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Published in: Thrombosis Journal 1/2024

Open Access 01-12-2024 | Rivaroxaban | Research

Clot time ratio (CTR) and relation to treatment outcome in patients with atrial fibrillation treated with Rivaroxaban

Authors: Liselotte Onelöv, Elvar Theodorsson, Mojca Božič-Mijovski†, Alenka Mavri

Published in: Thrombosis Journal | Issue 1/2024

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Abstract

Background

There are situations where information about the anticoagulant effects of Rivaroxaban could be clinically useful. Methods for measuring Rivaroxaban concentrations are not available at all medical laboratories while the test MRX PT DOAC for measuring the functional effects of Rivaroxaban, in CTR (Clot Time Ratio), can be made available around the clock. The objectives of this study were to investigate CTR in trough and peak samples during Rivaroxaban treatment of atrial fibrillation and to correlate the findings to bleeding episodes.

Methods

3 trough- and 3 peak samples from 60 patients (30 on 20 mg daily and 30 on 15 mg daily) were analyzed with PT DOAC. Patients were monitored for 20 months, and bleeding and thrombotic events were documented. Descriptive statistics were used to summarize the data and non-parametric t-test for comparison between groups. ROC curves for the prediction of DOAC plasma levels > 50 ng/mL as determined with LC-MS/MS and anti-FXa methods were computed.

Results

There was a significant difference between trough and peak CTR (median CTR 1.33 vs. 3.57, p < 0.001). 28 patients suffered bleeds. Patients on 20 mg Rivaroxaban with bleeds had higher mean peak CTR than patients without bleeds (CTR 4.11 vs. CTR 3.47, p = 0.040). There was no significant difference in mean CTR between patients on 15 mg Rivaroxaban with or without bleeds (CTR 3.81 vs. 3.21, p = 0.803), or when considering all patients (CTR 3.63 vs. 3.56, p = 0.445). Five out of seven patients on Rivaroxaban 20 with mean peak CTR above the dose specific first to third quartile range (Q1-Q3) suffered bleeds, while 7/16 patients with mean peak CTR within, and 1/7 patients with mean peak CTR below the Q1-Q3 suffered bleeds. The area under the ROC curve was > 0.98 at the upper limit of the PT DOAC reference interval and the negative predictive value of PT DOAC for the prediction of DOAC plasma levels > 50 ng/mL was > 0.96.

Conclusions

The sample size was too low to draw any firm conclusions but is seems that MRX PT DOAC might be a useful laboratory test in situations where the effect of Rivaroxaban needs evaluation.
Literature
2.
go back to reference Douxfils J, Adcock DM, Bates SM, Favaloro EJ, Gouin-Thibault I, Guillermo C, et al. 2021 update of the International Council for Standardization in Haematology Recommendations for Laboratory Measurement of direct oral anticoagulants. Thromb Haemost. 2021;121(8):1008–20.CrossRefPubMed Douxfils J, Adcock DM, Bates SM, Favaloro EJ, Gouin-Thibault I, Guillermo C, et al. 2021 update of the International Council for Standardization in Haematology Recommendations for Laboratory Measurement of direct oral anticoagulants. Thromb Haemost. 2021;121(8):1008–20.CrossRefPubMed
3.
go back to reference Abelius M, Theodorsson ERM, Lindahl T. A Novel Prothrombin Time (PT) assay - A Tool for Rapid Screening of all non‐vitamin K‐Dependent oral anticoagulants (NOACs). Thromb Haemost. 2018;2:1. Abelius M, Theodorsson ERM, Lindahl T. A Novel Prothrombin Time (PT) assay - A Tool for Rapid Screening of all non‐vitamin K‐Dependent oral anticoagulants (NOACs). Thromb Haemost. 2018;2:1.
4.
go back to reference Lindahl TL, Arbring K, Wallstedt M, Ranby M. A novel prothrombin time method to measure all non-vitamin K-dependent oral anticoagulants (NOACs). Ups J Med Sci. 2017;122(3):171–6.CrossRefPubMedPubMedCentral Lindahl TL, Arbring K, Wallstedt M, Ranby M. A novel prothrombin time method to measure all non-vitamin K-dependent oral anticoagulants (NOACs). Ups J Med Sci. 2017;122(3):171–6.CrossRefPubMedPubMedCentral
5.
go back to reference Miklic M, Mavri A, Vene N, Soderblom L, Bozic-Mijovski M, Pohanka A, et al. Intra- and inter- individual rivaroxaban concentrations and potential bleeding risk in patients with atrial fibrillation. Eur J Clin Pharmacol. 2019;75(8):1069–75.CrossRefPubMed Miklic M, Mavri A, Vene N, Soderblom L, Bozic-Mijovski M, Pohanka A, et al. Intra- and inter- individual rivaroxaban concentrations and potential bleeding risk in patients with atrial fibrillation. Eur J Clin Pharmacol. 2019;75(8):1069–75.CrossRefPubMed
6.
go back to reference Mueck W, Stampfuss J, Kubitza D, Becka M. Clinical pharmacokinetic and pharmacodynamic profile of rivaroxaban. Clin Pharmacokinet. 2014;53(1):1–16.CrossRefPubMed Mueck W, Stampfuss J, Kubitza D, Becka M. Clinical pharmacokinetic and pharmacodynamic profile of rivaroxaban. Clin Pharmacokinet. 2014;53(1):1–16.CrossRefPubMed
7.
go back to reference Talerico R, Pola R, Huisman MV, Klok FA. DOACs plasma levels in relation to clinical outcome. How far have we come? Thromb Res. 2023;225:16–21.CrossRefPubMed Talerico R, Pola R, Huisman MV, Klok FA. DOACs plasma levels in relation to clinical outcome. How far have we come? Thromb Res. 2023;225:16–21.CrossRefPubMed
8.
go back to reference Jakowenko N, Nguyen S, Ruegger M, Dinh A, Salazar E, Donahue KR. Apixaban and rivaroxaban anti-xa level utilization and associated bleeding events within an academic health system. Thromb Res. 2020;196:276–82.CrossRefPubMedPubMedCentral Jakowenko N, Nguyen S, Ruegger M, Dinh A, Salazar E, Donahue KR. Apixaban and rivaroxaban anti-xa level utilization and associated bleeding events within an academic health system. Thromb Res. 2020;196:276–82.CrossRefPubMedPubMedCentral
9.
go back to reference Testa S, Paoletti O, Legnani C, Dellanoce C, Antonucci E, Cosmi B, et al. Low drug levels and thrombotic complications in high-risk atrial fibrillation patients treated with direct oral anticoagulants. J Thromb Haemost. 2018;16(5):842–8.CrossRefPubMed Testa S, Paoletti O, Legnani C, Dellanoce C, Antonucci E, Cosmi B, et al. Low drug levels and thrombotic complications in high-risk atrial fibrillation patients treated with direct oral anticoagulants. J Thromb Haemost. 2018;16(5):842–8.CrossRefPubMed
10.
go back to reference Testa S, Legnani C, Antonucci E, Paoletti O, Dellanoce C, Cosmi B, et al. Drug levels and bleeding complications in atrial fibrillation patients treated with direct oral anticoagulants. J Thromb Haemost. 2019;17(7):1064–72.CrossRefPubMedPubMedCentral Testa S, Legnani C, Antonucci E, Paoletti O, Dellanoce C, Cosmi B, et al. Drug levels and bleeding complications in atrial fibrillation patients treated with direct oral anticoagulants. J Thromb Haemost. 2019;17(7):1064–72.CrossRefPubMedPubMedCentral
11.
go back to reference Wada S, Toyoda K, Sato S, Matsuki T, Okata T, Kumamoto M, et al. Anti-xa activity and event risk in patients with direct factor xa inhibitors initiated early after stroke. Circ J. 2018;82(11):2872–9.CrossRefPubMed Wada S, Toyoda K, Sato S, Matsuki T, Okata T, Kumamoto M, et al. Anti-xa activity and event risk in patients with direct factor xa inhibitors initiated early after stroke. Circ J. 2018;82(11):2872–9.CrossRefPubMed
12.
go back to reference Bonar RA, Favaloro E, Marsden K, Sioufi J. The effects of direct oral anticoagulants apixaban and rivaroxaban on haemostasis tests: results from a comprehensive cross-laboratory exercise. J Thromb Haemost. 2015;13:640. Bonar RA, Favaloro E, Marsden K, Sioufi J. The effects of direct oral anticoagulants apixaban and rivaroxaban on haemostasis tests: results from a comprehensive cross-laboratory exercise. J Thromb Haemost. 2015;13:640.
13.
go back to reference Bonar R, Favaloro EJ, Mohammed S, Pasalic L, Sioufi J, Marsden K. The effect of dabigatran on haemostasis tests: a comprehensive assessment using in vitro and ex vivo samples. Pathology. 2015;47(4):355–64.CrossRefPubMed Bonar R, Favaloro EJ, Mohammed S, Pasalic L, Sioufi J, Marsden K. The effect of dabigatran on haemostasis tests: a comprehensive assessment using in vitro and ex vivo samples. Pathology. 2015;47(4):355–64.CrossRefPubMed
14.
go back to reference Gosselin RC, Adcock DM, Bates SM, Douxfils J, Favaloro EJ, Gouin-Thibault I, et al. International Council for Standardization in Haematology (ICSH) recommendations for Laboratory Measurement of direct oral anticoagulants. Thromb Haemostasis. 2018;118(3):437–50.CrossRef Gosselin RC, Adcock DM, Bates SM, Douxfils J, Favaloro EJ, Gouin-Thibault I, et al. International Council for Standardization in Haematology (ICSH) recommendations for Laboratory Measurement of direct oral anticoagulants. Thromb Haemostasis. 2018;118(3):437–50.CrossRef
15.
go back to reference Exner T, Ellwood L, Dangol M, Favaloro EJ. Mixing factor xa and thrombin inhibiting direct oral anticoagulants produces a synergistic prolonging effect on most clotting tests. Int J Lab Hematol. 2023. Exner T, Ellwood L, Dangol M, Favaloro EJ. Mixing factor xa and thrombin inhibiting direct oral anticoagulants produces a synergistic prolonging effect on most clotting tests. Int J Lab Hematol. 2023.
16.
go back to reference Exner T, Ellwood L, Rubie J, Barancewicz A. Testing for new oral anticoagulants with LA-resistant russells viper venom reagents. An in vitro study. Thromb Haemostasis. 2013;109(4):762–5.CrossRef Exner T, Ellwood L, Rubie J, Barancewicz A. Testing for new oral anticoagulants with LA-resistant russells viper venom reagents. An in vitro study. Thromb Haemostasis. 2013;109(4):762–5.CrossRef
17.
go back to reference Altman R, Gonzalez CD. Simple and rapid assay for effect of the new oral anticoagulant (NOAC) rivaroxaban: preliminary results support further tests with all NOACs. Thromb J. 2014;12(1):7.CrossRefPubMedPubMedCentral Altman R, Gonzalez CD. Simple and rapid assay for effect of the new oral anticoagulant (NOAC) rivaroxaban: preliminary results support further tests with all NOACs. Thromb J. 2014;12(1):7.CrossRefPubMedPubMedCentral
18.
go back to reference Altman R, Gonzalez CD. Supporting the use of a coagulometric method for rivaroxaban control: a hypothesis-generating study to define the safety cut-offs. Thromb J. 2015;13:26.CrossRefPubMedPubMedCentral Altman R, Gonzalez CD. Supporting the use of a coagulometric method for rivaroxaban control: a hypothesis-generating study to define the safety cut-offs. Thromb J. 2015;13:26.CrossRefPubMedPubMedCentral
19.
go back to reference Colombini MP, Derogis P, de Aranda VF, de Campos Guerra JC, Hamerschlak N, Mangueira CLP. Comparison of different laboratory tests in the evaluation of hemorrhagic risk of patients using rivaroxaban in the critical care setting: diagnostic accuracy study. Thromb J. 2017;15:21.CrossRefPubMedPubMedCentral Colombini MP, Derogis P, de Aranda VF, de Campos Guerra JC, Hamerschlak N, Mangueira CLP. Comparison of different laboratory tests in the evaluation of hemorrhagic risk of patients using rivaroxaban in the critical care setting: diagnostic accuracy study. Thromb J. 2017;15:21.CrossRefPubMedPubMedCentral
Metadata
Title
Clot time ratio (CTR) and relation to treatment outcome in patients with atrial fibrillation treated with Rivaroxaban
Authors
Liselotte Onelöv
Elvar Theodorsson
Mojca Božič-Mijovski†
Alenka Mavri
Publication date
01-12-2024
Publisher
BioMed Central
Published in
Thrombosis Journal / Issue 1/2024
Electronic ISSN: 1477-9560
DOI
https://doi.org/10.1186/s12959-024-00591-x

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