The Heavy Toll of Lifeline: An Analysis of the Multidimensional Experience and Interaction Mechanisms of Establishing Arteriovenous Fistula in Patients Receiving Haemodialysis

IF 2 4区 医学 Q3 NURSING
Longfei Wang, Lijuan Zhao, Chen Zhang, Wenwen Lu, Yin Zheng, Bihong Huang
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引用次数: 0

Abstract

Background

The arteriovenous fistula, while serving as a vital ‘lifeline’ for haemodialysis, poses significant clinical challenges; it can extend beyond local dysfunction to adversely affect patients’ physiological, psychological and social well-being.

Objective

This study explored the multidimensional experiences of patients receiving haemodialysis regarding the creation and maintenance of an arteriovenous fistula, based on the biopsychosocial model.

Design

This study employed the biopsychosocial model as a theoretical framework and an interpretive phenomenological qualitative analysis methodology.

Participants

Participants (N = 23) were recruited from two haemodialysis centres and a nephrology department.

Approach

Data were collected through semi-structured interviews and analysed using interpretive phenomenological analysis. NVivo 11 was used to manage the qualitative data.

Findings

The arteriovenous fistula experience was interconnected across biological, psychological and social domains. Physically, patients reported frequent somatic symptoms and arteriovenous fistula-related complications. Psychologically, they underwent a process of cognitive restructuring while contending with persistent negative emotions. Socially, the arteriovenous fistula impaired daily functioning and challenged trust in healthcare, yet also highlighted the crucial role of social support.

Conclusion

For patients receiving haemodialysis, the arteriovenous fistula represents both a lifeline and a source of ongoing distress. A multidimensional understanding of this experience is essential for guiding more patient-centred, targeted and humane clinical management.

生命的沉重代价:血液透析患者建立动静脉瘘的多维体验及其相互作用机制分析。
背景:动静脉瘘作为血液透析的重要“生命线”,提出了重大的临床挑战;它可以超越局部功能障碍,对患者的生理、心理和社会福祉产生不利影响。目的:本研究基于生物心理社会模型,探讨血液透析患者在动静脉瘘形成和维持方面的多维体验。设计:本研究采用生物心理社会模型作为理论框架和解释性现象学定性分析方法。参与者:参与者(N = 23)从两个血液透析中心和一个肾脏病科招募。方法:通过半结构化访谈收集数据,并使用解释现象学分析进行分析。采用NVivo 11对定性数据进行管理。研究结果:动静脉瘘的经历是相互关联的跨生物,心理和社会领域。在身体方面,患者经常报告躯体症状和动静脉瘘相关并发症。在心理上,他们经历了一个认知重构的过程,同时与持续的负面情绪作斗争。在社会方面,动静脉瘘损害了日常功能,挑战了对医疗保健的信任,但也突出了社会支持的关键作用。结论:对于接受血液透析的患者,动静脉瘘既是生命线,也是持续窘迫的来源。对这一经验的多维理解对于指导更加以患者为中心、有针对性和人性化的临床管理至关重要。
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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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