A67 REDUCING INAPPROPRIATE GAMMA-GLUTAMYL TRANSFERASE TESTING FOR INPATIENTS: A QUALITY IMPROVEMENT INITIATIVE IN LAB WASTE REDUCTION APPLYING THE MODEL FOR CONTINUOUS IMPROVEMENT

T. Afzaal, R. AlRamdan, H. Bualbanat, N. C. Howarth, G. Malhi, D. Hudson, I. ChinYee, A. Teriaky
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Abstract

Abstract Background Review of the literature identifies a rising trend in laboratory testing, with over 30% of tests estimated to be inappropriately repeated. Laboratory overutilization increases healthcare costs, and can lead to overdiagnosis, overtreatment and negative health outcomes. Indications for repeat Gamma Glutamyl Transferase (GGT) testing in adults are limited, particularly repeat testing within the same admission. Aims Our aim was to reduce the inappropriate ordering of repeat GGT testing by 25% for all inpatients at the London Health Sciences Centre (LHSC) over a one-year study period. Methods An interprofessional team was created to help engage relevant stakeholders, collect baseline data and reassess the indications for GGT testing. A combination of root cause analysis tools, specifically the Ishikawa diagram and Pareto chart, were employed to identify potential factors contributing to the overutilization of GGT testing. After prioritizing potential solutions, intervention bundles were developed, and Plan-Do-Study-Act (PDSA) cycles were created to target correctable factors. In PDSA cycle #1, the process started by eliminating GGT as a laboratory testing option in the three most commonly used admission order care sets. Considering the hierarchy of intervention effectiveness, PDSA cycle #2 involved implementing a computerized Clinical Decision Support (CDS) system to restrict the reordering of GGT tests within 72 hours of the same admission. Results Baseline data showed that in 2022, a total of 62,542 GGT tests were ordered, with an average of approximately 5,200 GGT tests ordered per month. Of these, 16.4% were ordered through the top 3 most prevalent admission order care sets, and around 25% of all GGT tests were repeats within 72 hours of admission. Referring to Figure 1, PDSA cycle #1 yielded no significant reduction in GGT testing. PDSA cycle #2 successfully reduced the proportion of repeat GGT tests ordered by 12% within two months of implementation, leading to an estimated annualized cost savings of approximately $37,440. Conclusions Our results establish the effectiveness of CDS systems in reducing laboratory testing overutilization, suggesting their superiority to individual care set targeting interventions, and emphasize the potential for cost-effective CDS development in contemporary healthcare. Funding Agencies None
A67 减少住院病人不适当的γ-谷氨酰转移酶检测:应用持续改进模式减少实验室浪费的质量改进举措
摘要 背景 文献综述发现,实验室检测呈上升趋势,估计有超过 30% 的检测项目被不适当地重复使用。实验室过度使用增加了医疗成本,并可能导致过度诊断、过度治疗和不良健康后果。成人γ-谷氨酰转肽酶(GGT)重复检测的指征有限,尤其是在同一入院时间内重复检测。目的 我们的目标是在为期一年的研究期间,将伦敦健康科学中心(LHSC)所有住院病人重复伽马谷氨酰转肽酶检测的不当指令减少 25%。方法 我们成立了一个跨专业团队,帮助相关利益方参与进来,收集基线数据并重新评估 GGT 检测的适应症。研究人员采用了多种原因分析工具,特别是石川图表和帕累托图表,以确定导致 GGT 检测使用率过高的潜在因素。在对潜在的解决方案进行优先排序后,制定了干预措施捆绑包,并创建了 "计划-实施-研究-行动"(PDSA)循环,以针对可纠正的因素。在 PDSA 循环 #1 中,首先在三个最常用的入院医嘱中取消了 GGT 作为实验室检测选项。考虑到干预效果的层次性,PDSA 循环 #2 涉及实施计算机化的临床决策支持(CDS)系统,以限制在同一入院 72 小时内重新开具 GGT 检测单。结果 基线数据显示,2022 年共订购了 62,542 次 GGT 检测,平均每月订购约 5,200 次 GGT 检测。其中,16.4% 的 GGT 检测是通过前 3 个最常见的入院医嘱护理组下达的,约 25% 的 GGT 检测是在入院 72 小时内重复进行的。参照图 1,PDSA 循环 #1 没有显著减少 GGT 检测。PDSA 循环 #2 在实施后的两个月内成功地将重复 GGT 检测的比例降低了 12%,估计每年可节约成本约 37,440 美元。结论 我们的研究结果证实了 CDS 系统在减少实验室检测过度使用方面的有效性,表明其优于针对个人护理的干预措施,并强调了在当代医疗保健领域开发具有成本效益的 CDS 的潜力。资助机构 无
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