Literature DB >> 29455081

Quality of life and level of burden in primary caregivers of patients with epilepsy: Effect of neuropsychiatric comorbidity.

Ana Maria Gutierrez-Angel1, Iris Enriqueta Martinez-Juarez2, Laura Elena Hernandez-Vanegas3, Daniel Crail-Melendez4.   

Abstract

BACKGROUND: Few studies are focused on the quality of life (QOL) of primary caregivers and the effects of the clinical variables of epilepsy and patient psychiatric comorbidity on primary caregivers.
PURPOSE: Our main objective was to describe QOL and level of burden (LB) in caregivers of people with epilepsy (PWE) at a tertiary-care hospital in Mexico City. A secondary purpose was to determine if LB and QOL were different between caregivers of patients with neuropsychiatric comorbidity and caregivers of patients without neuropsychiatric comorbidity.
METHODS: One hundred and fifty-one caregivers of PWE were assessed with the short version of the World Health Organization Quality of Life (WHOQOL) scale (WHOQOL-BREF) and the Zarit Burden Interview. Patients' clinical and demographic data, along with their psychiatric histories, were collected.
RESULTS: One hundred and twelve patients had psychiatric comorbidity. The mean LB score of the caregivers was 26.25±16.28. The mean scores for the WHOQOL-BREF domains were as follows: physical health, 47.8±10.7; psychological health, 55.4±11.5; social relationships, 47.23±18.6; and environment, 48.7±11.6. The caregivers of patients with psychiatric comorbidity had lower scores in the domains of psychological health (p=0.034) and social relationships (p=0.029) compared with caregivers of PWE without comorbidity. On adjusted multivariate analysis, aggressiveness (p=0.008), age at onset of epilepsy (p=0.02), and years with epilepsy (p=0.01) were associated with higher caregiver LB scores; higher caregiver years of education were associated with better psychological health (p=0.002) and more years with epilepsy (p=0.03) with lower QOL scores.
CONCLUSION: Aggressive behavior was the psychiatric comorbidity most clearly associated with lower QOL and higher LB. Longer duration of epilepsy was related to higher burden and lower QOL. More years of education of the caregiver were associated with better QOL. We found no significant correlation between seizure control and QOL or LB.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Caregiver; Epilepsy; Level of burden; Neuropsychiatric comorbidity; Quality of life

Mesh:

Year:  2018        PMID: 29455081     DOI: 10.1016/j.yebeh.2018.01.034

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  4 in total

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Authors:  Marcus-Alexander Wörns; Christian Labenz; Michael Nagel; Vanessa Weidner; Sina Schulz; Jens U Marquardt; Peter R Galle; Jörn M Schattenberg; Marc Nguyen-Tat
Journal:  Health Qual Life Outcomes       Date:  2022-02-08       Impact factor: 3.186

Review 2.  A Comprehensive Literature Search of Digital Health Technology Use in Neurological Conditions: Review of Digital Tools to Promote Self-management and Support.

Authors:  John Henry Spreadbury; Alex Young; Christopher Myles Kipps
Journal:  J Med Internet Res       Date:  2022-07-28       Impact factor: 7.076

3.  Cognitive deficiency, parental relationship, and coping strategies are related with anxiety and depression among parents of children with epilepsy.

Authors:  Zhengjia Ren; Chunsong Yang; Dan Yu
Journal:  Chronic Dis Transl Med       Date:  2022-06-06

4.  Quality of life among caregivers of children with epilepsy: A cross-sectional study at Eastern Nepal.

Authors:  Rita Pokharel; Prakash Poudel; Sami Lama
Journal:  Epilepsia Open       Date:  2021-01-08
  4 in total

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