Real-life evaluation of a hypersensitive troponin I measurement on a point-of-care analyzer in an emergency unit (notice n° 136025)

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control field 20250112021444.0
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Language code of text/sound track or separate title fre
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100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Mottin, Léo
Relator term author
245 00 - TITLE STATEMENT
Title Real-life evaluation of a hypersensitive troponin I measurement on a point-of-care analyzer in an emergency unit
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2023.<br/>
500 ## - GENERAL NOTE
General note 19
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Summary, etc. European Society of Cardiology (ESC) guidelines introduce the possibility of a rule-in and rule-out algorithm with rapid troponin kinetics to be created in order to manage suspected Non ST-elevation acute coronary syndrome. These recommendations allow the use of point-of-care testing (POCT) systems provided that they have sufficient analytical performance. The aim of our study was to evaluate in real life the feasibility and performance of using a high-sensitivity cardiac troponin I POCT system assay (hs-cTnI, Atellica® VTLi, Siemens) compared to values obtained by a high-sensitivity cardiac troponin T test (hs-cTnT, e602®, Roche) for patients admitted to the emergency department. Analytical verification showed a coefficient of variation below 10% for hs-cTnI. Comparison of both troponins was moderate (r = 0.7). The study included 117 patients with a median age of 65 years, 30% of whom had kidney failure and 36% of whom presented with chest pain. In this study, the hs-cTnT value was more often above the 99th percentile than the hs-cTnl value, even for an age-adjusted 99th percentile hs-cTnT value. The concordance of the results was moderate (Cohen’s Kappa: 0.54), with age remaining the most important explanatory value of discordance. Only hs-cTnT had a predictive value for hospitalization. We did not observe any interpretation discrepancies for patients who had troponin kinetics. This study confirms the feasibility of using a POCT analyzer in the emergency department, provided that it performs a high-sensitivity troponin test. However, some data are missing to be able to use it as part of a rapid algorithm. Finally, the implementation of POCT requires collaboration between biologists and emergency physicians in terms of organization and interpretation of values, for the overall benefit of the patient.
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Kassimy, Iliasse Idrissi
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Girot, Hélène
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Leguillon, Romain
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Joly, Luc Marie
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Brunel, Valery
Relator term author
786 0# - DATA SOURCE ENTRY
Note Annales de Biologie Clinique | 81 | 2 | 2023-03-01 | p. 145-155 | 0003-3898
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Uniform Resource Identifier <a href="https://shs.cairn.info/journal-annales-de-biologie-clinique-2023-2-page-145?lang=en">https://shs.cairn.info/journal-annales-de-biologie-clinique-2023-2-page-145?lang=en</a>

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