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已确立的药学照护路径对 ICU 中药物相关问题的影响。

The Impact of an Established Pharmaceutical Care Pathway on Drug Related Problems in an Intensive Care Unit.

机构信息

Clinical Pharmacy Department, Al Haram Hospital, Giza, Egypt.

Anesthesia and Intensive Care Department, Faculty of Medicine, AL-Azhar University, Cairo, Egypt.

出版信息

Am J Med Sci. 2021 Aug;362(2):143-153. doi: 10.1016/j.amjms.2021.03.007. Epub 2021 Mar 19.

Abstract

BACKGROUND

The incidence of drug related problems (DRPs) in intensive care units (ICU) is higher compared to any other wards in the hospital, requiring a structured pathway to ensure optimum detection of DRPs. The study aimed to evaluate the impact of implementing a pharmaceutical care pathway on the detection and management of DRPs in an ICU.

METHODS

The study was conducted in a general ICU and included three phases: tool preparation phase included the development of a core measures reference pathway and daily working scenario flow-charts, a control phase where the patient files and pharmacists' case assessment notes were retrospectively reviewed to detect the rate of DRPs before pathway implementation and a prospective phase similar to the control phase but with the implementation of the new pathway. The number and classification of DRPs and required core measures in the control and implementation phases were documented.

RESULTS

Using the new pathway, the detection of unmet core measures increased from 7.3% in the control phase to 99% in the implementation phase (p-value <0.001). The prevalence of unidentified DRPs/1000 patients' service days decreased from 98.1 in the control phase to 27.08 in the implementation phase (p-value <0.001). However, there was no significant difference between the phases regarding mortality rate and length of ICU stay.

CONCLUSIONS

The implementation of a unified pharmaceutical care pathway improved the detection of DRPs in ICU patients.

摘要

背景

与医院的其他病房相比,重症监护病房(ICU)的药物相关问题(DRP)发生率更高,需要建立结构化的途径来确保最佳地发现 DRP。本研究旨在评估在 ICU 实施药物治疗管理路径对 DRP 的检测和管理的影响。

方法

该研究在普通 ICU 进行,包括三个阶段:工具准备阶段包括制定核心措施参考路径和日常工作情景流程图;控制阶段,回顾患者病历和药师案例评估记录,以检测实施路径之前的 DRP 发生率;以及与控制阶段相似但实施新路径的前瞻性阶段。记录控制和实施阶段的 DRP 数量和分类以及所需的核心措施。

结果

使用新路径,未满足的核心措施的检测率从控制阶段的 7.3%增加到实施阶段的 99%(p 值<0.001)。未识别的 DRP/1000 患者服务日的发生率从控制阶段的 98.1 下降到实施阶段的 27.08(p 值<0.001)。然而,在死亡率和 ICU 停留时间方面,两个阶段之间没有显著差异。

结论

实施统一的药物治疗管理途径可提高 ICU 患者 DRP 的检测率。

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