Article

Once or Twice-daily NOAC Therapy – Theory and Practice

Register or Login to View PDF Permissions
Permissions× For commercial reprint enquiries please contact Springer Healthcare: ReprintsWarehouse@springernature.com.

For permissions and non-commercial reprint enquiries, please visit Copyright.com to start a request.

For author reprints, please email rob.barclay@radcliffe-group.com.
Information image
Average (ratings)
No ratings
Your rating

Abstract

On 12 November 2014, Radcliffe Cardiology, in association with Arrhythmia & Electrophysiology Review (AER) journal, held a roundtable discussion in London, UK. The discussion held between an expert group of physicians was moderated by Professor A John Camm, a renowned authority in anticoagulation and atrial fibrillation. The meeting comprised a series of seven presentations and subsequent panel discussions on a range of topical issues related to the use of non-vitamin K antagonist (novel) oral anticoagulants (NOACs): real-world versus clinical trial data; once or twice daily dosing regimens; spot checks or monitoring for anticoagulation status; antidotes for NOACs; NOACs and dual antiplatelet therapy; NOAC treatment in chronic renal impairment; and choosing between NOACs. This paper summarises the presentations and presents key highlights from the subsequent discussions.

Disclosure:Professor Camm is a consultant/advisor/speaker for Actelion, Astellas, AstraZeneca, Bayer, Boehringer Ingelheim, Boston Scientific, Biotronik, BMS, ChanRX, Daiichi Sankyo, Gilead, GSK, InfoBionic, Incarda, Johnson and Johnson, Medtronic, Menarini, Merck, Mitsubishi, Novartis, Otsuka, Pfizer, Sanofi, Servier, St. Jude Medical, Takeda and Xention; Doctor Alings is a consultant/advisor for Bayer, Boehringer Ingelheim, BMS/Pfizer, Daiichi Sankyo; Professor De Caterina has received a research grant from Boehringer Ingelheim, and is a consultant/advisor/speaker for Bayer, Boehringer Ingelheim, BMS/Pfizer, Daiichi Sankyo, Novartis; Professor Kirchhof has received research grants from BMS/Pfizer, Cardiovascular Therapeutics, Daiichi Sankyo, Sanofi, St. Jude Medical, and is consultant/advisor/speaker for Bayer, Boehringer Ingelheim, BMS, Daiichi Sankyo, Johnson & Johnson, Medtronic, MSD, Pfizer and Servier; Professor Le Heuzey is a consultant/advisor for Bayer, Boehringer Ingelheim, BMS/Pfizer and Daiichi Sanyo; Professor Verheugt is consultant/advisor for Bayer, Boehringer Ingelheim, BMS/Pfizer, Daiichi Sankyo

Received:

Accepted:

Published online:

Support:The roundtable was supported by an unrestricted educational grant from Daiichi-Sankyo.

Copyright Statement:

The copyright in this work belongs to Radcliffe Medical Media. Only articles clearly marked with the CC BY-NC logo are published with the Creative Commons by Attribution Licence. The CC BY-NC option was not available for Radcliffe journals before 1 January 2019. Articles marked ‘Open Access’ but not marked ‘CC BY-NC’ are made freely accessible at the time of publication but are subject to standard copyright law regarding reproduction and distribution. Permission is required for reuse of this content.

Professor Camm began by highlighting the decisions that need to be made when developing NOACs. Among the four available NOACs, two are taken once daily and two are taken twice daily. Since the half-life of each NOAC is around 12 h, the decision regarding whether to administer once or twice daily is a borderline one. Data from the EUropean Patient Survey in Atrial Fibrillation (EUPS-AF) regarding patient preferences for taking medication once daily or twice daily, show that, overall, 81 % stated a clear preference for once daily anticoagulation.16 However, the pharmacokinetics of these drugs is interesting. A drug given once daily has a much lower trough level after 24 h than a drug administered twice daily. If a once daily drug is missed, a very low trough level results, whereas the impact of missing a twice daily drug is of less concern since the patient remains presumably better anticoagulated. As a result, there is considerable debate about whether missing a single dose is more hazardous when a drug is given once or twice a day. However, in a phase II dose-finding study of edoxaban, the bleeding frequency was higher in the 30 mg twice daily group than in the 60 mg once daily group.17 Although studies with other NOACs did not show this effect, this intriguing finding has led physicians to question whether a once daily or twice daily regimen is preferable for NOACs.

Surveys have found that once daily regimens are associated with greater adherence than twice daily regimens: a database analysis of cardiovascular patients found that adherence to all agents was 16 % greater for once daily versus twice daily. (p<0.01).18 Another study found that nonvalvular AF patients treated with once daily dosing regimens for chronic medications were associated with approximately 26 % higher likelihood of adherence compared with subjects on twice daily regimens.19 Starting patients on rivaroxaban may decrease the number of total ischaemic strokes relative to warfarin treatment.20 It has been argued that if a patient is already taking medication on a twice daily basis, as many CV patients are, then giving another drug twice daily does not produce any issues, whereas others point out that once daily is more convenient, as most people can generally be in the same place once a day but not twice.

The panel reached no consensus on this controversial matter. In the experience of Professor Le Heuzey, patients who have previously taken once daily VKA have expressed reluctance to switch to a twice daily NOAC. Switching drugs from once daily to twice daily is more of an issue than initiation on a twice daily regimen. Other panellists considered that adherence to NOACs is essential and finding ways to improve adherence is a more important challenge than deciding whether once daily or twice daily dosing is better. Professor Kirchhof underlined the consistent signal from various phase III trials of less intracerebral haemorrhage with NOACs in comparison with VKA, irrespective of dosages, even the total dosages in some cases. In addition to pharmacokinetics, practical factors such as tablet size contribute to the totality of drug exposure. In terms of electrophysiology, missing a once-daily dose before a procedure could result in patients being suboptimally anticoagulated, e.g. for an ablation procedure, but whether once or twice a day, adherence in general remains a difficult matter. The panel agreed that it requires further study. Professor Camm concluded by stating that adherence is the key mediator between medical practice and patient outcomes.

References

  1. Camm AJ, Lip GY, De Caterina R, et al. 2012 focused update of the ESC Guidelines for the management of atrial fibrillation: an update of the 2010 ESC Guidelines for the management of atrial fibrillation. Developed with the special contribution of the European Heart Rhythm Association. Eur Heart J 2012;33:2719–47.
    Crossref | Pubmed
  2. Heidbuchel H, Verhamme P, Alings M, et al. EHRA practical guide on the use of new oral anticoagulants in patients with non-valvular atrial fibrillation: executive summary. Eur Heart J 2013;34:2094–106.
    Crossref | Pubmed
  3. Mohl W, Komamura K, Kasahara H, et al. Myocardial protection via the coronary sinus. Circ J 2008;72:526–33.
    Crossref | Pubmed
  4. Mant J, Hobbs FD, Fletcher K, et al. Warfarin versus aspirin for stroke prevention in an elderly community population with atrial fibrillation (the Birmingham Atrial Fibrillation Treatment of the Aged Study, BAFTA): a randomised controlled trial. Lancet 2007;370:493–503.
    Crossref | Pubmed
  5. Connolly SJ, Eikelboom J, Joyner C, et al. Apixaban in patients with atrial fibrillation. N Engl J Med 2011;364:806–17.
    Crossref | Pubmed
  6. Singer DE, Hylek EM. Optimal oral anticoagulation for patients with nonrheumatic atrial fibrillation and recent cerebral ischemia. N Engl J Med 1995;333:1504.
    Crossref | Pubmed
  7. Kirchhof P, Curtis AB, Skanes AC, et al. Atrial fibrillation guidelines across the Atlantic: a comparison of the current recommendations of the European Society of Cardiology/European Heart Rhythm Association/European Association of Cardiothoracic Surgeons, the American College of Cardiology Foundation/American Heart Association/Heart Rhythm Society, and the Canadian Cardiovascular Society. Eur Heart J 2013;34:1471–4.
    Crossref | Pubmed
  8. Connolly SJ, Ezekowitz MD, Yusuf S, et al. Dabigatran versus warfarin in patients with atrial fibrillation. N Engl J Med 2009;361:1139–51.
    Crossref | Pubmed
  9. Patel MR, Mahaffey KW, Garg J, et al. Rivaroxaban versus warfarin in nonvalvular atrial fibrillation. N Engl J Med 2011;365:883–91.
    Crossref | Pubmed
  10. Granger CB, Alexander JH, McMurray JJ, et al. Apixaban versus warfarin in patients with atrial fibrillation. N Engl J Med 2011;365:981–92.
    Crossref | Pubmed
  11. Giugliano RP, Ruff CT, Braunwald E, et al. Edoxaban versus warfarin in patients with atrial fibrillation. N Engl J Med 2013;369:2093–104.
    Crossref | Pubmed
  12. Ruff CT, Giugliano RP, Braunwald E, et al. Comparison of the efficacy and safety of new oral anticoagulants with warfarin in patients with atrial fibrillation: a meta-analysis of randomised trials. Lancet 2014;383:955–62.
    Crossref | Pubmed
  13. Kakkar AK, Mueller I, Bassand JP, et al. Risk profiles and antithrombotic treatment of patients newly diagnosed with atrial fibrillation at risk of stroke: perspectives from the international, observational, prospective GARFIELD registry.
    PLoS One 2013;8:e63479.
    Crossref | Pubmed
  14. Lip GY, Laroche C, Ioachim PM, et al. Prognosis and treatment of atrial fibrillation patients by European cardiologists: one year follow-up of the Eurobservational Research Programme-Atrial Fibrillation General Registry pilot phase (EORP-AF Pilot registry), Eur Heart J 2014;35:3365–76.
    Crossref | Pubmed
  15. Kirchhof P, Ammentorp B, Darius H, et al. Management of atrial fibrillation in seven European countries after the publication of the 2010 ESC Guidelines on atrial fibrillation: primary results of the Prevention of Thromboembolic Events – European Registry in Atrial Fibrillation (PREFER in AF). Europace 2014;16:6–14.
    Crossref | Pubmed
  16. Zamorano JL, Greiner W, Sandberg A, et al. Patient preferences for chronic treatment for stroke prevention: results from the European Patient Survey in Atrial Fibrillation (EUPS-AF). Poster P1789. Presented at European Society of Cardiology Congress, 25–29 August 2012; Munich, Germany.
  17. Weitz JI, Connolly SJ, Patel I, et al. Randomised, parallel-group, multicentre, multinational phase 2 study comparing edoxaban, an oral factor Xa inhibitor, with warfarin for stroke prevention in patients with atrial fibrillation. Thromb Haemost 2010;104:633–41.
    Crossref | Pubmed
  18. Bae JP, Dobesh PP, Klepser DG, et al. Adherence and dosing frequency of common medications for cardiovascular patients. Am J Manag Care 2012;18:139–46.
    Pubmed
  19. Laliberte F, Nelson WW, Lefebvre P, et al. Impact of daily dosing frequency on adherence to chronic medications among nonvalvular atrial fibrillation patients. Adv Ther 2012;29:675–90.
    Crossref | Pubmed
  20. Evers T, Diamantopoulos A. Clinical impact of treatment persistence in patients with atrial fibrillation. Value in Health 2013;16:A276.
    Crossref
  21. Douxfils J, Mullier F, Robert S, et al. Impact of dabigatran on a large panel of routine or specific coagulation assays. Laboratory recommendations for monitoring of dabigatran etexilate. Thromb Haemost 2012;107:985–97.
    Crossref | Pubmed
  22. Douxfils J, Mullier F, Loosen C, et al. Assessment of the impact of rivaroxaban on coagulation assays: laboratory recommendations for the monitoring of rivaroxaban and review of the literature. Thromb Res 2012;130:956–66.
    Crossref | Pubmed
  23. Becker RC, Yang H, Barrett Y, et al. Chromogenic laboratory assays to measure the factor Xa-inhibiting properties of apixaban – an oral, direct and selective factor Xa inhibitor.
    J Thromb Thrombolysis 2011;32:183–7.
    Crossref | Pubmed
  24. Cuker A, Siegal DM, Crowther MA, et al. Laboratory measurement of the anticoagulant activity of the non-vitamin K oral anticoagulants. J Am Coll Cardiol 2014;64:1128–39.
    Crossref | Pubmed
  25. Blann AD, Lip GY. Laboratory monitoring of the non-vitamin K oral anticoagulants. J Am Coll Cardiol 2014;64:1140–2.
    Crossref | Pubmed
  26. Makris M, Van Veen JJ, Tait CR, et al. Guideline on the management of bleeding in patients on antithrombotic agents. Br J Haematol 2013;160:35–46.
    Crossref | Pubmed
  27. Phase 2 healthy volunteer study to evaluate the ability of prt064445 to reverse the effects of several blood thinner drugs on laboratory tests. Available at: http://clinicaltrials.gov/ct2/show/NCT01758432?term=NCT01758432&rank=1 (accessed 27 November 2014).
  28. Crowther M, Vandana M, Michael K, et al. A phase 2 randomized, double-blind, placebo-controlled trial demonstrating reversal of rivaroxaban-induced anticoagulation in healthy subjects by andexanet alfa (PRT064445), an antidote for Fxa inhibitors. Abstract no 3636. Presented at the 55th Americal Society of Haematology (ASH) Annual Meeting and Exposition 7–10 December 2013; New Orleans, LA, US.
  29. US National Institutes of Health. A study in older subject to evaluate the safety and ability of andexanet alfa to reverse the anticoagulation effect of rivaroxaban. http://clinicaltrials.gov/ct2/show/NCT02220725 (accessed 27 November 2014).
  30. US National Institutes of Health. Study to evaluate the safety, pharmacokinetics and pharmacodynamics of BI 655075 administered alone or with dabigatran etexilate. Available at: http://clinicaltrials.gov/ct2/show/NCT01688830 (accessed 27 November 2014).
  31. US National Institutes of Health. Reversal of dabigatran anticoagulant effect with idarucizumab. Available at: http://clinicaltrials.gov/ct2/show/NCT02104947 (accessed 27 November 2014).
  32. US National Institutes of Health. Effects of a double-blind, single dose of per977 administered alone, and following a single dose of edoxaban (PER977-P1). Available at: http://clinicaltrials.gov/ct2/show/NCT01826266 (accessed 27 November 2014).
  33. Boehringer Ingelheim. US FDA grants breakthrough therapy designation to Pradaxa® (dabigatran etexilate) specific investigational antidote. Press release. Available at: www.boehringer-ingelheim.com/news/news_releases/press_releases/2014/30_june_2014_dabigatranetexilate.html (accessed 27 November 2014).
  34. van Ryn J, Sghmoll M, Pillu H, et al. Effect of dabigatran on the ability to generate fibrin at a wound site and its reversal by idarucizumab, the antidote to dabigatran, in healthy volunteers: an exploratory marker of blood loss. Abstract no 18403. Presented at the American Heart Association Scientific Sessions, 18 November 2014; Chicago, USA.
  35. Lip GY, Huber K, Andreotti F, et al. Antithrombotic management of atrial fibrillation patients presenting with acute coronary syndrome and/or undergoing coronary stenting: executive summary – A consensus document of the European Society of Cardiology Working Group on Thrombosis, endorsed by the European Heart Rhythm Association (EHRA) and the European Association of Percutaneous Cardiovascular Interventions (EAPCI), Eur Heart J 2010;31:1311–8.
    Crossref | Pubmed
  36. Hansen ML, Sorensen R, Clausen MT, et al. Risk of bleeding with single, dual, or triple therapy with warfarin, aspirin and clopidogrel in patients with atrial fibrillation. Arch Intern Med 2010;170:1433–41.
    Crossref | Pubmed
  37. European Heart Rhythm Association, European Association for Cardio-Thoracic Society, Camm AJ, et al. Guidelines for the management of atrial fibrillation: the Task Force for the Management of Atrial Fibrillation of the European Society of Cardiology (ESC). Eur Heart J 2010;31:2369–429.
    Crossref | Pubmed
  38. Faxon DP, Eikelboom JW, Berger PB, et al. Antithrombotic therapy in patients with atrial fibrillation undergoing coronary stenting: a North American perspective: executive summary. Circ Cardiovasc Interv 2011;4:522–34.
    Crossref | Pubmed
  39. US National Institutes of Health. A study exploring two strategies of rivaroxaban (JNJ39039039; BAY-59-7939) and one of oral vitamin K antagonist in patients with atrial fibrillation who undergo percutaneous coronary intervention. Available at: https://clinicaltrials.gov/ct2/show/NCT01830543 (accessed 17 March 2015).
  40. US National Institutes of Health. Evaluation of dual therapy with dabigatran vs. triple therapy with warfarin in patients with af that undergo a pci with stenting (REDUAL-PCI). Available at: http://clinicaltrials.gov/ct2/show/NCT02164864 (accessed 1 December 2014).
  41. Ogata K, Mendell-Harary J, Tachibana M, et al. Clinical safety, tolerability, pharmacokinetics, and pharmacodynamics of the novel factor Xa inhibitor edoxaban in healthy volunteers. J Clin Pharmacol 2010;50:743–53.
    Crossref | Pubmed
  42. Peacock WF, Gearhart MM, Mills RM. Emergency management of bleeding associated with old and new oral anticoagulants. Clin Cardiol 2012;35:730–7.
    Crossref | Pubmed