Caregiver burden in Parkinson's disease
Identifieur interne : 002F71 ( Main/Exploration ); précédent : 002F70; suivant : 002F72Caregiver burden in Parkinson's disease
Auteurs : Pablo Martínez-Martín [Espagne] ; Maria João Forjaz [Espagne] ; Belén Frades-Payo [Espagne] ; Angels Bayés Rusi Ol [Espagne] ; José Manuel Fernández-García [Espagne] ; Julián Benito-Le N [Espagne] ; Víctor Campos Arillo [Espagne] ; Miquel Aguilar Barberá [Espagne] ; Margarita Pondal Sordo [Espagne] ; María José Catalán [Espagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-05-15.
English descriptors
- KwdEn :
- Aged, Aged, 80 and over, Caregivers (psychology), Cross-Sectional Studies, Factor Analysis, Statistical, Female, Health Status, Humans, Male, Middle Aged, Parkinson Disease (nursing), Parkinson Disease (psychology), Parkinson's disease, Quality of Life, Questionnaires, Self-Assessment, Severity of Illness Index, Zarit caregiver burden inventory, caregiver burden, health‐related quality of life.
- MESH :
Abstract
Parkinson's disease (PD) is a neurodegenerative disorder that imposes an important burden upon the patient's caregiver. This study aims at assessing caregiver burden (CB) and analyzing its relationship with sociodemographic, emotional, and functional factors, as well as health‐related quality of life (HRQoL). The following measures were applied to 80 patients with PD: the Hospital Anxiety and Depression Scale (HADS); the EuroQoL (for HRQoL); and PD‐specific measures (Hoehn and Yahr staging and SCOPA‐Motor ADL subscale). Patients' main caregivers completed the HADS, SF‐36, EuroQoL, and Zarit CB Inventory (ZCBI). The ZCBI was found to be a valid and reliable measure in the context of PD. There was a significant association between CB and caregivers' HRQoL (r = −0.29 to −0.64). Mental aspects of caregivers' HRQoL and burden were affected by disability and disease severity. The presence of caregivers' depression had a significant negative effect on both CB and HRQoL. The main predictors of CB were caregivers' psychological well‐being, patients' mood and clinical aspects of PD (disability and severity), and HRQoL of patients and caregivers. This study underscores the need to consider the impact of PD on caregivers' well‐being. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21355
Affiliations:
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Le document en format XML
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<term>Factor Analysis, Statistical</term>
<term>Female</term>
<term>Health Status</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (nursing)</term>
<term>Parkinson Disease (psychology)</term>
<term>Parkinson's disease</term>
<term>Quality of Life</term>
<term>Questionnaires</term>
<term>Self-Assessment</term>
<term>Severity of Illness Index</term>
<term>Zarit caregiver burden inventory</term>
<term>caregiver burden</term>
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<front><div type="abstract" xml:lang="en">Parkinson's disease (PD) is a neurodegenerative disorder that imposes an important burden upon the patient's caregiver. This study aims at assessing caregiver burden (CB) and analyzing its relationship with sociodemographic, emotional, and functional factors, as well as health‐related quality of life (HRQoL). The following measures were applied to 80 patients with PD: the Hospital Anxiety and Depression Scale (HADS); the EuroQoL (for HRQoL); and PD‐specific measures (Hoehn and Yahr staging and SCOPA‐Motor ADL subscale). Patients' main caregivers completed the HADS, SF‐36, EuroQoL, and Zarit CB Inventory (ZCBI). The ZCBI was found to be a valid and reliable measure in the context of PD. There was a significant association between CB and caregivers' HRQoL (r = −0.29 to −0.64). Mental aspects of caregivers' HRQoL and burden were affected by disability and disease severity. The presence of caregivers' depression had a significant negative effect on both CB and HRQoL. The main predictors of CB were caregivers' psychological well‐being, patients' mood and clinical aspects of PD (disability and severity), and HRQoL of patients and caregivers. This study underscores the need to consider the impact of PD on caregivers' well‐being. © 2007 Movement Disorder Society</div>
</front>
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<name sortKey="Arillo, Victor Campos" sort="Arillo, Victor Campos" uniqKey="Arillo V" first="Víctor Campos" last="Arillo">Víctor Campos Arillo</name>
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<name sortKey="Benito E N, Julian" sort="Benito E N, Julian" uniqKey="Benito E N J" first="Julián" last="Benito-Le N">Julián Benito-Le N</name>
<name sortKey="Catalan, Maria Jose" sort="Catalan, Maria Jose" uniqKey="Catalan M" first="María José" last="Catalán">María José Catalán</name>
<name sortKey="Fernandez Arcia, Jose Manuel" sort="Fernandez Arcia, Jose Manuel" uniqKey="Fernandez Arcia J" first="José Manuel" last="Fernández-García">José Manuel Fernández-García</name>
<name sortKey="Forjaz, Maria Joao" sort="Forjaz, Maria Joao" uniqKey="Forjaz M" first="Maria João" last="Forjaz">Maria João Forjaz</name>
<name sortKey="Frades Ayo, Belen" sort="Frades Ayo, Belen" uniqKey="Frades Ayo B" first="Belén" last="Frades-Payo">Belén Frades-Payo</name>
<name sortKey="Rusi Ol, Angels Bayes" sort="Rusi Ol, Angels Bayes" uniqKey="Rusi Ol A" first="Angels Bayés" last="Rusi Ol">Angels Bayés Rusi Ol</name>
<name sortKey="Sordo, Margarita Pondal" sort="Sordo, Margarita Pondal" uniqKey="Sordo M" first="Margarita Pondal" last="Sordo">Margarita Pondal Sordo</name>
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