Experiences of Post-treatment Patients with Systemic Lupus in Indonesia

M. Judha, Elizabeth C. Baua, Josephine D. Lorica
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引用次数: 1

Abstract

Background: Indonesia is currently associated with lupus disease that tends to increase in number, based on data from the Lupus Indonesia Foundation. About 90% of women are with lupus. Most women with reproductive status are inactive, and most want to have basic needs fulfillment disorders. As a result of the changes that arise and because of the long healing process and the disruption basic needs can cause prolonged sadness for the sufferer. Aims: To develop the concept of nursing theory through research from participants suffering from Lupus. Methods: This research is qualitative research to explore the experience of participants looking for the meaning of life. The study consisted of nine participants with purposive samples. Results: In this study data was obtained nine themes, among others: (1) Responses consisted of experience with Lupus disease, (2) Types of support obtained from the environment 3) Discrimination experienced (4) Efforts made to achieve recovery, (5) Ability to recognize signs and symptoms, (6) Changes in basic needs, and Effects of Lupus on activities (7) The effect of using drugs (8) Health services and resources(9) Changes in values, and beliefs. Conclusion: The results of the study contained the response of patients in dealing with Lupus disease related to physical activity, psychological and environmental changes as well as changes in the value, beliefs, and beliefs of Lupus sufferers Recommendation: The results suggest that healthcare workers must perform comprehensive care. Education awareness must be provided also. Holistic nursing care to be conducted. Future researchers must consider increasing the gender variation of participants in order to obtain a variety of themes.
印度尼西亚系统性狼疮患者治疗后的经验
背景:根据印度尼西亚狼疮基金会的数据,印度尼西亚目前与数量趋于增加的狼疮疾病有关。大约90%的女性患有狼疮。大多数有生育能力的女性是不活跃的,大多数有基本需求满足障碍。由于出现的变化,由于长期的治疗过程和中断,基本需求可能导致患者长期悲伤。目的:通过对狼疮患者的研究,发展护理理论的概念。方法:本研究为质性研究,探讨被试寻找生命意义的经验。该研究由9名参与者组成,有目的的样本。结果:本研究收集了九个主题的数据,其中:(1)反馈包括狼疮疾病的经历;(2)从环境中获得的支持类型;(3)经历的歧视;(4)为实现康复所做的努力;(5)识别体征和症状的能力;(6)基本需求的变化;狼疮对活动的影响;(7)使用药物的影响;(8)卫生服务和资源;(9)价值观和信仰的变化。结论:本研究结果包含了狼疮患者在处理狼疮疾病时的反应与身体活动、心理和环境变化以及狼疮患者的价值观、信念和信念的变化有关。建议:结果提示医护人员必须进行综合护理。还必须提供教育意识。进行整体护理。未来的研究者必须考虑增加参与者的性别差异,以获得多样化的主题。
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CiteScore
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