Hematology laboratory, University Hospital Pontchaillou, Rennes, France.
Cytometry A. 2010 Jun;77(6):552-63. doi: 10.1002/cyto.a.20893.
A Complete Blood Count performed by an automated hematology analyzer frequently needs a microscopic slide review. This step is time consuming and requires experienced personnel. Recently, several teams have proposed and validated convenient combinations of monoclonal antibodies for an extended white blood cell (WBC) differential by flow cytometry. The aim of this study was to evaluate the usefulness of this approach in the routine workflow of a hematology laboratory. We compared a workflow chain comprised of a robotic blood preparation system (for antibody labeling), a flow cytometer, and data management software to the standard manual review of a blood film and evaluated the diagnostic quality, the turnaround time, and the labor needed for the two different approaches. The study on 1,973 samples was organized, firstly, to determine analytic thresholds and these settings were then validated. The flow cytometric data management software automatically validated 52% of the samples without significant numbers of false negatives. Of the remaining specimens, an operator validated a further 33% of the samples and 15% needed a manual microscopic review. These results were obtained in a mean timeline similar to the traditional microscopic manual review. Our study demonstrates, for the first time, the efficiency of a flow cytometer integrated into a WBC differential workflow in a routine hematology laboratory.
自动化血液分析仪进行全血细胞计数(CBC)后通常需要进行显微镜镜检。这一步骤耗时且需要经验丰富的人员。最近,有几个团队已经提出并验证了通过流式细胞术进行扩展的白细胞(WBC)分类的方便的单克隆抗体组合。本研究旨在评估这种方法在常规血液学实验室工作流程中的实用性。我们将由机器人血液制备系统(用于抗体标记)、流式细胞仪和数据管理软件组成的工作流程链与血液涂片的标准手动检查进行了比较,并评估了两种不同方法的诊断质量、周转时间和所需的劳动力。该研究对 1973 个样本进行了组织,首先确定了分析阈值,然后对这些设置进行了验证。流式细胞术数据管理软件自动验证了 52%的样本,没有明显数量的假阴性。在其余的标本中,操作人员进一步验证了 33%的样本,15%的样本需要进行手动显微镜检查。这些结果是在与传统的显微镜手动检查相似的平均时间线上获得的。我们的研究首次证明了流式细胞仪集成到常规血液学实验室的 WBC 分类工作流程中的效率。