Children’s disability and caregivers’ health-related quality of life in Australia: A nationwide longitudinal study
摘要
Childhood disability is a significant health concern with profound implications for caregivers’ well-being. This study examines the association between children’s cumulative disability profile, encompassing disability status, types, and multiplicity, and caregivers’ health-related quality of life (HRQoL) in a cross-sectional Australian setting. Utilising data from the Longitudinal Study of Australian Children (LSAC), this study examined the association between children’s cumulative disability profile and caregivers’ cross-sectional HRQoL. Caregivers’ HRQoL was assessed using the Assessment of Quality of Life-8 Dimensions (AQoL-8D) instrument. Multivariable linear regression models were estimated to assess these associations, adjusting for sociodemographic and economic covariates. Overall, 25% of children experienced at least one form of disability. A significant lower mean utility score was observed (mean difference = 0.034; 95% confidence interval [CI], [0.018, 0.050]; p < 0.001) among caregivers of children with disabilities compared with caregivers of children without disabilities. After adjusting for covariates, caregivers of children with disabilities had significant lower utility (β = − 0.0230; 95% CI, [− 0.0376, − 0.0084]; p = 0.002), physical super dimension (β = − 0.0339; 95% CI, [− 0.0497, − 0.0182]; p < 0.001), and psychological super dimension (β = − 0.0181; 95% CI, [− 0.0353, − 0.0009]; p = 0.039) scores than caregivers of children without disabilities. Similarly, children experiencing physical, sensory, psychosocial disabilities, or multiple coexisting disabilities were associated with lower HRQoL among their caregivers compared with caregivers of children without disabilities.
Conclusion: Childhood disability is associated with a lower HRQoL for the caregivers. These findings highlight the need for targeted support services, particularly for families caring for children with physical, sensory, psychosocial, and multiple disabilities, and provide estimates of reductions in health state utility scores to inform future cost-utility analyses of caregiver-focused interventions.