Clinical review

New anticoagulants in combination with antiplatelet agents

Norwegian
    Henriette Johansen, Ole-Christian Walter Rutherford, Anne Hege Aamodt, David Russell, Dan Atar, Waleed Ghanima
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    Henriette Johansen

    Henriette Johansen (born 1983) Specialty registrar and research fellow specialising in neurology. She and Ole-Christian Rutherford are the joint principal authors of the manuscript.

    The author has completed the ICMJE form and reports no conflicts of interest.

    Department of Neurology

    Division of Surgery and Clinical Neuroscience

    Oslo University Hospital, Rikshospitalet

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    Ole-Christian Walter Rutherford

    Ole-Christian Walter Rutherford (born 1981) Specialist in internal medicine and senior consultant in charge of Medical Intensive Care. He and Henriette Johansen are the joint principal authors of the manuscript.

    The author has completed the ICMJE form and reports no conflicts of interest.

    Email: ole-christian.rutherford@so-hf.no

    Department of Medicine

    Østfold Hospital

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    Anne Hege Aamodt
    Orcid

    Anne Hege Aamodt (born 1972) Specialist in neurology, senior consultant and post-doctoral researcher. She is chairman of the Norwegian Neurological Association. She contributed to the conception and design of the manuscript, made contributions during its preparation and has taken part in the revision.

    The author has completed the ICMJE form and reports the following conflicts of interest: she has received lecture fees from Boehringer-Ingelheim, BMS/Pfizer and Bayer Healthcare.

    Department of Neurology

    Division of Surgery and Clinical Neuroscience

    Oslo University Hospital, Rikshospitalet

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    David Russell

    David Russell (born 1948) Specialist in neurology, senior consultant and professor. He heads the cerebrovascular research at Oslo University Hospital. He made contributions during the preparation of the manuscript and participated in the revision.

    The author has completed the ICMJE form and reports the following conflicts of interest: he has received lecture fees from Boehringer-Ingelheim, BMS/Pfizer and Bayer Healthcare.

    Department of Neurology

    Division of Surgery and Clinical Neuroscience

    Oslo University Hospital, Rikshospitalet

    and

    Institute of Clinical Medicine

    University of Oslo

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    Dan Atar
    Orcid

    Dan Atar (born 1959) Specialist in internal medicine and in cardiology, senior consultant and professor. Head of research at the Medical Division, Oslo University Hospital. He contributed to the conception and design of the manuscript, made contributions during its preparation and took part in the revision.

    The author has completed the ICMJE form and reports the following conflicts of interest: he has received lecture fees from Boehringer-Ingelheim, BMS/Pfizer, Bayer Healthcare and Cardiome.

    Cardiology Department B

    Oslo University Hospital, Ullevål

    and

    Institute of Clinical Medicine

    University of Oslo

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    Waleed Ghanima

    Waleed Ghanima (born 1964) Specialist in internal medicine and blood diseases, head of the Blood Diseases Section and head of research at Østfold Hospital Trust. He contributed to the conception and design of the manuscript, made contributions during its preparation and took part in the revision.

    The author has completed the ICMJE form and reports the following conflicts of interest: he has received lecture fees from Boehringer-Ingelheim, BMS/Pfizer, Bayer Healthcare, Novartis and Roche.

    Department of Medicine

    Østfold Hospital

    and

    Institute of Clinical Medicine

    University of Oslo

    ()

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    Article

    The use of new, direct anticoagulants is increasing. Data from both controlled trials and clinical practice have shown that these drugs are as efficacious and safe as warfarin for deep vein thrombosis and pulmonary embolism, and as stroke prophylaxis for patients with atrial fibrillation. But what if platelet inhibition is also indicated? In the following, the combination of antiplatelets and the new anticoagulants is discussed for various indications.

    The new non-vitamin K oral anticoagulants (NOACs) or direct oral anticoagulants (DOACs) are included in the guidelines for thrombosis prophylaxis after hip and knee surgery, for preventing and treating venous thromboembolism (deep vein thrombosis and pulmonary embolism), for preventing stroke and TIA in connection with atrial fibrillation, and as secondary prophylaxis after mycoardial infarction (1). Apixaban, rivaroxaban and dabigatran are the three new drugs that have so far been approved for use in Norway. Edoxaban is approved in Europe, but not yet marketed in Norway (expected from the end of 2016).

    Since no randomised trials exist of the risk of bleeding inherent in using the new drugs in combination with antiplatelet agents, the evidence basis for this treatment is based on post-hoc analyses of phase 3 studies and expert consensus. We will review the evidence base and safety of combination therapy for the indications in question.

    The article is based on Norwegian, European and US guidelines (1) – (4), searches in PubMed for articles published from 1980 to November 2015 with combinations of relevant keywords, searches in the authors’ own literature archives and our clinical experience. Several of the authors have been involved in working on the European and Norwegian guidelines for the use of new anticoagulants (4, 5).

    Prevention of stroke and TIA in atrial fibrillation cases

    Prevention of stroke and TIA in atrial fibrillation cases

    Lifelong anticoagulation treatment is recommended for patients with atrial fibrillation and at least two risk factors for thromboembolism (CHA₂DS₂-VASc score ≥ 2). An individual evaluation should be made of those with only one risk factor (CHA₂DS₂-VASc score = 1). Female gender alone is not an indication for anticoagulation treatment (4).

    Dabigatran, rivaroxaban and apixaban are approved in Norway as stroke prophylaxis for patients with non-valvular atrial fibrillation (5). The randomised controlled trials that formed the basis for the approval revealed lower incidences of stroke, systemic embolism and serious bleeding in connection with the use of the new anticoagulants compared with warfarin. This effect was also seen in the subgroups of patients with concomitant use of acetylsalicylic acid (aspirin). This is the reason that new drugs are now being recommended as the first choice for atrial fibrillation cases (4). However, concomitant use of anticoagulants and antiplatelet agents entails an extra risk of bleeding, and the underlying data are therefore discussed in more detail in the following.

    The RE-LY study (6), in which dabigatran was compared with warfarin, revealed an approximately 50  % higher risk of clinically relevant bleeding in those who received both antiplatelet and anticoagulant, compared with those who only received an anticoagulant. Triple therapy, i.e. dual antiplatelet therapy with acetylsalicylic acid and clopidogrel in addition to an anticoagulant, doubled the risk of bleeding in both groups. There was no difference in risk of bleeding between the warfarin and dabigatran groups who received combination treatment with an antiplatelet agent. The use of aspirin was the most important independent and modifiable risk factor for intracranial haemorrhage (7).

    Using aspirin concomitantly with new anticoagulants was also found to be a risk factor for severe haemorrhage in the ROCKET-AF trial, in which rivaroxaban and warfarin were compared.

    In the ARISTOTLE trial, in which the efficacy and safety of apixaban were compared with warfarin, 24  % of the patients used aspirin (9). The incidence of severe haemorrhage was higher for those who used aspirin in addition to warfarin (3.9  %) or apixaban (3.1  %) than for those who used only one anticoagulant (2.7  % and 1.8  %, respectively). There was lower risk of stroke, systemic embolism and major bleeding in the apixaban group than in the warfarin group. This difference was independent of whether the patients took aspirin or not (10).

    Peripheral vascular and cerebrovascular disease without atrial fibrillation

    Peripheral vascular and cerebrovascular disease without atrial fibrillation

    Antiplatelet agents (in this patient group aspirin and clopidogrel) are recommended as prophylactic treatment for peripheral vascular disease, symptomatic carotid stenoses and other types of cerebral infarction/TIA without detected atrial fibrillation.

    No randomised, controlled trials have yet been conducted to study the efficacy and safety of the new anticoagulants for this patient group (Fig. 1) (11, 12).

    Figure 1 Overview of conditions that indicate anticoagulation therapy or platelet inhibition as monotherapy or in…
    Figure 1 Overview of conditions that indicate anticoagulation therapy or platelet inhibition as monotherapy or in combination
    Coronary disease

    Coronary disease

    New anticoagulants for acute coronary disease

    New anticoagulants for acute coronary disease

    Patients with both acute and stable coronary disease who have stent implantation are normally treated with aspirin and a class P2Y12 antiplatelet agent (clopidogrel, prasugrel or ticagrelor) for a period, depending on the revascularisation strategy that has been chosen, the stent type and comorbidity/risk of haemorrhage (13). Despite dual antiplatelet therapy, a substantial proportion of patients nonetheless experience new ischaemic events (approximately 10  % within a year) (14).

    It is well known that anticoagulation therapy with warfarin in addition to antiplatelet agents results in fewer new ischaemic events in coronary disease patients, but the combination entails a significant risk of bleeding (15). The role of the new anticoagulants after acute coronary disease is subject to debate.

    In the APPRAISE II trial, full-dose apixaban (5 mg × 2) was added to aspirin or aspirin in combination with P2Y12 inhibitor for high-risk patients with acute coronary syndrome. The trial was stopped prematurely because of the increased incidence of major haemorrhages without a corresponding reduction in the number of ischaemic events (16).

    In the ATLAS-ACS 2 trial, rivaroxaban (2.5 mg × 2 or 5 mg × 2) was added to aspirin and clopidogrel following acute coronary syndrome, and rivaroxaban was found to reduce the risk of the combined end-point death due to cardiovascular causes, myocardial infarction or stroke (hazard ratio 0.84). Only the low dose 2.5 mg × 2 daily resulted in significantly reduced all-cause mortality (17).

    New anticoagulants for acute coronary syndrome and atrial fibrillation

    New anticoagulants for acute coronary syndrome and atrial fibrillation

    The potential role of the new drugs for patients with acute coronary syndrome and atrial fibrillation has not been investigated in separate trials. Available data are limited to post-hoc analyses of randomised, controlled trials of the new drugs in cases of non-valvular atrial fibrillation and follow-up data from randomised, controlled trials of new anticoagulants and antiplatelet agents for acute coronary syndrome (18).

    If patients undergoing treatment with new anticoagulants develop myocardial infarction with ST elevation, percutaneous coronary intervention (PCI) is recommended rather than thrombolysis (3). In patients with unstable angina pectoris or non-ST-elevation myocardial infarction, a switch to low-molecular heparin is recommended in the acute phase, and reversion to the new drugs either after five days, or immediately after successful revascularisation (13). Low-molecular heparin can be administered 12 hours after the last dose of new anticoagulants.

    There are no studies in which new anticoagulants have been combined with the newer, more potent, P2Y12 inhibitors (ticagrelor and prasugrel), so the primary recommendation is aspirin and clopidogrel when anticoagulation therapy (warfarin or new anticoagulants) is indicated in addition (Fig. 1) (5).

    New anticoagulants with stable coronary disease

    New anticoagulants with stable coronary disease

    At present, new anticoagulants are not indicated for stable coronary disease (> 12 months since acute coronary syndrome) alone.

    The new European guidelines propose using anticoagulation therapy (new anticoagulants or warfarin) alone, without the addition of antiplatelet agent, for stable coronary disease and concurrent atrial fibrillation, except in quite special cases, such as main stem stenosis, poor stent apposition, complex bifurcation stenosis, first- generation stents or repeated myocardial infarctions despite secondary prophylaxis (3).

    Venous thromboembolism – treatment and prophylaxis

    Venous thromboembolism – treatment and prophylaxis

    Treatment of venous thromboembolism

    Treatment of venous thromboembolism

    Patients with acute venous thromboembolism (deep vein thrombosis or pulmonary embolism) should receive anticoagulation therapy for at least three months. If the risk of bleeding is regarded as high, it is recommended that treatment be terminated after three months (Fig. 1) (1).

    Clinical trials to study the efficacy and safety of the new anticoagulants in cases of venous thromboembolism allowed combination therapy with new anticoagulants and dual platelet inhibition (Einstein trials) or aspirin (Amplify, Amplify-Extension, RE-COVER trials). There was increased incidence of clinically relevant (hazard ratio 1.81) and severe haemorrhages (hazard ratio 1.50) in both the rivaroxaban and the warfarin group in the Einstein trial in patients who used aspirin in addition (19). The efficacy and risk of bleeding in patients who used aspirin concomitantly was not analysed in the other trials.

    Prophylactic treatment for orthopaedic patients

    Prophylactic treatment for orthopaedic patients

    Approximately 4  % of the participants in the thromboprophylaxis trials with dabigatran and enoxaparin for patients undergoing knee and hip arthroplasty were taking aspirin concomitantly. Post-hoc analyses revealed no significantly increased risk of bleeding with concomitant aspirin compared with anticoagulation treatment as monotherapy, but the follow-up time was short – only 28 – 35 days (20).

    Nor did sub-group analyses of the RECORD trials reveal any significant difference between rivaroxaban and enoxaparin in terms of bleeding risk (21). The risk of bleeding in connection with short-term use of a low-dose new anticoagulant in combination with aspirin accordingly appears to be limited.

    New information

    New information

    Since the acceptance of the manuscript, new guidelines have been published (27 August 2016) by the European Society of Cardiology (ESC) for the treatment of patients with atrial fibrillation (1). They contain a few changes in the recommendations for stroke prophylaxis for atrial fibrillation patients. It is particularly important to note that there are now more detailed recommendations regarding CHA₂DS₂-VASc scores (the recommendation for women with only one additional risk factor has been downgraded from Class I to Class IIa). The article must therefore be read and interpreted in light of these new recommended classifications.

    References

    References

    1. Kirchhof P, Benussi S, Kotecha D et al. 2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS: The Task Force for the management of atrial fibrillation of the European Society of Cardiology (ESC) Developed with the special contribution of the European Heart Rhythm Association (EHRA) of the ESC Endorsed by the European Stroke Organisation (ESO). Eur Heart J 2016. E-published 27 August 2016.

    Henriette Johansen and Ole-Christian Walter Rutherford have contributed equally to this article.

    Comments  ( 1 )
    Dette kommentarfeltet modereres, men kommentarer blir ikke redaksjonelt behandlet ut over å sikre at de følger retningslinjer for vårt kommentarfelt.
    This article was published more than 12 months ago and we have therefore closed it for new comments.
    Published: 11 October 2016
    Tidsskr Nor Legeforen 11 October 2016
    doi:
    10.4045/tidsskr.15.1356

    Received 21 December 2015, first revision submitted 3 June 2016, accepted 23 June 2016. Editor: Martine Rostadmo.
    PlumX
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    1543-6
    Published: 11 October 2016
    Tidsskr Nor Legeforen 2016
    136
    : 
    1543-6
    doi: 10.4045/tidsskr.15.1356

    Received 21 December 2015, first revision submitted 3 June 2016, accepted 23 June 2016. Editor: Martine Rostadmo.
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