Senapaty Aishwarya, Srivastava Preeti, Swaroop Shikha, Mohanty Roshan, Mishra Adyasha
Department of Paediatrics, AIIMS, Bhubaneshwar, India.
Tata Main Hospital, Jamshedpur, India.
Niger Med J. 2025 Apr 3;66(1):225-234. doi: 10.71480/nmj.v66i1.690. eCollection 2025 Jan-Feb.
Epilepsy is a chronic neurological disorder that disrupts daily life and negatively impacts quality of life (QOL). While most medical approaches focus on seizure control, there is limited attention to the QOL of children with epilepsy (CWE) in eastern India. This study aimed to assess QOL among CWE and examine the influence of sociodemographic factors, seizure characteristics, and parental awareness of a seizure action plan (SAP).
This cross-sectional study was conducted in the Department of Paediatrics at a tertiary care teaching hospital in eastern India from December 2020 to May 2022. Eighty children aged 5-15 years, all diagnosed with epilepsy and on antiepileptic medication for at least six months, participated. Approval was obtained from the Institutional Ethics Committee of the hospital concerned. The participants were interviewed using a structured pre-tested schedule. The QOL of the participants was evaluated using the Quality of Life in Childhood Epilepsy (QOLCE-55) questionnaire. Parental awareness of SAP was assessed based on their knowledge of essential seizure management actions. Kruskal Wallis test was used to identify factors associated with QOL.
The mean age in the study population was 9.37 ± 3.57 years, with 56.45% males. The mean QOL scores in cognitive, emotional, social, and physical domains were 59.41, 55.11, 56.40, and 65.11, respectively. QOL steadily declined with age, with emotional and social domains more impacted on older children. Maternal illiteracy, low socioeconomic status, and earlier onset of epilepsy were significantly associated with poorer QOL (p<0.001). Only 21.25% of parents had complete awareness of SAP, and the children of these parents had relatively better QOL scores.
QOL was better in CWE who were younger, had late-onset epilepsy, belonged to the upper socioeconomic class, and whose mothers were educated. Interventions enhancing parental awareness about SAP may lead to improvement in the QOL of CWE.
癫痫是一种慢性神经系统疾病,会扰乱日常生活并对生活质量(QOL)产生负面影响。虽然大多数医学方法侧重于控制癫痫发作,但印度东部对癫痫患儿(CWE)的生活质量关注有限。本研究旨在评估CWE的生活质量,并探讨社会人口学因素、癫痫发作特征以及父母对癫痫发作行动计划(SAP)的认知的影响。
本横断面研究于2020年12月至2022年5月在印度东部一家三级护理教学医院的儿科进行。80名年龄在5至15岁之间、均被诊断为癫痫且服用抗癫痫药物至少六个月的儿童参与了研究。获得了相关医院机构伦理委员会的批准。使用经过预测试的结构化问卷对参与者进行访谈。使用儿童癫痫生活质量(QOLCE - 55)问卷评估参与者的生活质量。根据父母对癫痫发作基本管理措施的了解情况评估其对SAP的认知。采用Kruskal Wallis检验来确定与生活质量相关的因素。
研究人群的平均年龄为9.37 ± 3.57岁,男性占56.45%。认知、情感、社会和身体领域的平均生活质量得分分别为59.41、55.11、56.40和65.11。生活质量随年龄稳步下降,情感和社会领域对年龄较大的儿童影响更大。母亲文盲、社会经济地位低以及癫痫发作早与较差的生活质量显著相关(p<0.001)。只有21.25%的父母对SAP有全面的认知,这些父母的孩子生活质量得分相对较高。
年龄较小、癫痫发作晚、属于社会经济上层阶级且母亲受过教育的CWE生活质量较好。提高父母对SAP的认知的干预措施可能会改善CWE的生活质量。