护理干预方案对癫痫患儿照顾者负担感及应对的影响

M. El-malky, Magda M Mohsen, H. Amer
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引用次数: 8

摘要

癫痫是最常见的儿科神经系统疾病之一,提供护理会产生负面的心理、情绪和身体后果。护理干预是管理这些患者及其家属的关键因素,以减少负担感并加强照顾者之间的应对。目的:评价护理干预对癫痫患儿照料者负担感及应对的影响。设计:采用准实验设计(一组前测后测设计)达到研究目的。环境:这项研究是在Menoufia省Shebin El-Kom区医疗保险机构的门诊诊所进行的。对象:选取80名护理人员作为方便样本。工具:1 -研究人员制定了一份构建的访谈问卷,以评估社会人口统计数据、病史和家庭照顾者对癫痫儿童的知识、做法和意见。修改了Zarit负担访谈问卷,以评估负担感。家长应对健康量表评估照顾者的应对模式。结果:本研究的主要发现是,在护理人员的知识和实践方面存在统计学意义差异。护理干预后患者负担感减轻,应对方式改善。照料者的知识、实践与负担感呈负相关,照料者的KPO与应对呈正相关。研究对象以母亲居多(76%),平均年龄(37.21±5.22),中等文化程度过半,无业人员居多(75%)。结论:护理干预对改善照顾者的知识、做法和意见,提高癫痫患儿照顾者的负担感,提高应对能力有较好的效果。建议:在诊断前后需要额外的护理策略,对照顾者及其子女进行纵向评估和随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effectiveness of the nursing intervention program on feeling of burden and coping among caregivers of children with epilepsy
Epilepsy is one of the most common pediatric neurological disorders, which have negative psychological, emotional, and physical consequences of providing care. Nursing intervention is a key element of managing these patients and their families in order to reduce feelings of burden and enhancing coping among caregivers. Aim: To evaluate the effectiveness of nursing intervention on a feeling of burden and coping among caregivers of children with epilepsy. Design: A quasi-experimental design (one group pretest-posttest design) was used to achieve the aim of the study. Setting: The study was conducted at the outpatient clinic at the health insurance institute in Shebin El-Kom district, Menoufia Governorate. Subject: A convenience sample of 80 caregivers was used. Tool: I- A constructed interviewing questionnaire was developed by researchers to assess socio demographic data, medical history and family caregiver’s knowledge, practices and opinions regarding child with epilepsy. II- Modified version of the Zarit burden interviewing questionnaire to assess feeling of burden. III- Coping Health Inventory for Parents to assess coping patterns of care giver’s. The Results: the main finding of this study illustrated that, there were statistical significance differences regarding caregivers’ knowledge and practices. Reduction of the feeling of burden and improvement of coping patterns after nursing intervention than before. There was a negative correlation between caregiver’s knowledge, practice and feeling of burden and there was a positive correlation between (KPO) and coping among caregivers. The majority of the studied caregivers were mothers (76%) with mean age score37.21±5.22, more than half were secondary education, and the majority (75%) was not working. Conclusion: Nursing intervention was effective in improving caregiver’s knowledge, practices and opinions, feeling of burden and raising coping abilities for caregivers of children with epilepsy. Recommendation: additional nursing strategies are needed around the time of the diagnosis with longitudinal assessment and follow up for both caregivers and their children.
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