Cargando…

Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment

BACKGROUND/OBJECTIVES: To analyse the relationship between caregiver burden and severity of patients’ cognitive impairment. DESIGN: Data were drawn from the cross-sectional 2015/2016 Adelphi Real World Dementia Disease-Specific Programme. SETTING: This research was multi-national and studied physici...

Descripción completa

Detalles Bibliográficos
Autores principales: Black, Christopher M., Ritchie, Craig W., Khandker, Rezaul K., Wood, Robert, Jones, Eddie, Hu, Xiaohan, Ambegaonkar, Baishali M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283568/
https://www.ncbi.nlm.nih.gov/pubmed/30521532
http://dx.doi.org/10.1371/journal.pone.0204110
_version_ 1783379184640327680
author Black, Christopher M.
Ritchie, Craig W.
Khandker, Rezaul K.
Wood, Robert
Jones, Eddie
Hu, Xiaohan
Ambegaonkar, Baishali M.
author_facet Black, Christopher M.
Ritchie, Craig W.
Khandker, Rezaul K.
Wood, Robert
Jones, Eddie
Hu, Xiaohan
Ambegaonkar, Baishali M.
author_sort Black, Christopher M.
collection PubMed
description BACKGROUND/OBJECTIVES: To analyse the relationship between caregiver burden and severity of patients’ cognitive impairment. DESIGN: Data were drawn from the cross-sectional 2015/2016 Adelphi Real World Dementia Disease-Specific Programme. SETTING: This research was multi-national and studied physicians and their consulting patients with cognitive impairment. PARTICIPANTS: 1,201 caregivers completed self-assessment forms. MEASUREMENTS: Validated instruments of caregiver wellbeing and burden (EQ-5D-3L questionnaire, EQ-VAS, Zarit Burden Interview, and Work Productivity and Activity Impairment questionnaire) and number of caregiver hours were analysed by severity of patients’ cognitive impairment, categorised according to the Mini-Mental State Examination. Data were analysed using Spearman’s rank correlation coefficients and ordinary least squares regression models, to compare outcomes between caregivers of patients with prodromal, mild, moderate, and severe dementia. RESULTS: The majority of caregivers were female (69.1%), lived with the patient they cared for (75.8%), and only approximately one third (28.3%) were in part- or full-time employment. There were statistically significant (p<0.001) increases in caregiver time (36.9 versus 108.6 hours per week for prodromal versus severe dementia, respectively) and measures of caregiver burden and health status (EQ-5D-3L, EQ-VAS, and Zarit Burden Interview) and increases in measures of work productivity and activity impairment with increasing severity of patients’ disease. CONCLUSION: This study of real-world data confirmed an association between increased caregiver burden and severity of patients’ cognitive impairment by analysis of a wide range of validated measures of caregiver burden. These findings suggest that maintaining patients in the earliest stages of their disease for as long as possible may potentially help to protect caregiver wellbeing, although further research is required to confirm this hypothesis.
format Online
Article
Text
id pubmed-6283568
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-62835682018-12-20 Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment Black, Christopher M. Ritchie, Craig W. Khandker, Rezaul K. Wood, Robert Jones, Eddie Hu, Xiaohan Ambegaonkar, Baishali M. PLoS One Research Article BACKGROUND/OBJECTIVES: To analyse the relationship between caregiver burden and severity of patients’ cognitive impairment. DESIGN: Data were drawn from the cross-sectional 2015/2016 Adelphi Real World Dementia Disease-Specific Programme. SETTING: This research was multi-national and studied physicians and their consulting patients with cognitive impairment. PARTICIPANTS: 1,201 caregivers completed self-assessment forms. MEASUREMENTS: Validated instruments of caregiver wellbeing and burden (EQ-5D-3L questionnaire, EQ-VAS, Zarit Burden Interview, and Work Productivity and Activity Impairment questionnaire) and number of caregiver hours were analysed by severity of patients’ cognitive impairment, categorised according to the Mini-Mental State Examination. Data were analysed using Spearman’s rank correlation coefficients and ordinary least squares regression models, to compare outcomes between caregivers of patients with prodromal, mild, moderate, and severe dementia. RESULTS: The majority of caregivers were female (69.1%), lived with the patient they cared for (75.8%), and only approximately one third (28.3%) were in part- or full-time employment. There were statistically significant (p<0.001) increases in caregiver time (36.9 versus 108.6 hours per week for prodromal versus severe dementia, respectively) and measures of caregiver burden and health status (EQ-5D-3L, EQ-VAS, and Zarit Burden Interview) and increases in measures of work productivity and activity impairment with increasing severity of patients’ disease. CONCLUSION: This study of real-world data confirmed an association between increased caregiver burden and severity of patients’ cognitive impairment by analysis of a wide range of validated measures of caregiver burden. These findings suggest that maintaining patients in the earliest stages of their disease for as long as possible may potentially help to protect caregiver wellbeing, although further research is required to confirm this hypothesis. Public Library of Science 2018-12-06 /pmc/articles/PMC6283568/ /pubmed/30521532 http://dx.doi.org/10.1371/journal.pone.0204110 Text en © 2018 Black et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Black, Christopher M.
Ritchie, Craig W.
Khandker, Rezaul K.
Wood, Robert
Jones, Eddie
Hu, Xiaohan
Ambegaonkar, Baishali M.
Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
title Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
title_full Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
title_fullStr Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
title_full_unstemmed Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
title_short Non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
title_sort non-professional caregiver burden is associated with the severity of patients’ cognitive impairment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283568/
https://www.ncbi.nlm.nih.gov/pubmed/30521532
http://dx.doi.org/10.1371/journal.pone.0204110
work_keys_str_mv AT blackchristopherm nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment
AT ritchiecraigw nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment
AT khandkerrezaulk nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment
AT woodrobert nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment
AT joneseddie nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment
AT huxiaohan nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment
AT ambegaonkarbaishalim nonprofessionalcaregiverburdenisassociatedwiththeseverityofpatientscognitiveimpairment