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患者参与血液透析的叙述。

Narratives of patient participation in haemodialysis.

机构信息

Møre and Romsdal Hospital Trust, Ålesund, Norway.

Department of Circulation and Medical Imaging, Faculty of Medicine and Health Science, Norwegian University of Science and Technology, Trondheim, Norway.

出版信息

J Clin Nurs. 2020 Jul;29(13-14):2293-2305. doi: 10.1111/jocn.15238. Epub 2020 Apr 2.

Abstract

AIM AND OBJECTIVE

To explore how working-age adults experience patient participation in hospital haemodialysis.

BACKGROUND

End-stage kidney disease is a progressive, chronic condition imposing patients with high treatment burdens and low health-related quality of life. Patients face multiple medical decisions related to living with kidney failure. Given their frequent interaction with health services, patient participation may be of special value.

DESIGN

Qualitative design with a narrative approach.

METHODS

In 2018, eleven patients aged 35-64 years undergoing hospital haemodialysis participated in individual interviews. All interviews were analysed using a narrative approach. Reporting followed the Consolidated criteria for Reporting Qualitative Research guidelines.

FINDINGS

The patients' narratives of participation comprised three themes following their healthcare trajectory: Informed, but not involved in treatment choices; Duality of care and control; and Frail trust reflecting collaborative deficiencies. The patients received good information about dialysis, but were not involved in choice of treatment modality. Professional work, as well as the nature of treatment, contributed to restricted patient autonomy. Patients' trust suffered from collaborative deficiency generating delays in their treatment trajectories, and patients extended their responsibility into the coordination of transitions as a way of coping with these issues.

CONCLUSIONS

The study identified challenges related to patient involvement and interdisciplinary collaboration. Involving patients through dialogue and acknowledging their experiences, preferences and lifestyles may strengthen the mutual patient-professional understanding of treatment. Despite increased focus on seamless trajectories, patients face obstacles regarding interdisciplinary collaboration and coordination of health services.

RELEVANCE TO CLINICAL PRACTICE

The findings indicate a want of individually customised care for people requiring dialysis. Patients need to be involved in the choice of treatment modality as well as decisions related to the current treatment. Information must include potential consequences of the different treatment modalities. Health services need to strengthen collaboration in order to secure treatment continuity and patient involvement.

摘要

目的

探讨处于工作年龄的成年人如何体验医院血液透析中的患者参与。

背景

终末期肾病是一种进行性、慢性疾病,给患者带来了沉重的治疗负担和较低的健康相关生活质量。患者面临与肾衰竭共存相关的多种医疗决策。鉴于他们与卫生服务的频繁互动,患者参与可能具有特殊价值。

设计

具有叙述方法的定性设计。

方法

2018 年,11 名年龄在 35-64 岁之间正在接受医院血液透析的患者参与了个人访谈。所有访谈均采用叙述方法进行分析。报告遵循了定性研究报告的统一标准。

结果

患者的参与叙述包括三个主题,遵循他们的医疗轨迹:接受信息,但不参与治疗选择;护理和控制的双重性;脆弱的信任反映了协作缺陷。患者接受了关于透析的良好信息,但不参与治疗方式的选择。专业工作以及治疗性质限制了患者的自主权。患者的信任因协作缺陷而受损,导致治疗轨迹延迟,患者将其责任扩展到过渡的协调中,作为应对这些问题的一种方式。

结论

该研究确定了与患者参与和跨学科合作相关的挑战。通过对话让患者参与,并承认他们的经验、偏好和生活方式,可以增强患者与专业人员对治疗的相互理解。尽管越来越关注无缝轨迹,但患者在跨学科合作和卫生服务协调方面仍面临障碍。

临床意义

研究结果表明需要为需要透析的人提供个性化的护理。患者需要参与治疗方式的选择以及与当前治疗相关的决策。信息必须包括不同治疗方式的潜在后果。卫生服务机构需要加强合作,以确保治疗的连续性和患者的参与。

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