LIVED EXPERIENCES OF PATIENTS WITH HEMODIALYSIS IN CHITWAN

S. Bhattarai, K. Sharma
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Abstract

Background: Chronic Kidney Disease is a serious, long-term illness that is increasing rapidly worldwide. Hemodialysis is the treatment option for the patients with this disease, which affects their daily life in both positive and negative perspective. This study was undertaken to explore the lived experiences of patients with hemodialysis in Chitwan. Methods: Qualitative descriptive phenomenological study was used and a total twelve patients receiving hemodialysis from 11th August 2019 to 9th September 2019 were selected purposively for the study. Data were collected using in-depth interview guidelines and analyzed using Colaizzi’s seven steps of analysis. Results: Five themes and eighteen subthemes were extracted from the study. They were i) perception about chronic kidney disease (irremediable condition, lethal illness and strenuous ailment with living in confinement) ii) pathway to illness identification (symptoms experience, diagnostic journey and treatment options iii) meaning of living with hemodialysis (renewed hope of survival, uncertainty of life, restricted lifestyle and substandard quality of living) iv) impact of hemodialysis on daily life (soothing effect on body, physical discomfort due to side-effects, mental anguish, social detachment, breach in relationship and economic adversity) and v) journey towards adaptation (acceptance of illness and inability of coping). Conclusions: Patients perceive hemodialysis as a hope for survival and tool for relieving their physical tribulations. But they also experience various physical, psychological, social and financial troubles in their daily life. Hence, it is mandatory for health care providers to understand their experiences to provide them need based holistic care. Nepal government also needs to formulate health policy addressing the need of hemodialysis patients.
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奇旺省血液透析患者的生活经历
背景:慢性肾脏疾病是一种严重的长期疾病,在世界范围内迅速增加。血液透析是本病患者的治疗选择,对患者的日常生活既有积极的影响,也有消极的影响。本研究旨在探讨奇旺省血液透析患者的生活经验。方法:采用定性描述现象学研究方法,有意选择2019年8月11日至2019年9月9日接受血液透析治疗的患者12例进行研究。使用深度访谈指南收集数据,并使用Colaizzi的七个分析步骤进行分析。结果:从研究中提取了5个主题和18个副主题。它们是:i)对慢性肾脏疾病的认识(无法治愈的疾病、致命的疾病和与禁闭生活有关的严重疾病)ii)疾病识别途径(症状经历、诊断过程和治疗方案)iii)血液透析生活的意义(生存的新希望、生活的不确定性、生活方式的限制和生活质量的不合格)iv)血液透析对日常生活的影响(对身体的舒缓作用、副作用引起的身体不适、精神痛苦,社会疏远,关系破裂和经济困境)和v)适应之旅(接受疾病和无法应对)。结论:患者将血液透析视为生存的希望和减轻身体痛苦的工具。但他们在日常生活中也会遇到各种各样的身体、心理、社会和经济问题。因此,医疗保健提供者必须了解他们的经历,为他们提供基于需求的整体护理。尼泊尔政府还需要制定卫生政策,解决血液透析患者的需要。
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