Effective stewardship strategies to enhance appropriateness of refer-out test requests in a Canadian tertiary centre laboratory

IF 2.5 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinical biochemistry Pub Date : 2024-06-08 DOI:10.1016/j.clinbiochem.2024.110777
Amy Lou, Andrea Thoni, Nafisa Shandi, Zhifeng Yang, Bassam A. Nassar, Manal Elnenaei
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Abstract

Objectives

Specialized testing conducted in reference laboratories is costly and often not optimally directed. Since 2016, our institution has worked to ensure the appropriateness of refer-out (RO) tests. We examine the impact of utilization initiatives on the patterns of requests and completed tests.

Design and methods

In 2016, 81 RO tests were selected for a more rigorous approval process. Physicians not pre-approved for testing received a prompt to consult with laboratory subject matter experts (SMEs) for further detail. After review, SMEs provided responses, approving or rejecting requests based on clinical relevance. Stewardship activities also included: repatriating tests locally, preferring Canadian over foreign institutions, unbundling tests, distributing educational memos, and introducing staged testing. We collected data on the number of requested (NoR) and number of completed (NoC) tests in 2015, before the implementation of the new vetting procedures, and for the post-implementation phase from 2016−2022.

Results

For 62 targeted RO tests (including trace metals, vitamins, antibodies, and endocrine-related tests), there was a 33% reduction in NoR and a 51% reduction in NoC in 2022 compared to 2015. The total savings for the study period based on NoC was $807,736. The NoC rate for Neuronal antibody tests decreased to 48.6% in 2022, with cost savings of $17,123, and an additional $50,000 saved by changing the testing site. Insourcing apolipoprotein B and fecal calprotectin tests resulted in cost savings of $3,380 and $3,371, respectively, in 2022.

Conclusions

Automated messaging followed by a formal review of RO test requests is an effective utilization strategy that prevents redundant or clinically unjustified testing. This approach leads to significant economic savings and is expected to improve the efficiency of patient care.

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加拿大一家三级中心实验室提高转出检验申请适当性的有效管理策略。
目标:参考实验室进行的专业化检测成本高昂,而且往往不能得到最佳指导。自 2016 年以来,我院一直致力于确保转出(RO)检验的适当性。我们研究了利用举措对申请和完成检验模式的影响:2016 年,我们选择了 81 项转诊检验进行更严格的审批。未预先批准检测的医生收到了向实验室主题专家(SMEs)咨询进一步细节的提示。经审查后,SME 做出答复,根据临床相关性批准或拒绝申请。管理活动还包括:将检验项目运回本地、优先选择加拿大机构而非外国机构、拆分检验项目、分发教育备忘录以及引入分阶段检验。我们收集了 2015 年(新审核程序实施前)和 2016-2022 年(实施后阶段)申请的检测数量(NoR)和完成的检测数量(NoC)的数据:对于 62 项目标 RO 检测(包括微量金属、维生素、抗体和内分泌相关检测),与 2015 年相比,2022 年的 NoR 减少了 33%,NoC 减少了 51%。根据 NoC,研究期间共节省 807,736 美元。2022 年,神经元抗体检测的 NoC 率降至 48.6%,节约成本 17 123 美元,通过更换检测地点还可额外节约 50 000 美元。通过内包载脂蛋白 B 和粪便钙蛋白检测,2022 年分别节约成本 3,380 美元和 3,371 美元:自动发送信息,然后对 RO 检验申请进行正式审查,是一种有效的利用策略,可防止重复检验或临床上不合理的检验。这种方法可节省大量经济成本,并有望提高病人护理的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical biochemistry
Clinical biochemistry 医学-医学实验技术
CiteScore
5.10
自引率
0.00%
发文量
151
审稿时长
25 days
期刊介绍: Clinical Biochemistry publishes articles relating to clinical chemistry, molecular biology and genetics, therapeutic drug monitoring and toxicology, laboratory immunology and laboratory medicine in general, with the focus on analytical and clinical investigation of laboratory tests in humans used for diagnosis, prognosis, treatment and therapy, and monitoring of disease.
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