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DOI: 10.1055/a-2695-2674
Usefulness and Limits of DOAC Removal Agents Based on Activated Charcoal in Thrombophilia Testing: Literature Review and Expert Proposals
Authors

Abstract
Although inherited and acquired thrombophilia screening should ideally be performed outside of any direct oral anticoagulant (DOAC) therapy, it is sometimes performed in patients who are anticoagulated. However, DOACs have been shown to interfere with many hemostasis tests, with a risk of false-positive/negative results in lupus anticoagulant testing and overestimation of natural coagulation inhibitor levels, which may lead to misdiagnosis. Devices have been developed to overcome DOAC interference but their role in thrombophilia testing is not clearly established. In this comprehensive review, we provide an in-depth overview of the literature on the impact of DOACs on thrombophilia assays, including lupus anticoagulant testing, antithrombin, protein C, and protein S assessment. DOACs can interfere with the results of thrombophilia testing even at low concentrations; therefore information on current or recently discontinued anticoagulant treatment should be provided when prescribing thrombophilia testing. Data on the usefulness of the most used DOAC removal systems based on activated charcoal to circumvent DOAC interference are heterogeneous. They are summarized in this critical review. Although activated charcoal could be useful to remove DOACs from plasma prior to thrombophilia testing, it may not be completely effective, particularly with apixaban. Hence, and in the light of the available literature, we provide 22 practical proposals for reliable thrombophilia testing and accurate result interpretation in samples from patients receiving DOACs and treated in vitro with activated charcoal.
Contributions' Statement
G.J., C.F., E.D.M., N.G., V.E., and L.M. reviewed the literature; G.J., C.F., E.D.M., N.G., V.E., and L.M. wrote the manuscript. All authors reviewed the manuscript and approved the submitted version.
Publication History
Received: 02 June 2025
Accepted: 03 September 2025
Article published online:
29 September 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
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References
- 1 Sanchez O, Benhamou Y, Bertoletti L. et al. [Recommendations for best practice in the management of venous thromboembolic disease in adults. Long version]. Rev Mal Respir 2021; 38 (Suppl. 01) e1-e6
- 2 Trillot N, Marlu R, Suchon P. et al. Prescription et réalisation d'un bilan biologique à la recherche d'une thrombophilie: propositions du GFHT 2022 Partie I: aspects cliniques et prescription dans la maladie thromboembolique veineuse classique. Revue Francophone d'Hémostase et Thrombose. Accessed February 23, 2024 at: https://www.rfht.fr/publication/prescription-et-realisation-dun-bilan-biologique-a-la-recherche-dune-thrombophilie-propositions-du-gfht-2022-partie-i-aspects-cliniques-et-prescription-dans-la-maladie-thromboemb/
- 3 Middeldorp S, Nieuwlaat R, Baumann Kreuziger L. et al. American Society of Hematology 2023 guidelines for management of venous thromboembolism: thrombophilia testing. Blood Adv 2023; 7 (22) 7101-7138
- 4 Arachchillage DJ, Mackillop L, Chandratheva A, Motawani J, MacCallum P, Laffan M. Thrombophilia testing: a British Society for Haematology guideline. Br J Haematol 2022; 198 (03) 443-458
- 5 Mannucci PM, Franchini M. Classic thrombophilic gene variants. Thromb Haemost 2015; 114 (05) 885-889
- 6 Schreiber K, Sciascia S, de Groot PG. et al. Antiphospholipid syndrome. Nat Rev Dis Primers 2018; 4: 18005
- 7 Khider L, Gendron N, Mauge L. Inherited thrombophilia in the era of direct oral anticoagulants. Int J Mol Sci 2022; 23 (03) 1821
- 8 Di Minno MND, Ambrosino P, Ageno W, Rosendaal F, Di Minno G, Dentali F. Natural anticoagulants deficiency and the risk of venous thromboembolism: a meta-analysis of observational studies. Thromb Res 2015; 135 (05) 923-932
- 9 Simone B, De Stefano V, Leoncini E. et al. Risk of venous thromboembolism associated with single and combined effects of factor V Leiden, prothrombin 20210A and methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls. Eur J Epidemiol 2013; 28 (08) 621-647
- 10 Konstantinides SV, Meyer G, Becattini C. et al; ESC Scientific Document Group. 2019 ESC Guidelines for the diagnosis and management of acute pulmonary embolism developed in collaboration with the European Respiratory Society (ERS). Eur Heart J 2020; 41 (04) 543-603
- 11 van Es N, Coppens M, Schulman S, Middeldorp S, Büller HR. Direct oral anticoagulants compared with vitamin K antagonists for acute venous thromboembolism: evidence from phase 3 trials. Blood 2014; 124 (12) 1968-1975
- 12 Ageno W, Caramelli B, Donadini MP, Girardi L, Riva N. Changes in the landscape of anticoagulation: a focus on direct oral anticoagulants. Lancet Haematol 2024; 11 (12) e938-e950
- 13 Gosselin RC, Adcock DM, Douxfils J. An update on laboratory assessment for direct oral anticoagulants (DOACs). Int J Lab Hematol 2019; 41 (Suppl. 01) 33-39
- 14 Moore GW, Jones PO, Platton S. et al. International multicenter, multiplatform study to validate Taipan snake venom time as a lupus anticoagulant screening test with ecarin time as the confirmatory test: communication from the ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies. J Thromb Haemost 2021; 19 (12) 3177-3192
- 15 Godier A, Dincq AS, Martin AC. et al. Predictors of pre-procedural concentrations of direct oral anticoagulants: a prospective multicentre study. Eur Heart J 2017; 38 (31) 2431-2439
- 16 Prescription et réalisation d'un bilan biologique à la recherche d'une thrombophilie: propositions du GFHT 2022 Partie II: aspects méthodologiques et biologiques - v2.1. Revue Francophone d'Hémostase et Thrombose. Accessed March 16, 2025 at: https://www.rfht.fr/publication/prescription-et-realisation-dun-bilan-biologique-a-la-recherche-dune-thrombophilie-propositions-du-gfht-2022-partie-ii-aspects-methodologiques-et-biologiques-v2-1/
- 17 Van Cott EM, Orlando C, Moore GW, Cooper PC, Meijer P, Marlar R. Subcommittee on Plasma Coagulation Inhibitors. Recommendations for clinical laboratory testing for antithrombin deficiency; communication from the SSC of the ISTH. J Thromb Haemost 2020; 18 (01) 17-22
- 18 Lindahl TL, Baghaei F, Blixter IF. et al; Expert Group on Coagulation of the External Quality Assurance in Laboratory Medicine in Sweden. Effects of the oral, direct thrombin inhibitor dabigatran on five common coagulation assays. Thromb Haemost 2011; 105 (02) 371-378
- 19 Adcock DM, Gosselin R, Kitchen S, Dwyre DM. The effect of dabigatran on select specialty coagulation assays. Am J Clin Pathol 2013; 139 (01) 102-109
- 20 Van Blerk M, Bailleul E, Chatelain B. et al. Influence of dabigatran and rivaroxaban on routine coagulation assays. A nationwide Belgian survey. Thromb Haemost 2015; 113 (01) 154-164
- 21 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 (04) 355-364
- 22 Douxfils J, Mullier F, Robert S, Chatelain C, Chatelain B, Dogné JM. Impact of dabigatran on a large panel of routine or specific coagulation assays. Laboratory recommendations for monitoring of dabigatran etexilate. Thromb Haemost 2012; 107 (05) 985-997
- 23 Kim YA, Gosselin R, Van Cott EM. The effects of dabigatran on lupus anticoagulant, diluted plasma thrombin time, and other specialized coagulation assays. Int J Lab Hematol 2015; 37 (04) e81-e84
- 24 Hillarp A, Baghaei F, Fagerberg Blixter I. et al. Effects of the oral, direct factor Xa inhibitor rivaroxaban on commonly used coagulation assays. J Thromb Haemost 2011; 9 (01) 133-139
- 25 Bonar R, Favaloro EJ, Mohammed S. et al. The effect of the direct factor Xa inhibitors apixaban and rivaroxaban on haemostasis tests: a comprehensive assessment using in vitro and ex vivo samples. Pathology 2016; 48 (01) 60-71
- 26 Gosselin R, Grant RP, Adcock DM. Comparison of the effect of the anti-Xa direct oral anticoagulants apixaban, edoxaban, and rivaroxaban on coagulation assays. Int J Lab Hematol 2016; 38 (05) 505-513
- 27 Gerotziafas GT, Baccouche H, Sassi M. et al. Optimisation of the assays for the measurement of clotting factor activity in the presence of rivaroxaban. Thromb Res 2012; 129 (01) 101-103
- 28 Douxfils J, Chatelain C, Chatelain B, Dogné JM, Mullier F. Impact of apixaban on routine and specific coagulation assays: a practical laboratory guide. Thromb Haemost 2013; 110 (02) 283-294
- 29 Van Blerk M, Bailleul E, Chatelain B. et al. Influence of apixaban on commonly used coagulation assays: results from the Belgian national External Quality Assessment Scheme. Int J Lab Hematol 2017; 39 (04) 402-408
- 30 Hillarp A, Gustafsson KM, Faxälv L. et al. Effects of the oral, direct factor Xa inhibitor apixaban on routine coagulation assays and anti-FXa assays. J Thromb Haemost 2014; 12 (09) 1545-1553
- 31 Rühl H, Reda S, Müller J, Oldenburg J, Pötzsch B. Activated factor X-based versus thrombin-based antithrombin testing in thrombophilia workup in the DOAC era. Thromb Haemost 2018; 118 (02) 381-387
- 32 Vercruyssen J, Meeus P, Bailleul E. Resolving DOAC interference on antithrombin activity testing on a FXa based method by the use of activated carbon. Clin Chim Acta 2023; 538: 216-220
- 33 Jacquemin M, Toelen J, Schoeters J. et al. The addition of idarucizumab to plasma samples containing dabigatran allows the use of routine coagulation assays for the diagnosis of hemostasis disorders. J Thromb Haemost 2015; 13 (11) 2087-2092
- 34 Hillarp A, Strandberg K, Baghaei F, Fagerberg Blixter I, Gustafsson KM, Lindahl TL. Effects of the oral, direct factor Xa inhibitor edoxaban on routine coagulation assays, lupus anticoagulant and anti-Xa assays. Scand J Clin Lab Invest 2018; 78 (7-8): 575-583
- 35 Douxfils J, Chatelain B, Chatelain C, Dogné JM, Mullier F. Edoxaban: impact on routine and specific coagulation assays. A practical laboratory guide. Thromb Haemost 2016; 115 (02) 368-381
- 36 Douxfils J, Mullier F, Loosen C, Chatelain C, Chatelain B, Dogné JM. Assessment of the impact of rivaroxaban on coagulation assays: laboratory recommendations for the monitoring of rivaroxaban and review of the literature. Thromb Res 2012; 130 (06) 956-966
- 37 Buckley GT, Murphy B, Fleming N, Crowley MP, Harte JV. Removing direct oral factor Xa inhibitor interferences from routine and specialised coagulation assays using a raw activated charcoal product. Clin Chim Acta 2023; 550: 117565
- 38 Mani H, Hesse C, Stratmann G, Lindhoff-Last E. Rivaroxaban differentially influences ex vivo global coagulation assays based on the administration time. Thromb Haemost 2011; 106 (01) 156-164
- 39 Cooper PC, Pavlova A, Moore GW, Hickey KP, Marlar RA. Recommendations for clinical laboratory testing for protein C deficiency, for the subcommittee on plasma coagulation inhibitors of the ISTH. J Thromb Haemost 2020; 18 (02) 271-277
- 40 Marlar RA, Gausman JN, Tsuda H, Rollins-Raval MA, Brinkman HJM. Recommendations for clinical laboratory testing for protein S deficiency: communication from the SSC committee plasma coagulation inhibitors of the ISTH. J Thromb Haemost 2021; 19 (01) 68-74
- 41 Smock KJ, Plumhoff EA, Meijer P. et al. Protein S testing in patients with protein S deficiency, factor V Leiden, and rivaroxaban by North American specialized coagulation laboratories. Thromb Haemost 2016; 116 (01) 50-57
- 42 Maryamchik E, Rosenbaum MW, Van Cott EM. Rivaroxaban causes missed diagnosis of protein S deficiency but not of activated protein C resistance (factor V Leiden). Arch Pathol Lab Med 2018; 142 (01) 70-74
- 43 Maryamchik E, Van Cott EM. Apixaban does not interfere with protein S or activated protein C resistance (factor V Leiden) testing using aPTT-based methods. Arch Pathol Lab Med 2020; 144 (11) 1401-1407
- 44 Gessoni G, Valverde S, Gessoni F, Valle R. The effect of dabigatran and rivarovaban on a prothrombinase-based assay for activated protein C resistance: a preliminary study in subjects heterozygous for factor V Leiden. Blood Transfus 2015; 13 (04) 666-668
- 45 Gessoni G, Valverde S, Valle L, Caruso P, Gessoni F, Valle R. Effect of dabigatran on a prothrombinase-based assay for detecting activated protein C resistance: an ex vivo and in vitro study in normal subjects and factor V Leiden carriers. Blood Transfus 2017; 15 (06) 562-567
- 46 Gessoni G, Valverde S, Valle L, Gessoni F, Caruso P, Valle R. Lack of rivaroxaban influence on a prothrombinase-based assay for the detection of activated C protein resistance: an Italian ex vivo and in vitro study in normal subjects and factor V Leiden carriers. Int J Lab Hematol 2017; 39 (04) 418-422
- 47 Barbhaiya M, Zuily S, Naden R. et al; ACR/EULAR APS Classification Criteria Collaborators. The 2023 ACR/EULAR antiphospholipid syndrome classification criteria. Arthritis Rheumatol 2023; 75 (10) 1687-1702
- 48 Cervera R. Antiphospholipid syndrome. Thromb Res 2017; 151 (Suppl. 01) S43-S47
- 49 Keeling D, Mackie I, Moore GW, Greer IA, Greaves M. British Committee for Standards in Haematology. Guidelines on the investigation and management of antiphospholipid syndrome. Br J Haematol 2012; 157 (01) 47-58
- 50 Pengo V, Tripodi A, Reber G. et al; Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibody of the Scientific and Standardisation Committee of the International Society on Thrombosis and Haemostasis. Update of the guidelines for lupus anticoagulant detection. J Thromb Haemost 2009; 7 (10) 1737-1740
- 51 Devreese KMJ, Bertolaccini ML, Branch DW. et al. An update on laboratory detection and interpretation of antiphospholipid antibodies for diagnosis of antiphospholipid syndrome: guidance from the ISTH-SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies. J Thromb Haemost 2025; 23 (02) 731-744
- 52 Favaloro EJ, Mohammed S, Curnow J, Pasalic L. Laboratory testing for lupus anticoagulant (LA) in patients taking direct oral anticoagulants (DOACs): potential for false positives and false negatives. Pathology 2019; 51 (03) 292-300
- 53 Martinuzzo ME, Barrera LH, D'adamo MA, Otaso JC, Gimenez MI, Oyhamburu J. Frequent false-positive results of lupus anticoagulant tests in plasmas of patients receiving the new oral anticoagulants and enoxaparin. Int J Lab Hematol 2014; 36 (02) 144-150
- 54 Ratzinger F, Lang M, Belik S. et al. Lupus-anticoagulant testing at NOAC trough levels. Thromb Haemost 2016; 116 (02) 235-240
- 55 Antovic A, Norberg EM, Berndtsson M. et al. Effects of direct oral anticoagulants on lupus anticoagulant assays in a real-life setting. Thromb Haemost 2017; 117 (09) 1700-1704
- 56 Malik NEH, Ward A, Erskine B. Comparing the effect of DOAC-Stop® and DOAC-Remove® on apixaban, rivaroxaban and dabigatran prior to thrombophilia and lupus testing. Br J Biomed Sci 2024; 81: 13359
- 57 Jacquemin M, Toelen J, Feyen L. et al. The adsorption of dabigatran is as efficient as addition of idarucizumab to neutralize the drug in routine coagulation assays. Int J Lab Hematol 2018; 40 (04) 442-447
- 58 Flieder T, Weiser M, Eller T. et al. Interference of DOACs in different DRVVT assays for diagnosis of lupus anticoagulants. Thromb Res 2018; 165: 101-106
- 59 Depreter B, Devreese KMJ. Dilute Russell's viper venom time reagents in lupus anticoagulant testing: a well-considered choice. Clin Chem Lab Med 2017; 55 (01) 91-101
- 60 Merriman E, Kaplan Z, Butler J, Malan E, Gan E, Tran H. Rivaroxaban and false positive lupus anticoagulant testing. Thromb Haemost 2011; 105 (02) 385-386
- 61 van Os GMA, de Laat B, Kamphuisen PW, Meijers JCM, de Groot PG. Detection of lupus anticoagulant in the presence of rivaroxaban using Taipan snake venom time. J Thromb Haemost 2011; 9 (08) 1657-1659
- 62 Martinuzzo ME, Forastiero R, Duboscq C. et al. False-positive lupus anticoagulant results by DRVVT in the presence of rivaroxaban even at low plasma concentrations. Int J Lab Hematol 2018; 40 (05) e99-e101
- 63 Gay J, Duchemin J, Imarazene M, Fontenay M, Jourdi G. Lupus anticoagulant diagnosis in patients receiving direct oral FXa inhibitors at trough levels: a real-life study. Int J Lab Hematol 2019; 41 (06) 738-744
- 64 Reda S, Brügelmann A, Müller J, Oldenburg J, Pötzsch B, Rühl H. Functional lupus anticoagulant testing in a large retrospective cohort of thrombosis patients with direct oral anticoagulants. Sci Rep 2020; 10 (01) 12221
- 65 Arachchillage DRJ, Gomez K, Alikhan R, Anderson JAM, Lester W, Laffan M. British Society for Haematology Haemostasis and Thrombosis Taskforce. Addendum to British Society for Haematology Guidelines on Investigation and Management of Antiphospholipid syndrome, 2012 (Br. J. Haematol. 2012; 157: 47-58): use of direct acting oral anticoagulants. Br J Haematol 2020; 189 (02) 212-215
- 66 Mani H, Hesse C, Stratmann G, Lindhoff-Last E. Ex vivo effects of low-dose rivaroxaban on specific coagulation assays and coagulation factor activities in patients under real life conditions. Thromb Haemost 2013; 109 (01) 127-136
- 67 De Kesel PM, Devreese KMJ. Direct oral anticoagulant adsorption: impact on lupus anticoagulant testing-Review of the literature and evaluation on spiked and patient samples. J Thromb Haemost 2020; 18 (08) 2003-2017
- 68 Favresse J, Lardinois B, Sabor L. et al. Evaluation of the DOAC-Stop® procedure to overcome the effect of DOACs on several thrombophilia screening tests. TH Open 2018; 2 (02) e202-e209
- 69 Thiriet A, Poindron V, Sattler L. et al. Evaluation of an integrated activated partial thromboplastin time (Cephen LS/Cephen) for the detection of lupus anticoagulant. Int J Lab Hematol 2024; 46 (06) 1109-1117
- 70 Favaloro EJ, Gilmore G, Arunachalam S, Mohammed S, Baker R. Neutralising rivaroxaban induced interference in laboratory testing for lupus anticoagulant (LA): a comparative study using DOAC Stop and andexanet alfa. Thromb Res 2019; 180: 10-19
- 71 Gendron N, Billoir P, Siguret V. et al; French Society on Thrombosis and Haemostasis. Is there a role for the laboratory monitoring in the management of specific antidotes of direct oral anticoagulants?. Thromb Res 2024; 237: 171-180
- 72 Frackiewicz A, Kalaska B, Miklosz J, Mogielnicki A. The methods for removal of direct oral anticoagulants and heparins to improve the monitoring of hemostasis: a narrative literature review. Thromb J 2023; 21 (01) 58
- 73 Exner T, Dangol M, Favaloro EJ. Simplified method for removing direct oral anticoagulant interference in mechanical coagulation test systems—a proof of concept. J Clin Med 2024; 13 (04) 1042
- 74 Sevenet PO, Cucini V, Hervé T. et al. Evaluation of DOAC Filter, a new device to remove direct oral anticoagulants from plasma samples. Int J Lab Hematol 2020; 42 (05) 636-642
- 75 Farkh C, Ellouze S, Gounelle L. et al. A diagnostic solution for lupus anticoagulant testing in patients taking direct oral FXa inhibitors using DOAC filter. Front Med (Lausanne) 2021; 8: 683357
- 76 Linskens EA, De Kesel P, Devreese KMJ. Direct oral anticoagulant removal by a DOAC filter: impact on lupus anticoagulant testing—evaluation on spiked and patient samples. Res Pract Thromb Haemost 2022; 6 (02) e12633
- 77 Savola P, Lemponen M, Joutsi-Korhonen L, Helin TA. Novel ex vivo DOAC removal methods reduce interference in lupus anticoagulant testing. Diagnostics (Basel) 2022; 12 (10) 2520
- 78 Douxfils J, Adcock DM, Bates SM. et al. 2021 update of the International Council for Standardization in Haematology recommendations for laboratory measurement of direct oral anticoagulants. Thromb Haemost 2021; 121 (08) 1008-1020
- 79 Jourdi G, Delrue M, Stepanian A. et al. Potential usefulness of activated charcoal (DOAC remove®) for dRVVT testing in patients receiving direct oral anticoagulants. Thromb Res 2019; 184: 86-91
- 80 Melicine S, Habay C, Ghammad W. et al. DOAC-Remove to counteract the interference of anti-Xa oral anticoagulants on the monitoring of heparin. Int J Lab Hematol 2024; 46 (05) 953-962
- 81 Favre R, Zia-Chahabi S, Talb Y, de Gunzburg N, Flaujac C. Direct oral anticoagulant neutralization by activated charcoal DOAC-Remove for thrombophilia screening. Blood Coagul Fibrinolysis 2021; 32 (05) 356-358
- 82 Raulet-Bussian C, Launois A, Perez F. et al. Reducing factor V Leiden interference in clotting-based protein C activity assays, including in patients with direct factor Xa oral anticoagulant. Int J Lab Hematol 2025; 47 (03) 544-547
- 83 Platton S, Hunt C. Influence of DOAC Stop on coagulation assays in samples from patients on rivaroxaban or apixaban. Int J Lab Hematol 2019; 41 (02) 227-233
- 84 Novelli C, Pradella P, Papandrea M, Montaruli B. Direct oral anticoagulant adsorption and laboratory detection of lupus anticoagulant. Blood Coagul Fibrinolysis 2023; 34 (03) 199-205
- 85 Tripodi A, Scalambrino E, Chantarangkul V. et al. Impact of a commercially available DOAC absorbent on two integrated procedures for lupus anticoagulant detection. Thromb Res 2021; 204: 32-39
- 86 Cox-Morton S, MacDonald S, Thomas W. A diagnostic solution for haemostasis laboratories for patients taking direct oral anticoagulants using DOAC-Remove. Br J Haematol 2019; 187 (03) 377-385
- 87 Baker SA, Jin J, Pfaffroth C, Vu T, Zehnder JL. DOAC-Stop in lupus anticoagulant testing: direct oral anticoagulant interference removed in most samples. Res Pract Thromb Haemost 2021; 5 (02) 314-325
- 88 Monteyne T, De Kesel P, Devreese KMJ. Interference of DOAC stop and DOAC remove in the thrombin generation assay and coagulation assays. Thromb Res 2020; 192: 96-99
- 89 Ząbczyk M, Natorska J, Kopytek M, Malinowski KP, Undas A. The effect of direct oral anticoagulants on antithrombin activity testing is abolished by DOAC-Stop in venous thromboembolism patients. Arch Pathol Lab Med 2021; 145 (01) 99-104
- 90 Kopytek M, Ząbczyk M, Malinowski KP, Undas A, Natorska J. DOAC-Remove abolishes the effect of direct oral anticoagulants on activated protein C resistance testing in real-life venous thromboembolism patients. Clin Chem Lab Med 2020; 58 (03) 430-437
- 91 Tripodi A, Cohen H, Devreese KMJ. Lupus anticoagulant detection in anticoagulated patients. Guidance from the Scientific and Standardization Committee for lupus anticoagulant/antiphospholipid antibodies of the International Society on Thrombosis and Haemostasis. J Thromb Haemost 2020; 18 (07) 1569-1575
- 92 Slavik L, Jacova J, Friedecky D. et al. Evaluation of the DOAC-Stop procedure by LC-MS/MS assays for determining the residual activity of dabigatran, rivaroxaban, and apixaban. Clin Appl Thromb Hemost 2019; 25: 1076029619872556
- 93 Skaugen JM, Sayre C, Hassett AC. et al. Performance characteristics of DOAC-Remove for neutralization of the effects of apixaban and rivaroxaban in lupus anticoagulant assays. Am J Clin Pathol 2022; 157 (03) 457-469
- 94 Riva N, Vella K, Hickey K. et al. The effect of DOAC-Stop® on several oral and parenteral anticoagulants. Int J Lab Hem 2021; 43: O171-O175
- 95 Frans G, Meeus P, Bailleul E. Resolving DOAC interference on aPTT, PT, and lupus anticoagulant testing by the use of activated carbon. J Thromb Haemost 2019; 17 (08) 1354-1362
- 96 White D, Moore GW, Besser M, MacDonald S, Thomas W. Direct oral anticoagulants-Remove versus Taipan snake venom time for detection of a lupus anticoagulant in patients taking oral direct factor Xa inhibitors. Res Pract Thromb Haemost 2022; 6 (01) e12648
- 97 Favaloro EJ, Pasalic L. Lupus anticoagulant testing during anticoagulation, including direct oral anticoagulants. Res Pract Thromb Haemost 2022; 6 (02) e12676