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在电子健康记录中实施药物不良事件报告表之前进行预试验。

Pilot-testing an adverse drug event reporting form prior to its implementation in an electronic health record.

作者信息

Chruscicki Adam, Badke Katherin, Peddie David, Small Serena, Balka Ellen, Hohl Corinne M

机构信息

Faculty of Medicine, Queen's University, 15 Arch Street, Kingston, ON K7L 3N8 Canada.

Department of Emergency Medicine, University of British Columbia, 855 West 12th Avenue, Vancouver, BC V5Z 1M9 Canada.

出版信息

Springerplus. 2016 Oct 11;5(1):1764. doi: 10.1186/s40064-016-3382-z. eCollection 2016.

Abstract

BACKGROUND

Adverse drug events (ADEs), harmful unintended consequences of medication use, are a leading cause of hospital admissions, yet are rarely documented in a structured format between care providers. We describe pilot-testing structured ADE documentation fields prior to integration into an electronic medical record (EMR).

METHODS

We completed a qualitative study at two Canadian hospitals. Using data derived from a systematic review of the literature, we developed screen mock-ups for an ADE reporting platform, iteratively revised in participatory workshops with diverse end-user groups. We designed a paper-based form reflecting the data elements contained in the mock-ups. We distributed them to a convenience sample of clinical pharmacists, and completed ethnographic workplace observations while the forms were used. We reviewed completed forms, collected feedback from pharmacists using semi-structured interviews, and coded the data in NVivo for themes related to the ADE form.

RESULTS

We completed 25 h of clinical observations, and 24 ADEs were documented. Pharmacists perceived the form as simple and clear, with sufficient detail to capture ADEs. They identified fields for omission, and others requiring more detail. Pharmacists encountered barriers to documenting ADEs including uncertainty about what constituted a reportable ADE, inability to complete patient follow-up, the need for inter-professional communication to rule out alternative diagnoses, and concern about creating a permanent record.

CONCLUSION

Paper-based pilot-testing allowed planning for important modifications in an ADE documentation form prior to implementation in an EMR. While paper-based piloting is rarely reported prior to EMR implementations, it can inform design and enhance functionality. Piloting with other groups of care providers and in different healthcare settings will likely lead to further revisions prior to broader implementations.

摘要

背景

药物不良事件(ADEs)是药物使用产生的有害意外后果,是导致住院的主要原因,但在医护人员之间很少以结构化格式记录。我们描述了在将结构化ADE文档字段集成到电子病历(EMR)之前进行的试点测试。

方法

我们在两家加拿大医院完成了一项定性研究。利用对文献系统评价得出的数据,我们开发了一个ADE报告平台的屏幕原型,并在与不同最终用户群体的参与式研讨会上进行了反复修订。我们设计了一份纸质表格,反映原型中包含的数据元素。我们将表格分发给临床药师的便利样本,并在使用表格时完成人种学工作场所观察。我们审查了已填写的表格,通过半结构化访谈收集药师的反馈,并在NVivo中对与ADE表格相关的主题进行数据编码。

结果

我们完成了25小时的临床观察,记录了24起ADEs。药师认为该表格简单明了,有足够的细节来记录ADEs。他们指出了需要遗漏的字段,以及其他需要更多细节的字段。药师在记录ADEs时遇到了障碍,包括对可报告的ADEs的构成不确定、无法完成患者随访、需要跨专业沟通以排除其他诊断,以及对创建永久记录的担忧。

结论

纸质试点测试允许在将ADE文档表格实施到EMR之前规划重要的修改。虽然在EMR实施之前很少报告纸质试点测试,但它可以为设计提供信息并增强功能。在更广泛实施之前,与其他医护人员群体以及在不同医疗环境中进行试点可能会导致进一步修订。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f9/5056922/7b7cbab40b40/40064_2016_3382_Fig1_HTML.jpg

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