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An Automated Software Application Reduces Controlled Substance Discrepancies in Perioperative Areas

机译:自动化软件应用减少了围手术期地区的受控物质差异

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Background: Perioperative controlled substance diversion and tracking have received increased regulatory focus throughout the United States. The authors' institution developed and implemented an automated web-based software application for perioperative controlled substance management. The authors hypothesized that implementation of such a system reduces errors as measured by missing controlled substance medications, missing controlled substance kits (a package of multiple controlled substance medications), and missing witness signatures during kit return. Methods: From December 1, 2014 to March 31, 2017, the authors obtained missing controlled substance medication, controlled substance kit, and witness return signature data during the preimplementation, implementation, and study period of the controlled substance management application at a single university hospital. This before and after study was based on a QI project at the authors' institution. The authors included all cases requiring anesthesia services. The primary outcome of this study was the rate of missing controlled substance medications. Secondary outcomes included rates for kits not returned to pharmacy and missing kit return witness signatures. Results: There were 54,302 cases during the preimplementation period, 57,670 cases during the implementation period, and 65,911 cases during the study period. The number of missing controlled substance medication (difference 0.7 per 1,000 cases; 95% CI, 0.38-1.02; P < 0.001) and kit return errors (difference 0.45 per 1,000 cases; 95% CI, 0.24-0.66, P < 0.001) declined after implementation of the application. There was no difference in the number of missing witness return signatures (difference 0.09 per 1,000 cases; 95% CI, -0.08 to 0.26, P = 0.350). A user survey with 206 of 485 (42%) response rate demonstrated that providers believed the new application managed controlled substances better than the previous system. Conclusions: A software application that tracks perioperative controlled substance kits with deep integration into the electronic health record and pharmacy systems is associated with a decrease in management errors.
机译:背景:围手术期受控物质转移和跟踪已收到全部监管重点。作者的机构制定并实施了一种自动化的基于网络的软件应用,可用于围手术期控制物质管理。作者假设这种系统的实施减少了缺失受控物质药物,缺失受控物质试剂盒(多种受控物质药物包装)测量的误差,以及在套件返回期间缺少见证签名。方法:2014年12月1日至2017年3月31日,作者在一所大学医院的预体检,实施和研究期间,作者获得了受控物质药物,受控物质套件和证人返回签名数据。此前和之后的研究是基于作者机构的QI项目。作者包括所有需要麻醉服务的案例。本研究的主要结果是缺失受控物质药物的速度。二次结果包括套件的税率,而没有返回药房,缺失套件返回证人签名。结果:在挽救期间有54,302例,实施期间57,670例,研究期间65,911例。受控物质药物的数量(差异为0.7每1,000例; 95%CI,0.38-1.02; P <0.001)和套件返回误差(差异为0.45,每1,000例; 95%CI,0.24-0.66,P <0.001)下降实施申请后。缺失证人返回签名的数量没有差异(每1000例差异为0.09例; 95%CI,-0.08至0.26,P = 0.350)。用户调查,共有206名485(42%)响应率显示,提供者认为新申请管理的受管物质比以前的系统更好。结论:一种跟踪具有深度集成到电子健康记录和药房系统的围手术期控制物质套件的软件应用与管理误差的减少有关。

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  • 来源
    《Anesthesiology》 |2019年第6期|共12页
  • 作者单位

    Univ Michigan Dept Anesthesiol 1H247 UH SPC 5048 1500 East Med Ctr Dr Ann Arbor MI 48109 USA;

    Univ Michigan Dept Anesthesiol 1H247 UH SPC 5048 1500 East Med Ctr Dr Ann Arbor MI 48109 USA;

    Univ Michigan Dept Anesthesiol 1H247 UH SPC 5048 1500 East Med Ctr Dr Ann Arbor MI 48109 USA;

    Univ Michigan Dept Anesthesiol 1H247 UH SPC 5048 1500 East Med Ctr Dr Ann Arbor MI 48109 USA;

    Univ Michigan Dept Anesthesiol 1H247 UH SPC 5048 1500 East Med Ctr Dr Ann Arbor MI 48109 USA;

    Univ Michigan Dept Anesthesiol 1H247 UH SPC 5048 1500 East Med Ctr Dr Ann Arbor MI 48109 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 麻醉学;
  • 关键词

  • 入库时间 2022-08-20 01:00:57

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