如何在Sysmex血液学分析仪上处理血脂性CBC样本?

IF 1.1 Q4 MEDICAL LABORATORY TECHNOLOGY
Advances in laboratory medicine Pub Date : 2025-03-20 eCollection Date: 2025-06-01 DOI:10.1515/almed-2024-0206
Vanja Radišić Biljak, Lucija Dolovčak, Iva Bakarić, Ana Nikler, Andrea Saračević, Marija Grdić Rajković
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引用次数: 0

摘要

目的:由于识别和去除的方法有限且不标准化,脂血症对全血细胞计数(CBC)测量造成了重大的分析前问题。我们旨在验证Sysmex XN-1000血液学分析仪(HA)上的光学血红蛋白(Hb-O)测量作为管理血脂性CBC样本的可能可靠方法。方法:90份不同Hb浓度的CBC样品逐渐加入脂质乳状液。重复测量并记录Hb-O浓度。加入的CBC样品离心(400 g/10 min)。小心地取出血浆,测量Hb浓度。根据血浆中的测量值调整从血脂样品获得的值。取下的血浆用分析仪的稀释液代替,重复测量。在血脂血浆样本中测量甘油三酯浓度。结果:根据最严格的可接受标准,Hb- o与初始Hb测量相比具有统计学不显著性和可接受偏差(-0.4 %,95 % CI: -1.2-0.3, p=0.2447)。观察到的偏倚与血脂的程度无关(rho=-0.072, 95 % CI: -0.295至0.157,p=0.537)。在用分析仪稀释液代替血脂血浆的样品中测量的血红蛋白显示出最小的偏差,尽管具有统计学意义(-1.1 %,95 % CI: -2.0至(-0.1),p=0.025)。观察到的偏倚与血脂程度负相关(rho=-0.369, 95 % CI: -0.550至(-0.155),p=0.001)。根据测定的血浆血红蛋白重新计算的血红蛋白值发现了最高的不可接受偏差(-3.5 %,95% % CI: -4.1至(-2.9))。结论:Hb-O测量是Sysmex XN-1000 HA上CBC样品中脂血症去除的最可靠测量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How to handle lipemic CBC samples on Sysmex hematology analyzers?

How to handle lipemic CBC samples on Sysmex hematology analyzers?

How to handle lipemic CBC samples on Sysmex hematology analyzers?

How to handle lipemic CBC samples on Sysmex hematology analyzers?

Objectives: Lipemia poses a significant preanalytical problem for complete blood count (CBC) measurement due to limited and non-standardized methods for recognition and removal. We aimed to verify the optical hemoglobin (Hb-O) measurements on the Sysmex XN-1000 hematology analyzer (HA) as a possible reliable method for managing lipemic CBC samples.

Methods: Ninety CBC samples with varying Hb concentrations were gradually spiked with a lipid emulsion. Measurements were repeated and Hb-O concentrations were recorded. Spiked CBC samples were centrifuged (400 g/10 min). Plasma was carefully removed, and Hb concentration was measured. The values obtained from the lipemic samples were adjusted according to the measurements in the plasma. The removed plasma was substituted with the analyzer's diluent, and measurements were repeated. Triglyceride concentrations were measured in lipemic plasma samples.

Results: Hb-O showed statistically insignificant and acceptable bias compared to the initial Hb measurement according to the strictest acceptability criteria (-0.4 %, 95 % CI: -1.2-0.3, p=0.2447). The observed bias did not correlate with the degree of lipemia (rho=-0.072, 95 % CI: -0.295 to 0.157, p=0.537). Hemoglobin measured in samples with lipemic plasma replaced by analyzer diluent exhibited minimal, albeit statistically significant, bias (-1.1 %, 95 % CI: -2.0 to (-0.1), p=0.025). The observed bias negatively correlated with the degree of lipemia (rho=-0.369, 95 % CI: -0.550 to (-0.155), p=0.001). The highest unacceptable bias was found in the recalculated hemoglobin values based on the measured plasma hemoglobin (-3.5 %, 95 % CI: -4.1 to (-2.9), p<0.0001).

Conclusions: Hb-O measurement is the most reliable measure of lipemia removal in CBC samples on the Sysmex XN-1000 HA.

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