Department of Pathology & Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Department of Pathology & Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Int J Lab Hematol. 2024 Apr;46(2):266-274. doi: 10.1111/ijlh.14209. Epub 2023 Dec 6.
The International Council for Standardization in Haematology convened a working group to assess and propose improvements upon the state of standardization and harmonization of reticulocyte parameters among commercial hematology analyzers.
An international group of laboratory hematologists prospectively collected and analyzed clinical samples using locally available IVD commercial hematology analyzers. Eight hundred and fifty-five total samples were collected at 6 sites using 9 distinct analyzer types. Samples were assessed for reticulocyte percent (RET%), immature reticulocyte fraction (IRF), and reticulocyte hemoglobin content (RHC). Method comparison and regression statistics were calculated. These analyses were used to determine whether statistical recalibration offered a potential avenue for increasing comparability between these methods.
While methods producing reticulocyte percent were the most comparable in this study, the state of harmonization for the IRF and RHC was reduced with pearson correlation coefficients ranging from 0.955 to 0.77 and 0.927 and 0.680, respectively. Nevertheless, use of parameters from the Passing Bablok regression substantially improved the comparability of the results. In addition, precision data was derived which also demonstrated substantial differences between analyzer systems.
While reticulocyte counting is correlated between the automated methods evaluated in this study, the current state of harmonization of other reticulocyte parameters is not as strong. A major challenge in moving this field forward is the need for commutable materials to facilitate comparisons between analyzers not co-located. A potential alternate approach to improve the current state would be instrument re-calibration. However, this is challenging both technically and due to national regulatory frameworks.
国际血液学标准化委员会召集了一个工作组,以评估和提出改进商业血液分析仪网织红细胞参数标准化和协调化的方法。
一个国际实验室血液学家小组使用当地可用的体外诊断商业血液分析仪前瞻性地收集和分析临床样本。在 6 个地点使用 9 种不同的分析仪类型共采集了 855 个总样本。评估网织红细胞百分率(RET%)、不成熟网织红细胞分数(IRF)和网织红细胞血红蛋白含量(RHC)。计算方法比较和回归统计。这些分析用于确定统计重新校准是否为提高这些方法之间的可比性提供了潜在途径。
虽然在这项研究中产生网织红细胞百分率的方法最具可比性,但 IRF 和 RHC 的协调状态降低,Pearson 相关系数分别为 0.955 至 0.77 和 0.927 至 0.680。然而,使用 Passing Bablok 回归的参数大大提高了结果的可比性。此外,还得出了精密度数据,也证明了分析系统之间存在很大差异。
虽然在这项研究中评估的自动方法之间的网织红细胞计数具有相关性,但其他网织红细胞参数的协调状态并不强。推动这一领域向前发展的一个主要挑战是需要可交换材料,以促进不在同一地点的分析仪之间的比较。改善当前状态的一种潜在方法是仪器重新校准。然而,这在技术上和由于国家监管框架都具有挑战性。