Pierre R V
Blood Cells. 1985;11(1):11-23.
The clinical use of the proposed performance standards for differential leukocyte counts is determined by multiple factors. Their use must be considered according to the specific use of the differential count, the sources of variability in differential counting, the relation between specific use and sources of variability, the role of analytic errors in the detection of nonspecific changes, the use of qualitative vs quantitative data, the sensitivity and specificity of the routine eye count, the role of disease or specific cell prevalence in determination of predictive value, the effect on use of automated instruments for screening, and whether abnormal specimen flagging can be done. The routine eye-count differential method, as performed by a well-trained technologist or technician, seems to lack both sensitivity and specificity. Because of the magnitude of technique- and method-related and biologic sources of variability, the 100- or 200-cell eye-count differential method is not a good screening method for detection of hematologic illnesses, particularly those that are uncommon. The automated differential leukocyte instruments address many of the technique- and method-related errors and are thus able to equal or exceed the performance of the routine eye-count differential method.
所提议的白细胞分类计数性能标准的临床应用由多种因素决定。其使用必须根据白细胞分类计数的具体用途、分类计数中的变异性来源、具体用途与变异性来源之间的关系、分析误差在非特异性变化检测中的作用、定性与定量数据的使用、常规人工计数的敏感性和特异性、疾病或特定细胞患病率在预测值确定中的作用、对使用自动化仪器进行筛查的影响以及是否可以进行异常标本标记来考虑。由训练有素的技术专家或技术人员执行的常规人工分类计数方法似乎缺乏敏感性和特异性。由于技术和方法相关以及生物学变异性来源的程度,100 或 200 个细胞的人工分类计数方法不是检测血液疾病,特别是那些罕见疾病的良好筛查方法。自动化白细胞分类仪器解决了许多技术和方法相关的误差,因此能够达到或超过常规人工分类计数方法的性能。