在供应商编程的液体处理机上出现偷偷摸摸的移液错误

IF 3.1 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Kelly Britt-Rodriquez , Jamie Daniel , Joshua Hayden
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引用次数: 0

摘要

液体处理仪(LH)已成为临床和学术实验室制备和处理样本的常用设备。从理论上讲,由于消除了误吸误操作,这些系统有可能减少误差。但实际上,这些系统仍然存在误吸的可能性,需要最终用户仔细验证。在本案例报告中,我们描述了两个观察到的由供应商编程的 LH 错误移液的实例。在这两个案例中,从 LH 中获得的工作清单都未能反映出实际的移液情况,因此这些情况都是重大的险情,极有可能对患者造成伤害。实验室在对 LH 进行验证研究时都没有发现这些情况。实验室应意识到 LH 误吸的可能性。LH 供应商应努力确保工作清单能反映出所移取的内容(而不是本应移取的内容),而最终用户则必须确保进行稳健的验证研究,尽可能多地考虑到 "真实世界 "的各种情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surreptitious pipetting errors on a vendor-programmed liquid handler

Liquid handlers (LHs) have become common in both clinical and academic laboratories for the preparation and manipulation of samples. In theory, these systems offer the potential for reduced error due to the elimination of mis-pipetting errors. In reality, these systems still have potential for mis-pipetting and require careful validation by the end user. In this case report, we describe two instances where inappropriate pipetting by a vendor-programmed LH were observed. In each case, the worklist that was obtained from the LH failed to reflect what had actually been pipetted and as such these instances represented significant near misses with substantial potential for patient harm. Neither of these instances were caught during the laboratory’s validation studies of the LH. Laboratories should be aware of the potential for mis-pipetting by LHs. LH vendors should work to ensure the worklists reflect what was pipetted (instead of what was intended to be pipetted) and end users must ensure robust validation studies that take into account as many “real world” scenarios as possible.

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来源期刊
Journal of Mass Spectrometry and Advances in the Clinical Lab
Journal of Mass Spectrometry and Advances in the Clinical Lab Health Professions-Medical Laboratory Technology
CiteScore
4.30
自引率
18.20%
发文量
41
审稿时长
81 days
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