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创建一个区域性危害药物处理工作队。

Creation of a regional hazardous drug handling task force.

机构信息

Department of Pharmacy, Children's Mercy, Kansas City, MO, USA.

Department of Pharmacy, The University of Kansas Medical Center, Kansas City, KS, USA.

出版信息

Am J Health Syst Pharm. 2021 Jun 23;78(13):1233-1237. doi: 10.1093/ajhp/zxab181.

Abstract

PURPOSE

A regional task force of health-system pharmacy leaders was created to assist with successful adoption of United States Pharmacopeia (USP) general chapter <800>.

SUMMARY

A group of pharmacy leaders in the Kansas City region identified potential benefits to healthcare personnel and patients if hazardous drug handling procedures were standardized. A task force was created, a preimplementation survey was distributed, and meetings were held monthly to discuss sections of USP <800> identified as the most challenging to implement. The task force focused on an assessment of risk tool, hot topics, cleanroom design, and a detailed analysis of controversial medications. After the first year of meetings, a postimplementation survey was distributed, and the results were analyzed. The task force created significant value for the participants and achieved the goal of facilitating efficient USP <800> implementation resulting in greater compliance and consistency across the multiple health systems represented. Over 5,100 beds and 200 clinic sites were affected by this task force's efforts. Nearly three-fourths (73%) of respondents reported that the task force was "extremely helpful," and the majority (64%) of respondents adopted most or all (81%-100%) of the task force's assessment of risk choices. Prioritization of tasks, information sharing, and decision-making were areas where the individual leaders were most supported.

CONCLUSION

Creating a structure to eliminate barriers and facilitate collaboration among regional pharmacy leaders provided a framework for successful implementation of USP <800> requirements. This interdependent leadership model produced innovative and standardized solutions and should be considered when addressing complicated initiatives that impact the profession.

摘要

目的

成立了一个卫生系统药学领导者区域工作组,以协助成功采用美国药典(USP)通则<800>。

摘要

堪萨斯城地区的一群药学领导者确定,如果危险药物处理程序标准化,将为医疗保健人员和患者带来潜在益处。成立了一个工作组,分发了实施前调查,并每月举行会议,讨论被认为最具挑战性的 USP<800>实施部分。该工作组专注于风险评估工具、热点话题、洁净室设计以及有争议药物的详细分析。在会议的第一年结束后,分发了实施后调查,并对结果进行了分析。该工作组为参与者创造了巨大的价值,并实现了促进 USP<800>高效实施的目标,从而在多个代表的卫生系统中实现了更高的合规性和一致性。超过 5100 张床位和 200 个诊所受到该工作组努力的影响。近四分之三(73%)的受访者表示,工作组“非常有帮助”,大多数(64%)受访者采用了工作组风险评估选择的大部分或全部(81%-100%)。任务的优先级、信息共享和决策制定是个别领导者最受支持的领域。

结论

创建一个消除障碍和促进区域药学领导者之间协作的结构,为成功实施 USP<800>要求提供了框架。这种相互依存的领导模式产生了创新和标准化的解决方案,在处理影响专业的复杂倡议时应予以考虑。

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