A102嵌入电子病历到整个英格兰东南部的常规医疗模拟培训,一个开创性的区域合作

Andy Buttery, Rosie Courtney, Alastair Kirby, Benjamin Repton, Charlotte Roberts, Arron Thind
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引用次数: 0

摘要

电子病历(EPR)系统在临床环境中越来越普遍,但英国医学模拟培训继续使用过时的纸质方法来培训医疗保健人员。虽然已发表的文献强调了将epr纳入医学模拟培训的培训益处[1,2],但由于缺乏定制软件,这种过渡以前受到阻碍。为了解决这个问题,一种新型的教育EPR(名为SimEPR)被创建,这是一种定制的培训软件,设计用于人体模型床边的计算机上,具有可定制的临床场景(SimEPR预览,为英国医学模拟培训设计的新型教育电子病历系统)。该项目旨在将SimEPR纳入英格兰东南部的常规医学模拟培训中,并报告学员使用该软件的经验。反馈数据是通过电子反馈表格从使用SimEPR作为模拟训练一部分的受训者那里收集的。从2021年2月11日起,SimEPR最初在一所医学院和两个NHS信托基金部署,然后从2023年1月3日起,该项目扩大到另外六个教育中心(一所大学和五个NHS信托基金)。收集了209名学员的数据,其中16%为医学生,82%为基础医生,2%为基础后医生。其中,86%的人报告说,与使用纸质笔记相比,教育EPR创造了更真实的培训体验。同时,83%的患者表示使用SimEPR有助于改善他们的临床学习。最后,87%的人表示他们会建议模拟部门继续使用SimEPR。SimEPR是第一个专门为英国医学教育设计的同类软件,是与许多模拟领导和nhs附属组织合作的产品。除了支持更高保真度培训体验的数据外,SimEPR还将数字技能纳入实践培训,从而支持数字化劳动力的发展。此外,通过消除纸张的使用,SimEPR有助于可持续地提供基于模拟的教育。作为这一开创性区域项目的一部分,进一步的评估工作旨在收集培训前和培训后的反馈、医学教育者的反馈和其他保健学科的反馈。从长远来看,SimEPR将为NHS员工提供模拟培训。该软件的“场景共享”功能允许在机构之间共享模拟患者记录,支持培训的标准化,同时节省员工构建培训场景的时间。此外,正在探索诸如培训学员反馈的绩效分析和生成交互式场景的人工智能技术等功能。作者确认已符合研究行为和传播的所有相关伦理标准。提交作者确认已获得相关的伦理批准(如适用)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A102 Embedding Electronic Patient Records Into Routine Medical Simulation Training Across the South East of England, a Pioneering Regional Collaboration
Electronic patient record (EPR) systems are increasingly prevalent in clinical settings, yet UK medical simulation training continues to use outdated paper-based methods for training healthcare staff. While published literature has highlighted the training benefits of incorporating EPRs into medical simulation training [1, 2], the transition has previously been hampered by a lack of bespoke software. To address this, a novel educational EPR (named SimEPR) was created, a bespoke training software designed to be used on a computer at the manikin’s bedside, which features customizable clinical scenarios ( A preview of SimEPR, a novel educational electronic patient record system designed for UK medical simulation training This project aimed to incorporate SimEPR into routine medical simulation training in the South East of England, and report trainee experience using the software. Feedback data was collected from trainees who used SimEPR as part of their simulation training using an electronic feedback form. SimEPR was initially deployed in a medical school and two NHS trusts from 11th February 2021, before the project was scaled up to six additional educational centres (one university and five NHS trusts) from 3rd January 2023. Data from 209 trainees was collected, of which 16% were medical students, 82% were foundation doctors and 2% were post-foundation doctors. Out of these, 86% reported that, compared to using paper notes, the educational EPR created a more realistic training experience. Meanwhile, 83% reported that the use of SimEPR helped improve their clinical learning. Last, 87% reported that they would recommend the simulation department to continue using SimEPR. SimEPR is the first software of its kind designed specifically for UK medical education, and is the product of collaboration with a number of simulation leads and NHS-affiliated organizations. As well as data supporting a higher fidelity training experience, SimEPR incorporates digital skills into practical training, thus supporting the development of a digitally-ready workforce. In addition, by eliminating the use of paper, SimEPR contributes to the sustainable delivery of simulation-based education. Further evaluation work as part of this pioneering regional project aims to collect pre- and post-training feedback, feedback from medical educators and feedback from other healthcare disciplines. In the longer term, SimEPR offers to transform the delivery of simulation training for the NHS workforce. The software’s ‘scenario-sharing’ function allows sharing of simulated patient records between institutions, supporting the standardization of training while saving staff time in building training scenarios. Furthermore, features such as performance analytics for trainee feedback, and AI technology to generate interactive scenarios, are being explored. Authors confirm that all relevant ethical standards for research conduct and dissemination have been met. The submitting author confirms that relevant ethical approval was granted, if applicable.
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