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充分利用远程护理:共同开发工具包,以改善为服务不足群体提供远程肾脏护理预约服务。

Getting the most out of remote care: Co-developing a Toolkit to improve the delivery of remote kidney care appointments for underserved groups.

机构信息

Institute of Health and Social Care, London South Bank University, London, UK.

Renal Patient Led Advisory Network (R-PLAN), Blackburn, UK.

出版信息

J Ren Care. 2024 Dec;50(4):413-425. doi: 10.1111/jorc.12504. Epub 2024 Jun 4.

Abstract

BACKGROUND

Telephone and video appointments are still common post-pandemic, with an estimated 25%-50% of kidney appointments in the United Kingdom still conducted remotely. This is important as remote consultations may exacerbate pre-existing inequalities in those from underserved groups. Those from underserved groups are often not represented in health research and include those with learning disability, mental health needs, hearing/sight problems, young/older people, those from ethnic minority groups.

OBJECTIVES

The aim was to develop a Toolkit to improve the quality of remote kidney care appointments for people from different underserved groups.

DESIGN

A parallel mixed methods approach with semistructured interviews/focus groups and survey. We also conducted workshops to develop and validate the Toolkit.

PARTICIPANTS

Seventy-five renal staff members completed the survey and 21 patients participated in the interviews and focus groups. Patients (n = 11) and staff (n = 10) took part in the Toolkit development workshop, and patients (n = 13) took part in the Toolkit validation workshop.

RESULTS

Four themes from interviews/focus groups suggested areas in which remote appointments could be improved. Themes were quality of appointment, patient empowerment, patient-practitioner relationship and unique needs for underserved groups. Staff reported difficulty building rapport, confidentiality issues, confidence about diagnosis/advice given, technical difficulties and shared decision making.

CONCLUSION

This study is the first to explore experiences of remote appointments among both staff and those from underserved groups living with kidney disease in the United Kingdom. While remote appointments can be beneficial, our findings indicate that remote consultations need optimisation to meet the needs of patients. The project findings informed the development of a Toolkit which will be widely promoted and accessible in the United Kingdom during 2024.

摘要

背景

电话和视频预约在疫情后仍然很常见,据估计,英国仍有 25%-50%的肾脏预约是远程进行的。这很重要,因为远程咨询可能会加剧服务不足群体中已经存在的不平等。服务不足的群体通常在健康研究中没有代表性,包括有学习障碍、心理健康需求、听力/视力问题、年轻人/老年人、少数族裔群体的人。

目的

旨在开发一个工具包,以提高不同服务不足群体远程肾脏护理预约的质量。

设计

采用平行混合方法,包括半结构式访谈/焦点小组和调查。我们还举办了研讨会来开发和验证工具包。

参与者

75 名肾脏科工作人员完成了调查,21 名患者参加了访谈和焦点小组。11 名患者和 10 名工作人员参加了工具包开发研讨会,13 名患者参加了工具包验证研讨会。

结果

访谈/焦点小组的四个主题提出了可以改进远程预约的领域。主题包括预约质量、患者赋权、医患关系以及服务不足群体的独特需求。工作人员报告说,建立融洽关系、保密性问题、对诊断/建议的信心、技术困难和共同决策方面存在困难。

结论

这项研究首次探索了英国工作人员和患有肾脏疾病的服务不足群体在远程预约方面的经验。虽然远程预约可能是有益的,但我们的研究结果表明,远程咨询需要优化,以满足患者的需求。该项目的研究结果为开发一个工具包提供了信息,该工具包将于 2024 年在英国广泛推广和使用。

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