Startseite Medizin Detecting paraprotein interference on a direct bilirubin assay by reviewing the photometric reaction data
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Detecting paraprotein interference on a direct bilirubin assay by reviewing the photometric reaction data

  • Elena García-González , Maite Aramendía , Ricardo González-Tarancón , Naiara Romero-Sánchez und Luis Rello EMAIL logo
Veröffentlicht/Copyright: 11. Januar 2017

Abstract

Background:

The direct bilirubin (D-Bil) assay on the AU Beckman Coulter instrumentation can be interfered by paraproteins, which may result in spurious D-Bil results. In a previous work, we took advantage of this fact to detect this interference, thus helping with the identification of patients with unsuspected monoclonal gammopathies. In this work, we investigate the possibility to detect interference based on the review of the photometric reactions, regardless of the D-Bil result.

Methods:

The D-Bil assay was carried out in a set of 2164 samples. It included a group of 164 samples with paraproteins (67 of which caused interference on the assay), as well as different groups of samples for which high absorbance background readings could also be expected (i.e. hemolyzed, lipemic, or icteric samples). Photometric reaction data were reviewed and receiver operating characteristics (ROC) curves were used to establish a cut-off for absorbance that best discriminates interference.

Results:

The best cut-off was 0.0100 for the absorbance at the first photometric point of the complementary wavelength in the blank cuvette. Once the optimal cut-off for probable interference was selected, all samples analyzed in our laboratory that provided absorbance values above this cut-off were further investigated to try to discover paraproteins. During a period of 6 months, we detected 44 samples containing paraproteins, five of which belonged to patients with non-diagnosed monoclonal gammopathies.

Conclusions:

Review of the photometric reaction data permits the systematic detection of paraprotein interference on the D-Bil AU assay, even for samples for which reasonable results are obtained.

Acknowledgments

The authors acknowledge the funding from CTQ2015-64684-P (MINECO/FEDER) and from the Aragón Government (Fondo Europeo de Desarrollo Regional).

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

  2. Research funding: CTQ2015-64684-P (MINECO/FEDER), Aragón Government (Fondo Europeo de Desarrollo Regional).

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Bakker AJ, Muecke M. Gammopathy interference in clinical chemistry assays: mechanisms, detection and prevention. Clin Chem Lab Med 2007;45:1240–3.10.1515/CCLM.2007.254Suche in Google Scholar

2. Dalal BI, Brigden ML. Factitious biochemical measurements resulting from hematologic conditions. Am J Clin Pathol 2009;131:195–204.10.1309/AJCPY9RP5QYTYFWCSuche in Google Scholar

3. Nauti A, Barassi A, Merlini G, d’Eril GV. Paraprotein interference in an assay of conjugated bilirubin. Clin Chem 2005;51:1076–7.10.1373/clinchem.2005.048710Suche in Google Scholar

4. Yang Y, Howanitz PJ, Howanitz JH, Gorfajn H, Wong K. Paraproteins are a common cause of interferences with automated chemistry methods. Arch Pathol Lab Med 2008;132:217–23.10.5858/2008-132-217-PAACCOSuche in Google Scholar

5. Song L, Kelly KA, Butch AW. Monoclonal and polyclonal immunoglobulin interference in a conjugated bilirubin assay. Arch Pathol Lab Med 2014;138:950–4.10.5858/arpa.2013-0042-OASuche in Google Scholar

6. García-González E, González-Tarancón R, Aramendía M, Rello L. Analytical interference by monoclonal immunoglobulins on the direct bilirubin AU Beckman Coulter assay: the benefit of unsuspected diagnosis from spurious results. Clin Chem Lab Med 2016;54:1329–35.10.1515/cclm-2015-0608Suche in Google Scholar

7. Seimiya M, Suzuki Y, Yoshida T, Sawabe Y, Matsushita K, Nomura F. The abnormal reaction data-detecting function of the automated biochemical analyzer was useful to prevent erroneous total-bilirubin measurement and to identify monoclonal proteins. Clin Chim Acta 2015;441:44–6.10.1016/j.cca.2014.12.013Suche in Google Scholar

8. DeLong ER, DeLong DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics 1998;44:837–45.10.2307/2531595Suche in Google Scholar

9. Alberti MO, Drake TA, Song L. The pH of chemistry assays plays an important role in monoclonal immunoglobulin interferences. Pract Lab Med 2015;3:8–16.10.1016/j.plabm.2015.09.001Suche in Google Scholar

10. McQueen MJ. Some ethical and design challenges of screening programs and screening tests. Clin Chim Acta 2002;315:41–8.10.1016/S0009-8981(01)00719-7Suche in Google Scholar

11. Wijeratne N, Benatar SR. Ethical issues in laboratory medicine. J Clin Pathol 2010;63:97–8.10.1136/jcp.2007.054494Suche in Google Scholar PubMed

12. Kyle RA, Rajkumar SV. Monoclonal gammopathies of undetermined significance. Best Pract Res Clin Haematol 2005;18:689–707.10.1016/j.beha.2005.01.025Suche in Google Scholar PubMed

Received: 2016-8-4
Accepted: 2016-11-14
Published Online: 2017-1-11
Published in Print: 2017-7-26

©2017 Walter de Gruyter GmbH, Berlin/Boston

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