消费者合作与临床治理的交响乐:使用 RE-AIM 框架进行组织审查。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Jodie Nixon, Emily Steel, Warren Stubbs, Amber Williamson, Javed Khan, Phillip Carswell, Anne Coccetti
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引用次数: 0

摘要

导言:在许多国家,医疗保健系统中与消费者建立合作伙伴关系已被广泛接受和强制执行。尽管已被接受,但关于如何成功建立系统将这一做法纳入医疗系统的最佳做法的信息却少之又少:本次评估采用 RE-AIM 实施框架,对 3 年时间内的数据进行回顾性分析,以回顾与消费者伙伴计划向临床治理部门过渡有关的事件。数据来源包括:第一阶段--焦点小组,以确定 3 年间的事件、促进因素和障碍;第二阶段--定量和定性半结构式访谈,以回顾为支持将消费者合作嵌入临床治理而开发的系统:结果:确定了成功将消费者合作团队纳入临床治理单位的五个主要促进因素和五个障碍。有利因素包括:行政人员对与消费者建立伙伴关系的价值的支持和所有权、行政领导对地方区域采纳情况的影响、全组织范围的网络、通过薪酬给予的重视,以及为消费者合作伙伴提供的集中指导和入职培训计划。障碍包括委员会主席的技能和态度、总局的规模(较小的地方区域可能更容易影响变革)、患者反馈数据需要解释才能发挥作用、人员流动会减少与消费者合作伙伴的关系,以及财政不稳定是实施和维护的障碍:本文介绍了澳大利亚卫生服务机构如何将消费者合作伙伴团队嵌入临床治理部门,以确保合作伙伴关系成为常规做法。促进因素、障碍和意外后果可作为其他组织开发类似方法的借鉴:患者或公众的贡献:评估小组中有两名具有医疗服务生活经验的消费者伙伴和组织委员会成员。作为团队成员,消费者以平等的身份参与了评估设计、焦点小组和访谈数据的分析,以及手稿的撰写和审阅。两名具有医疗服务生活经验的消费者伙伴和委员会成员参与了焦点小组和访谈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Symphony of Consumer Partnering and Clinical Governance: An Organizational Review Using the RE-AIM Framework

The Symphony of Consumer Partnering and Clinical Governance: An Organizational Review Using the RE-AIM Framework

Introduction

Partnering with Consumers in healthcare systems is now widely accepted and mandated in many countries. Despite this acceptance, there is minimal information regarding the best practice of how to successfully establish systems to embed this practice into healthcare systems.

Methods

This evaluation used the RE-AIM implementation framework to retrospectively analyse data from a 3-year timeline to review the events relating to the transition of Consumer Partnering into a Clinical Governance Unit. Data was sourced via Phase 1 – a focus group to establish a 3-year timeline of events, enablers and barriers, and Phase 2 – a quantitative and qualitative semi-structured interview to review systems that had been developed to support embedding partnering with consumers into Clinical Governance.

Results

Five primary enablers and five barriers to successfully embedding a Consumer Partnering Team into a Clinical Governance Unit were identified. Enablers included Executive sponsorship and ownership of the value of partnering with consumers, Executive leadership influence on local area uptake, an organization-wide network, valuing via remuneration, and a centralized orientation and onboarding programme for Consumer Partners. Barriers included skills and attitudes of committee chairs, the size of the Directorate (smaller local areas can be easier to influence change), patient feedback data requires interpretation to be useful, staff turnover can reduce the relationships with Consumer Partners, and financial insecurity is a barrier to implementation and maintenance.

Conclusions

This article described how an Australian Health Service embedded a Consumer Partnering Team into a Clinical Governance Unit to ensure that partnering became business as usual practice. Enablers, barriers, and unintended consequences can be used as learnings for other organizations to develop a similar approach.

Patient or Public Contribution

Two Consumer Partners with lived experience of the health service, and members of the organizations committee structures are part of the evaluation team. As team members, the consumers participated as equal contributors in evaluation design, analysis of the focus group and interview data, and contribution to the writing and review of the manuscript. Two Consumer Partners with lived experience of the health service, and members of the committee structures participated in the focus groups and the interviews.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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