Reproducibility and stability of the immature platelet fraction using Sysmex XN-10.

IF 1.3 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Usman Ali, Gavin Knight, Mridula Chopra, Dimitris A Tsitsikas
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引用次数: 0

Abstract

Background: The Immature Platelet Fraction (IPF) is an indicator of thrombopoiesis which is a useful parameter in thrombocytopenia. It demonstrates compensatory mechanisms in production of platelets, but currently not implemented in routine clinical practice. The aim of this study was to establish the reproducibility and stability of IPF, for both percentage (%-IPF) and absolute (A-IPF) measurements.Material/methods: A total of 71 samples, of which 45 for reproducibility and 26 for stability analysis, were assayed for full blood count using the Sysmex XN-10 analyser at room temperature (RT:19-25 °C). For reproducibility analysis, IPF measurements were analysed 11 times by different appraisers using the same sample, while for stability analysis, IPF was measured over fourteen hourly-intervals up to 24 h (n = 21) and then separately extended beyond the point of stability to 72 h (n = 5).

Results: Reproducibility analysis of %-IPF and A-IPF (n = 45) showed very reliable results, with the range of mean CV% values between 1.25-8.90% and 1.70-9.96%, respectively. On the other hand, overall, stability analysis of %-IPF and A-IPF (n = 21) at RT over 24 h showed reliable results, with pooled mean CV% values of 1.32% and 1.43%, respectively, with no significant difference between %-IPF and A-IPF (p = 0.767 and p = 0.821). All %-IPF and A-IPF values had exceeded the set acceptance criterion of stability (CV% ≥ 10.0%) before 72 h.

Conclusions: Overall, %-IPF and A-IPF reproducibility and storage at RT for 24 h predominantly demonstrates the suitability of their usage for testing on the Sysmex XN-series analysers.

使用 Sysmex XN-10 检测未成熟血小板部分的可重复性和稳定性。
背景:未成熟血小板比例(IPF)是血小板生成的一个指标,是血小板减少症的一个有用参数。它显示了血小板生成的代偿机制,但目前尚未在常规临床实践中应用。本研究旨在确定 IPF 百分比(%-IPF)和绝对值(A-IPF)测量的可重复性和稳定性:使用 Sysmex XN-10 分析仪在室温(RT:19-25 °C)下对 71 份样本进行了全血细胞计数分析,其中 45 份用于重现性分析,26 份用于稳定性分析。在重现性分析中,由不同的鉴定人员使用同一样本进行了 11 次 IPF 测量分析;而在稳定性分析中,IPF 的测量时间间隔为每小时 14 次,直至 24 小时(n = 21),然后在稳定点之后分别延长至 72 小时(n = 5):结果:%-IPF 和 A-IPF 的重现性分析(n = 45)显示结果非常可靠,平均 CV% 值范围分别为 1.25-8.90% 和 1.70-9.96%。另一方面,总体而言,RT 24 小时内 %-IPF 和 A-IPF(n = 21)的稳定性分析结果可靠,汇总平均 CV% 值分别为 1.32% 和 1.43%,%-IPF 和 A-IPF 之间无显著差异(p = 0.767 和 p = 0.821)。所有 %-IPF 和 A-IPF 值在 72 小时前都超过了设定的稳定性接受标准(CV% ≥ 10.0%):总体而言,%-IPF 和 A-IPF 的重现性和在 RT 条件下保存 24 小时的稳定性表明,它们适合在 Sysmex XN 系列分析仪上进行测试。
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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来源期刊
CiteScore
3.50
自引率
4.80%
发文量
85
审稿时长
4-8 weeks
期刊介绍: The Scandinavian Journal of Clinical and Laboratory Investigation is an international scientific journal covering clinically oriented biochemical and physiological research. Since the launch of the journal in 1949, it has been a forum for international laboratory medicine, closely related to, and edited by, The Scandinavian Society for Clinical Chemistry. The journal contains peer-reviewed articles, editorials, invited reviews, and short technical notes, as well as several supplements each year. Supplements consist of monographs, and symposium and congress reports covering subjects within clinical chemistry and clinical physiology.
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