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Determination of Anti-Xa Inhibitor Plasma Concentrations Using a Universal Edoxaban Calibrator

Authors :
Nagler, Annika Burger
Jan-Dirk Studt
Adriana Mendez
Lorenzo Alberio
Pierre Fontana
Walter A. Wuillemin
Adrian Schmidt
Lukas Graf
Bernhard Gerber
Cédric Bovet
Thomas C. Sauter
Nikolaus B. Binder
Michael
Source :
Diagnostics; Volume 13; Issue 12; Pages: 2128
Publication Year :
2023
Publisher :
Multidisciplinary Digital Publishing Institute, 2023.

Abstract

A universal calibrator for the determination of all anti-Xa inhibitors would support laboratory processes. We aimed to test the clinical performance of an anti-Xa assay utilizing a universal edoxaban calibrator to determine clinically relevant concentrations of all anti-Xa inhibitors. Following a pilot study, we enrolled 553 consecutive patients taking rivaroxaban, edoxaban, or apixaban from nine study centers in a prospective cross-sectional study. The Technochrom® anti-Xa assay was conducted using the Technoview® edoxaban calibrator. Using ultra-high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS), anti-Xa inhibitor drug concentrations were determined. Sensitivities and specificities to detect three clinically relevant drug concentrations (30 µgL−1, 50 µgL−1, 100 µgL−1) were determined. Overall, 300 patients treated with rivaroxaban, 221 with apixaban, and 32 with edoxaban were included. The overall correlation coefficient (rs) was 0.95 (95% CI 0.94, 0.96). An area under the receiver operating characteristic curve of 0.96 for 30 µgL−1, 0.98 for 50 µgL−1, and 0.99 for 100 µgL−1 was found. The sensitivities were 92.3% (95% CI 89.2, 94.6), 92.7% (89.4, 95.1), and 94.8% (91.1, 97.0), respectively (specificities 82.2%, 93.7%, and 94.4%). In conclusion, the clinical performance of a universal, edoxaban-calibrated anti-Xa assay was solid and most drug concentrations were predicted correctly.

Details

Language :
English
ISSN :
20754418
Database :
OpenAIRE
Journal :
Diagnostics; Volume 13; Issue 12; Pages: 2128
Accession number :
edsair.multidiscipl..7c6f10980fc4c7a0d60211ffc8dc7faa
Full Text :
https://doi.org/10.3390/diagnostics13122128