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利用溶血指数检查功能自动测量血浆无细胞血红蛋白。

Automated Measurement of Plasma Cell-Free Hemoglobin Using the Hemolysis Index Check Function.

机构信息

Department of Pathology and Laboratory Medicine, Pennsylvania State University College of Medicine, Hershey, PA.

出版信息

J Appl Lab Med. 2020 Mar 1;5(2):281-289. doi: 10.1093/jalm/jfz006.

Abstract

BACKGROUND

The Roche Cobas chemistry analyzer's hemolysis index (HI) check function can directly report hemoglobin (Hb) concentrations. We aimed to validate the HI check function for the measurement of plasma cell-free Hb.

METHODS

Plasma samples (6 μl) were taken by the analyzer and diluted in normal saline to measure the absorbance for Hb at 570 and 600 nm. Hb concentrations were calculated based on the molar extinction coefficient. Imprecision, lower limit of quantification (LLOQ), and analytical measurement range (AMR) of the assay were evaluated. The accuracy was determined by comparing the results between the new method and an existing spectrophotometric method. We further studied interference of icterus and lipemia and carryover. The performance of the assay in proficiency testing was also evaluated. The reference range was transferred from the existing method.

RESULTS

Within-run and total CVs were 1.7%-4.2% and 2.1%-7.0%, respectively (n = 20). The LLOQ was 11 mg/dL (CV = 8.1%) with the upper limit of AMR of 506 mg/dL. The results of the new method correlated well with the existing reference assay: Y (new method) = 0.974 x (reference method) + 4.9, r = 0.9990, n = 52. Bilirubin with a concentration up to 60 mg/dL and lipemic index up to 389 did not show significant interference. No significant carryover was detected. The average standard deviation index in proficiency testing was 0.03 ± 0.29. The reference range was <22 mg/dL.

CONCLUSIONS

Plasma cell-free Hb measurement using the HI check function meets the analytical requirements of the plasma cell-free Hb assays. It is simple and cost-effective.

摘要

背景

罗氏 Cobas 化学分析仪的溶血指数 (HI) 检查功能可直接报告血红蛋白 (Hb) 浓度。我们旨在验证 HI 检查功能用于测量血浆游离 Hb。

方法

分析仪采集 6 μl 血浆样品,用生理盐水稀释后测量 570nm 和 600nm 处的 Hb 吸光度。根据摩尔消光系数计算 Hb 浓度。评估该方法的不精密度、定量下限 (LLOQ) 和分析测量范围 (AMR)。通过比较新方法和现有的分光光度法的结果来确定准确性。我们还进一步研究了黄疸和脂血以及携带污染的干扰。还评估了该方法在能力验证中的性能。参考范围从现有的方法转移而来。

结果

批内和总 CV 分别为 1.7%-4.2%和 2.1%-7.0%(n=20)。LLOQ 为 11mg/dL(CV=8.1%),AMR 的上限为 506mg/dL。新方法的结果与现有的参考测定法相关性良好:Y(新方法)= 0.974x(参考方法)+4.9,r=0.9990,n=52。胆红素浓度高达 60mg/dL 和脂血指数高达 389 时无明显干扰。未检测到明显的携带污染。能力验证中的平均标准偏差指数为 0.03±0.29。参考范围为<22mg/dL。

结论

使用 HI 检查功能测量血浆游离 Hb 符合血浆游离 Hb 测定的分析要求。它简单且具有成本效益。

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