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UF-1000i:体液模式用于体液中细胞计数的验证。

UF-1000i: validation of the body fluid mode for counting cells in body fluids.

出版信息

Clin Chem Lab Med. 2014 Dec;52(12):1781-90. doi: 10.1515/cclm-2014-0512.

Abstract

BACKGROUND

We evaluated the new body fluid mode on the UF-1000i urinalysis analyzer for counting total white blood cells (WBC) and red blood cells (RBC) in continuous ambulatory peritoneal dialysis (CAPD), ascites and pleural fluids.

METHODS

We collected 154 body fluid samples, and compared the results of the UF-1000i BF mode with the Fuchs-Rosenthal counting chamber and the XN-1000 BF mode. Linearity, carry over and precision were also assessed.

RESULTS

Method comparison results showed acceptable WBC agreement between UF-1000i and chamber (y=1.27x+3.13, n=135, r=0.99) and between UF-1000i and XN (y=1.15x+0.31, n=135, r=1.00). Comparison between the UF-1000i and both comparison methods showed good agreement for RBC counts. Overall results were better when UF-1000i was compared with the XN-1000 than with the Fuchs-Rosenthal chamber. The lower limit of quantitation was defined at 9×106 WBC/L and at 25×106 RBC/L. Linearity for both WBC (r=1.00) and RBC (r=0.99) was good. Carry over was negligible, and it never exceeded 0.01%. In one sample, a high discrepancy was observed between WBC results for both automated analyzers and the counting chamber. This discrepancy was due to interfering factors, such as bacteria and yeast cells, and it led to a false increased WBC count on both automated systems.

CONCLUSIONS

The UF-1000i BF mode offers rapid and reliable total WBC and RBC counts for initial screening of CAPD, ascites and pleural fluid, and can improve the workflow in a routine laboratory; however, when using automated analyzers, the inspection of scattergrams is required to ensure the most accurate results are obtained.

摘要

背景

我们评估了 UF-1000i 尿液分析仪新的体液模式,用于连续不卧床腹膜透析(CAPD)、腹水和胸腔液中总白细胞(WBC)和红细胞(RBC)的计数。

方法

我们收集了 154 份体液样本,将 UF-1000i BF 模式的结果与 Fuchs-Rosenthal 计数室和 XN-1000 BF 模式进行比较。还评估了线性、携带和精密度。

结果

方法比较结果显示 UF-1000i 与室(y=1.27x+3.13,n=135,r=0.99)和 UF-1000i 与 XN(y=1.15x+0.31,n=135,r=1.00)之间的 WBC 具有可接受的一致性。UF-1000i 与两种比较方法之间的 RBC 计数也具有良好的一致性。UF-1000i 与 XN-1000 相比与 Fuchs-Rosenthal 室相比,总体结果更好。WBC(r=1.00)和 RBC(r=0.99)的定量下限定义为 9×106 WBC/L 和 25×106 RBC/L。WBC(r=1.00)和 RBC(r=0.99)的线性均良好。携带量可以忽略不计,从不超过 0.01%。在一个样本中,两种自动分析仪和计数室的白细胞结果之间观察到明显的差异。这种差异是由于细菌和酵母细胞等干扰因素所致,导致两种自动系统的白细胞计数均出现假性增加。

结论

UF-1000i BF 模式可快速可靠地进行初始筛选,用于 CAPD、腹水和胸腔液中的总 WBC 和 RBC 计数,可改善常规实验室的工作流程;但是,使用自动分析仪时,需要检查散点图以确保获得最准确的结果。

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