What factors contribute to the quality of life among caregivers of children with epilepsy worldwide?
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Caregivers' quality of life (QoL) in epilepsy care is influenced by various factors. Knowledge levels, illness perceptions, and caregiver activation play crucial roles. Adherence to medication regimens significantly impacts caregivers' QoL, with forgetfulness or inconsistency leading to decreased QoL. Additionally, demographic factors like gender, religion, education level, income, and seizure type can negatively affect caregivers' QoL. Providing emotional and practical support through epilepsy support groups and interventions that help caregivers reframe negative experiences and engage in enjoyable activities can enhance their QoL. Ensuring seizure control, improving compliance, and reducing stigma through education and empowerment are vital for optimizing caregivers' QoL worldwide.
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| Papers (5) | Insight |
|---|---|
| Factors influencing the quality of life among caregivers of children with epilepsy include child's gender, caregiver's gender, education level, income, rural residence, seizure type, frequency, and medication complexity. | |
| Adherence to medication plays a crucial role in the quality of life among caregivers of children with epilepsy worldwide, as shown in the study conducted in the Aseer region. | |
| Factors contributing to caregivers' quality of life for children with epilepsy include stigma, seizure control, education, compliance, rescue treatment availability, and minimizing restrictions to enable regular activities. | |
| Factors contributing to caregivers' quality of life for children with developmental and epileptic encephalopathy include cognitive and emotional illness perceptions, while health literacy and caregiver activation show no significant correlation. | |
| Caregivers' quality of life is influenced by their knowledge of epilepsy. Factors like marital status, education level, religion, and income also impact caregivers' quality of life. |
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