Cox C J, Habermann T M, Payne B A, Klee G G, Pierre R V
Am J Clin Pathol. 1985 Sep;84(3):297-306. doi: 10.1093/ajcp/84.3.297.
Evaluation of linearity, carry-over, precision, and accuracy of a Coulter Counter model S-Plus IV prototype showed that they meet the manufacturer's specifications. The instrument also was compared with an earlier model. Correlations of the lymphocyte and granulocyte values in the three-part differential count with manual eye-count and a Technicon Hemalog D90 results were very close to the correlation of eye-count to Hemalog D90 results. The percentage of mononuclear cells showed acceptable correlation to the manual eye-count when monocytes were combined with blasts, eosinophils, and basophils. The medical effectiveness of the three-part differential was determined by comparison with manual eye-counts in 1,084 samples. The false positive and false negative values were 7.38% and 7.84%, respectively. The instrument has acceptable limits of operation. When combined with analysis of histograms by trained personnel, the three-part differential count is capable of screening for abnormalities that require further analysis.
对库尔特S-Plus IV型血细胞计数仪原型机的线性、携带污染、精密度和准确度进行评估,结果表明其符合制造商的规格要求。该仪器还与早期型号进行了比较。三分群白细胞分类计数中淋巴细胞和粒细胞值与人工镜检计数以及Technicon Hemalog D90结果的相关性,与人工镜检计数和Hemalog D90结果之间的相关性非常接近。当单核细胞与原始细胞、嗜酸性粒细胞和嗜碱性粒细胞合并时,单核细胞百分比与人工镜检计数显示出可接受的相关性。通过与1084份样本的人工镜检计数比较,确定了三分群白细胞分类计数的医学有效性。假阳性和假阴性值分别为7.38%和7.84%。该仪器具有可接受的操作限度。当由经过培训的人员结合直方图分析时,三分群白细胞分类计数能够筛查出需要进一步分析的异常情况。