A multinational interlaboratory task force explored the important variables of platelet reference counting and developed a candidate flow cytometric reference method based on the RBC/platelet ratio. A multicenter comparison was performed to determine whether the method met the necessary criteria and was precise enough to be recommended as a new reference method. Each laboratory analyzed serial dilutions of normal specimens, stabilized material, and at least 60 patient specimens with a range of platelet counts from 1 to 400 × 103/μ (1-400 × 109/L). Pooled analysis of the serial dilutions showed that RBC-platelet and RBC-RBC coincidence events became negligible at sufficiently high dilutions (ie, > 1:1,000). All laboratories demonstrated excellent intra-assay and acceptable interlaboratory precision. Two antibodies (CD61 and CD41) were used for identifying platelets and individually gave acceptable results, but in a minority of samples, staining differences were observed. The optimum method thus uses a double-labeling procedure with a final dilution factor of 1:1,000. The study demonstrated that this method meets the criteria for a reference platelet count.
CITATION STYLE
Harrison, P., Ault, K. A., Chapman, S., Charie, L., Davis, B., Fujimoto, K., … Van Assendelft, O. W. (2001). An Interlaboratory Study of a Candidate Reference Method for Platelet Counting. American Journal of Clinical Pathology, 115(3), 448–459. https://doi.org/10.1309/91PR-E4G6-XBAF-N8DY
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