育龄期癫痫妇女的生活质量和耻辱。

Journal of epilepsy research Pub Date : 2021-06-30 eCollection Date: 2021-06-01 DOI:10.14581/jer.21009
Pallerla Srikanth, Mysore Narasimha Vranda, Priya Treesa Thomas, Kenchaiah Raghvendra
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引用次数: 3

摘要

背景与目的:本研究的目的是了解育龄妇女癫痫患者生活质量与病耻感之间的关系。方法:横断面描述性研究进行了评估数据从49名妇女癫痫从三级保健医院在印度。用癫痫生活质量-31问卷评价生活质量,用癫痫病耻感量表评价病耻感。数据还包括社会人口统计学和临床特征。结果:参与者平均年龄24.67±3.72岁。生活质量总分(r=-0.485**)和癫痫焦虑域(r=-0.427**)与病耻感总分(p10年)呈显著负相关,服用左乙拉西坦、抗癫痫药物(AED)是育龄期癫痫女性生活质量低下的显著影响因素。社会经济地位较低和服用两种以上抗癫痫药也与癫痫妇女的生活质量较低有关,这一趋势越来越明显。结论:本研究评估了生活质量与癫痫病耻感量表之间的关系,并论证了病耻感和生活质量对育龄妇女癫痫患者社会人口学和临床变量的影响。为了提高女性癫痫患者的生活质量和降低耻辱感,多学科卫生保健专业人员可以根据目前的研究结果考虑一些可修改的参数。
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Quality of Life and Stigma among Women with Epilepsy during Their Reproductive Years.

Background and purpose: The purpose of this study was to understand the relationship between quality of life and stigma among reproductive age group women with epilepsy.

Methods: A cross-sectional descriptive study was conducted to assess the data from the 49 women with epilepsy from a tertiary care hospital in India. Quality of life was evaluated with the quality of life in epilepsy-31 questionnaire and stigma was evaluated with the stigma scale of epilepsy. Data also included socio-demographic and clinical characteristics.

Results: The mean age of the participants was 24.67±3.72 years. Quality of life total score (r=-0.485**) and seizure worry domain (r=-0.427**) were significantly negatively correlated with stigma total score at p<0.01 level. Being uneducated, married, unemployed, having children, having generalized tonic-clonic seizures, duration of illness (>10 years), and consuming levetiracetam, anti-epileptic drug (AED), were the significant contributing factors for low quality of life among women with epilepsy during the reproductive age group. Belonging to lower socio-economic status and taking more than two AEDs were also associated with lower quality of life among women with epilepsy, which are trending towards significance.

Conclusions: The study assessed the relationship between the quality of life and the Stigma scale of epilepsy and demonstrated the impact of stigma and quality of life on socio-demographic and clinical variables of women with epilepsy under the reproductive age group. To enhance the quality of life and reduce the stigma levels among women with epilepsy, some of the modifiable parameters can be considered by the multidisciplinary health care professionals from the findings of the current research.

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