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Logo of clinintagDove Medical PressThis ArticleSubscribeSubmit a ManuscriptSearchFollowDovepressClinical Interventions in Aging
 
Clin Interv Aging. 2013; 8: 75–84.
Published online Jan 22, 2013. doi:  10.2147/CIA.S37818
PMCID: PMC3556861
Oral anticoagulation to reduce risk of stroke in patients with atrial fibrillation: current and future therapies
Alpesh Amin
Hospitalist Program, University of California, Irvine, Orange, CA, USA
Correspondence: Alpesh Amin, University of California, Irvine, 101 The City Drive South, Building 26, Room 1005, ZC-4076H, Orange, CA 92868, USA, Tel +1 714 456 3785, Email anamin/at/uci.edu
Atrial fibrillation (AF) is associated with an increased incidence and severity of strokes. The burden of AF-related stroke is expected to increase in parallel with the aging of the population. Oral anticoagulation with warfarin has been the pharmacologic standard for stroke risk reduction in patients with AF. When used with close attention to dosing and monitoring, warfarin is effective prophylactic therapy against thromboembolic stroke. However, it is underused by physicians, in part because of the known risks of adverse events with warfarin. Consequently, many patients with AF live with an avoidably elevated risk of stroke. New options, ie, oral anticoagulants with novel mechanisms of action, have recently been approved to reduce the risk of stroke in AF, and others are in development. These newer agents may address some of the complexities of warfarin use while providing similar or better efficacy and safety.
Keywords: atrial fibrillation, stroke, oral anticoagulants
Atrial fibrillation (AF), the most common type of sustained cardiac arrhythmia, is characterized on electrocardiography by rapid, irregular waves that vary in size, form, and timing.1 AF is associated with a high risk of thromboembolism and stroke. The thrombogenic effect is derived from a number of pathologic mechanisms, in particular, flow abnormalities resulting in stasis in the left atrium, as well as abnormal changes in the vessel walls and constituents of the blood.2 The frequency of AF, which is estimated to account for 15% of strokes in the US annually, is projected to more than double by mid-century as more Americans survive to the ninth decade and beyond.3,4 The 2.6 million who experienced AF in 2010 will increase to about 12 million by 2050 as the population ages.4 The lifetime risk for AF is one in four for Americans older than 40 years.5 Approximately 70% of patients with AF are aged 65–85 years.6
AF is associated with higher medical costs as well as an increased risk of disability and death from stroke.7 Stroke imposes a severe and growing burden on individuals and society, with the incidence of stroke continuing to rise as the population ages and risk-control initiatives are weakly implemented.7 The results of numerous studies have shown that therapeutic and behavioral approaches to management of risk factors can bring about marked reductions in most types of cardiovascular disease, including stroke, not only at the population level but also for individual patients at high risk.7,8 As a leading risk factor for stroke, AF is an important target for prevention by pharmacologic means.
The annual economic burden of stroke in the US was estimated at $54 billion in 2010. Direct costs of stroke are on track to grow by 238% over the 20-year period up to 2030, a rate much higher than all other categories of cardiovascular disease.8 By 2030, direct costs of stroke will sap $95.6 billion from the US annual health care budget, and indirect costs, another $44.4 billion.8 It should be noted that indirect costs, based largely on productivity, grow more slowly than direct costs, mainly because relatively few older Americans, ie, those in the age group most vulnerable to strokes, are active in the workforce.8 It is also noteworthy that the US health care system spends less than $600 million a year on preventive care for patients at risk for thrombotic events.9
The costs and hazards of AF are exacerbated by comorbid conditions that are common in the older population and also increase the risk of stroke. A study of hospitalized Medicare patients found that the presence of AF plus a concomitant cardiovascular diagnosis increased the risk of stroke by 10% in men and 25% in women compared with patients who had AF in the absence of coronary artery disease.10 The odds of experiencing an AF-related stroke are also influenced by patient characteristics. For example, in the ATRIA (Anticoagulation and Risk Factors in Atrial Fibrillation) study, among patients who did not receive anticoagulant therapies, women had a 1.6-fold higher annual incidence of ischemic stroke and peripheral thromboembolism than men;11 however, female gender has inconsistently been found to be a risk factor in other studies.7
The risk of stroke increases along with AF as patients grow older, even when no other stroke risk factors are present.12 However, generally, the age-related increase in stroke risk is attributable to a higher prevalence of AF-related predisposing conditions, as well as conditions that are associated with increased stroke risk but independent of AF.7
The CHADS2 score is a risk assessment scheme widely used to identify patients with AF who are likely to benefit from anticoagulant prophylaxis against stroke. CHADS2 assigns one point each to four of five critical risk factors, ie, congestive heart failure (C), hypertension (H), age ≥ 75 years (A), and diabetes mellitus (D), and two points to the fifth, ie, previous stroke (S) or transient ischemic attack.13
The original CHADS2 had relatively modest predictive value for stroke, especially for patients at intermediate risk.13 Therefore, the CHA2DS2-Vasc scheme was developed to address the deficiencies of CHADS2 by incorporating one point each for additional risk factors, including vascular disease (V: prior myocardial infarction, peripheral arterial disease or aortic plaque) and female gender (S2), as well as by stratifying patients into age groups (A2) of 65–74 years (1 point) or ≥ 75 years (2 points).13 CHA2DS2-Vasc has better predictive value for thromboembolism than CHADS2, particularly for patients at lower and intermediate stroke risk levels. When CHA2DS2-Vasc was compared with CHADS2 in a real-world cohort of 1084 AF patients who did not receive anticoagulation at baseline, the schemes identified 9.2% and 20.4% of patients as having low risk (a score of 0), respectively.13 Thromboembolic events occurred in 0% of low-risk CHA2DS2-Vasc patients compared with 1.4% of low-risk CHADS2 patients.13 Thus, CHA2DS2-Vasc recognizes a higher risk level for many patients considered at low risk according to CHADS2. The advantages of CHA2DS2-Vasc must be weighed against its greater complexity as a means for nonspecialists to assess stroke risk.13
Framingham Heart Study investigators developed a score to predict the 5-year risk of stroke alone and stroke or death in patients with new onset AF.14 Overlapping somewhat with CHADS2 and CHAsDS2-Vasc, the Framingham scheme scores advancing age, female gender, increasing systolic blood pressure, prior stroke/transient ischemic attack, and diabetes, and clinical evaluation also takes account of smoking history. Using the system, the investigators developed risk scores for stroke and stroke or death at the time of warfarin initiation for 705 of 868 patients with new-onset AF and examined event rates in low-risk individuals, as defined by the Framingham risk score and four earlier risk schemes, during a mean follow-up of 4 years. According to the Framingham risk score, 14.3% of the cohort had a predicted 5-year stroke rate ≤ 7.5% (average annual rate ≤ 1.5%) and 30.6% had a predicted 5-year stroke rate ≤ 10% (average annual rate ≤ 2.0%). Actual stroke rates in these low-risk groups were 1.1 and 1.5 per 100 person-years, respectively. According to the earlier risk schemes, 6.4%–17.3% of patients were classified as low-risk, with actual stroke rates ranging from 0.9 to 2.3 per 100 person-years. The investigators noted that the flexible Framingham score provides for use of different thresholds of risk, which is important when tolerability may vary according to the clinical situation. They suggested that the score, which allows stratification at the time of diagnosis, may be helpful both in counseling patients and in making treatment decisions.14
In addition to risk stratification scores that offer a means of identifying patients likely to benefit from anticoagulation, other schemes, which calculate the risk of major hemorrhage during anticoagulant therapy, may add further precision to the selection of medication. HAS-BLED (Hypertension, Abnormal renal/liver function, Stroke, Bleeding history/disposition, Labile international normalized ratio [INR], Elderly [.65 years], Drugs/alcohol concomitantly) is one bleeding risk score.15 Another is HEMORR2HAGES (Hepatic or renal disease, Ethanol abuse, Malignancy, Older [age > 75 years], Reduced platelet count or function, Hypertension [uncontrolled], Anemia, Genetic factors, Excessive fall risk, Stroke), based on data from quality improvement organizations in seven states and comprising a registry of 3791 Medicare beneficiaries with AF.16 The predictive schemes in current use do not equip physicians to achieve the goal of identifying the restricted but significant group of patients with AF who will experience stroke and thus limiting anticoagulation to such patients.13,15 The considerable overlap between risk factors for stroke and bleeding may present a confounding challenge. However, investigators suggest that physicians combine use of a bleeding risk score, such as HEMORR2HAGES, with a clinical prediction rule for stroke, and thus “trade off the risks and benefits” of prescribing anticoagulants versus antiplatelet therapy to select the most appropriate therapies for individual patients.16
Anticoagulation is an established therapeutic strategy to reduce the risk of stroke in AF patients.17 Anticoagulants are prescribed to mitigate hypercoagulable states and reduce the risk of cardioembolic stroke as well as to prevent or treat postoperative deep vein thrombosis and pulmonary embolism (Table 1).17,18
Table 1
Table 1
Oral agents to reduce the risk of stroke in atrial fibrillation
Stroke risk reduction with warfarin
Physicians and patients alike prefer oral medications because they are convenient to administer outside the hospital setting.18 Oral anticoagulants (often warfarin, a vitamin K epoxide reductase inhibitor, commonly referred to as a vitamin K antagonist) are recommended for long-term stroke risk reduction in AF patients. A meta-analysis of 29 trials evaluated more than 28,000 elderly patients with nonvalvular AF over a mean follow-up of 1.5 years.19 With adjusted-dose warfarin, stroke was reduced by 64%, compared with 22% for antiplatelet therapy (relative risk reduction 39%; 95% confidence interval [CI] 22–52; 12 trials, 12,963 patients).19 While the methodology and quality of reporting varied among trials in this analysis, warfarin anticoagulation was substantially more effective than antiplatelet therapy in reducing stroke risk; however, other randomized comparisons, including those for adverse events, were inconclusive.19
Despite its acknowledged efficacy over more than half a century, warfarin is associated with a number of challenges that may make clinicians reluctant to prescribe it. Most importantly, the blood concentration must be maintained within a narrow therapeutic window to balance antithrombotic benefit against the risk of bleeding, a process that is complicated by substantial heterogeneity of response.20 Between 30% and 50% of variability in the response to warfarin is attributable to variants in two genes, CYP2C9 and VKORC1.20 Routine genotyping to determine sensitivity to warfarin is not recommended at present, but the US Food and Drug Administration (FDA) has revised the label, advising clinicians to select one of three initial dose ranges, based on the results of clinical trials, when a patient’s CYP2C9/VKORC1 genotype is known.20 Patients’ responses to warfarin are influenced by dietary vitamin K.21 Warfarin also competes with dietary flavonoids.21
Tight INR control is necessary if stroke is to be prevented effectively and the risk of bleeding reduced, but tight control is sometimes difficult to achieve with warfarin. In a retrospective study of 488 Medicare patients with a history of AF before hospitalization, only 38% (117/304) of those eligible for anticoagulation had been prescribed warfarin, and patients admitted with a stroke were likely to be significantly undercoagulated, with INR < 1.5 (43.5% compared with 20.9% of those without stroke; P < 0.005).22 In this sample, 60% of AF patients who were candidates for anticoagulation were not prescribed warfarin, while those who received warfarin were undertreated according to clinical guidelines.22 Conversely, nearly 9% of the patients on anticoagulation had INR that exceeded the upper limit of the therapeutic range.22 In a survey of 309 warfarin-treated patients with AF admitted with stroke to six US tertiary care institutions, 40%–70% had an INR outside the therapeutic range.23 The level of anticoagulation is inversely associated with stroke and especially with the risk for intracranial hemorrhage, and stroke risk increases dramatically when the INR is <2.24 Bleeding risk rises when the INR exceeds 3.0, and rises steeply at INR values > 4.0.25
The efficacy of warfarin demonstrated in controlled conditions during clinical trials has not always been translated sufficiently to the real-world conditions of clinical practice. A retrospective analysis of health care claims stratified patients with nonvalvular AF into new-to-warfarin (n = 4895) and non-warfarin-treated (n = 7644) cohorts.26 For warfarin-treated patients, risks for ischemic stroke and thromboembolism were reduced by 22% (hazards ratio 0.78; 95% CI 0.65–0.93) and 34% (hazards ratio 0.66; 95% CI 0.59–0.75), respectively, over a follow-up of ≤720 days, with no increase in the risk for hemorrhage. Results were adjusted for age, gender, and other risk factors. The observed reductions for stroke and thromboembolism, while considerable, were lower than others reported in clinical trials, leading the authors to infer that “warfarin was used conservatively and dosed cautiously”.26
One possible explanation for the gap between evidence and practice is that INR monitoring, provided reliably and consistently in a clinical trial, may not be used optimally in the real-world setting. In a survey of 2587 residents of a long-term care facility in Connecticut, 83 were identified as ideal candidates for stroke prevention with warfarin.27 However, only about half the patients received warfarin and their INR values were maintained in the therapeutic range only about half of the time.27 A record-linkage retrospective study in the United Kingdom of 2223 patients with AF showed that warfarin-treated patients were outside the target INR range one third of the time, and that the quartile with poorest control was out of target range almost three quarters of the time.28 Interestingly, time outside target range decreased with duration of INR monitoring, from 52% in the first 3 months, which corresponds to the initial period of warfarin dose adjustment, to 30% after 2 years.28 Results of a multivariate logistic regression analysis showed that a 10% increase in time out of range was associated with an increased risk of death (P < 0.001) and/or ischemic stroke (P < 0.006) and other thromboembolic events (P < 0.001).28
Use of point-of-care INR testing devices and attendance at anticoagulation clinics that provide INR testing as part of coordinated care have been associated with better outcomes from warfarin therapy.29 Several studies have indicated a positive cost benefit of anticoagulation clinics versus usual care, as reflected in lower rates of adverse events and recourse to hospital services.29 However, costs of coordinated care at anticoagulation clinics vary widely; in a review of 29 studies, the cost of a single INR monitoring test ranged from $6.19 to $145.70 (2006 US dollars).30 Although elderly patients are those most in need of chronic oral anticoagulant therapy, they were often the least likely to receive it, partly because there was until recently a dearth of evidence from controlled clinical trials to support the positive risk-benefit of thromboprophylaxis in the elderly. In the BAFTA (Birmingham Atrial Fibrillation Treatment of the Aged) trial, dose-adjusted warfarin with a target INR of 2.5 was compared with acetylsalicylic acid 75 mg/day in patients aged > 75 years in the primary care setting.31 Warfarin was associated with a significant reduction in the occurrence of fatal or nonfatal disabling stroke (ischemic or hemorrhagic, or significant arterial embolism; odds ratio 0.48; 95% CI 0.28–0.80; number needed to treat, 80) with no difference between the warfarin-treated and acetylsalicylic acid-treated groups in the risk of intracerebral hemorrhage and all other major hemorrhages.31 These persuasive findings may have contributed to positive changes in clinical management of elderly patients at risk for thrombotic events.
Numerous studies have demonstrated that acetylsalicylic acid provides only modest stroke prevention compared with the effect achievable when warfarin is administered with meticulous attention to dosing and monitoring. In 2011, the American College of Cardiology/American Heart Association/American Stroke Association updated their joint practice guidelines to suggest that, as an alternative to acetylsalicylic acid monotherapy, acetylsalicylic acid may be combined with the thienopyridine antiplatelet agent, clopidogrel, to prevent stroke in patients who are not candidates for warfarin, whether because of patient preference or the physician’s clinical assessment.32 The American College of Chest Physicians recommends acetylsalicylic acid monotherapy 75 mg to 325 mg per day in AF patients with a CHADS2 score of 0, or combined with clopidogrel as an alternative to warfarin in patients with a CHADS2 score of 1.33 The American College of Chest Physicians recommends use of warfarin or acetylsalicylic acid combined with clopidogrel for patients with a CHADS2 score ≥ 2.33 The physician’s choice of acetylsalicylic acid in patients at low or moderate risk must take into account patient preference, the likely bleeding risk if warfarin is the concurrent anticoagulant, and the availability of access to high-quality monitoring of anticoagulation.33 For many patients considered to be at high or moderate risk, adjusted-dose warfarin to a target INR in the 2.0–3.0 range is recommended.32,33 For high-risk patients who prefer not to be treated with warfarin or for whom warfarin is unsuitable, the ACC/AHA/ASA guidelines suggest that dual antiplatelet therapy with clopidogrel and acetylsalicylic acid is reasonable.32 However, the risk of hemorrhage is not lower with dual antiplatelet therapy than with warfarin, and dual antiplatelet therapy provides greater protection against stroke than acetylsalicylic acid alone at the price of a higher risk of major bleeding.32
Prevention of major vascular events with acetylsalicylic acid alone and with acetylsalicylic acid plus clopidogrel were compared in ACTIVE A (the Atrial Fibrillation Clopidogrel Trial with Irbesartan for Prevention of Vascular Events).34 Patients with AF (n = 7554, mean age 71 years) who were not candidates for warfarin therapy were randomized to treatment with acetylsalicylic acid plus either clopidogrel (n = 3772) or placebo (n = 3782). Patients enrolled between June 2003 and May 2006 were followed until the conclusion of the study in November 2008. Median duration of follow-up was 3.6 years. The primary endpoint for the study was any major vascular event (stroke, non-central nervous system systemic embolism, myocardial infarction, or death from vascular causes) and the most important secondary outcome was stroke. The primary endpoint occurred in 832 patients receiving clopidogrel (6.8% per year) compared with 924 patients on placebo (7.6% per year; relative risk 0.89, 95% CI 0.81–0.98, P = 0.01). The reduction in risk of major vascular events among clopidogrel-treated patients was mainly the result of a lower incidence of stroke, which occurred in 296 patients on clopidogrel compared with 408 on placebo (relative risk 0.72, 95% CI 0.62–0.83; P < 0.001). Major bleeding occurred in 251 patients in the clopidogrel group (2.0% per year) versus 162 patients in the placebo group (1.3% per year, relative risk 1.57; 95% CI 1.29–1.92; P < 0.001). Clopidogrel-treated patients experienced an excess of 83 major bleeding episodes not related to stroke, including 62 episodes classified as severe and an excess of 13 fatal episodes. When major vascular episodes and hemorrhage were considered together, there was no significant difference in the overall event rate between the group treated with acetylsalicylic acid alone and the group treated with acetylsalicylic acid plus clopidogrel (968 versus 996 events; relative risk 0.97, 95% CI 0.89–1.06; P = 0.54).34
The 2010 European Society of Cardiology guidelines largely dispensed with categorizations of high, medium, and low risk. Instead, they encouraged physicians to view risk as a continuum and advocated an approach to clinical assessment and management based on the cumulative presence or absence of risk factors.35 This risk factor-based approach corresponds to the CHA2DS2-Vasc scoring system previously described. The European Society of Cardiology guidelines were updated, according to the results of several large-scale clinical trials, shortly before the approval of new oral anticoagulants. For patients with a CHA2DS2-Vasc score of 0 and no risk factors other than AF, they recommend either acetylsalicylic acid 72–325 mg/day or no antithrombotic therapy, with a preference for the latter. The authors of the guidelines considered that for this group, data on acetylsalicylic acid were insufficient to show benefit, whereas the potential for adverse effects, especially bleeding, was known. For patients with one clinically relevant but “nonmajor” risk factor, they advised either an oral anticoagulant such as a vitamin K antagonist adjusted to a target INR of 2.0–3.0, or acetylsalicylic acid 72–325 mg/day, but preferably the former. For patients with one major risk factor and at least two clinically relevant, nonmajor risk factors, they recommended an oral anticoagulant (target INR 2.0–3.0). Anticipating approval of the new oral anticoagulants, the 2010 European Society of Cardiology guidelines advised that dabigatran etexilate may be considered as an alternative to adjusted-dose vitamin K antagonist therapy. The authors of the guidelines also urged use of the HAS-BLED score, described earlier, in assessing bleeding risk, selecting medication, and monitoring anticoagulant therapy.35 Revised European Society of Cardiology guidelines were published in late August 2012.
More than a decade ago, leading investigators in antithrombotic therapy emphasized the need for development of orally active anticoagulants with at least comparable efficacy, and superior safety, to the standard coumarin derivatives in long-term stroke risk reduction therapy.25,29 Targets for anticoagulant intervention in the coagulation cascade are shown schematically in Figure 1.36 A number of parenterally administered agents have been introduced to practice in recent years. However, the need for innovative oral anticoagulant strategies has been met by the direct thrombin inhibitor, dabigatran etexilate, and the factor Xa inhibitor, rivaroxaban. Both of these agents are approved by the FDA for reducing the risk of stroke and systemic embolism in patients with nonvalvular AF; rivaroxaban is also indicated for the prophylaxis of deep vein thrombosis, which may lead to pulmonary embolism in patients undergoing knee or hip replacement surgery.37,38 A second factor Xa inhibitor, apixaban, has recently been approved by the FDA.
Figure 1
Figure 1
Coagulation cascade: targets for antithrombotic intervention.
Direct thrombin inhibitors have a well defined mechanism of action. Thrombin, central to the clotting process, converts soluble fibrinogen to fibrin and activates other clotting factors, which, in turn, generate more thrombin and stimulate platelets. Thrombin also activates factor XIII, which facilitates bonding among fibrin molecules and stabilizes the clot.36 Direct thrombin inhibitors prevent thrombin activity by occupying catalytic binding sites, fibrinogen binding sites, or both; inhibit thrombin in both the inactive fluid phase and the stabilized fibrin-bound state; and inhibit surface-bound thrombin, with the effect of attenuating thrombus growth.36
Several direct thrombin inhibitors (hirudin, bivalirudin, argatroban) have been in use for a number of years but must be administered parenterally.39 In late-stage clinical trials, ximelagatran, the first oral direct thrombin inhibitor, was equivalent to warfarin for stroke prevention in AF patients and was subsequently marketed in Europe for the prevention of primary venous thromboembolism.40 However, postmarketing reports of hepatotoxicity resulted in withdrawal of this agent from the market.
The new oral direct thrombin inhibitor, dabigatran etexilate, in contrast with warfarin, has a rapid onset of anticoagulant effect, predictable pharmacodynamics, and few drug–drug interactions. Dabigatran etexilate is a prodrug that is rapidly converted into its active form, dabigatran, by esterases.41 The 2011 focused update to the 2006 ACC/AHA/ESC guidelines recommends dabigatran etexilate as a useful alternative to warfarin to reduce the risk of stroke and systemic thromboembolism in patients with AF and at least one additional risk factor for stroke and systemic thromboembolism.32 Contraindications include active pathological bleeding or a history of a serious hypersensitivity reaction to dabigatran.37 Dabigatran etexilate is approved for use without routine coagulation monitoring.37,41
The 2011 update to the ACC/AHA/ESC guidelines is based on the results of the RE-LY (Randomized Evaluation of Long-term anticoagulant therapY) study.42,43 In this trial, 18,113 patients with nonvalvular AF and at least one additional risk factor for stroke were randomized either to blinded treatment with fixed-dose oral dabigatran (110 mg or 150 mg twice daily) or to adjusted-dose warfarin (warfarin treatment was well controlled; mean time in therapeutic range was 64%). Patients were followed for a median of 2 years for the composite endpoint of stroke and systemic thromboembolism. At study endpoint, the rate of stroke and systemic thromboembolism was 1.71% per year among patients randomized to warfarin versus 1.54% per year in patients randomized to dabigatran 110 mg twice daily (relative risk for dabigatran 110 mg, 0.90; 95% CI 0.74 –1.10; P < 0.001 for noninferiority) and 1.11% per year in patients who received dabigatran 150 mg twice daily (relative risk for dabigatran 150 mg, 0.65; 95% CI 0.52–0.81; P < 0.001 for superiority). The rate of major bleeding was 3.57% per year with warfarin versus 2.87% per year with dabigatran 110 mg (P = 0.003) and 3.32% per year in the dabigatran 150 mg group (P = 0.32). The rate of hemorrhagic stroke was significantly lower among patients who received dabigatran (110 mg, 0.12%; 150 mg, 0.10%) than in those who received warfarin (0.38%; P < 0.001 for both comparisons).42 There were significant reductions in intracranial hemorrhage, which occurred at annual rates of 0.23% and 0.32%, respectively, for dabigatran 110 mg bid and dabigatran 150 mg bid, compared with 0.76% for warfarin (P < 0.0001).44 The mortality rate was 4.13% per year with warfarin versus 3.75% per year with dabigatran 110 mg (P = 0.13) and 3.64% per year with dabigatran 150 mg (P = 0.051).42,43 Using insurance claims and administrative data from the Mini-Sentinel pilot of the Sentinel Initiative, the FDA compared the actual rates of gastrointestinal bleeding for new users of dabigatran versus new users of warfarin during the period from 19 October 2010 (dabigatran’s FDA approval date) through 31 December 2011.45 The incidence rate of gastrointestinal bleeding events per 100,000 days at risk was 1.6–2.2 times higher for new warfarin users than for new dabigatran users, consistent with observations from the RE-LY trial.45
Overall, the results indicated that in patients with AF, dabigatran at the dose of 150 mg twice daily was superior to warfarin in preventing stroke and systemic thromboembolism, caused significantly less intracranial bleeding and comparable extracranial bleeding, and was associated with less cardiovascular mortality.4245 The FDA approved dabigatran etexilate 150 mg twice daily to reduce the risk of stroke and systemic thromboembolism in patients with nonvalvular AF and normal renal function or moderate renal impairment (creatinine clearance > 30 mL per minute).37 Dabigatran etexilate 75 mg twice daily is recommended for patients with a creatinine clearance of 15–30 mL per minute.37
Results of a meta-analysis of seven noninferiority trials indicated an increase in the risk of myocardial infarction or acute coronary syndrome with dabigatran therapy compared with controls including warfarin.46 Although the increase in relative risk compared with warfarin was 33%, the absolute risk increase was very small, at 0.27%.46 Warfarin is known to prevent myocardial infarction, as is acetylsalicylic acid, which was allowed concurrently in all the trials. The authors suggested that dabigatran may not directly increase the risk of myocardial infarction, but may lack the beneficial effects of warfarin in prevention of myocardial infarction.46 The reduction in ischemic stroke risk with dabigatran therapy appears to confer a favorable benefit to risk balance. However, selection guidelines should be closely followed, especially among patients at high risk for myocardial infarction or acute coronary syndrome.46
A double-blind Phase III trial, ROCKET-AF (Rivaroxaban Once-daily oral direct factor Xa inhibition Compared with vitamin K antagonism for the prevention of stroke and Embolism Trial in Atrial Fibrillation), compared the oral direct factor Xa inhibitor rivaroxaban at a dose of 20 mg/day with dose-adjusted warfarin for stroke prevention in patients with nonvalvular AF. For warfarin-treated patients, mean time in therapeutic range was 55%.47 The composite primary efficacy and safety endpoints were all-cause stroke and noncentral nervous system systemic embolism, and major and clinically relevant nonmajor bleeding events, respectively.47 In the primary analysis, the primary endpoint occurred in 188 rivaroxaban-treated patients (1.7% per year) compared with 241 warfarin-treated patients (2.2% per year; P < 0.001 for noninferiority).47 In the intention-to-treat analysis, the primary endpoint occurred in 269 rivaroxaban-treated patients compared with 306 warfarin-treated patients (2.1% per year and 2.4% per year, respectively; P < 0.001 for noninferiority, P = 0.12 for superiority).47 Major and nonmajor clinically relevant bleeding occurred in 1475 patients in the rivaroxaban group compared with 1449 in the warfarin group (14.9% per year and 14.5% per year, respectively; P = 0.44). There were significant reductions in intracranial hemorrhage (0.5% versus 0.7%, P = 0.02) and fatal bleeding (0.2% versus 0.5%, P = 0.003) in the rivaroxaban group.47
In a randomized comparison, 1584 patients received oral rivaroxaban 10 mg once daily and 1564 received subcutaneous enoxaparin 30 mg every 12 hours.48 The primary efficacy outcome was the composite of deep vein thrombosis, nonfatal pulmonary embolism, or all-cause mortality ≤ 17 days after knee arthroplasty. The primary efficacy outcome occurred in 6.9% of rivaroxaban-treated patients and 10.1% of those treated with enoxaparin, for an absolute risk reduction of 3.19% (P = 0.0118). Major bleeding was observed in 0.7% of rivaroxaban-treated patients compared with 0.3% of enoxaparin-treated patients (P = 0.1096).48
In a further comparison study, patients scheduled for elective total hip arthroplasty were randomly assigned to treatment with oral rivaroxaban 10 mg once daily (n = 1252) or subcutaneous enoxaparin 40 mg once daily (n = 1257).49 The primary efficacy outcome was the composite of deep vein thrombosis, nonfatal pulmonary embolism, or all-cause mortality ≤ 30–42 days after surgery. In the modified intention-to-treat analysis, the primary outcome occurred in 2.0% of rivaroxaban-treated patients compared with 9.3% of enoxaparin-treated patients, for an absolute risk reduction of 7.3% (P < 0.0001). The incidence of any bleeding on treatment did not differ significantly between the groups (P = 0.25).49
Apixaban, another factor Xa inhibitor in development to reduce the risk of stroke in AF, is currently under FDA review. The AVERROES (Apixaban VERsus acetylsalicylic acid to pRevent strOkES) study, conducted in patients in whom vitamin K antagonist therapy failed or was deemed unsuitable, evaluated apixaban as a substitute for acetylsalicylic acid in patients with AF.50 The study was halted early due to preliminary findings of a risk reduction of more than 50% with apixaban versus acetylsalicylic acid, with no increase in major bleeding or liver toxicity.50 The ARISTOTLE (Apixaban for the pReventIon of Stroke in subjecTs with aTrial fibriLLation) study compared the efficacy and safety of apixaban 5 mg twice daily (n = 9120) and warfarin to an INR of 2.0–3.0 (n = 9081) for stroke prevention in AF.51 A predefined group of patients > 80 years, with low body weight and/or impaired renal function received half the test dose, ie, 2.5 mg twice daily. In this trial, which was designed to test for noninferiority, the primary outcome was ischemic or hemorrhagic stroke or systemic embolism, and the secondary objectives were to test for superiority with respect to the primary outcome and rates of major bleeding and all-cause mortality. Over a median follow-up of 1.8 years, the primary outcome occurred at a rate of 1.27% per year in the apixaban group compared with 3.09% per year in the warfarin group (P < 0.001), and the rates of all-cause mortality were 3.52% and 3.94%, respectively. Hemorrhagic stroke occurred at a rate of 0.24% per year in the apixaban group compared with 0.47% per year in the warfarin group (P < 0.0001), and the rate of ischemic/uncertain stroke type was 0.95% per year in the apixaban group and 1.05% per year in the warfarin group (P = 0.42).51 The results indicated that, in patients with atrial fibrillation, apixaban was superior to warfarin in preventing stroke and systemic thromboembolism, caused less bleeding, and was associated with a lower mortality rate.51 Other factor Xa inhibitors are in various stages of development.
To date, relatively limited evidence is available to inform decisions around management of new anticoagulants. However, expert opinion recommends that bleeding events should be risk-stratified.52 Minor bleeding, such as epistaxis or menorrhagia, can be managed with withdrawal of the agent for one or more days, allowing for interventions as indicated. Moderate bleeding can be managed with drug withdrawal, clinical monitoring, symptomatic treatment, mechanical compression or surgical intervention, fluid replacement, and hemodynamic support and/or transfusion of blood products. Major bleeding should be managed with drug withdrawal, monitoring, hospital admission if required for stabilization, and administration of coagulation factors in case of life-threatening bleeding.52
Warfarin has a long history of attenuating the risk of stroke in patients with AF; however, its limitations lead to both overcoagulation and undercoagulation and, in some cases, failure to use anticoagulation at all. Alternative anticoagulant modalities, such as direct thrombin inhibitors and factor Xa inhibitors, have the potential to improve outcomes in patients with AF and reduce the burdens associated with coagulation monitoring and dose adjustment. Dabigatran etexilate demonstrated equivalent or superior efficacy and safety to warfarin without the need for routine coagulation monitoring during clinical trials and was the first FDA-approved alternative to vitamin K antagonist therapy to reduce the risk of stroke in patients with nonvalvular AF. The factor Xa inhibitor rivaroxaban is also FDA-approved for this indication, and apixaban is now available. New oral anticoagulants appear to have a pivotal role in reducing the risk of stroke for patients with AF.
Footnotes
Disclosure
The author acknowledges the writing and editorial assistance of UBC-Envision Group, the services of which were funded by Boehringer Ingelheim Pharmaceuticals Inc. The author meets criteria for authorship as recommended by the International Committee of Medical Journal Editors (ICMJE), was fully responsible for all content and editorial decisions, and was involved in all stages of manuscript development. The author received no compensation related to the development of the manuscript. Otherwise, the author reports no conflicts of interest in this work.
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