首页> 外文期刊>Scandinavian journal of clinical and laboratory investigation. >Six-day stability of erythrocyte and reticulocyte parameters in-vitro: A comparison of blood samples from healthy, iron-deficient, and thalassemic individuals
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Six-day stability of erythrocyte and reticulocyte parameters in-vitro: A comparison of blood samples from healthy, iron-deficient, and thalassemic individuals

机译:体外红细胞和网织红细胞参数的六天稳定性:来自健康,铁缺乏和地中海贫血个体的血液样本比较

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Introduction. Stability for up to 6 days' storage of erythrocyte and reticulocyte parameters in samples from iron-deficient and thalassemic individuals has not yet been reported. This lack of knowledge challenges evaluation of the full blood count in referral samples for hemoglobinopathy evaluation. We therefore hereby present such sample stability data. Methods. We included fresh (less than 4 hours old) blood samples from eight healthy, eight iron-deficient, and 11 thalassemic individuals. A full blood count, including reticulocyte parameters, was performed on a Sysmex XE-2100 once daily during a 6-day storage period at room temperature. For healthy individuals, we also studied stability of refrigerated samples and investigated analytical and biological variation. Results. Hemoglobin concentration, erythrocyte count, and mean corpuscular hemoglobin were stable for 6 days in all diagnostic groups. Mean corpuscular volume increased less in samples from iron-deficient individuals while the number of reticulocytes increased more in samples from thalassemic, as compared to healthy individuals. Ret-He stability depended on its baseline value. Within-person biological variation in samples from healthy individuals was low both for erythrocyte parameters and for reticulocyte hemoglobin, while higher for reticulocyte counts. Conclusion. Results for hemoglobin concentration, erythrocyte count, and mean corpuscular hemoglobin are reliable in hemoglobinopathy investigation of referred samples for up to 6 days. Storage time-dependent changes of other erythrocyte and reticulocyte parameters in blood samples from iron-deficient and thalassemic individuals differ from those of healthy individuals.
机译:介绍。尚未报道铁缺乏症和地中海贫血患者样品中红细胞和网织红细胞参数最多可保存6天的稳定性。这种知识的缺乏挑战了在转诊样本中对全血细胞计数进行血红蛋白病评估的评估。因此,我们特此提出此类样品稳定性数据。方法。我们纳入了来自八名健康,八名铁缺乏症和十一例地中海贫血患者的新鲜(不到4小时)血液样本。在室温下保存6天期间,每天对Sysmex XE-2100进行一次全血细胞计数,包括网状细胞参数。对于健康个体,我们还研究了冷藏样品的稳定性,并研究了分析和生物学差异。结果。在所有诊断组中,血红蛋白浓度,红细胞计数和平均红细胞血红蛋白稳定6天。与健康个体相比,铁缺乏者的样本中平均红细胞体积增加较少,而地中海贫血者的样本中网织红细胞数量增加较多。 Ret-He的稳定性取决于其基线值。健康个体样品的人内生物学变异在红细胞参数和网织红细胞血红蛋白方面均较低,而网织红细胞计数则较高。结论。血红蛋白浓度,红血球计数和平均红细胞血红蛋白的结果在长达6天的参考样本血红蛋白病调查中是可靠的。缺铁和地中海贫血患者血液样本中其他红细胞和网织红细胞参数的储存时间依赖性变化与健康个体不同。

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