VITAMIN D LEVELS IN PEDIATRIC EPILEPSY PATIENTS ON THE ANTI-EPILEPTIC DRUGS AT TIKUR ANBESSA SPECIALIZED HOSPITAL, ADDIS ABABA, ETHIOPIA

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Abstract

Background: Epilepsy is a common neurological disorder of childhood repeatedly necessitating prolonged use of anticonvulsants. This study was done to evaluate the status of vitamin D in epileptic children. We targeted to describe the prevalence and risk factors for vitamin D deficiency among children with epilepsy. Methods: A hospital-based descriptive cross-sectional study design with prospective data collection was used among children with epilepsy on anti-epileptic drugs attending the Pediatric Neurology Clinic and their primary caretakers. For this study, a sample of 226 children and adolescents were included in the study and a blood sample for the determination of serum vitamin D was taken. The participants were interviewed, and medical records were thoroughly reviewed. Descriptive statistics and binary logistic regression analysis was done to assess determinants of vitamin D deficiency. . Results: In this study, the prevalence of vitamin D deficiency was found to be 42%. Children on polytherapy (AOR = 4.3 (1.2-16)), 3 or more AEDs (AOR = 0.1 (0.0-0.8)), female sex (AOR = 1.8 (1.7-2.6)), age >15 years (AOR = 2.12 (1.0-1.5)), 4 months of exclusive breastfeeding (AOR = 5.6 (4.9-36)), family diet (AOR = 0.3 (0.1-0.8)) and non-ambulation (AOR = 1.7 (1.8-3.6)) were factors associated with being in the vitamin D deficiency group.Conclusion: According to this study patients who take Anti-Epilepsy drugs are at a higher risk of a poor vitamin D status. Based on this finding, the need for timely and appropriate vitamin D supplementation and periodic follow-up seems to be very evident.

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APA

Miftah, M., Tefera, M., Legas, M., & Moges, A. (2023). VITAMIN D LEVELS IN PEDIATRIC EPILEPSY PATIENTS ON THE ANTI-EPILEPTIC DRUGS AT TIKUR ANBESSA SPECIALIZED HOSPITAL, ADDIS ABABA, ETHIOPIA. Ethiopian Journal of Pediatrics and Child Health, 18(2), 131–147. https://doi.org/10.4314/ejpch.v18i2.4

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