Division of Anatomic Pathology, Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Science Center, Toronto, ON, M4N 3M5, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
Virchows Arch. 2024 May;484(5):743-751. doi: 10.1007/s00428-023-03611-9. Epub 2023 Aug 7.
Pre-analytical deficiencies (PADs) are a major source of errors in anatomical pathology, accounting for about 70% of laboratory deficiencies. These can lead to incorrect diagnoses, delayed treatments, and increased healthcare costs. As part of a quality improvement initiative, we retrospectively identified and characterized 237 PADs documented over a 1-year period in a tertiary care academic center. The most common PADs were errors in specimen procurement (56%), handling of samples within the lab (16%), accessioning (10%), incomplete requisitions (9%), and transportation-related issues (7%). Strategies were then devised to mitigate these errors. Categorization of pre- and intra-laboratory PADs was refined into eight categories (collection, requisition, specimen container, transportation, receiving, accessioning, preparation, and communications) in the laboratory information system. Mandatory PAD documentation was implemented for accessioning staff. Post-implementation, prospective analysis identified that the most common PADs were related to surgical requisitions (75%). Among these, missing ordering physician's signature was the most common, accounting for 67.7% of requisition-related PADs and 50.8% of all PADs. Other common PADs included incomplete information of specimens, clinical information, patient information, physician information, source location, collection time, incorrect requisition forms, and illegible handwritten information. This study highlights the importance of identifying and addressing PADs in the anatomical pathology laboratory setting as well as the potential benefits of implementing standardized documentation and quality improvement processes to address these deficiencies.
分析前缺陷(PADs)是解剖病理学中误差的主要来源,约占实验室缺陷的 70%。这些缺陷可能导致错误诊断、治疗延误和增加医疗保健成本。作为质量改进计划的一部分,我们回顾性地确定并描述了在一个三级护理学术中心的 1 年期间记录的 237 个 PAD。最常见的 PAD 是标本获取(56%)、实验室样本处理(16%)、标本登记(10%)、不完整的医嘱(9%)和与运输相关的问题(7%)。然后制定了策略来减少这些错误。在实验室信息系统中,将分析前和实验室内 PAD 分类细化为八个类别(采集、医嘱、标本容器、运输、接收、登记、准备和沟通)。对登记人员实施了 PAD 强制性记录。实施后,前瞻性分析确定最常见的 PAD 与手术医嘱有关(75%)。在这些 PAD 中,缺失开单医生签名是最常见的,占医嘱相关 PAD 的 67.7%,占所有 PAD 的 50.8%。其他常见的 PAD 包括标本、临床信息、患者信息、医生信息、来源位置、采集时间、不正确的医嘱单、手写信息不清晰等信息不完整。本研究强调了在解剖病理学实验室环境中识别和解决 PAD 的重要性,以及实施标准化文档和质量改进流程以解决这些缺陷的潜在益处。