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Caregiver burden and its predictors in adult epilepsy patients.
Yeni, Kubra; Tulek, Zeliha; Cavusoglu, Aysel; Dunya, Cansu Polat; Erden, Sevda Ozturk; Bostan, Nur Sena; Bebek, Nerses; Baykan, Betul.
Afiliação
  • Yeni K; Ondokuz Mayis University, Faculty of Health Sciences, Samsun, Turkey. Electronic address: kubra.yeni@omu.edu.tr.
  • Tulek Z; Istanbul University-Cerrahpasa, Florence Nightingale Faculty of Nursing, Istanbul, Turkey.
  • Cavusoglu A; Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey.
  • Dunya CP; Istanbul University, Faculty of Nursing, Istanbul, Turkey.
  • Erden SO; Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey.
  • Bostan NS; Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey.
  • Bebek N; Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey; Istanbul University, Center for Research in Epilepsy, Istanbul, Turkey.
  • Baykan B; Istanbul University, Istanbul Medical Faculty, Department of Neurology, Istanbul, Turkey; Istanbul University, Center for Research in Epilepsy, Istanbul, Turkey.
Epilepsy Behav ; 153: 109685, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38368790
ABSTRACT

OBJECTIVE:

The aim of this study was to evaluate caregiver burden and factors associated with caregiver burden in caregivers of adults with epilepsy. MATERIALS AND

METHODS:

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.

RESULTS:

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, R2 = 0.61).

CONCLUSION:

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.
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Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Qualidade de Vida / Epilepsia Limite: Adult / Humans Idioma: En Revista: Epilepsy Behav Assunto da revista: CIENCIAS DO COMPORTAMENTO / NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Qualidade de Vida / Epilepsia Limite: Adult / Humans Idioma: En Revista: Epilepsy Behav Assunto da revista: CIENCIAS DO COMPORTAMENTO / NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article