The experience of transitioning into life-sustaining treatment: A systematic literature review

IF 1.5 4区 医学 Q3 NURSING
Annica Sedin RN, BSc, MSc, Johan Isaksson RN, BSc, MSc, Harshida Patel RN, APN, PhD
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引用次数: 1

Abstract

Background

Being informed about treatment options for kidney failure and included in the related decision-making process can facilitate a smooth transition. Among patients with kidney failure the initiation of kidney failure replacement therapy is considered a traumatic event, causing physical and emotional distress and disrupting several aspects of one's social life. In order to ease the transition, health care personnel must ensure that the patient understands the parameters of each treatment option. It is imperative to increase the knowledge of patients' lived experiences around initiating kidney failure replacement therapy.

Objectives

To explore how adults with kidney failure describe the lived experience of transitioning into life-sustaining kidney failure replacement therapy.

Design

A systematic review of qualitative literature.

Methods

Primary qualitative studies published in English between 2010 and 2020 from CINAHL, PubMed and PsycINFO were included. Content analysis summarised the patients' lived experience.

Findings

From 959 records screened, 17 studies were eligible for inclusion. A total of 5 themes that described the patients' lived experience were identified: an existential transformative feeling, a change in quality of life, limitation, safety, and ambivalence.

Conclusion

Being prepared and receiving emotional, physical, and social support can ease the transition for the patient. Among all available treatment options, dialysis and transplantation, the transition into kidney failure replacement therapy is experienced as a life-changing event. With this knowledge, it is imperative to clarify the importance of providing a patient with adequate support during the transition.

Abstract Image

过渡到维持生命治疗的经验:系统的文献综述
背景了解肾衰竭的治疗方案并参与相关决策过程可以促进平稳过渡。在肾衰竭患者中,开始肾衰竭替代治疗被认为是一种创伤事件,会导致身体和情绪困扰,并扰乱社会生活的几个方面。为了简化过渡,卫生保健人员必须确保患者了解每种治疗方案的参数。必须增加对患者开始肾衰竭替代治疗的生活经历的了解。目的探讨成年肾衰竭患者如何描述过渡到维持生命的肾衰竭替代治疗的生活经历。设计对定性文献的系统综述。方法纳入CINAHL、PubMed和PsycINFO在2010年至2020年间以英文发表的初步定性研究。内容分析总结了患者的生活经历。结果从959份筛查记录中,有17项研究符合入选条件。共确定了5个描述患者生活经历的主题:生存的变革感、生活质量的变化、局限性、安全性和矛盾心理。结论做好准备并接受情感、身体和社会支持可以缓解患者的过渡。在所有可用的治疗选择中,透析和移植,向肾衰竭替代治疗的过渡是一个改变生活的事件。有了这些知识,就必须澄清在过渡期间为患者提供足够支持的重要性。
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来源期刊
Journal of renal care
Journal of renal care Nursing-Advanced and Specialized Nursing
CiteScore
3.50
自引率
5.30%
发文量
36
期刊介绍: The Journal of Renal Care (JORC), formally EDTNA/ERCA Journal, is the official publication of the European Dialysis and Transplant Nursing Association/European Renal Care Association (EDTNA/ERCA). The Journal of Renal Care is an international peer-reviewed journal for the multi-professional health care team caring for people with kidney disease and those who research this specialised area of health care. Kidney disease is a chronic illness with four basic treatments: haemodialysis, peritoneal dialysis conservative management and transplantation, which includes emptive transplantation, living donor & cadavaric transplantation. The continuous world-wide increase of people with chronic kidney disease (CKD) means that research and shared knowledge into the causes and treatment is vital to delay the progression of CKD and to improve treatments and the care given. The Journal of Renal Care is an important journal for all health-care professionals working in this and associated conditions, such as diabetes and cardio-vascular disease amongst others. It covers the trajectory of the disease from the first diagnosis to palliative care and includes acute renal injury. The Journal of Renal Care accepts that kidney disease affects not only the patients but also their families and significant others and provides a forum for both the psycho-social and physiological aspects of the disease.
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