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Sociodemographic Factors Influencing Health Care-Seeking Behavior for Pediatric Epilepsy in Southeast Nigeria
Wilson C Igwe1, Esther N Umeadi1, Sylvia T Echendu2
1Department of Paediatrics, Faculty of Medicine, College of Health Sciences, Nnamdi Azikiwe University, Awka, Nigeria.
Insights
Caregivers in Southeast Nigeria often use unorthodox home treatments for pediatric epilepsy. Strengthening primary and secondary care is crucial for timely diagnosis and effective management of childhood epilepsy.
Area of Science:
- Pediatric Neurology
- Public Health
- Global Health
Background:
- Early diagnosis and treatment of epilepsy are vital for reducing associated morbidity and mortality.
- Pediatric epilepsy management requires understanding caregiver health-seeking behaviors.
Purpose of the Study:
- To evaluate health-seeking behaviors for pediatric epilepsy among caregivers in Southeast Nigeria.
- To identify sociodemographic factors influencing these behaviors.
Main Methods:
- A cross-sectional, descriptive, questionnaire-based study was conducted.
- Participants were recruited consecutively.
Main Results:
- Most caregivers were mothers with some education and employment.
- Half of caregivers used unorthodox home treatments; primary and secondary care were common first points of contact.
- Caregivers sought tertiary care due to advice from health workers and families, with 45% presenting within 6 months.
Conclusions:
- Primary and secondary healthcare levels require strengthening through continuous medical education for health workers.
- Effective management of pediatric epilepsy necessitates prompt diagnosis, classification, and appropriate therapy initiation.
Abstract:
Background Early presentation and initiation of appropriate anticonvulsants help in controlling epilepsy and reducing morbidity and mortality associated with epilepsy. Objectives This study aimed to assess the health-seeking behavior for pediatric epilepsy among caregivers in Southeast Nigeria and the associated sociodemographic factors. Methodology This study was a cross-sectional descriptive and questionnaire-based study. The participants were recruited consecutively. Results Majority of the caregivers were mothers, had some formal education, and were employed. While 50% of these caregivers did not seek any home treatment for seizures, the other half offered various types of unorthodox home treatments. Treatments in primary and secondary levels of care were the most common form of first point of care outside the home. The most common reasons for the choice of care outside the home were advice from relations and belief in the efficacy of care offered. About 45% of the caregivers presented to tertiary level of care within 6 months of seizure onset. The major motivators for seeking care in tertiary level of care were health workers and families of children with epilepsy. Conclusion There is a need to strengthen the primary and secondary levels of care through continuous medical education of health workers in these levels of care for effective management of epilepsy. This will help in making prompt and correct diagnosis, classification, and initiation of appropriate therapy in epilepsy.
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