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实施试验的过程评估,以改善急诊科中风患者的分诊、治疗和转院(T 试验):一项定性研究。

Process evaluation of an implementation trial to improve the triage, treatment and transfer of stroke patients in emergency departments (T trial): a qualitative study.

机构信息

Nursing Research Institute - St Vincent's Health Network Sydney, St Vincent's Hospital Melbourne & Australian Catholic University, School of Nursing, Midwifery & Paramedicine, Australian Catholic University, Level 4, Daniel Mannix Building, Brunswick Street, Fitzroy, Victoria, 3065, Australia.

Nursing Research Institute - St Vincent's Health Network Sydney, St Vincent's Hospital Melbourne & Australian Catholic University, Level 5, deLacy Building, Victoria Street, Darlinghurst, New South Wales, 2010, Australia.

出版信息

Implement Sci. 2020 Nov 4;15(1):99. doi: 10.1186/s13012-020-01057-0.

Abstract

BACKGROUND

The implementation of evidence-based protocols for stroke management in the emergency department (ED) for the appropriate triage, administration of tissue plasminogen activator to eligible patients, management of fever, hyperglycaemia and swallowing, and prompt transfer to a stroke unit were evaluated in an Australian cluster-randomised trial (T trial) conducted at 26 emergency departments. There was no reduction in 90-day death or dependency nor improved processes of ED care. We conducted an a priori planned process influential factors that impacted upon protocol uptake.

METHODS

Qualitative face-to-face interviews were conducted with purposively selected ED and stroke clinicians from two high- and two low-performing intervention sites about their views on factors that influenced protocol uptake. All Trial State Co-ordinators (n = 3) who supported the implementation at the 13 intervention sites were also interviewed. Data were analysed thematically using normalisation process theory as a sensitising framework to understand key findings, and compared and contrasted between interviewee groups.

RESULTS

Twenty-five ED and stroke clinicians, and three Trial State Co-ordinators were interviewed. Three major themes represented key influences on evidence uptake: (i) Readiness to change: reflected strategies to mobilise and engage clinical teams to foster cognitive participation and collective action; (ii) Fidelity to the protocols: reflected that beliefs about the evidence underpinning the protocols impeded the development of a shared understanding about the applicability of the protocols in the ED context (coherence); and (iii) Boundaries of care: reflected that appraisal (reflexive monitoring) by ED and stroke teams about their respective boundaries of clinical practice impeded uptake of the protocols.

CONCLUSIONS

Despite initial high 'buy-in' from clinicians, a theoretically informed and comprehensive implementation strategy was unable to overcome system and clinician level barriers. Initiatives to drive change and integrate protocols rested largely with senior nurses who had to overcome contextual factors that fell outside their control, including low medical engagement, beliefs about the supporting evidence and perceptions of professional boundaries. To maximise uptake of evidence and adherence to intervention fidelity in complex clinical settings such as ED cost-effective strategies are needed to overcome these barriers.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry ( ACTRN12614000939695 ).

摘要

背景

在澳大利亚的一项 26 个急诊部参与的聚类随机试验(T 试验)中,评估了在急诊科(ED)实施基于证据的中风管理方案,包括适当分诊、为符合条件的患者使用组织型纤溶酶原激活剂、管理发热、高血糖和吞咽问题,以及迅速转至中风单元,以实现适当的转介。该试验并未降低 90 天死亡率或依赖性,也未改善 ED 护理流程。我们进行了一项事先计划的过程影响因素研究,以评估影响方案采用的因素。

方法

我们对来自两个高绩效和两个低绩效干预地点的 ED 和中风临床医生进行了定性面对面访谈,探讨了他们对影响方案采用的因素的看法。还对所有 13 个干预地点的试验州协调员(n=3)进行了访谈。采用常规化进程理论作为一个敏感框架对数据进行了主题分析,以了解关键发现,并对受访者组之间进行了比较和对比。

结果

共对 25 名 ED 和中风临床医生以及 3 名试验州协调员进行了访谈。三个主要主题代表了影响证据采用的关键因素:(i)改变的准备度:反映了动员和吸引临床团队的策略,以促进认知参与和集体行动;(ii)对方案的忠实度:反映了对方案所依据证据的信念阻碍了对 ED 背景下方案适用性的共同理解(一致性);(iii)护理边界:反映了 ED 和中风团队对各自临床实践边界的评估(反思性监测)阻碍了方案的采用。

结论

尽管临床医生最初表现出很高的“采纳意愿”,但理论上有依据且全面的实施策略仍无法克服系统和临床医生层面的障碍。推动变革和整合方案的举措主要依赖于高级护士,她们必须克服超出其控制范围的环境因素,包括医疗人员参与度低、对支持证据的信念以及对专业边界的看法。为了在 ED 等复杂临床环境中最大限度地采用证据并坚持干预的忠实度,需要采取具有成本效益的策略来克服这些障碍。

试验注册

澳大利亚新西兰临床试验注册(ACTRN12614000939695)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797e/7640433/1cefbcade529/13012_2020_1057_Fig1_HTML.jpg

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