Meyer-Massetti Carla, Cheng Christine M, Schwappach David L B, Paulsen Lynn, Ide Brigid, Meier Christoph R, Guglielmo B Joseph
Swiss Patient Safety Foundation, Zurich, Switzerland.
Am J Health Syst Pharm. 2011 Feb 1;68(3):227-40. doi: 10.2146/ajhp100019.
The accuracy, efficiency, and efficacy of four commonly recommended medication safety assessment methodologies were systematically reviewed.
Medical literature databases were systematically searched for any comparative study conducted between January 2000 and October 2009 in which at least two of the four methodologies-incident report review, direct observation, chart review, and trigger tool-were compared with one another. Any study that compared two or more methodologies for quantitative accuracy (adequacy of the assessment of medication errors and adverse drug events) efficiency (effort and cost), and efficacy and that provided numerical data was included in the analysis.
Twenty-eight studies were included in this review. Of these, 22 compared two of the methodologies, and 6 compared three methods. Direct observation identified the greatest number of reports of drug-related problems (DRPs), while incident report review identified the fewest. However, incident report review generally showed a higher specificity compared to the other methods and most effectively captured severe DRPs. In contrast, the sensitivity of incident report review was lower when compared with trigger tool. While trigger tool was the least labor-intensive of the four methodologies, incident report review appeared to be the least expensive, but only when linked with concomitant automated reporting systems and targeted follow-up.
All four medication safety assessment techniques-incident report review, chart review, direct observation, and trigger tool-have different strengths and weaknesses. Overlap between different methods in identifying DRPs is minimal. While trigger tool appeared to be the most effective and labor-efficient method, incident report review best identified high-severity DRPs.
对四种常用的药物安全评估方法的准确性、效率和效能进行系统评价。
系统检索医学文献数据库,查找2000年1月至2009年10月期间进行的任何比较研究,其中四种方法中的至少两种——事件报告审查、直接观察、病历审查和触发工具——相互进行了比较。任何比较两种或更多方法在定量准确性(药物错误和药物不良事件评估的充分性)、效率(工作量和成本)以及效能方面的研究,并提供了数值数据的研究都纳入了分析。
本综述纳入了28项研究。其中,22项比较了两种方法,6项比较了三种方法。直接观察发现的药物相关问题(DRP)报告数量最多,而事件报告审查发现的最少。然而,与其他方法相比,事件报告审查通常显示出更高的特异性,并且最有效地捕捉到严重的DRP。相比之下,与触发工具相比,事件报告审查的敏感性较低。虽然触发工具是四种方法中劳动强度最小的,但事件报告审查似乎是成本最低的,但只有在与伴随的自动报告系统和有针对性的随访相结合时才是如此。
所有四种药物安全评估技术——事件报告审查、病历审查、直接观察和触发工具——都有不同的优点和缺点。不同方法在识别DRP方面的重叠最小。虽然触发工具似乎是最有效和劳动效率最高的方法,但事件报告审查最能识别高严重性的DRP。