Ann Lab Med.  2021 Jul;41(4):419-423. 10.3343/alm.2021.41.4.419.

Concordance of Three Automated Procalcitonin Immunoassays at Medical Decision Points

Affiliations
  • 1Department of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
  • 2Department of Laboratory Medicine Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, Korea

Abstract

Procalcitonin (PCT) is a useful bacterial infection biomarker with the potential for guiding antibiotic therapy. We evaluated the concordance of three automated PCT immunoassays: Kryptor (BRAHMS GmbH, Hennigsdorf, Germany), Atellica IM 1600 (Siemens Healthcare Diagnostics, Munich, Germany), and Cobas e801 (Roche Diagnostics, Mannheim, Germany). In 119 serum samples with a PCT concentration < 5.00 μg/L, Kryptor (reference assay) was compared with the other two immunoassays by Spearman’s rank correlation, regression analysis, and concordance at two antibiotic stewardship medical decision points: 0.25 and 0.50 μg/L. The Atellica IM 1600 and Cobas e801 results showed high correlations with those of Kryptor, with correlation coefficient (ρ) values of 0.97 and 0.99, respectively. However, negative biases were observed in both immunoassays (slope/y-intercept: 0.75/–0.00 for Atellica IM 1600; 0.88/–0.01 for Cobas e801). Atellica IM 1600 and Cobas e801 demonstrated excellent concordance with Kryptor at both medical decision points, with linearly weighted κ values of 0.90 and 0.92, respectively, despite discrepancies, which were more prominent at the 0.25 μg/L medical decision point. Based on these biases and discrepancies, the alternate use of different PCT immunoassays in repeat examinations is inadvisable. Standardization is required before comparing the results of different PCT immunoassays.

Keyword

Procalcitonin; Standardization; Concordance; Immunoassay; Kryptor; Atellica IM 1600; Cobas e801

Figure

  • Fig. 1 Comparative analysis of PCT concentrations measured by Atellica IM 1600, Cobas e801, and Kryptor by Passing–Bablok regression (left) and Bland–Altman plots (right). (A) Atellica IM 1600 vs. Kryptor (n=107). (B) Cobas e801 vs. Kryptor (n=113). (C) Atellica IM 1600 vs. Cobas e801 (n=107). Abbreviations: PCT, procalcitonin; CI, confidence interval.


Reference

1. Samsudin I, Vasikaran SD. 2017; Clinical utility and measurement of procalcitonin. Clin Biochem Rev. 38:59–68.
2. Schuetz P, Beishuizen A, Broyles M, Ferrer R, Gavazzi G, Gluck EH, et al. 2019; Procalcitonin (PCT)-guided antibiotic stewardship: an international experts consensus on optimized clinical use. Clin Chem Lab Med. 57:1308–18. DOI: 10.1515/cclm-2018-1181. PMID: 30721141.
Article
3. Meisner M. 2014; Update on procalcitonin measurements. Ann Lab Med. 34:263–73. DOI: 10.3343/alm.2014.34.4.263. PMID: 24982830. PMCID: PMC4071182.
Article
4. Bouadma L, Luyt CE, Tubach F, Cracco C, Alvarez A, Schwebel C, et al. 2010; Use of procalcitonin to reduce patients' exposure to antibiotics in intensive care units (PRORATA trial): a multicentre randomised controlled trial. Lancet. 375:463–74. DOI: 10.1016/S0140-6736(09)61879-1.
Article
5. Schuetz P, Wirz Y, Sager R, Christ-Crain M, Stolz D, Tamm M, et al. 2018; Effect of procalcitonin-guided antibiotic treatment on mortality in acute respiratory infections: a patient level meta-analysis. Lancet Infect Dis. 18:95–107. DOI: 10.1016/S1473-3099(17)30592-3.
6. Christ-Crain M, Jaccard-Stolz D, Bingisser R, Gencay MM, Huber PR, Tamm M, et al. 2004; Effect of procalcitonin-guided treatment on antibiotic use and outcome in lower respiratory tract infections: cluster-randomised, single-blinded intervention trial. Lancet. 363:600–7. DOI: 10.1016/S0140-6736(04)15591-8.
Article
7. Heilmann E, Gregoriano C, Wirz Y, Luyt CE, Wolff M, Chastre J, et al. 2020; Association of kidney function with effectiveness of procalcitonin-guided antibiotic treatment: a patient-level meta-analysis from randomized controlled trials. Clin Chem Lab Med. doi:10.1515/cclm-2020-0931. DOI: 10.1515/cclm-2020-0931. PMID: 32986609.
8. Schuetz P, Bretscher C, Bernasconi L, Mueller B. 2017; Overview of procalcitonin assays and procalcitonin-guided protocols for the management of patients with infections and sepsis. Expert Rev Mol Diagn. 17:593–601. DOI: 10.1080/14737159.2017.1324299. PMID: 28443360.
Article
9. U.S. Food & Drug Administration. Medical device databases: CLIA-clinical laboratory improvement amendments. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCLIA/search.cfm. Updated on Dec 2020.
10. Schuetz P, Birkhahn R, Sherwin R, Jones AE, Singer A, Kline JA, et al. 2017; Serial procalcitonin predicts mortality in severe sepsis patients: results from the multicenter procalcitonin monitoring sepsis (MOSES) study. Crit Care Med. 45:781–9. DOI: 10.1097/CCM.0000000000002321. PMID: 28257335. PMCID: PMC5389588.
11. de Wolf HK, Gunnewiek JK, Berk Y, van den Ouweland J, de Metz M. 2009; Comparison of a new procalcitonin assay from Roche with the established method on the Brahms Kryptor. Clin Chem. 55:1043–4. DOI: 10.1373/clinchem.2008.117655. PMID: 19264851.
Article
12. Hausfater P, Brochet C, Freund Y, Charles V, Bernard M. 2010; Procalcitonin measurement in routine emergency medicine practice: comparison between two immunoassays. Clin Chem Lab Med. 48:501–4. DOI: 10.1515/CCLM.2010.091. PMID: 20148728.
Article
13. Dipalo M, Guido L, Micca G, Pittalis S, Locatelli M, Motta A, et al. 2015; Multicenter comparison of automated procalcitonin immunoassays. Pract Lab Med. 2:22–8. DOI: 10.1016/j.plabm.2015.07.001. PMID: 28932801. PMCID: PMC5597721.
Article
14. Kutz A, Hausfater P, Oppert M, Alan M, Grolimund E, Gast C, et al. 2016; Comparison between B·R·A·H·M·S PCT direct, a new sensitive point-of-care testing device for rapid quantification of procalcitonin in emergency department patients and established reference methods-a prospective multinational trial. Clin Chem Lab Med. 54:577–84. DOI: 10.1515/cclm-2015-0437. PMID: 26426890.
Article
15. Ceriotti F, Marino I, Motta A, Carobene A. 2017; Analytical evaluation of the performances of Diazyme and BRAHMS procalcitonin applied to Roche Cobas in comparison with BRAHMS PCT-sensitive Kryptor. Clin Chem Lab Med. 56:162–9. DOI: 10.1515/cclm-2017-0159. PMID: 28809746.
Article
16. Soh A, Binder L, Clough M, Hernandez MH, Lefèvre G, Mostert K, et al. 2018; Comparison of the novel ARCHITECT procalcitonin assay with established procalcitonin assay systems. Pract Lab Med. 12:e00110. DOI: 10.1016/j.plabm.2018.e00110. PMID: 30519621. PMCID: PMC6249413.
Article
17. Chambliss AB, Hayden J, Colby JM. 2019; Evaluation of procalcitonin immunoassay concordance near clinical decision points. Clin Chem Lab Med. 57:1414–21. DOI: 10.1515/cclm-2018-1362. PMID: 30763263.
Article
18. Gruzdys V, Cahoon K, Pearson L, Lehman CM. 2019; Method verification shows a negative bias between 2 procalcitonin methods at medical decision concentrations. J Appl Lab Med. 4:69–77. DOI: 10.1373/jalm.2018.028449. PMID: 31639709.
Article
19. Lippi G, Salvagno GL, Gelati M, Pucci M, Lo Cascio C, Demonte D, et al. 2019; Two-center comparison of 10 fully-automated commercial procalcitonin (PCT) immunoassays. Clin Chem Lab Med. 58:77–84. DOI: 10.1515/cclm-2019-0888. PMID: 31539351.
Article
20. Lippi G, Salvagno GL, Gelati M, Pucci M, Demonte D, Faggian D, et al. 2020; Analytical evaluation of the new Beckman Coulter Access procalcitonin (PCT) chemiluminescent immunoassay. Diagnostics (Basel). 10:128. DOI: 10.3390/diagnostics10030128. PMID: 32111028. PMCID: PMC7151122.
Article
21. Eidizadeh A, Asif AR, von Ahsen N, Binder L, Schnelle M. 2019; Differences in procalcitonin measurements between three BRAHMS-partnered immunoassays (Liaison, Elecsys and Architect). Clin Chem Lab Med. 57:e207–10. DOI: 10.1515/cclm-2018-0916. PMID: 30325730.
Article
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