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Multicenter comparison of automated procalcitonin immunoassays

OBJECTIVES: A multicenter study to compare results of BRAHMS Kryptor PCT with those obtained using four BRAHMS-partnered procalcitonin (PCT) automated immunoassays (DiaSorin Liaison, BioMérieux Vidas, Roche Cobas E601 and Siemens Advia Centaur) and the Diazyme immunotubidimetric assay implemented on...

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Autores principales: Dipalo, Mariella, Guido, Lorena, Micca, Gianmatteo, Pittalis, Salvatore, Locatelli, Massimo, Motta, Andrea, Bianchi, Vincenza, Callegari, Tiziana, Aloe, Rosalia, Da Rin, Giorgio, Lippi, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597721/
https://www.ncbi.nlm.nih.gov/pubmed/28932801
http://dx.doi.org/10.1016/j.plabm.2015.07.001
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author Dipalo, Mariella
Guido, Lorena
Micca, Gianmatteo
Pittalis, Salvatore
Locatelli, Massimo
Motta, Andrea
Bianchi, Vincenza
Callegari, Tiziana
Aloe, Rosalia
Da Rin, Giorgio
Lippi, Giuseppe
author_facet Dipalo, Mariella
Guido, Lorena
Micca, Gianmatteo
Pittalis, Salvatore
Locatelli, Massimo
Motta, Andrea
Bianchi, Vincenza
Callegari, Tiziana
Aloe, Rosalia
Da Rin, Giorgio
Lippi, Giuseppe
author_sort Dipalo, Mariella
collection PubMed
description OBJECTIVES: A multicenter study to compare results of BRAHMS Kryptor PCT with those obtained using four BRAHMS-partnered procalcitonin (PCT) automated immunoassays (DiaSorin Liaison, BioMérieux Vidas, Roche Cobas E601 and Siemens Advia Centaur) and the Diazyme immunotubidimetric assay implemented on four clinical chemistry platforms (Abbott Architect c16000, Siemens Advia 2400, Roche Cobas C501 and Beckman Coulter AU5800). DESIGN AND METHODS: One hundred serum samples from in-patients with PCT values between 0.10 and 58.7 ng/mL were divided into aliquots and tested with the nine different reagents and analyzers. BRAHMS PCT Kryptor results were used as reference. RESULTS: Compared to BRAHMS PCT Kryptor, significant differences in results were observed on Vidas, Advia Centaur, Architect, Cobas C501 and AU5800. However, the correlation coeffiecients (r) with BRAHMS PCT Kryptor were between 0.899 and 0.988. The mean bias was less than ±1.02 ng/mL, except for Vidas (2.70 ng/mL). The agreement at three clinically relevant cut-offs was optimal: between 83–98% at 0.50 ng/mL, 90–97% at 2.0 ng/mL, and 98% at 10 ng/mL. The comparison of Diazyme PCT across the four clinical chemistry analyzers yielded high correlation coefficients (r between 0.952 and 0.976), a mean bias less than ±0.9 ng/mL, acceptable agreement at 0.5 ng/mL (>82%), and high concordance at the 2.0 ng/mL (>97%) and 10 ng/mL (>98%) cut-offs. CONCLUSIONS: The methods and applications evaluated in this multicenter study are aligned with BRAHMS PCT Kryptor and can be used for predicting the risk of progression to systemic inflammation in patients with bacterial infections using the conventional PCT diagnostic thresholds.
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spelling pubmed-55977212017-09-20 Multicenter comparison of automated procalcitonin immunoassays Dipalo, Mariella Guido, Lorena Micca, Gianmatteo Pittalis, Salvatore Locatelli, Massimo Motta, Andrea Bianchi, Vincenza Callegari, Tiziana Aloe, Rosalia Da Rin, Giorgio Lippi, Giuseppe Pract Lab Med Research Article OBJECTIVES: A multicenter study to compare results of BRAHMS Kryptor PCT with those obtained using four BRAHMS-partnered procalcitonin (PCT) automated immunoassays (DiaSorin Liaison, BioMérieux Vidas, Roche Cobas E601 and Siemens Advia Centaur) and the Diazyme immunotubidimetric assay implemented on four clinical chemistry platforms (Abbott Architect c16000, Siemens Advia 2400, Roche Cobas C501 and Beckman Coulter AU5800). DESIGN AND METHODS: One hundred serum samples from in-patients with PCT values between 0.10 and 58.7 ng/mL were divided into aliquots and tested with the nine different reagents and analyzers. BRAHMS PCT Kryptor results were used as reference. RESULTS: Compared to BRAHMS PCT Kryptor, significant differences in results were observed on Vidas, Advia Centaur, Architect, Cobas C501 and AU5800. However, the correlation coeffiecients (r) with BRAHMS PCT Kryptor were between 0.899 and 0.988. The mean bias was less than ±1.02 ng/mL, except for Vidas (2.70 ng/mL). The agreement at three clinically relevant cut-offs was optimal: between 83–98% at 0.50 ng/mL, 90–97% at 2.0 ng/mL, and 98% at 10 ng/mL. The comparison of Diazyme PCT across the four clinical chemistry analyzers yielded high correlation coefficients (r between 0.952 and 0.976), a mean bias less than ±0.9 ng/mL, acceptable agreement at 0.5 ng/mL (>82%), and high concordance at the 2.0 ng/mL (>97%) and 10 ng/mL (>98%) cut-offs. CONCLUSIONS: The methods and applications evaluated in this multicenter study are aligned with BRAHMS PCT Kryptor and can be used for predicting the risk of progression to systemic inflammation in patients with bacterial infections using the conventional PCT diagnostic thresholds. Elsevier 2015-07-17 /pmc/articles/PMC5597721/ /pubmed/28932801 http://dx.doi.org/10.1016/j.plabm.2015.07.001 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Dipalo, Mariella
Guido, Lorena
Micca, Gianmatteo
Pittalis, Salvatore
Locatelli, Massimo
Motta, Andrea
Bianchi, Vincenza
Callegari, Tiziana
Aloe, Rosalia
Da Rin, Giorgio
Lippi, Giuseppe
Multicenter comparison of automated procalcitonin immunoassays
title Multicenter comparison of automated procalcitonin immunoassays
title_full Multicenter comparison of automated procalcitonin immunoassays
title_fullStr Multicenter comparison of automated procalcitonin immunoassays
title_full_unstemmed Multicenter comparison of automated procalcitonin immunoassays
title_short Multicenter comparison of automated procalcitonin immunoassays
title_sort multicenter comparison of automated procalcitonin immunoassays
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597721/
https://www.ncbi.nlm.nih.gov/pubmed/28932801
http://dx.doi.org/10.1016/j.plabm.2015.07.001
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