Establishing Referral Laboratory Testing Governance and Addressing "Miscellaneous" Test Orders across an Academic Health System.

IF 1.8 Q3 MEDICAL LABORATORY TECHNOLOGY
Allison B Chambliss, Joshua L Deignan, Charlemagne Isip, Monique Trinh, William Werre, Alyssa Ziman
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引用次数: 0

Abstract

Background: Referral (send-out) laboratories support clinical needs but may cause issues for hospitals or health systems related to regulations and governance, specimen logistics, test result availability, and cost and reimbursement. The use of a "miscellaneous" referral test order can increase risks of specimen collection or processing errors, result delays, and repeat testing.

Methods: We established an approved referral laboratory test list and a digital form for providers to request new referral tests. We collated laboratory stewardship committee decisions over a 20-month period. Separately, we retrospectively reviewed referral tests ordered as miscellaneous across our health system over 1 year. Subject matter experts identified appropriate tests to build as discretely orderable in the electronic health record. Following targeted provider notification of the new tests, we assessed their uptake and impact on result turnaround times for the first 5 built tests over 6 months.

Results: Our laboratory stewardship committee approved 16 of 27 provider requests to build new referral tests over the first 20 months following implementation of the new request process. In addition, 37 of the 100 most frequently ordered miscellaneous tests were recommended to be built as discrete orders. Uptake of the first 5 built tests (relative to providers continuing to use miscellaneous orders) averaged 64% over the first 6 months. Result turnaround times improved by an average of 1.1 days when the discrete orders were used.

Conclusions: We successfully established oversight of referral laboratory testing across our health system, pivoted orders away from miscellaneous, and observed improvements in turnaround times.

建立转诊实验室测试治理和解决跨学术卫生系统的“杂项”测试命令。
背景:转诊(送出)实验室支持临床需求,但可能给医院或卫生系统带来与法规和治理、标本物流、检测结果可用性以及成本和报销相关的问题。使用“杂项”转诊检测命令会增加标本采集或处理错误、结果延迟和重复检测的风险。方法:我们建立了一份经批准的转诊实验室检测清单和一份数字表格,供提供者申请新的转诊检测。我们在20个月的时间里整理了实验室管理委员会的决定。另外,我们回顾性地审查了1年来在我们的卫生系统中订购的杂项转诊检查。主题专家确定了在电子健康记录中建立可离散订购的适当测试。在有针对性的提供商通知新测试之后,我们评估了它们在6个月内对前5个构建测试的结果周转时间的吸收情况和影响。结果:在实施新的请求流程后的头20个月内,我们的实验室管理委员会批准了27个供应商建立新的转诊检测的请求中的16个。此外,在100个最常订购的杂项测试中,建议将37个作为离散订单建造。前6个月,前5个构建测试(相对于继续使用杂项订单的提供商)的平均使用率为64%。结果周转时间提高了平均1.1天,当离散的订单被使用。结论:我们成功地在整个卫生系统中建立了对转诊实验室检测的监督,减少了繁杂的订单,并观察到周转时间的改善。
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来源期刊
Journal of Applied Laboratory Medicine
Journal of Applied Laboratory Medicine MEDICAL LABORATORY TECHNOLOGY-
CiteScore
3.70
自引率
5.00%
发文量
137
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