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再保险部门的前瞻性风险分析:聚焦于药品配发流程

[Prospective risk analysis in a retrocession unit: Focus on drug dispensation process].

作者信息

Darcissac C, Duvert L, Hoegy D, Chappuy M, Pivot C, Janoly-Dumenil A

机构信息

Pharmacie hôpital Edouard-Herriot, hospices civils de Lyon, 5, place d'Arsonval, 69003 Lyon, France.

Pharmacie hôpital Edouard-Herriot, hospices civils de Lyon, 5, place d'Arsonval, 69003 Lyon, France.

出版信息

Ann Pharm Fr. 2020 Jan;78(1):12-20. doi: 10.1016/j.pharma.2019.06.006. Epub 2019 Sep 26.

Abstract

OBJECTIVES

Failure mode effect analysis (FMEA) improves safety in the drug life cycle. As the drug dispensation by hospital's pharmacy can be at risk, the FMEA tool has been used to evaluate and enhance the process.

METHODS

After detailing the process, a first FMEA has been run in 2015. Corrective actions were implemented every time criticality indexes (CI) were above 15. One year later, we have evaluated potential impacts of these actions by running a new FMEA.

RESULTS

In 2015, 11 failure modes were prioritized (CI>15) and the total CI for the overall process was 397. Corrective actions were implemented and one year later this amount has decreased by 14% (340) with 6 failure modes still prioritized. Thus, thanks to the FMEA, risks could be identified in year "y", they were taken into account and corrected and then effectively reassessed in year "y+1".

CONCLUSION

This study showed us the interest of performing FMEA analysis in the drug dispensation process by hospital. The renewal of this risk analysis after a year helped us to monitor corrective actions, to evaluate their effectiveness and to improve safety. Finally, FMEA seems to be an effective way to steer the drug dispensation process.

摘要

目的

失效模式与效应分析(FMEA)可提高药物生命周期中的安全性。由于医院药房的药品调配存在风险,因此已使用FMEA工具来评估和改进该流程。

方法

在详细描述该流程后,于2015年进行了首次FMEA。每当关键度指标(CI)高于15时,就会实施纠正措施。一年后,我们通过进行新的FMEA评估了这些措施的潜在影响。

结果

2015年,确定了11个优先失效模式(CI>15),整个流程的总CI为397。实施了纠正措施,一年后该数值下降了14%(340),仍有6个失效模式被列为优先。因此,借助FMEA,在“y”年能够识别风险,加以考虑并纠正,然后在“y+1”年进行有效重新评估。

结论

本研究向我们展示了在医院药品调配过程中进行FMEA分析的益处。一年后进行的这种风险分析更新有助于我们监测纠正措施,评估其有效性并提高安全性。最后,FMEA似乎是指导药品调配过程的有效方法。

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