Patients' perspectives on key aspects influencing needling for haemodialysis: A qualitative study

IF 1.5 4区 医学 Q3 NURSING
Currie Moore PhD, Helen Ellis-Caird ClinPsyD, Catherine Fielding PhD, Faizan Awan, Tarsem Paul, Rebecca Flanagan BSc, Shivani Sharma PhD, Kieran McCafferty MDRes, Sabine N. van der Veer PhD, Ken Farrington PhD, David Wellsted PhD
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引用次数: 0

Abstract

Background

For many patients, cannulation (‘needling’) is essential for haemodialysis. It is associated with anxiety and fear and contributes to the overall burden of treatment. Limited research exists on patient experience of needling and how this might vary by individual and clinical characteristics.

Objectives

To explore and identify key aspects of needling impacting patients' experiences.

Design

Qualitative, multicentre, cross-sectional, co-produced.

Participants

Adults on haemodialysis with working fistulae or grafts (n = 41).

Approach

We used interviews to explore patients' experiences of needling and key aspects contributing to this. Interviews were conducted in two sets: unstructured (n = 24, broadly investigated needling experience) and semistructured (n = 17, refined themes and assessed cultural relevance). Thematic analysis was used to identify themes driving experience and examine variation. A Patient Steering Group comprising people with lived experience of needling was integral to the study.

Findings

A thematic framework capturing patients' view of needling was developed. It defined a core theme (The Nature of needling) and five foundational aspects of needling (Health of the fistula or graft, Steps in needling, The needler, The patient, Organisational context). We identified two further themes important to overall experience, Learning from needling experience and Reciprocity (the two-way interaction between patient and needler). Both interrelated across themes, highlighting the complexity of needling and junctures where patient experience can be influenced.

Conclusions

Needling is shaped by multiple psychological and relational influences. These findings provide healthcare professionals with a basis to improve patient experience as part of a broader drive to enhance quality in healthcare delivery.

Abstract Image

患者对影响血液透析针刺的关键因素的看法:定性研究。
背景:对许多患者来说,插管("针刺")是血液透析的必要步骤。它与焦虑和恐惧有关,加重了治疗的总体负担。关于患者对针刺的体验以及这种体验如何因个体和临床特征而异的研究十分有限:探索并确定影响患者体验的针刺疗法的主要方面:设计:定性、多中心、横断面、共同制作:方法:我们采用访谈的方式探讨患者的针刺经历:方法:我们通过访谈来了解患者的针刺经历以及导致这种经历的关键因素。访谈分两组进行:无结构访谈(24 人,广泛调查针刺经验)和半结构访谈(17 人,细化主题并评估文化相关性)。采用主题分析法确定体验主题并研究差异。由具有针刺经验者组成的患者指导小组是本研究不可或缺的一部分:研究结果:研究制定了一个主题框架,反映了患者对针刺疗法的看法。该框架确定了一个核心主题(针刺的性质)和针刺的五个基本方面(瘘管或移植物的健康、针刺步骤、针刺者、患者、组织环境)。我们还确定了另外两个对总体经验非常重要的主题,即从针刺经验中学习和互惠(患者与针刺师之间的双向互动)。这两个主题相互关联,凸显了针刺的复杂性以及患者体验可能受到影响的关键点:结论:针刺受多种心理和关系影响。这些发现为医护人员提供了改善患者体验的基础,是提高医疗服务质量的广泛努力的一部分。
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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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