Caregiver burden and its predictors in adult epilepsy patients.

Anxiety Caregiving burden Depression Epilepsy Quality of life Stigma

Journal

Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858

Informations de publication

Date de publication:
17 Feb 2024
Historique:
received: 24 11 2023
revised: 02 02 2024
accepted: 03 02 2024
medline: 19 2 2024
pubmed: 19 2 2024
entrez: 18 2 2024
Statut: aheadofprint

Résumé

The aim of this study was to evaluate caregiver burden and factors associated with caregiver burden in caregivers of adults with epilepsy. This descriptive cross-sectional study was conducted with 107 patients with epilepsy and 107 their primary caregivers. Personal information form including sociodemographic data and Zarit Caregiver Burden Inventory (ZBI), were used for caregivers, and patient information form, Montreal Cognitive Assessment Scale (MoCA), Hospital Anxiety and Depression Scale (HADS), Epilepsy Quality of Life Scale (QoLIE-31) and Stigma Scale were used for patients. Caregiver burden was found to be related to gender (p = 0.047), marital status (p = 0.008), income (p = 0.003), education level (p = 0.05) age at onset of epilepsy (p = 0.025) and type of therapy (p = 0.005). The scale scores for cognitive functions (p < 0.001), stigma (p < 0.001), anxiety (p = 0.001), depression (p = 0.005), and quality of life (p < 0.001) of the patient showed significant correlations with caregiver burden. In addition, caregiver burden was found to correlate with some caregiver characteristics such as caregivers' age (p = 0.041), gender (p < 0.001), education (p < 0.001), income (p = 0.001) and relationship with the patient (p = 0.016). Time spent on caregiving per day was also positively correlated with caregiving burden (p < 0.001). In regression analysis, the gender of the caregiver, the gender of the patient, the stigma level of patient, and the type of treatment were found to be predictors of care burden (p < 0.05, R It was found that two-thirds of the families of patients with epilepsy experienced varying degrees of caregiver burden. In addition, it was determined that caregiver burden was associated with sociodemographic and numerous psychosocial factors of the patient as well as the caregiver. It is important that both the caregiver and the patient being cared for are closely evaluated in interventions to reduce the caregiver burden in patients with epilepsy.

Identifiants

pubmed: 38368790
pii: S1525-5050(24)00066-0
doi: 10.1016/j.yebeh.2024.109685
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109685

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kubra Yeni (K)

Ondokuz Mayis University, Faculty of Health Sciences, Samsun, Turkey. Electronic address: kubra.yeni@omu.edu.tr.

Zeliha Tulek (Z)

Istanbul University-Cerrahpasa, Florence Nightingale Faculty of Nursing, Istanbul, Turkey.

Aysel Cavusoglu (A)

Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey.

Cansu Polat Dunya (CP)

Istanbul University, Faculty of Nursing, Istanbul, Turkey.

Sevda Ozturk Erden (SO)

Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey.

Nur Sena Bostan (NS)

Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey.

Nerses Bebek (N)

Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey; Istanbul University, Center for Research in Epilepsy, Istanbul, Turkey.

Betul Baykan (B)

Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey; Istanbul University, Center for Research in Epilepsy, Istanbul, Turkey.

Classifications MeSH