Startseite Evaluation of hemolysis, lipemia, and icterus interference with common clinical immunoassays
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

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

  • Amir Karin , Victoria Higgins , Jessica Miller , Davor Brinc , Vathany Kulasingam und Rajeevan Selvaratnam ORCID logo EMAIL logo
Veröffentlicht/Copyright: 13. Januar 2023
Veröffentlichen auch Sie bei De Gruyter Brill

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.


Corresponding author: Rajeevan Selvaratnam, Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada; and Laboratory Medicine Program, Division of Clinical Biochemistry, University Health Network, Toronto, ON, Canada, E-mail:
Amir Karin and Victoria Higgins contributed equally to this work.
  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Not applicable.

  5. Ethical approval: Not applicable.

References

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.Suche in Google Scholar PubMed

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.Suche in Google Scholar PubMed

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.Suche in Google Scholar PubMed

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.Suche in Google Scholar

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.Suche in Google Scholar PubMed PubMed Central

6. CLSI. Interference testing in clinical chemistry; approved guideline. CLSI document EP07-A2. Wayne, PA: Clinical and Laboratory Standards Institute; 2005.Suche in Google Scholar

7. Aarsand, AK, Fernandez-Calle, P, Webster, C, Coskun, A, Gonzales-Lao, E, Diaz-Garzon, J, et al.. The EFLM Biological Variation Database [Internet]. Available from: https://biologicalvariation.eu/ [Accessed 22 Nov 2022].Suche in Google Scholar

8. Dimech, W, Vincini, G, Karakaltsas, M. Determination of quality control limits for serological infectious disease testing using historical data. Clin Chem Lab Med 2015;53:329–36. https://doi.org/10.1515/cclm-2014-0546.Suche in Google Scholar PubMed

9. Walker, S, Dimech, W, Kiely, P, Smeh, K, Francis, B, Karakaltsas, M, et al.. An international quality control programme for PRISM chemiluminescent immunoassays in blood service and blood product laboratories. Vox Sang 2009;97:309–16. https://doi.org/10.1111/j.1423-0410.2009.01218.x.Suche in Google Scholar PubMed

10. Sciacovelli, L, Lippi, G, Sumarac, Z, Del Pino Castro, IG, Ivanov, A, De Guire, V, et al., Working Group “Laboratory Errors and Patient Safety” of International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). Pre-analytical quality indicators in laboratory medicine: Performance of laboratories participating in the IFCC working group “Laboratory Errors and Patient Safety” project. Clin Chim Acta 2019;497:35–40. https://doi.org/10.1016/j.cca.2019.07.007. 31295446.Suche in Google Scholar PubMed

11. Barbato, L, Campelo, MD, Pigozzo, S, Realdon, N, Gandini, A, Barbazza, R, et al.. Rejection of hemolyzed samples can jeopardize patient safety. EJIFCC 2020;31:15–20. 32256285.Suche in Google Scholar

12. Zornitzki, T, Blaychfeld-Magnazi, M, Knobler, H, Ulman, M. The effect of phlebotomy-induced hemolysis on insulin level determination. Endocr Pract 2015;21:1093–7. https://doi.org/10.4158/ep15698.or.Suche in Google Scholar

13. Garinet, S, Fellahi, S, Marlin, G, Capeau, J, Lefèvre, G, Bastard, JP. Differential interferences of hemoglobin and hemolysis on insulin assay with the Abbott Architect-Ci8200 immunoassay. Clin Biochem 2014;47:445–7. https://doi.org/10.1016/j.clinbiochem.2014.01.026. 24486652.Suche in Google Scholar PubMed

14. Hasanato, R, Brearton, S, Alshebani, M, Bailey, L, Aldugashim, S, Alothaim, A, et al.. Effects of serum indices interference on hormonal results from the Abbott Architect i2000 immunoassay analyser. Br J Biomed Sci 2015;72:151–5. https://doi.org/10.1080/09674845.2015.11665744.Suche in Google Scholar PubMed

15. La’ulu, SL, Rawlins, ML, Pfeiffer, CM, Zhang, M, Roberts, WL. Performance characteristics of six homocysteine assays. Am J Clin Pathol 2008;130:969–75. https://doi.org/10.1309/ajcp64bjipnpsqdj.Suche in Google Scholar PubMed

16. Armbruster, DA, Jirinzu, DC, Williams, JV. Evaluation of enhanced luminescence immunoenzymometric assays (LIA) for ferritin and free T4. J Clin Lab Anal 1989;3:78–83. https://doi.org/10.1002/jcla.1860030203.Suche in Google Scholar PubMed

17. Saenger, AK, Jaffe, AS, Body, R, Collinson, PO, Kavsak, PA, Lam, CSP, et al.. Cardiac troponin and natriuretic peptide analytical interferences from hemolysis and biotin: educational aids from the IFCC Committee on Cardiac Biomarkers (IFCC C-CB). Clin Chem Lab Med 2019;57:633–40. https://doi.org/10.1515/cclm-2018-0905. 30291783.Suche in Google Scholar PubMed

18. Harley, K, Bissonnette, S, Inzitari, R, Schulz, K, Apple, FS, Kavsak, PA, et al.. Independent and combined effects of biotin and hemolysis on high-sensitivity cardiac troponin assays. Clin Chem Lab Med 2021;59:1431–43. https://doi.org/10.1515/cclm-2021-0124. 33761581.Suche in Google Scholar PubMed

19. Rotenberg, M, Rubin, M, Bor, A, Meyuhas, D, Talmon, Y, Lichtenberg, D. Physico-chemical characterization of IntralipidTM emulsions. Biochim Biophys Acta Lipids Lipid Metabol 1991;1086:265–72. https://doi.org/10.1016/0005-2760(91)90169-i.Suche in Google Scholar PubMed

20. Mainali, S, Davis, SR, Krasowski, MD. Frequency and causes of lipemia interference of clinical chemistry laboratory tests. Pract Lab Med 2017;8:1–9. https://doi.org/10.1016/j.plabm.2017.02.001.Suche in Google Scholar PubMed PubMed Central


Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2022-0924).


Received: 2022-09-16
Accepted: 2022-12-06
Published Online: 2023-01-13
Published in Print: 2023-05-25

© 2022 Walter de Gruyter GmbH, Berlin/Boston

Artikel in diesem Heft

  1. Frontmatter
  2. Editorial
  3. Improving access to diagnostic testing in conflict-affected areas: what is needed?
  4. Review
  5. Deciphering the role of monocyte and monocyte distribution width (MDW) in COVID-19: an updated systematic review and meta-analysis
  6. Opinion Paper
  7. From research cohorts to the patient – a role for “omics” in diagnostics and laboratory medicine?
  8. EFLM Paper
  9. The European Register of Specialists in Clinical Chemistry and Laboratory Medicine: code of conduct, version 3 – 2023
  10. Guidelines and Recommendations
  11. Cardiac troponin measurement at the point of care: educational recommendations on analytical and clinical aspects by the IFCC Committee on Clinical Applications of Cardiac Bio-Markers (IFCC C-CB)
  12. Genetics and Molecular Diagnostics
  13. A new and improved method of library preparation for non-invasive prenatal testing: plasma to library express technology
  14. Multiplex proteomics using proximity extension assay for the identification of protein biomarkers predictive of acute graft-vs.-host disease in allogeneic hematopoietic cell transplantation
  15. General Clinical Chemistry and Laboratory Medicine
  16. Assessment of laboratory capacity in conflict-affected low-resource settings using two World Health Organization laboratory assessment tools
  17. Challenge in hyponatremic patients – the potential of a laboratory-based decision support system for hyponatremia to improve patient’s safety
  18. Evaluation of hemolysis, lipemia, and icterus interference with common clinical immunoassays
  19. Serum bicarbonate stability study at room temperature – influence of time to centrifugation and air exposure on bicarbonate measurement reported according to the CRESS checklist
  20. Effects of lipemia on capillary serum protein electrophoresis in native ultra-lipemic material and intravenous lipid emulsion added sera
  21. C-reactive protein interacts with amphotericin B liposomes and its potential clinical consequences
  22. Evaluation of analytical performance of homocysteine LC-MS/MS assay and design of internal quality control strategy
  23. A reliable and high throughput HPLC–HRMS method for the rapid screening of β-thalassemia and hemoglobinopathy in dried blood spots
  24. Dynamics of the vitamin D C3-epimer levels in preterm infants
  25. Comparison of ANA testing by indirect immunofluorescence or solid-phase assays in a low pre-test probability population for systemic autoimmune disease: the Camargo Cohort
  26. Reference Values and Biological Variations
  27. LMS-based continuous reference percentiles for 14 laboratory parameters in the CALIPER cohort of healthy children and adolescents
  28. Indirectly determined reference intervals for automated white blood cell differentials of pediatric patients in Berlin and Brandenburg
  29. Infectious Diseases
  30. Evaluation of a high-sensitivity SARS-CoV-2 antigen test on the fully automated light-initiated chemiluminescent immunoassay platform
  31. Letters to the Editor
  32. Non-esterified fatty acids (NEFA): sample stability and effect of haemolysis and icterus
  33. Frozen serum sample pool should not be used as internal quality assessment for lipemia (L) index
  34. Stability of SARS-CoV-2 respiratory samples in non-freezing condition: importance for tropical countries under heavy diagnostic demand
  35. A rare case of both macro-TSH and macro-LH: laboratory analysis of the pathogenesis
  36. A new method for early cancer detection based on platelet transcriptomics will have low positive predictive value
  37. Comparison of near-infrared and UV–vis-based non-contact hematocrit prediction of dried blood spots from patients on immunosuppressants
  38. The diagnostics of heparin-induced thrombocytopenia in Italy and the possible impact of vaccine-induced immune thrombotic thrombocytopenia on it
  39. Pitfall in the analysis of the alcohol biomarkers ethyl glucuronide and ethyl sulfate by laboratory-caused contamination with disinfectants
  40. Growing your own food is like printing money, don’t let it make you mad as a hatter
  41. Congress Abstracts
  42. 43rd annual conference of the association of clinical biochemists in Ireland (ACBI 2021)
  43. 44th Annual Conference of the Association of Clinical Biochemists in Ireland (ACBI 2022)
Heruntergeladen am 18.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/cclm-2022-0924/html?lang=de
Button zum nach oben scrollen