癫痫儿童的生活质量:东印度社会人口因素的影响和父母对癫痫行动计划的认识

Aishwarya Senapaty, Preeti Srivastava, Shikha Swaroop, Roshan Mohanty, Adyasha Mishra
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引用次数: 0

摘要

背景: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产生负面影响。虽然大多数医疗方法侧重于癫痫发作控制,但对印度东部癫痫儿童(CWE)的生活质量关注有限。本研究旨在评估CWE的生活质量,并检查社会人口因素、癫痫发作特征和父母对癫痫发作行动计划(SAP)的认识的影响。方法: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5-15岁之间的儿童参与了这项研究,他们都被诊断患有癫痫,并且服用了至少6个月的抗癫痫药物。已获得有关医院机构伦理委员会的批准。参与者接受了结构化的预先测试时间表的采访。采用儿童癫痫生活质量(QOLCE-55)问卷评估受试者的生活质量。根据家长对癫痫发作基本管理措施的了解来评估他们对SAP的认识。采用Kruskal Wallis检验确定与生活质量相关的因素。结果:研究人群平均年龄为9.37±3.57岁,男性占56.45%。在认知、情感、社交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。生活质量随着年龄的增长而稳步下降,情绪和社会领域对年龄较大的儿童的影响更大。母亲文盲率低、社会经济地位低、早发性癫痫与较差的生活质量显著相关(p结论:年龄小、晚发性癫痫、社会经济地位高、母亲受教育程度高的CWE生活质量较好。干预措施可提高家长对SAP的认识,从而改善CWE的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of life in children with epilepsy: Effect of socio-demographic factors and Parental awareness of seizure action plan in Eastern India.

Background: 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).

Methodology: 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.

Results: 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.

Conclusion: 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.

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