Objective: The aim of this study was to evaluate chilhood absence epilepsy in the Middle Black Sea Region.
Methods: 14 pediatric patients who treated absence epilepsy between May 2018 and May 2020, and had adequate follow-up were included in the study. Medical record datas were reviewed age, gender, etiology, features of family, treatment, and results.
Results: 10 (71%) of the patients were female and 4 (29%) were male. Their average age was 9 years (6-15). Valproate was started in all patients at the time of diagnosis. In the controls 15 days later, no seizure was detected by the family of 5 patients. 5 patients stated that their seizures decreased but continued. In 4 patients, the family did not notice a decrease in seizure frequency. Ethosuximide was added to 9 patients who said that their seizures were still continuing. In the controls 15 days later, 6 patients were found to be cured. However, it was stated that 3 patients had intermittent seizures although they decreased. Lamutrigine was added as the third drug after checking the valproate drug level to these 3 patients, whose treatment was still unsuccessful. 3 patients still have electroencephalography disorder and seizures recognized by the family. With our treatment management, 11 of 14 patients were found to be seizure free.
Conclusion: We achieved high success with valproate and ethosuximide in the treatment management of pediatric absence epilepsy.
Primary Language | English |
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Subjects | Health Care Administration |
Journal Section | Research articles |
Authors | |
Publication Date | April 30, 2021 |
Published in Issue | Year 2021 Volume: 7 Issue: 1 |