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首页> 外文期刊>Journal of clinical laboratory analysis. >Discovery and Correction of Spurious Low Platelet Counts due to EDTA-Dependent Pseudothrombocytopenia
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Discovery and Correction of Spurious Low Platelet Counts due to EDTA-Dependent Pseudothrombocytopenia

机译:发现和纠正由于EDTA依赖的伪血小板减少症而导致的虚假的低血小板计数

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Background: Ethylene diamine tetraacetic acid dependent pseudothrombocytopenia (EDTA-PTCP) is a laboratory artifact that may lead to unnecessary evaluation and treatment of patients. The purpose of this article is to discuss how to identify EDTA-PTCP and correct spurious low platelet counts in clinical laboratories. Methods: We use two criteria to screen for platelet aggregation: (1) an abnormal platelet count in EDTA-treated blood from a patient lacking clinical signs of a platelet disorder, and (2) an instrument flag for platelet clumps. EDTA-PTCP was confirmed by microscopic examination for platelet agglutination and by platelet counts that corrected with citrate sample. In addition, the time course of EDTA-PTCP was investigated in samples from 26 patients anticoagulated with EDTA-K-2 and sodium citrate. Amikacin (5 mg/ml) was added to tubes with EDTA-K-2 or sodium citrate from seven additional cases in order to confirm its dissociative effect on platelet aggregation. Results: In our laboratory, the overall incidence of EDTA-PTCP was approximately 0.09%; and the duration was between 2 weeks and 6 months. EDTA-PTCP was time-dependent and occurred as early as 10 min after sample collection. Weaker agglutination could also occur in most corresponding citrate-treated samples. The dissociative effect of amikacin on platelet agglutination was case-specific and not concentration-dependent. Conclusions: The method of screening for platelet clumping with the help of XE5000 images is convenient. The decline in the platelet count is related to the length of time and the intensity of chelation. Amikacin supplement is not always effective for correcting platelet counts in vitro. (C) 2014 Wiley Periodicals, Inc.
机译:背景:乙二胺四乙酸依赖性假性血小板减少症(EDTA-PTCP)是实验室人工产物,可能导致不必要的患者评估和治疗。本文的目的是讨论如何在临床实验室中鉴定EDTA-PTCP并纠正虚假的低血小板计数。方法:我们使用两个标准来筛选血小板聚集:(1)来自缺乏血小板疾病临床体征的患者的EDTA处理的血液中血小板计数异常,以及(2)血小板凝块的仪器标记。 EDTA-PTCP通过显微镜检查血小板凝集和用柠檬酸盐样品校正的血小板计数来确认。此外,在来自EDTA-K-2和柠檬酸钠抗凝的26位患者的样本中研究了EDTA-PTCP的时程。从另外七个案例中,将阿米卡星(5 mg / ml)与EDTA-K-2或柠檬酸钠一起加入试管中,以确认其对血小板聚集的解离作用。结果:在我们的实验室中,EDTA-PTCP的总发生率约为0.09%;持续时间在2周到6个月之间。 EDTA-PTCP是时间依赖性的,最早发生在样品收集后10分钟。在大多数相应的柠檬酸盐处理过的样品中也可能发生较弱的凝集。阿米卡星对血小板凝集的解离作用是病例特异性的,而不是浓度依赖性的。结论:借助XE5000图像筛查血小板凝块的方法是方便的。血小板数量的减少与时间的长短和螯合的强度有关。阿米卡星补充剂并非总是能有效地校正体外血小板计数。 (C)2014威利期刊公司

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