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库尔特三分群血细胞分析仪的评估

Evaluation of the Coulter three-part differential screen.

作者信息

Ross D W, Watson J S, Davis P H, Tracy S L

出版信息

Am J Clin Pathol. 1985 Oct;84(4):481-4. doi: 10.1093/ajcp/84.4.481.

Abstract

An evaluation of the Coulter Electronics, Inc. (Hialeah, FL) three-part differential screen (3PD) was undertaken to determine the performance characteristics of this system. The 3PD measures white blood cell (WBC) volumes and, by automatic analysis of the resultant WBC histogram, produces a determination of the number and percent of lymphocytes, mononuclear cells, and granulocytes. A group of 984 random patient blood samples was tested. The overall review rate (samples requiring some further analysis or review) was 42%. The main source of false negatives on the 3PD was eosinophilia: 5 out of 22 instances of eosinophilia greater than 750/microL were not flagged. The precision of the three parameters, measured as percent coefficient of variation, was 3.3% for lymphocytes, 14.2% for mononuclear cells, 3.1% for granulocytes, and 2.4% for the total WBC. The stability of blood samples was acceptable for up to eight hours at room temperature (less at 4 degrees C).

摘要

对库尔特电子公司(位于佛罗里达州希亚莱)的三分群血细胞分析仪(3PD)进行了评估,以确定该系统的性能特征。3PD可测量白细胞(WBC)体积,并通过对所得WBC直方图进行自动分析,确定淋巴细胞、单核细胞和粒细胞的数量及百分比。对984份随机患者血样进行了检测。总体复查率(需要进一步分析或复查的样本)为42%。3PD假阴性的主要来源是嗜酸性粒细胞增多:在22例嗜酸性粒细胞计数大于750/微升的病例中,有5例未被标记。以变异系数百分比衡量的三个参数的精密度分别为:淋巴细胞3.3%,单核细胞14.2%,粒细胞3.1%,白细胞总数2.4%。血样在室温下长达8小时的稳定性是可接受的(在4摄氏度时稳定性稍差)。

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