Burden in Caregivers of Adults With Epilepsy at A Tertiary Hospital in North Western Nigeria.
Keywords:
Burden, caregivers, epilepsy, Health related quality of life, determinants.Abstract
Epilepsy has a great impact on the lives of the patients and their caregivers. Caring for patients with
epilepsy is challenging and associated with enormous burden. This cross-sectional study assessed the
determinants of burden among 103 caregivers of persons with epilepsy attending Neurology clinic of
Ahmadu Bello University Teaching Hospital (ABUTH) Zaria Nigeria. Ethical approval and
informed consent were obtained from the Health Research Ethical Committee (HREC) of ABUTH
and the participants respectively. Structured questionnaire, the Zarit Burden Interview (ZBI) and
WHOQoL Bref instruments were interviewer administered to the caregivers and people with
epilepsy (PWE) respectively. Data was analyzed using statistical package for social sciences (SPSS)
version 21 and statistical significance was set at p value < 0.05. The mean and range ages of
participants were 40.3 ±12.8 and 51 (18-67) years respectively. More than half were female 56
(54.4%).The mean ZBI of caregivers and HRQoL of PWE were 45.0 ± 16.7 and 65.2 ± 16.4
respectively. Median duration and caregiving hours daily were 7 days and 8 hours respectively.
Majority of caregivers, 96(93.2%) were either their first degree relatives or spouses. These
caregivers reported little or no burden in 3 (2.9%), mild to moderate burden in 47 (45.6%), moderate
to severe burden in 38 (36.9%) and severe burden in 15 (14.6%). Caregivers with lower monthly
income and those with informal employment had significantly higher mean ZBI of 47.95, p = 0.006
and 49.87, p = 0.008 respectively. There was a significant negative correlation between burden of
caregiving and health related quality of life (HRQoL) of persons with epilepsy (r = - 0.355, p =
0.0001). Equally, HRQoL was found to be a independent determinant of caregiving burden (t= -
3.082, p = 0.003)
Conclusion: Majority of the caregivers were first degree relatives or spouses of the PWE, they had
mild to moderate burden level and HRQoL of PWE was found to be an independent determinant of
caregiving burden among them. Mitigating caregivers' burden will be essential in comprehensive
epilepsy care