手术室医疗器械事件报告的路径图开发:改进现有系统的人为因素方法。

Arkeliana Tase, Massimo Micocci, Peter Buckle, Melody Ni, George Hanna
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引用次数: 0

摘要

目的:本研究旨在建立手术室医疗技术故障报告与信息传递的实际途径。这样做的目的是了解与NHS改进和改进点的识别所公布的途径的差异。设计:这是一项定性研究,涉及对医生、护士、制造商、医疗设备安全官员和药品和保健产品监管机构的利益相关者进行访谈。设置:收集手术室使用的报告路径数据。参与的临床工作人员在英国各地的不同信托机构工作,而制造商在英国和欧盟/美国提供设备。参与者:与15名临床医生和13名制造商完成半结构化访谈。调查由38名临床医生和5家制造商完成。使用公认的途径发展方法。适用于医疗保健的精益六西格玛原则被用于提出改进建议。主要结果衡量标准:确定工作人员报告的既定报告途径和信息传递与日常发生的情况之间的差异。确定路径中可以应用改进的点。结果:开发的路径显示了当前医疗器械报告系统的复杂性。它确定了在决策过程中产生问题和多重偏见的许多领域。这突出了导致设备性能和患者风险少报和缺乏知识的核心问题。根据最终用户的需求和发现的问题,提出了改进建议。结论:本研究详细了解了现行医疗器械和技术申报制度中存在的关键问题领域。制定的途径旨在解决改善报告结果的关键问题。识别“已完成的工作”和“想象中的工作”之间的路径差异可以导致可以系统应用的质量改进的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system.

Objectives: This study aimed to develop the actual pathway to reporting and information transfer in operating theatres in relation to medical technology malfunction/failure. This with the aim of understanding the differences with the pathway published by NHS Improvement and identification of points for improvement.

Design: This is a qualitative study involving stakeholder interviews with doctors, nurses, manufacturers, medical device safety officer and Medicines and Healthcare products Regulatory Agency.

Setting: Data were collected on reporting pathway used in operating theatres. Clinical staff who took part worked in different trusts throughout UK while manufacturers provided devices in UK and EU/USA.

Participants: Semistructured interviews were completed with 15 clinicians and 13 manufacturers. Surveys were completed by 38 clinicians and 5 manufacturers. Recognised methods of pathway development were used. The Lean Six Sigma principles adapted to healthcare were used to develop suggestions for improvement.

Main outcome measures: To identify the differences between the set pathway to reporting and information transfer to what is occurring on a day-to-day basis as reported by staff. Identify points in the pathway where improvements could be applied.

Results: The developed pathway demonstrated great complexity of the current reporting system for medical devices. It identified numerous areas that give rise to problems and multiple biases in decision making. This highlighted the core issues leading to under-reporting and lack of knowledge on device performance and patient risk. Suggestions for improvement were deduced based on end user requirements and identified problems.

Conclusions: This study has provided a detailed understanding of the key problem areas that exist within the current reporting system for medical devices and technology. The developed pathway sets to address the key problems to improve reporting outcomes. The identification of pathway differences between 'work as done' and 'work as imagined' can lead to development of quality improvements that could be systematically applied.

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来源期刊
CiteScore
2.80
自引率
0.00%
发文量
22
审稿时长
17 weeks
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