TY - JOUR
T1 - Laboratory Testing In Patients Treated With Direct Oral Anticoagulants
T2 - A Practical Guide For Clinicians
AU - Douxfils, Jonathan
AU - Ageno, Walter
AU - Samama, Charles-Marc
AU - Lessire, Sarah
AU - Ten Cate, Hugo
AU - Verhamme, Peter
AU - Dogné, Jean-Michel
AU - Mullier, François
N1 - Funding Information:
W. Ageno reports personal fees and non-financial support from Stago and Daiichi Sankyo; grants, personal fees and non-financial support from Bayer Pharma and Boehringer Ingelheim; and personal fees from BMS/Pfizer and Aspen, outside the submitted work. H. ten Cate reports personal fees for being a consultant to STAGO, during the conduct of the study. J. Douxfils is CEO and founder of QUALIblood sa and reports personal fees from Stago and Daiichi-Sankyo, outside the submitted work. P. Ver-hamme reports grants and personal fees from Bayer Pharma, Boehringer Ingelheim and LeoPharma; personal fees from Daiichi Sankyo, BMS/Pfizer and Portola; and grants from Sanofi, outside the submitted work. C.-M. Samama reports speaker’s fees from Bayer, BMS, Pfizer, Siemens and Stago; he has sat on advisory committees for Bayer, Daiichi-Sankyo, Portola and Roche, and has been a primary investigator for Bayer, BMS and Boehringer-Ingelheim.
Publisher Copyright:
© 2017 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals, Inc. on behalf of International Society on Thrombosis and Haemostasis.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Click to hear Dr Baglin's perspective on the role of the laboratory in treatment with new oral anticoagulants. Summary: One of the key benefits of the direct oral anticoagulants (DOACs) is that they do not require routine laboratory monitoring. Nevertheless, assessment of DOAC exposure and anticoagulant effects may become useful in various clinical scenarios. The five approved DOACs (apixaban, betrixaban, dabigatran etexilate, edoxaban and rivaroxaban) have different characteristics impacting assay selection and the interpretation of results. This article provides an updated overview on (i) which test to use (and their advantages and limitations), (ii) when to assay DOAC levels, (iii) how to interpret the results relating to bleeding risk, emergency situations and perioperative management, and (iv) what is the impact of DOACs on routine and specialized coagulation assays. Assays for anti-Xa or anti-IIa activity are the preferred methods when quantitative information is useful, although the situations in which to test for DOAC levels are still debated. Different reagent sensitivities and variabilities in laboratory calibrations impact assay results. International calibration standards for all specific tests for each DOAC are needed to reduce the inter-laboratory variability and allow inter-study comparisons. The impact of the DOACs on hemostasis testing may cause false-positive or false-negative results; however, these can be minimized by using specific assays and collecting blood samples at trough concentrations. Finally, prospective clinical trials are needed to validate the safety and efficacy of proposed laboratory thresholds in relation to clinical decisions. We offer recommendations on the tests to use for measuring DOACs and practical guidance on laboratory testing to help patient management and avoid diagnostic errors.
AB - Click to hear Dr Baglin's perspective on the role of the laboratory in treatment with new oral anticoagulants. Summary: One of the key benefits of the direct oral anticoagulants (DOACs) is that they do not require routine laboratory monitoring. Nevertheless, assessment of DOAC exposure and anticoagulant effects may become useful in various clinical scenarios. The five approved DOACs (apixaban, betrixaban, dabigatran etexilate, edoxaban and rivaroxaban) have different characteristics impacting assay selection and the interpretation of results. This article provides an updated overview on (i) which test to use (and their advantages and limitations), (ii) when to assay DOAC levels, (iii) how to interpret the results relating to bleeding risk, emergency situations and perioperative management, and (iv) what is the impact of DOACs on routine and specialized coagulation assays. Assays for anti-Xa or anti-IIa activity are the preferred methods when quantitative information is useful, although the situations in which to test for DOAC levels are still debated. Different reagent sensitivities and variabilities in laboratory calibrations impact assay results. International calibration standards for all specific tests for each DOAC are needed to reduce the inter-laboratory variability and allow inter-study comparisons. The impact of the DOACs on hemostasis testing may cause false-positive or false-negative results; however, these can be minimized by using specific assays and collecting blood samples at trough concentrations. Finally, prospective clinical trials are needed to validate the safety and efficacy of proposed laboratory thresholds in relation to clinical decisions. We offer recommendations on the tests to use for measuring DOACs and practical guidance on laboratory testing to help patient management and avoid diagnostic errors.
KW - apixaban
KW - dabigatran
KW - edoxaban
KW - laboratory testing
KW - practical management
KW - rivaroxaban
UR - http://www.scopus.com/inward/record.url?scp=85039159991&partnerID=8YFLogxK
U2 - 10.1111/jth.13912
DO - 10.1111/jth.13912
M3 - Review article
C2 - 29193737
SN - 1538-7933
VL - 16
SP - 209
EP - 219
JO - Journal of Thrombosis and Haemostasis
JF - Journal of Thrombosis and Haemostasis
IS - 2
ER -