共同设计和测试共同学习指导,以支持患者和家属参与患者安全调查:一项混合方法研究。

Jane O'Hara, Lauren Ramsey, Siobhan McHugh, Joseph Langley, Justin Waring, Ruth Simms-Ellis, Gemma Louch, Jenni Murray, Carl Macrae, John Baker, Rebecca Lawton, Daisy Halligan, Olivia Rogerson, Penny Phillips, Debra Hazeldine, Sarah Seddon, Joanne Hughes, Rebecca Partridge, Katherine Ludwin, Laura Sheard
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引用次数: 0

摘要

背景:在事故调查中涉及患者和家属有多种原因。在财政上,每年因临床疏忽索赔的费用约为40亿英镑。从逻辑上讲,患者和家属提供了有关患者安全事件的重要信息。从道义上讲,让受伤害的病人和家属参与进来有助于解决他们的关切。然而,很少有来自联合王国的证据支持有系统的参与。目的:共同设计流程和资源,以指导患者和家属参与国家和地方层面的事件调查,并测试这些流程,以了解它们对经验、学习和诉讼可能性的影响。设计和方法:进行了一项混合方法的研究方案。第一阶段包括对事件调查中患者/家属经验的证据进行范围审查,并对43项国家卫生服务信托基金事件调查政策进行文献分析。阶段2A进一步扩展,对患者/家属、医护人员和调查人员进行了41次定性访谈。阶段2B综合以往的资料,发展共同的原则和计划理论。第三阶段是为期6个月的协同设计阶段,由50个利益相关者组成“协同设计社区”。在第4和第5阶段,在四个国家保健服务信托基金和国家独立调查机构内,对共同设计的指导方针进行了为期15个月的人种学评估。实时跟踪29项调查,包括127次访谈和45小时的观察。四个最终的共同设计研讨会支持最终指南和网站的迭代。一个子研究通过访谈和一项涉及32人(医护人员、政策制定者和管理人员;因自杀而失去亲人的人)。发现:第一阶段发现利益相关者重视参与,但它没有得到当地政策的很好支持,尽管它可能减少诉讼。阶段2A发现对导航支持的需求,以及对其他需求的支持。在第2B阶段,制定了10项共同原则和一个方案理论,强调减少复合伤害的目标,同时促进组织学习。在第三阶段,编制了四份指导手册草案和一次培训课程。第4阶段发现这些是可行的,利益相关者对参与持积极态度,并且普遍认为它有助于组织学习。该指南支持参与的系统化,并鼓励关系型工作,但强调了更广泛的组织挑战。子研究发现,自杀被认为与其他安全事件有所不同。有意义的参与因一系列因素而复杂化,应与事后支助脱钩。局限性:在大流行期间进行研究可能会影响2A阶段样本的代表性。少数民族和社会经济地位较低的群体在整个方案中代表性不足。未来的研究:研究应该探索来自少数群体的人如何经历调查,以及对这种方法的任何必要的适应。研究还应该探索“以伤害为中心”而不是“以事件为中心”的安全响应的可能性。结论:调查是一个复杂的、相互关联的过程。我们的指导被认为是可行的,利益相关者对参与和对组织学习的影响持积极态度。这可能有助于减少对病人和家属造成严重和长期的复合伤害。然而,由于患者/家庭和组织的不同需求,参与可能总是具有挑战性。研究注册:本研究注册为当前对照试验ISRCTN14463242。资助:该奖项由国家卫生和保健研究所(NIHR)卫生和社会保健提供研究项目(NIHR奖励编号:18/10/02)资助,全文发表在《卫生和社会保健提供研究》上;第13卷,第18号有关进一步的奖励信息,请参阅美国国立卫生研究院资助和奖励网站。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-designing and testing the learn together guidance to support patient and family involvement in patient safety investigations: a mixed-methods study.

Background: There are multiple reasons for involving patients and families in incident investigations. Fiscally, costs due to clinical negligence claims approximate £4 billion annually. Logically, patients and families provide important information about patient safety incidents. Morally, involving harmed patients and families helps address their concerns. However, little United Kingdom-based evidence was available to support systematic involvement.

Objective: To co-design processes and resources to guide the involvement of patients and families in incident investigations at a national and local level, and to test these processes to understand their impact upon experience, learning and likelihood of litigation.

Design and methods: A mixed-methods programme of research was undertaken. Stage 1 comprised a scoping review of evidence for the experience of patients/families in incident investigations, and a documentary analysis of 43 National Health Service Trust incident investigation policies. Stage 2A extended this with 41 qualitative interviews with patients/families, healthcare staff and investigators. Stage 2B synthesised previous data to develop common principles and programme theory. Stage 3 involved a 6-month co-design phase with a 'co-design community' of > 50 stakeholders. In stages 4 and 5, co-designed guidance was evaluated in a 15-month ethnography, within four National Health Service Trusts and the national independent investigatory body. Twenty-nine investigations were followed in real time, including 127 interviews and 45 hours of observation. Four final co-design workshops supported iterations to the final guidance and website. A substudy explored meaningful involvement in, and learning from, investigations following suicide via interviews and a qualitative survey involving 32 people (healthcare staff, policy-makers and managers; people bereaved by suicide).

Findings: Stage 1 found stakeholders valued involvement, but it was not well supported by local policy, even though it likely reduces litigation. Stage 2A found a need for navigational support, and support for other needs. In stage 2B, 10 common principles and a programme theory were developed, emphasising the aim of reducing compounded harm, alongside promoting organisational learning. In stage 3, four draft guidance booklets and a training session were developed. Stage 4 found these to be feasible, with stakeholders positive about involvement, and generally agreed that it aided organisational learning. The guidance supported systematisation of involvement and encouraged relational working, but wider organisational challenges were highlighted. The substudy found that suicide was regarded as somewhat different to other safety events. Meaningful involvement was complicated by a range of factors and should be decoupled from postvention support.

Limitations: Undertaking research during the pandemic may have impacted sample representativeness in stage 2A. Ethnically minoritised and lower socioeconomic groups were under-represented across the programme.

Future research: Research should explore how people from minoritised groups experience investigations and any required adaptations to the approach. Research should also explore the possibilities for 'harm-centred' rather than 'incident-centred' responses to safety.

Conclusions: Investigations are complex, relational processes. Our guidance was found to be feasible, with stakeholders being positive about involvement and the impact on organisational learning. It may help to reduce the significant and long-lasting experience of compounded harm for patients and families. However, involvement may always be challenging due to the divergent needs of patients/families and organisations.

Study registration: This study is registered as Current Controlled Trials ISRCTN14463242.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme (NIHR award ref: 18/10/02) and is published in full in Health and Social Care Delivery Research; Vol. 13, No. 18. See the NIHR Funding and Awards website for further award information.

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