ExL-A with concomitant stroke indicating the need, in ageing patients, of differential diagnosis in or-der to achieve the best possible treatment. Bentham Science Publishers 2018-10 2018-10 /pmc/articles/PMC6388423/ /pubmed/30338749 http://dx.doi.org/10.2174/1874609811666181019103642 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Domínguez, Raúl O.
Marschoff, Enrique R.
Oudkerk, Liliana M.
Neira, Luis J.
Serra, Jorge A.
Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis
title Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis
title_full Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis
title_fullStr Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis
title_full_unstemmed Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis
title_short Daily Living Activities and Cognition in Aged Patients: Effect of Acute Systemic Diseases and Stroke on Leukoaraiosis
title_sort daily living activities and cognition in aged patients: effect of acute systemic diseases and stroke on leukoaraiosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388423/
https://www.ncbi.nlm.nih.gov/pubmed/30338749
http://dx.doi.org/10.2174/1874609811666181019103642
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