Effects of different blood storage conditions on leukocytes cell population data using the Sysmex XN hematological analyzer.

IF 1.8
Biochemia medica Pub Date : 2026-06-15 Epub Date: 2026-04-15 DOI:10.11613/BM.2026.020704
Vincenzo Roccaforte, Rossella Panella, Massimo Daves, Antonella De Martino, Erika Jani, Giovanni Sabbatini, Pierfrancesco Agostini, Floriana De Filippi, Paolo Formenti, Giuseppe Lippi, Matteo Vidali, Angelo Pezzi, Stefano Pastori
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Abstract

Introduction: The aim of this study was to investigate the stability of leukocyte cell population data (CPD) assessed on Sysmex XN-3000 hematological analyzer in samples stored for up to 24 h at different temperatures.

Materials and methods: Whole-blood samples from 25 donors were analyzed for 18 CPD parameters at baseline and after storage at room temperature (RT), 4 °C, or 37 °C for 3, 6, 12, and 24 h. Stability was assessed using three complementary approaches: paired Wilcoxon tests with Bonferroni correction, percent difference between medians > 10%, and per-sample percent change > 10% in ≥ 2 samples. In addition, the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) stability protocol was applied, modelling percent differences over time using linear regression through the origin to estimate the rate of change and the stability limit (SL), defined as the time required to exceed a maximum permissible error of 10%.

Results: According to predefined stability criteria, several CPD parameters exceeded stability limits within 24 h, particularly under storage at 37 °C. Parameters related to neutrophil, lymphocyte and monocyte complexity and size (e.g., neutrophils complexity (NE-SSC), neutrophils size (NE-FSC), monocytes complexity (MO-X), lymphocytes complexity (LY-X); where SSC = side scatter, FSC = forward scatter) showed slow rates of change with estimated stability limits beyond 24 h across storage conditions. In contrast, fluorescence- and dispersion-related parameters (e.g., neutrophils fluorescence intensity (NE-SFL), width of dispersion of neutrophils complexity (NE-WX), width of dispersion of lymphocytes fluorescence (LY-WY), width of dispersion of monocytes size (MO-WZ); where SFL = side fluorescence, W = width of dispersion) reached the stability limit within 24 h, most frequently at 37 °C. Lymphocyte size (LY-Z) exceeded the stability limit at 17 h also under storage at 4 °C.

Conclusions: Leukocyte CPD stability is strongly temperature- and parameter-dependent. Exposure to elevated temperature (37 °C) leads to early exceedance of predefined stability limits for several CPD parameters, whereas storage at RT preserves stability for longer time intervals. Avoiding prolonged exposure to high temperatures is therefore essential for reliable CPD assessment in routine laboratory practice.

使用Sysmex XN血液分析仪分析不同血液储存条件对白细胞群数据的影响。
本研究的目的是研究Sysmex XN-3000血液学分析仪在不同温度下保存24小时的样品中白细胞群数据(CPD)的稳定性。材料和方法:分析来自25名献血者的全血样本在基线和室温(RT)、4°C或37°C保存3、6、12和24小时后的18个CPD参数。使用三种互补方法评估稳定性:配对Wilcoxon试验与Bonferroni校正,中位数差异百分比> 10%,以及≥2个样本的单样本百分比变化> 10%。此外,应用了欧洲临床化学和实验室医学联合会(EFLM)稳定性方案,通过原点使用线性回归对随时间的百分比差异进行建模,以估计变化率和稳定性极限(SL),定义为超过最大允许误差10%所需的时间。结果:根据预先设定的稳定性标准,几个CPD参数在24 h内超过了稳定性限制,特别是在37℃的储存条件下。与中性粒细胞、淋巴细胞和单核细胞复杂性和大小相关的参数(例如,中性粒细胞复杂性(NE-SSC)、中性粒细胞大小(NE-FSC)、单核细胞复杂性(MO-X)、淋巴细胞复杂性(LY-X);其中SSC =侧散射,FSC =前向散射)在不同的储存条件下显示出缓慢的变化速率,估计的稳定性极限超过24小时。相比之下,荧光和弥散相关参数(如中性粒细胞荧光强度(NE-SFL)、中性粒细胞复杂性弥散宽度(NE-WX)、淋巴细胞荧光弥散宽度(LY-WY)、单核细胞大小弥散宽度(MO-WZ);其中SFL =侧荧光,W =色散宽度)在24 h内达到稳定极限,最常发生在37℃。淋巴细胞大小(LY-Z)在4℃下保存17 h时也超过了稳定性极限。结论:白细胞CPD稳定性强烈依赖于温度和参数。暴露在高温下(37℃)会导致几个CPD参数的早期稳定性超出预定的限制,而在室温下储存可以保持更长的稳定性。因此,避免长时间暴露在高温下对于在常规实验室实践中进行可靠的CPD评估至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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