Gupta Arunima, Aggarwal Anju, Sharma Sangeeta, Aaradhana Aaradhana
Pediatrics, University College of Medical Sciences and Guru Tegh Bahadur Hospital, Delhi, IND.
Neuropsychopharmacology, Institute of Human Behaviour and Allied Sciences, Delhi, IND.
Cureus. 2025 Jun 18;17(6):e86273. doi: 10.7759/cureus.86273. eCollection 2025 Jun.
Introduction Breakthrough seizures in children diagnosed with epilepsy pose a significant clinical challenge. Though valproate is effective in managing seizures, a subset of patients can still experience breakthrough seizures. It can cause increased morbidity, reduce the quality of life, and increase anxiety among parents. There is insufficient data in the Indian population regarding the cause of breakthrough seizures and their association with serum valproate levels; hence, we carried out this study. Objective Primary Objective To study the clinical profile and drug levels in children presenting with breakthrough seizures while receiving valproate therapy. Secondary Objective To find out the association of the clinical, demographic, and etiological profile of breakthrough seizures with valproate levels. Methods A group of 100 children, 2-12 years old, receiving valproate therapy and presenting to the hospital within 24 hours of a breakthrough seizure were studied. Clinical and demographic profiles were recorded. Valproate levels were estimated using recombinant DNA technology using an autoanalyzer (reference level 50-100 mcg/ml). Phenytoin levels were estimated in 10 children receiving dual therapy (reference level 10-20 mcg/mL). Results The mean age was 81.6±31.9 months (59 M, 41 F). The mean dose of valproate was 24.8±8.4 mg. Syrup formulation was used in 73 and tablets in 27. Non-compliance was observed in 19, and fever was identified as a possible precipitating factor in 18. Compliance was not affected by age, sex, socioeconomic status, education of parents, or type of seizure (p > 0.05). Valproate levels were below the reference range in 44, within the reference range in 47, and above the reference range in 9. There was no statistically significant association between valproate levels (therapeutic or subtherapeutic) and age, sex, socioeconomic status, parental education, seizure type, or the presence of precipitating factors (p > 0.05). Similarly, mean valproate levels were also not affected by these factors. The levels did not vary with drug formulations. Conclusion Breakthrough seizures in children on valproate therapy were not related to valproate levels. Valproate levels were not affected by clinical or demographic profile, drug formulation, change in formulation, compliance, etc.
引言
癫痫患儿出现的突破性癫痫发作是一项重大的临床挑战。尽管丙戊酸盐在控制癫痫发作方面有效,但仍有一部分患者会经历突破性癫痫发作。这可能导致发病率增加、生活质量下降以及家长焦虑情绪上升。在印度人群中,关于突破性癫痫发作的原因及其与血清丙戊酸盐水平的关联的数据不足;因此,我们开展了这项研究。
目的
主要目的
研究接受丙戊酸盐治疗时出现突破性癫痫发作的儿童的临床特征和药物水平。
次要目的
找出突破性癫痫发作的临床、人口统计学和病因学特征与丙戊酸盐水平之间的关联。
方法
对一组100名年龄在2至12岁、正在接受丙戊酸盐治疗且在突破性癫痫发作后24小时内入院的儿童进行研究。记录临床和人口统计学特征。使用自动分析仪通过重组DNA技术测定丙戊酸盐水平(参考水平为50 - 100 mcg/ml)。对10名接受联合治疗的儿童测定苯妥英水平(参考水平为10 - 20 mcg/mL)。
结果
平均年龄为81.6±31.9个月(59名男性,41名女性)。丙戊酸盐的平均剂量为24.8±8.4毫克。73名使用糖浆制剂,27名使用片剂。19名存在不依从情况,18名发现发热是可能的诱发因素。依从性不受年龄、性别、社会经济地位、家长教育程度或癫痫发作类型的影响(p > 0.05)。44名儿童的丙戊酸盐水平低于参考范围,47名在参考范围内,9名高于参考范围。丙戊酸盐水平(治疗性或亚治疗性)与年龄、性别、社会经济地位、家长教育程度、癫痫发作类型或诱发因素的存在之间无统计学显著关联(p > 0.05)。同样,平均丙戊酸盐水平也不受这些因素影响。水平不因药物制剂而变化。
结论
接受丙戊酸盐治疗的儿童出现的突破性癫痫发作与丙戊酸盐水平无关。丙戊酸盐水平不受临床或人口统计学特征、药物制剂、制剂变化、依从性等影响。