Evaluation of hemolysis, lipemia, and icterus interference with common clinical immunoassays

Author:

Karin Amir12,Higgins Victoria34,Miller Jessica5,Brinc Davor67,Kulasingam Vathany67,Selvaratnam Rajeevan67ORCID

Affiliation:

1. Division of Clinical Chemistry , Vancouver General Hospital , Vancouver , BC , Canada

2. Department of Pathology and Laboratory Medicine , University of British Columbia , Vancouver , BC , Canada

3. DynaLIFE Medical Labs , Edmonton , AB , Canada

4. Department of Laboratory Medicine and Pathology , University of Alberta , Edmonton , AB , Canada

5. Dynacare , Brampton , ON , Canada

6. Department of Laboratory Medicine and Pathobiology , University of Toronto , Toronto , ON , Canada

7. Laboratory Medicine Program, Division of Clinical Biochemistry , University Health Network , Toronto , ON , Canada

Abstract

Abstract Objectives Hemolysis, icterus, and lipemia (HIL) are common sources of endogenous interference in clinical laboratory testing. Defining the threshold of interference for immunoassays enables appropriate reporting of their results when they are affected by HIL. Methods Pools of residual patient serum samples were spiked with a known amount of interferent to create samples with varying concentrations of hemolysate, bilirubin, and Intralipid that mimicked the effects of endogenous HIL. Samples were analysed on the Alinity i analyser (Abbott Diagnostics) for more than 25 immunoassays. The average recovery relative to the non-spiked sample was calculated for each interference level and was compared to a predefined allowable bias. Results C-peptide, estradiol, serum folate, free T4, homocysteine, insulin, and vitamin B12 were found to be affected by hemolysis, at hemoglobin concentrations between 0.3 to 20 g/L. Immunoassays for BNP, estradiol, free T3, and homocysteine were affected by icterus at conjugated bilirubin concentrations between 50 to 1,044 μmol/L. BNP, serum folate, and homocysteine were affected by Intralipid with measured triglyceride concentrations between 0.8 to 10 mmol/L. Lastly, serological immunoassays for HIV and hepatitis A, B and C were also affected by interferences. Conclusions Immunoassays are impacted by varying degrees of HIL interference. Some measurands, in the presence of interference, are affected in a manner not previously indicated. The data presented herein provide an independent evaluation of HIL thresholds and will be of aid to resource-limited clinical laboratories that are unable to internally verify endogenous interferences when implementing the Alinity i analyser.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Reference20 articles.

1. Knezevic, CE, Ness, MA, Tsang, PHT, Tenney, BJ, Marzinke, MA. Establishing hemolysis and lipemia acceptance thresholds for clinical chemistry tests. Clin Chim Acta 2020;510:459–65. https://doi.org/10.1016/j.cca.2020.08.004.

2. Agarwal, S, Vargas, G, Nordstrom, C, Tam, E, Buffone, GJ, Devaraj, S. Effect of interference from hemolysis, icterus and lipemia on routine pediatric clinical chemistry assays. Clin Chim Acta 2015;438:241–5. https://doi.org/10.1016/j.cca.2014.08.008.

3. Lippi, G, Cadamuro, J, von Meyer, A, Simundic, AM, European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) Working Group for Preanalytical Phase (WG-PRE). Practical recommendations for managing hemolyzed samples in clinical chemistry testing. Clin Chem Lab Med 2018;56:718–27. https://doi.org/10.1515/cclm-2017-1104. 29373316.

4. CLSI. Hemolysis, icterus, and lipemia/turbidity indices as indicators of interference in clinical laboratory analysis; approved guideline. CLSI document C56-A. Wayne, PA: Clinical Laboratory Standard Institute; 2012.

5. Cadamuro, J, Lippi, G, von Meyer, A, Ibarz, M, van Dongen, E, Cornes, M, et al.. European survey on preanalytical sample handling - Part 2: Practices of European laboratories on monitoring and processing haemolytic, icteric and lipemic samples. On behalf of the European federation of clinical chemistry and laboratory medicine (EFLM) working group for the preanalytical phase (WG-PRE). Biochem Med (Zagreb) 2019;29:020705. https://doi.org/10.11613/BM.2019.020705. 31223259.

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