Tillati Silvia, Pati Ilaria, Delle Donne Michela, Meneghel Alessandra, Londero Donatella, De Angelis Vincenzo
Unit of Medical Statistics, Department of Clinical and Experimental Medicine, University of Pisa, 56121 Pisa, Italy.
National Blood Centre, Italian National Institute of Health, 00161 Rome, Italy.
Diagnostics (Basel). 2022 Oct 25;12(11):2586. doi: 10.3390/diagnostics12112586.
Background: Eligibility criteria for blood donation require hemoglobin levels of ≥12.5 g/dL for women and ≥13.5 g/dL for men, and a platelet count of ≥180 × 109/L. Screening methods before donation should ensure high accuracy, precision, and ease in operation. We assessed the performance, precision, and repeatability of the Horiba Micros ES 60 (Horiba) compared to the Beckman Coulter DXH 800. Methods: Performance was compared by testing samples for each of the 11 devices across 6 sites in the Transfusion Service of Friuli Venezia Giulia Region, Italy. We measured precision by calculating the coefficient of variation (CV), concordance with ρ-Pearson’s correlation coefficient, and accuracy with F-tests. The intra-assay agreement was examined in the 11 devices, and repeatability was performed by using CV and the Kruskal−Wallis test. Results: The precision of Horiba was acceptable. Overall, ρ-Pearson’s coefficients indicated a strong correlation and positive relationship between all variables. The Bland−Altman plots showed that most of the differences lay within the limits of agreement. All CV were below the reference threshold for all the parameters. Finally, the Kruskal−Wallis test reported non-significant statistical differences for all parameters, except platelet count (p < 0.000). Conclusions: Horiba is adequate for routine pre-donation screening. The intra-assay agreement further demonstrates the accuracy of the device.
献血的资格标准要求女性血红蛋白水平≥12.5 g/dL,男性≥13.5 g/dL,血小板计数≥180×10⁹/L。献血前的筛查方法应确保高准确性、精密度和操作简便性。我们将堀场Micros ES 60(Horiba)与贝克曼库尔特DXH 800进行了比较,评估了其性能、精密度和可重复性。方法:通过在意大利弗留利-威尼斯朱利亚地区输血服务中心的6个地点对11台设备的样本进行检测来比较性能。我们通过计算变异系数(CV)、与ρ-皮尔逊相关系数的一致性以及F检验的准确性来测量精密度。在11台设备中检查批内一致性,并使用CV和克鲁斯卡尔-沃利斯检验进行可重复性测试。结果:Horiba的精密度是可接受的。总体而言,ρ-皮尔逊系数表明所有变量之间存在强相关性和正相关关系。布兰德-奥特曼图显示,大多数差异在一致性限度内。所有参数的CV均低于参考阈值。最后,克鲁斯卡尔-沃利斯检验报告,除血小板计数外(p < 0.000),所有参数的统计学差异均不显著。结论:Horiba适用于常规献血前筛查。批内一致性进一步证明了该设备的准确性。