Evaluation of dabigatran, rivaroxaban and apixaban target-specific assays in a multicenter French study

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TitreEvaluation of dabigatran, rivaroxaban and apixaban target-specific assays in a multicenter French study
Type de publicationJournal Article
Year of Publication2017
AuteursGouin-Thibault I, Freyburger G, De Maistre E, Susen S, Delavenne X, Golmard J-L, Gruel Y, Sie P, Abecassis L, Aillaud M-F, Ajzenberg N, Alhenc-Gelas M, Flory AAppert, Bauters A, Biron C, Berruyer M, Jouvan FBlanc, Brionne-Francois M, d'Audigier C, Delahousse B, Donnard M, Eschwege V, Fischer F, Flaujac C, Fontana P, Galinat H, Hezard N, Huisse M-G, Le Cam-Duchez V, Le Flem L, Le Querrec A, Marlu R, Martin-Toutain I, Meley R, Menard-Deroure F, Meraud-Vialon G, Mourey G, Pineau-Vincent F, Sauget P, Toussaint-Hacquard M, Trichet C, Voisin S, DOAC GFHTStudy Grp
JournalTHROMBOSIS RESEARCH
Volume158
Pagination126-133
Date PublishedOCT
Type of ArticleArticle
ISSN0049-3848
Mots-clésAnti-Xa activity, aPTT, Dilute thrombin time, Direct factor Xa inhibitor, Direct thrombin inhibitor, DOAC measurement, Ecarin assay, PT
Résumé

Dabigatran etexilate, rivaroxaban and apixaban (DOACs) are widely used and measurement of their concentration is desirable in certain clinical situations. Target-specific assays are available but limited information exists on their performance especially in their ability to accurately measure low and high concentrations. Aims: To define, in a multicenter study, the precision and accuracy of DOAC measurements in daily practice. Methods: 15 plasma samples (kindly provided by Hyphen-Biomed) spiked with 5 blinded concentrations of dabigatran, rivaroxaban or apixaban (targeted 0-40-100-250-500 ng/mL, actual concentrations measured by HPLC-MS/MS), were sent to 30 haemostasis laboratories. DOAC concentration, PT and aPTT were measured once in each sample using local reagents. Interlaboratory precision was determined by its coefficient of variation (CV) and accuracy by its bias. Results: 464 DOAC measurements were performed in the 30 laboratories using 4 dabigatran and 5 rivaroxaban/apixaban calibrated assays on 3 analysers. Inter-laboratory CVs were below 18% for concentrations >= 100 ng/mL, and higher for concentrations similar to 40 ng/mL; biases were below 8% for all drugs and concentrations. In DOAC-free samples, concentrations were all below the lower limit of quantification except for one value (dabigatran: 35 ng/mL). Depending on the concentrations, significant differences were found between reagents in rivaroxaban and apixaban concentration values. PT and aPTT ratios displayed a low sensitivity to apixaban. Conclusion: Our results suggest that calibrated DOAC assays allow the reliable measurement of a wide range of drug concentrations, even though improvement of their performances is necessary, especially for measuring low concentrations.

DOI10.1016/j.thromres.2017.09.001