Knowledge about Epilepsy among Patients under Community Care

A. Królikowska, K. Filipska, Alina Laskowska, R. Jabłońska, B. Haor, Robert Ślusarz
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Abstract

Introduction. Insufficient knowledge and misconception about epilepsy causes the development of negative attitudes towards epilepsy patients, increases stigmatization and psychosocial problems, and consequently affects their quality of life.Aim. The aim of the study was to assess the state of knowledge of primary care patients on epilepsy.Material and Methods. The study included a group of 149 patients from three primary health care facilities in the city of Bydgoszcz. The study population consisted of 99 women (66%) and 50 men (34%). Adults predominated, the mean age of the respondents was 43.91 years (SD = 13.03). The research used the method of diagnostic survey, the research tool was the original questionnaire. The research was carried out in a correlation model. The non-parametric Spearman rank test was used to determine the significance of the relationship between demographic variables and knowledge about epilepsy. The significance level p < 0.05 was considered statistically significant.Results. The bast majority of respondents (97%) have heard about epilepsy in their lives and believe that they have knowledge about this disease (90%) and know the main cause (76%). Moreover, most of the respondents (96%, 97%) know that during an attack, the patient should be safely positioned and their head protected against injuries. Unfortunately, only 47% of the respondents were ready to help the sick.Conclusions. Most of the respondents have heard about epilepsy in their lifetime and believe they have knowledge of epilepsy. More than half of the respondents witnessed an epileptic seizure. Readiness to provide first aid during an epileptic seizure is declared by nearly half of the respondents. The vast majority of respondents accept people with epilepsy in the work environment as well as in the social environment. There is a relationship between gender, age and education, and some aspects of knowledge about epilepsy and the presented opinion about the disease. (JNNN 2021;10(3):105–111)
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社区护理患者对癫痫的认识
介绍。对癫痫的认识不足和误解导致对癫痫患者产生消极态度,增加对癫痫患者的污名化和社会心理问题,从而影响他们的生活质量。该研究的目的是评估初级保健患者对癫痫的认识状况。材料和方法。这项研究包括来自比得哥什市三家初级卫生保健机构的149名患者。研究人群包括99名女性(66%)和50名男性(34%)。调查对象以成人为主,平均年龄43.91岁(SD = 13.03)。本研究采用诊断调查的方法,研究工具为原始问卷。研究是在一个相关模型中进行的。采用非参数Spearman秩检验来确定人口统计变量与癫痫知识之间关系的显著性。p < 0.05为差异有统计学意义。绝大多数答复者(97%)在生活中听说过癫痫,并认为自己了解这种疾病(90%),知道主要原因(76%)。此外,大多数受访者(96%,97%)知道,在攻击期间,患者应安全放置,头部应保护以免受伤。不幸的是,只有47%的受访者愿意帮助病人。大多数受访者一生中听说过癫痫,并认为自己对癫痫有了解。超过一半的受访者目睹了癫痫发作。近一半的答复者表示准备好在癫痫发作时提供急救。绝大多数答复者在工作环境和社会环境中接受癫痫患者。性别、年龄和教育程度与癫痫知识的某些方面以及对该病的看法之间存在关系。(JNNN 2021; 10 (3): 105 - 111)
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