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The Beckman Coulter® DXH900 uses the impedance method to measure the total leukocytes count. In presence of platelet aggregates, the device identifies the structural changes and associates an alarm with the leukocytes result. The aim of this study was to evaluate the influence of platelet aggregates using the principle of flow cytometry as a second assessment of the white blood cell count. Total leukocytes count was evaluated in 49 specimens with presence of platelet aggregates and 32 without anomaly. The differences between total leukocyte count by the two automatic methods (impedance and flow cytometry) and the microscopic method were compared. Without platelet aggregates, the median values were 5.6 (microscopic cell count), 5.4 (impedance) and 5.4 (flow cytometry) and no discordance was observed. In presence of platelet aggregates, the median values were 5.6, 6.4 and 5.1 respectively. The graphical analysis with the allowable total error range of ± 25.7% showed substantial analytical discrepancies (15/49) using impedance method while the flow cytometry method revealed minor disagreements (3/49). Analytical discordances versus WBC reference ranges showed 88% agreement and a substantial Kappa coefficient of 0.70 by impedance, while the flow cytometry method had 94% agreement and a perfect Kappa coefficient of 0.83. The formation of platelet aggregates increased the total leukocyte count performed DXH900 impedance method. Our study has shown that DXH 900 flow cytometry method may be an alternative to exclude the presence of pseudoleukocytosis. In case flags are generated, the microscopic method may be needed for the confirmation of WBC count. [ABSTRACT FROM AUTHOR]

Platelet clumps present in anticoagulant specimens may generate a falsely decreased platelet count and lead to an incorrect diagnosis. A clear understanding of the ability of a haematology analyser (HA) to detect platelet clumps is important for routine work in the clinical laboratory. Citrate-anticoagulated whole-blood samples were collected from various patients as a negative group. Adenosine diphosphate (ADP)-induced platelet aggregation was performed on those negative samples to mimic platelet-clump-containing (positive) samples. The 'platelet clumps' and 'platelet abnormal' flags generated by the Sysmex XN-10 instrument were used to assess the flagging performance of this HA and demonstrate its flagging features. The complete blood count (CBC) results of paired negative and positive samples were compared to evaluate the impact of platelet clumps on the CBC parameters. A total of 187 samples were eligible for this study. The total accuracy, sensitivity, and specificity of the platelet clumps flag were 0.786, 0.626, and 0.947, respectively. The total accuracy, sensitivity, and specificity of the platelet abnormal flag were 0.631, 0.348, and 0.914, respectively. A separate assessment focusing on the positive samples with low platelet counts showed that the total sensitivities of the platelet clumps and platelet abnormal flags were 0.801 and 1.000, respectively. Platelet clumps may interfere with the leukocyte count and with platelet and erythrocyte indices. Platelet clumps can influence not only platelet indices but also leukocyte and erythrocyte counts. The Sysmex XN-10 instrument is sensitive to positive samples with low platelet counts but insensitive to those with high platelet counts. [ABSTRACT FROM AUTHOR]

The article presents a letter to the editor in response to a study which compared the performance of the low platelet count by two detection methods, the impedance method and the optical method, between a novel hematological analyzer Mindray and the used Sysmex XE-2100 analyzer.