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Living with epilepsy in adolescence-A qualitative study of young people's experiences in Singapore: Peer socialization, autonomy, and self-esteem

机译:与癫痫患者在青春期生活 - 在新加坡的年轻人经历的定性研究:同伴社会化,自主和自尊

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Background Systematic reviews of quantitative research on the effects of childhood epilepsy have established its association with higher levels of psychiatric diagnosis, externalizing and internalizing problems, lower health-related quality of life, social competence, and poorer academic achievements, compared with their peers. However, much less is known about young people's experiences of living with epilepsy and its impact on their development from their own perspectives. Methods Semistructured interviews were conducted with 15 young people aged between 13 and 16 years. Participants were recruited as part of a larger mixed methods study examining individual and family influences on outcomes for young people with epilepsy. These young people attended an epilepsy clinic in KK Women's and Children's Hospital, Singapore. The framework approach to data management and analyses involved both inductive and deductive generation of themes. Results Findings from young people's interviews provided in-depth descriptions of stressful circumstances encountered. Interconnectedness between severity of the impairment and its impact on key developmental tasks, such as independence, autonomy, and social development, were emphasized. Seizures and illness-related demands disrupted their day-to-day functioning and challenged their abilities to meet these tasks. In addition to these impairment effects, young people's experiences of social exclusion were also affected by social and environmental factors, which act as systemic barriers to participation. In turn, this has an effect on their self-esteem. Nevertheless, young people reported positive experiences, such as support from both family and friends, which served as protective factors against the stress of living with a chronic medical condition. Conclusion The demands of epilepsy affect various domains of young people's lives. In order to obtain a holistic understanding of young people's inclusion or exclusion to participation, it is necessary to consider impairment effects, barriers to doing, and barriers to being.
机译:背景技术对儿童癫痫效应的定量研究已经建立了其与对同龄人相比较高的精神诊断,外部化和内化问题,较低的健康相关质量,社会能力和较差的学术成就的关联。然而,关于年轻人患有癫痫的经历以及从他们自己的角度对他们的发展的影响,更少。方法使用13至16岁以下的15名年轻人进行半系统访谈。作为一个更大的混合方法的一部分招募了参与者,研究审查个人和家庭对癫痫的年轻人的结果。这些年轻人参加了新加坡KK女子和儿童医院的癫痫诊所。数据管理和分析的框架方法涉及归纳和演绎的主题。结果年轻人访谈的结果在遇到的压力情况下提供了深入的描述。强调,损害严重程度与其对关键发展任务的影响之间的相互关联性,例如独立,自主权和社会发展。癫痫发作和疾病相关的要求扰乱了他们的日常运作,并挑战他们满足这些任务的能力。除了这些减值效应外,年轻人的社会排斥经验也受到社会和环境因素的影响,这是参与的全身障碍。反过来,这对自己的自尊产生了影响。尽管如此,年轻人报告了积极的经历,例如家庭和朋友的支持,这是针对慢性医学条件的生活压力的保护因素。结论癫痫的需求影响年轻人生活的各个领域。为了获得对年轻人纳入或排斥的全面了解,有必要考虑减值影响,障碍以及存在的障碍。

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