急诊科的人为因素与质量改进:减少采血的潜在错误。

O. Bashkin, Sigalit Caspi, Assaf Swissa, Amitai Amedi, Shai Zornano, R. Stalnikowicz
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引用次数: 2

摘要

目的:血液采集过程中的不良事件,如不匹配或未标记的样本,可能对患者安全产生重大影响(如错误的诊断和治疗)。目前的研究检查了急诊科在应用人为因素方法提高表现质量和预防不良事件之前和之后的采血程序。方法对某社区护理医院急诊科190例采血事件进行分析,分为干预前和干预后2个阶段。对两项质量措施进行如下测试:质量措施1,根据方案执行采血程序的所有7个阶段;质量措施2,根据方案按正确顺序执行采血程序的各个阶段。此外,医务人员匿名回答了关于他们采血程序的问卷。结果对干预前收集的数据进行分析后发现,只有2例患者的手术方案中7个阶段全部完成,只有1例患者的7个阶段按正确顺序完成。在91%的事件中,患者没有被完全识别。基于这些发现,我们开发了一种使用人为因素方法的干预措施来提高表现质量。干预后收集的数据分析显示,干预开始前(mean [SD], 4.8[0.6])和干预开始后(mean [SD], 6.4[0.8])的质量测量1有显著差异(t188 = -14.9, ρ < 0.01),这意味着干预实施后效率有所提高。质量测量2也有所改善。结论本研究阐明了采血效能中潜在错误的性质,为提高采血效能的正确率提供了积极的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human Factors and Quality Improvement in the Emergency Department: Reducing Potential Errors in Blood Collection.
OBJECTIVES Adverse events in blood collection procedures such as mismatched or unlabeled samples may have critical implications on patient safety (such as wrong diagnosis and treatments). The current study examined blood collection procedures in an emergency department before and after the application of a human factors approach for improving performance quality and preventing adverse events. METHODS In the emergency department of a community care hospital, 190 blood collection events were observed in 2 phases: preintervention and postintervention. Two quality measures were tested as follows: quality measure 1, performing all 7 stages in the procedure of blood collection according to protocol, and quality measure 2, performing the stages of the procedure in the correct sequence according to the protocol. In addition, medical staff anonymously answered questionnaires about their procedure for collecting blood. RESULTS Analyses of data collected before the intervention revealed only 2 events in which all 7 stages in the protocol of the procedure were performed and only 1 event in which the 7 stages of the procedure were performed in the correct sequence. In 91% of the events, the patient was not fully identified. Based on these findings, we developed an intervention using a human factors approach to improve the quality of performance. Analyses of data collected after the intervention revealed significant differences (t188 = -14.9, ρ < 0.01) in quality measure 1 before (mean [SD], 4.8 [0.6]) and after (mean [SD], 6.4 [0.8]) the intervention was initiated, which implies improvement on efficiency subsequent to the implementation of the intervention. Improvement also appeared in quality measure 2. CONCLUSIONS This study illustrates the nature of potential errors in blood collection performance, offering a proactive approach to improve the rate of proper performance.
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