MovDisordV3, Main, Exploration, bibRecord, 002A82

Burden, Perceived Health Status, and Mood Among Caregivers of Parkinson's Disease Patients

Identifieur interne : 002A82 ( Main/Exploration ); précédent : 002A81; suivant : 002A83

Burden, Perceived Health Status, and Mood Among Caregivers of Parkinson's Disease Patients

Auteurs : Pablo Martinez-Martin [Espagne] ; Susana Arroyo [Espagne] ; Jose Manuel Rojo-Abuin [Espagne] ; Carmen Rodriguez-Blazquez [Espagne] ; Belen Frades [Espagne] ; Jesus De Pedro Cuesta [Espagne]

Source :

Movement disorders [ 0885-3185 ] ; 2008.

RBID : Pascal:08-0487369

Descripteurs français

Pascal (Inist)
- Maladie de Parkinson, Pathologie du système nerveux, Etat sanitaire, Humeur, Aidant, Homme, Soin, Coût.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Care, Caregiver, Costs, Health status, Human, Mood, Nervous system diseases, Parkinson disease.

Abstract

The objective of this study is to describe the characteristics of the caregivers of patients with Parkinson's disease (PD) and to analyze the association between these characteristics and caregiver burden, perceived health and mood status, and identify their predictors. A multicenter, nationwide, observational, cross-sectional study that included 289 patient-caregiver pairs was conducted. Caregiver self-assessments were the Hospital Anxiety and Depression Scale (HADS), EuroQol (EQ), and Zarit Caregiver Burden Inventory (ZCBI). Most caregivers in the study were women aged 60 years or thereabouts. Over two thirds were gainfully employed or housewives, 75% were patients' spouses, and the majority (96.5%) had been permanently taking care of the patient for 6 ± 5.4 years. Less than 5% of patients were in the most advanced stages of disease, and direct costs were 6,350 euros per patient per year. Caregivers had more mood disorders and worse health-related quality of life (HRQol; EQ-Tariff) than did the general population. Caregiver HADS and EuroQol scores displayed a weak correlation (r_S = 0.01-0.28) with patient-related variables (disease duration, HY, SCOPA-Motor, SCOPA-AUT, HADS, PPRS, and CISI-PD) whereas the ZCBI correlated moderately (r_S = 0.27-0.47). Among caregivers, the EQ-Tariff was significantly lower and the HADS-Anxiety scores significantly higher for women. ZCBI and HADS-depression, though not EuroQol and HADS-anxiety, scores significantly increased with increasing PD severity levels. Caregivers' affective status proved the most important factor influencing their burden and perceived health, whereas patient-related variables influenced caregiver burden and mood but not health status. In PD, prevalence of affective disorders among patients' caregivers is high and influences both burden and HROoL. © 2008 Movement Disorder Society burden and HRQoL.

Affiliations:

Links toward previous steps (curation, corpus...)

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Le document en format XML

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<author><name sortKey="Rodriguez Blazquez, Carmen" sort="Rodriguez Blazquez, Carmen" uniqKey="Rodriguez Blazquez C" first="Carmen" last="Rodriguez-Blazquez">Carmen Rodriguez-Blazquez</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>Department of Applied Epidemiology, National Center for Epidemiology, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Carlos III Institute of Health</s1>
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<author><name sortKey="Frades, Belen" sort="Frades, Belen" uniqKey="Frades B" first="Belen" last="Frades">Belen Frades</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>Department of Applied Epidemiology, National Center for Epidemiology, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Carlos III Institute of Health</s1>
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</author>
<author><name sortKey="Cuesta, Jesus De Pedro" sort="Cuesta, Jesus De Pedro" uniqKey="Cuesta J" first="Jesus De Pedro" last="Cuesta">Jesus De Pedro Cuesta</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>Department of Applied Epidemiology, National Center for Epidemiology, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Carlos III Institute of Health</s1>
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<series><title level="j" type="main">Movement disorders</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Care</term>
<term>Caregiver</term>
<term>Costs</term>
<term>Health status</term>
<term>Human</term>
<term>Mood</term>
<term>Nervous system diseases</term>
<term>Parkinson disease</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Maladie de Parkinson</term>
<term>Pathologie du   système nerveux</term>
<term>Etat sanitaire</term>
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<term>Aidant</term>
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<front><div type="abstract" xml:lang="en">The objective of this study is to describe the characteristics of the caregivers of patients with Parkinson's disease (PD) and to analyze the association between these characteristics and caregiver burden, perceived health and mood status, and identify their predictors. A multicenter, nationwide, observational, cross-sectional study that included 289 patient-caregiver pairs was conducted. Caregiver self-assessments were the Hospital Anxiety and Depression Scale (HADS), EuroQol (EQ), and Zarit Caregiver Burden Inventory (ZCBI). Most caregivers in the study were women aged 60 years or thereabouts. Over two thirds were gainfully employed or housewives, 75% were patients' spouses, and the majority (96.5%) had been permanently taking care of the patient for 6 ± 5.4 years. Less than 5% of patients were in the most advanced stages of disease, and direct costs were 6,350 euros per patient per year. Caregivers had more mood disorders and worse health-related quality of life (HRQol; EQ-Tariff) than did the general population. Caregiver HADS and EuroQol scores displayed a weak correlation (r<sub>S</sub>
 = 0.01-0.28) with patient-related variables (disease duration, HY, SCOPA-Motor, SCOPA-AUT, HADS, PPRS, and CISI-PD) whereas the ZCBI correlated moderately (r<sub>S</sub>
 = 0.27-0.47). Among caregivers, the EQ-Tariff was significantly lower and the HADS-Anxiety scores significantly higher for women. ZCBI and HADS-depression, though not EuroQol and HADS-anxiety, scores significantly increased with increasing PD severity levels. Caregivers' affective status proved the most important factor influencing their burden and perceived health, whereas patient-related variables influenced caregiver burden and mood but not health status. In PD, prevalence of affective disorders among patients' caregivers is high and influences both burden and HROoL. © 2008 Movement Disorder Society burden and HRQoL.</div>
</front>
</TEI>
<affiliations><list><country><li>Espagne</li>
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<tree><country name="Espagne"><region name="Communauté de Madrid"><name sortKey="Martinez Martin, Pablo" sort="Martinez Martin, Pablo" uniqKey="Martinez Martin P" first="Pablo" last="Martinez-Martin">Pablo Martinez-Martin</name>
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<name sortKey="Arroyo, Susana" sort="Arroyo, Susana" uniqKey="Arroyo S" first="Susana" last="Arroyo">Susana Arroyo</name>
<name sortKey="Cuesta, Jesus De Pedro" sort="Cuesta, Jesus De Pedro" uniqKey="Cuesta J" first="Jesus De Pedro" last="Cuesta">Jesus De Pedro Cuesta</name>
<name sortKey="Frades, Belen" sort="Frades, Belen" uniqKey="Frades B" first="Belen" last="Frades">Belen Frades</name>
<name sortKey="Rodriguez Blazquez, Carmen" sort="Rodriguez Blazquez, Carmen" uniqKey="Rodriguez Blazquez C" first="Carmen" last="Rodriguez-Blazquez">Carmen Rodriguez-Blazquez</name>
<name sortKey="Rojo Abuin, Jose Manuel" sort="Rojo Abuin, Jose Manuel" uniqKey="Rojo Abuin J" first="Jose Manuel" last="Rojo-Abuin">Jose Manuel Rojo-Abuin</name>
</country>
</tree>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Burden, Perceived Health Status, and Mood Among Caregivers of Parkinson's Disease Patients

Burden, Perceived Health Status, and Mood Among Caregivers of Parkinson's Disease Patients

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri