Literature DB >> 34147043

Harmonization status of procalcitonin measurements: what do comparison studies and EQA schemes tell us?

Huu-Hien Huynh1,2, Amandine Bœuf1, Jens Pfannkuche3, Philipp Schuetz4,5, Marc Thelen6, Gunnar Nordin7, Eline van der Hagen8, Patricia Kaiser9, Dagmar Kesseler10, Tony Badrick11, Bernard Poggi12,13, Ulla Tiikkainen14, Gareth J Davies15, Anja Kessler16, Mario Plebani17, Joëlle Vinh2, Vincent Delatour1.   

Abstract

Sepsis represents a global health priority because of its high mortality and morbidity. The key to improving prognosis remains an early diagnosis to initiate appropriate antibiotic treatment. Procalcitonin (PCT) is a recognized biomarker for the early indication of bacterial infections and a valuable tool to guide and individualize antibiotic treatment. To meet the increasing demand for PCT testing, numerous PCT immunoassays have been developed and commercialized, but results have been questioned. Many comparison studies have been carried out to evaluate analytical performance and comparability of results provided by the different commercially available immunoassays for PCT, but results are conflicting. External Quality Assessment Schemes (EQAS) for PCT constitute another way to evaluate results comparability. However, when making this comparison, it must be taken into account that the variety of EQA materials consist of different matrices, the commutability of which has not yet been investigated. The present study gathers results from all published comparison studies and results from 137 EQAS surveys to describe the current state-of-the-art harmonization of PCT results. Comparison studies globally highlight a significant variability of measurement results that nonetheless seem to have a moderate impact on medical decision-making. For their part, EQAS for PCT provides highly discrepant estimates of the interlaboratory CV. Due to differences in commutability of the EQA materials, the results from different peer groups could not be compared. To improve the informative value of the EQA data, the existing limitations such as non-harmonized conditions and suboptimal and/or unknown commutability of the EQA materials have to be overcome. The study highlights the need for commutable reference materials that could be used to properly evaluate result comparability and possibly standardize calibration, if necessary. Such an initiative would further improve the safe use of PCT in clinical routine.
© 2021 Walter de Gruyter GmbH, Berlin/Boston.

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Keywords:  equivalence; external-quality-assessment; harmo-nization; method comparison; procalcitonin; sepsis

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Year:  2021        PMID: 34147043     DOI: 10.1515/cclm-2021-0566

Source DB:  PubMed          Journal:  Clin Chem Lab Med        ISSN: 1434-6621            Impact factor:   3.694


  2 in total

1.  Candidate High-Resolution Mass Spectrometry-Based Reference Method for the Quantification of Procalcitonin in Human Serum Using a Characterized Recombinant Protein as a Primary Calibrator.

Authors:  Huu-Hien Huynh; Vincent Delatour; Maxence Derbez-Morin; Qinde Liu; Amandine Boeuf; Joëlle Vinh
Journal:  Anal Chem       Date:  2022-03-02       Impact factor: 6.986

2.  Comparison of a novel automated DiaSys procalcitonin immunoassay with four different BRAHMS-partnered immunoassays.

Authors:  Abass Eidizadeh; Mechthild Wiederhold; Moritz Schnelle; Lutz Binder
Journal:  Pract Lab Med       Date:  2022-04-12
  2 in total

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