1 Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, US.
Am J Clin Pathol. 2024 Oct 3;162(4):356-368. doi: 10.1093/ajcp/aqae040.
The aims of this study were to (1) establish the maximum allowable interference limits for hemolysis, lipemia, and icterus for chemistry analytes tested in body fluid samples and (2) assess the effectiveness of serial dilution to mitigate spectral interferences.
Residual body fluids from clinically ordered testing were mixed (<10% by volume) with stock solutions of interferent (spiked) and compared with a control spiked with an equal volume of 0.9% saline. The analytes were measured on the Roche cobas c501 instrument. Difference and percentage difference were calculated and compared with allowable total error limits. A subset of samples were serially diluted with 0.9% saline. Mean (SD) difference and percentage difference were calculated.
The interference thresholds were lower than the package insert for lactate dehydrogenase, cholesterol, triglycerides, and total protein for hemolysis; amylase, cholesterol, and total protein for icterus; and albumin for lipemia. Only cholesterol and triglyceride results returned to baseline upon dilution of icteric samples.
Interference thresholds in body fluids were lower than blood for 6 analytes. Diluting interferences that surpass these limits does not produce reliable results that are comparable to the baseline results before spiking in the interferent.
本研究旨在(1)确定体液样本中检测的化学分析物发生溶血、脂血和黄疸时的最大允许干扰限度,以及(2)评估连续稀释在减轻光谱干扰方面的效果。
将临床订购检测的剩余体液与干扰物(加标)的储备溶液混合(体积<10%),并与用等量 0.9%生理盐水加标的对照物进行比较。罗氏 cobas c501 仪器上测量分析物。计算差异和百分比差异,并与允许的总误差限度进行比较。将部分样本用 0.9%生理盐水连续稀释。计算平均(SD)差异和百分比差异。
溶血时的干扰阈值低于乳酸脱氢酶、胆固醇、甘油三酯和总蛋白的试剂盒说明,黄疸时的干扰阈值低于淀粉酶、胆固醇和总蛋白,脂血时的干扰阈值低于白蛋白。只有当稀释黄疸样本时,胆固醇和甘油三酯的结果才会恢复到基线。
体液中的干扰阈值低于血液中的 6 种分析物。当干扰超过这些限度时,即使进行稀释,也无法得到与加标前基线结果可比的可靠结果。