Bulduk Mehmet, Can Veysel
Van Yuzuncu Yil University, Faculty of Health Sciences, Department of Pediatric Nursing, 65000, Van, Turkey.
Heliyon. 2024 Aug 3;10(15):e35525. doi: 10.1016/j.heliyon.2024.e35525. eCollection 2024 Aug 15.
The aim of this study was to examine the factors that affect stigma perceptions and health fatalism of parents of children with epilepsy in eastern Turkey, the relationship between these and the impact of these on their social lives.
This descriptive and cross-sectional study was conducted between August 2022 and January 2023 with the parents of children under the age of 18 who had been diagnosed with epilepsy for at least 1 year and who were followed up in the only hospital with a paediatric neurology outpatient clinic in Van province of Turkey. No sample selection was made in the study. Healthy parents (n = 123) who presented to the outpatient clinic within the specified time period and who agreed to participate in the study after being explained the purpose of the study participated in the study.
In this study, parental age was found to have a statistically weak positive correlation with Health Fatalism Scale (HFS) (r = 0.251; p = 0.005). A weak positive correlation was also found between the years patients had epilepsy and Parent Stigma Scale (PSS) (r = 0.275; p = 0.002). In addition, a statistically positive and weak relationship was found between Parent Stigma Scale scores and Health Fatalism Scale scores (r = 0.212; p = 0.018). This study found significant relationships between stigma perception and health fatalism in parents of epileptic children. Stigma perception increased with disease duration and lower parental education levels.
While providing an important basis for understanding the difficulties experienced by parents and developing support mechanisms, the present study can contribute to more informed support for parents of patients with epilepsy in the community. Nurses can contribute to ending stigma and discrimination by identifying patients' and parents' perceptions of epilepsy, focusing on addressing gaps in knowledge and raising awareness in the community.
本研究旨在探讨影响土耳其东部癫痫患儿家长耻辱感认知和健康宿命论的因素、这些因素之间的关系及其对患儿家长社交生活的影响。
本描述性横断面研究于2022年8月至2023年1月期间开展,研究对象为土耳其凡省唯一一家设有儿科神经科门诊的医院中,年龄未满18岁、已被诊断患有癫痫且至少随访1年的患儿的家长。本研究未进行样本选择。在规定时间段内到门诊就诊、在了解研究目的后同意参与研究的健康家长(n = 123)参与了本研究。
在本研究中,发现家长年龄与健康宿命论量表(HFS)存在统计学意义上的弱正相关(r = 0.251;p = 0.005)。还发现患者患癫痫的年限与家长耻辱感量表(PSS)之间存在弱正相关(r = 0.275;p = 0.002)。此外,家长耻辱感量表得分与健康宿命论量表得分之间存在统计学意义上的正相关且较弱(r = 0.212;p = 0.018)。本研究发现癫痫患儿家长的耻辱感认知与健康宿命论之间存在显著关系。耻辱感认知随疾病持续时间的延长和家长教育水平的降低而增加。
本研究在为理解家长所经历的困难及制定支持机制提供重要依据的同时,有助于为社区中癫痫患者的家长提供更明智的支持。护士可以通过识别患者及其家长对癫痫的认知、关注知识差距并提高社区意识,为消除耻辱感和歧视做出贡献。