Quality of Life in Caregivers of Children with Cerebral Palsy in Rivers State, Nigeria

Abstract

Introduction: Cerebral palsy (CP) is a common neurologic disorder which leads to physical disability in children. Children with CP require more care and attention from their care givers. Hence the quality of life (QoL) of the care givers can be adversely affected. Aim: The aim of this study is to assess the QoL and its determinants among caregivers of children with CP in Port Harcourt, Nigeria. Materials and Methods: Using a convenience sampling method, a hospital based cross-sectional descriptive study was carried out, participants were 96 caregivers of children on follow up for CP. The English Version of the World Health Organization Quality of Life-Bref (WHOQOL-Bref) was used to evaluate the QoL of the participants. A structured questionnaire was used to obtain socio- demographic characteristic of the participants and children with CP, while the patients hospital record was used to obtain the medical history of the patients. The functional disability level of the child was measured by the Gross Motor Function Classification System (GMFCS levels I-V) scale. Multiple regression analysis was carried out to determine the predictors of the care givers QoL on all four domains of the WHOQOL-Bref. Results: The ages of the participants ranged from 23 -58 years with a mean age of 37.67± 8.27 years. Seventy-eight (81.3%) were females, 77(80.0%) had secondary education and above while 56 (58.3%) of the patients had co-morbidity. The care givers had lower level of QoL < 60 points in all domains except for Physical Health Domain which had mean point of 61.3. The GMFCS level of the patients with CP and the marital status of the caregivers significantly determined the different domains of the caregivers QoL (p ≤ 0.05). Age of care giver (p 0.00), presence of comorbidity (0.03) significantly predicted the psychological domain of the QoL of the care givers. In addition, the socioeconomic class significantly predicted the environment and psychological domains of the caregivers QoL (p < 0.05). Conclusion: The quality of life in caregivers of children with cerebral palsy is low. The predictors include GMFCS level of the patient, age of the care giver, marital status, presence of comorbidity and socioeconomic status. The treatment of CP should include strategies to enhance the health and quality of life of caregivers of children with the condition.