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用于常规血液学检测的低采血量采血管的验证

Validation of low-volume blood collection tubes for routine hematologic testing.

作者信息

Lippi Giuseppe, Martini Loredana, Cortivo Barbara, Zecchetto Chiara, Ferrari Anna

机构信息

University of Verona, Section of Clinical Biochemistry, Verona, Italy.

General Hospital of Verona, Service of Laboratory Medicine, Verona, Italy.

出版信息

J Med Biochem. 2024 Nov 16;43(6):955-959. doi: 10.5937/jomb0-51438.

Abstract

BACKGROUND

Low-volume blood tubes offer several advantages in facilitating blood collection, reducing iatrogenic anemia and spurious hemolysis, but their clinical reliability must be validated. We planned this investigation for establishing the reliability of routine hematologic testing in low-volume tubes before their implementation into clinical practice.

METHODS

Blood was drawn from 44 ostensibly healthy laboratory professionals into three blood tubes, as follows: 3.0 mL of blood into a 3.0 mL K2EDTA standard reference blood tube, 0.5 mL of blood into a second 3.0 mL K2EDTA standard blood tube, and 0.5 mL of blood into a 0.25-0.5 mL K2EDTA low-volume blood tube. Hematologic testing was performed on Sysmex XN-10 hematology analyzer.

RESULTS

Statistically significant differences were observed in total white blood cell count, neutrophil count, lymphocyte count, red blood cell count, platelet count, hemoglobin, hematocrit, mean corpuscular volume (MCV), mean corpuscular hemoglobin concentration (MCHC), and mean platelet volume in both 0.5 mL-filled 3.0 mL standard blood tubes and 0.5 mL-filled low-volume blood tubes. Although none of these variations was found to be clinically significant in the 0.5 mL-filled low-volume blood tube compared to the desirable specifications, hematocrit, MCV and MCHC displayed a clinically significant bias in the 0.5 mL filled 3.0 mL K2EDTA standard blood tube.

CONCLUSIONS

These results suggests that K2EDTA low-volume blood tubes could safely replace standard blood tubes for preventing the receipt of insufficient samples, but also for facilitating blood collection in patients with difficult veins and reducing the risk of iatrogenic anemia and spurious hemolysis.

摘要

背景

微量采血管在促进血液采集、减少医源性贫血和假性溶血方面具有诸多优势,但其临床可靠性必须得到验证。我们开展此项研究旨在确定微量采血管在临床应用前常规血液学检测的可靠性。

方法

从44名表面健康的实验室工作人员采集血液,分别注入三种采血管:3.0毫升血液注入3.0毫升K2EDTA标准参考采血管;0.5毫升血液注入另一支3.0毫升K2EDTA标准采血管;0.5毫升血液注入0.25 - 0.5毫升K2EDTA微量采血管。使用Sysmex XN - 10血液分析仪进行血液学检测。

结果

在总白细胞计数、中性粒细胞计数、淋巴细胞计数、红细胞计数、血小板计数、血红蛋白、血细胞比容、平均红细胞体积(MCV)、平均红细胞血红蛋白浓度(MCHC)和平均血小板体积方面,0.5毫升装的3.0毫升标准采血管和0.5毫升装的微量采血管均存在统计学显著差异。尽管与理想规格相比,0.5毫升装的微量采血管中这些差异均未发现具有临床意义,但血细胞比容、MCV和MCHC在0.5毫升装的3.0毫升K2EDTA标准采血管中显示出具有临床意义的偏差。

结论

这些结果表明,K2EDTA微量采血管不仅可以安全地替代标准采血管以防止采集到不足的样本,还可便于为静脉穿刺困难的患者采血,并降低医源性贫血和假性溶血的风险。

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