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Bir, S. Antithrombotic Therapy in the Prevention of Stroke. Encyclopedia. Available online: https://encyclopedia.pub/entry/18095 (accessed on 23 April 2024).
Bir S. Antithrombotic Therapy in the Prevention of Stroke. Encyclopedia. Available at: https://encyclopedia.pub/entry/18095. Accessed April 23, 2024.
Bir, Shyamal. "Antithrombotic Therapy in the Prevention of Stroke" Encyclopedia, https://encyclopedia.pub/entry/18095 (accessed April 23, 2024).
Bir, S. (2022, January 12). Antithrombotic Therapy in the Prevention of Stroke. In Encyclopedia. https://encyclopedia.pub/entry/18095
Bir, Shyamal. "Antithrombotic Therapy in the Prevention of Stroke." Encyclopedia. Web. 12 January, 2022.
Antithrombotic Therapy in the Prevention of Stroke
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This entry is adapted from the peer-reviewed paper 10.3390/biomedicines9121906

 Ischemic stroke is a leading cause of death and disability throughout the world. Antithrombotic therapy, which includes both antiplatelet and anticoagulant agents, is a primary medication of choice for the secondary prevention of stroke. However, the choices vary with the need to incorporate evolving, newer information into the clinical scenario. There is also the need to factor in co-morbid medical conditions as well as the cost ramifications for a particular patient as well as compliance with the regimen. 

antiplatelet therapy stroke prevention TIA minor stroke anticoagulant therapy atrial fibrillation aspirin clopidogrel ticagrelor

1. Introduction

Stroke is a leading cause of death and neurological disability in the world. Stroke prevention is, therefore, a high priority in removing this substantial burden. The typical approach to acute ischemic stroke or transient ischemic attack (TIA) is to identify the mechanism of the ischemic insult as rapidly and accurately as possible. Typical mechanisms include small vessel (penetrating artery) ischemic stroke commonly referred to as lacunar-type infarct; large vessel athero-thrombotic stroke, which can result in large vessel occlusion (LVO); artery-to-artery embolic stroke; cardioembolic stroke; and embolic stroke of undetermined source (ESUS). Less common mechanisms include vascular dissection, vasculitis, and infectious vascular occlusive disease such as meningo-vascular syphilis. The mechanism can be compounded by underlying disorders such as a pro-thrombotic state or familial dyslipidemias, which can result in accelerated atherosclerosis.
Antithrombotic agents, either antiplatelet or anticoagulant, are a main stay of the prevention of ischemic stroke [1]. Evolving information has brought to the forefront the selection of dual antiplatelet therapy, such as aspirin and clopidogrel or aspirin and ticagrelor, in the acute setting of minor ischemic stroke or TIA if no clear contraindications are encountered. An embolic mechanism often calls for consideration of anticoagulant therapy, but this is impacted by the scenario such as high-grade carotid stenosis associated to artery-to-artery embolism, which generally is most effectively managed either with timely carotid endarterectomy or carotid angioplasty with stenting. A particularly challenging scenario can be the choice of antithrombotic regimen in ESUS [2].

2. Antithrombotic Agents

As mentioned previously, antithrombotic agents represent both antiplatelet agents and anticoagulant agents. Antiplatelet agents typically function by blocking the activation pathway of platelets while anticoagulants typically interfere with the coagulation cascade for clot formation. Antiplatelets are primarily used for the prevention of non-cardioembolic stroke while anticoagulants tend to be most efficacious for the prevention of cardioembolic stroke. Commonly used antiplatelet agents include aspirin; clopidogrel; dipyridamole; and a combination of low dose aspirin and clopidogrel, cilostazol, and ticagrelor. Antiplatelet agents either not commonly used or not of proven efficacy include ticlopidine, prasugrel, and eptifibatide. Anticoagulant choices include warfarin, rivaroxaban, apixaban, edoxaban, and dabigatran.

3. Antiplatelet Therapy for the Prevention of Stroke

3.1. Aspirin

Aspirin is the most commonly used antiplatelet agent used for stroke prevention. This reflects its established efficacy, low cost, relative safety, and ease of use with generally limited drug–drug interaction. It is available without a prescription, which is beneficial in terms of cost and availability. However, this can also translate into a variable pattern of administration with medication reconciliation efforts. A not uncommon scenario, in the acute ischemic stroke setting, is trying to determine whether the patient is actually taking the medication, and how regularly, as the use of such an agent may not be recorded on the medication list of prescribed medications and its as often as necessary use, for pain, may cause it to be confused with acetaminophen or a non-steroidal anti-inflammatory agent when trying to obtain this information in the acute setting.
In terms of mechanism of action, aspirin administration results in the irreversible blockage of both cyclo-oxygenase (COX) enzymes. COX 1 blockage causes inhibition of platelet thromboxane A2 (TXA2) [3]. The half-life of aspirin is 2 to 3 h [4][5]. The more common side effects of aspirin include dyspepsia and gastrointestinal bleeding. It is uncommon to see easy bruising reflective of its antiplatelet effect, and this may provide reassurance that it is being taken regularly. Fortunately, intracranial hemorrhage is an uncommon complication [4][5][6]. Aspirin is contraindicated if there is a reported history of significant allergic reaction. A history of asthma, nasal polyps, and rhinitis can be associated with an enhanced risk of bronchospasm, urticaria, and angioedema although significant allergic reactions are not commonly observed.
A combined analysis of 40,000 patients from CAST (Chinese Acute Stroke Trial) and IST (International Stroke Trial) demonstrated that early initiation of aspirin, at 160 to 300 mg a day, reduces the risk of stroke recurrence compared to control [7]. In the CAPRIE trial [8], comparison of clopidogrel at 75 mg daily versus aspirin at 325 mg daily showed no significant difference in the recurrence rate of stroke, MI, and vascular death in the 19,183 ischemic stroke patients reported. Therefore, aspirin is typically viewed as first-line antiplatelet therapy for stroke prevention in non-cardioembolic ischemic stroke [7]. In meta-analysis data, aspirin, in a dosage range of 81 to 325 mg a day, was associated with an approximately 13% relative reduction of recurrence of stroke [8]. There has been no reported efficacy difference between 81 and 325 mg a day for protection against vascular events including stroke [9].
Aspirin is of limited efficacy for stroke prevention in embolic stroke with a cardiogenic source. The Stroke Prevention in Atrial Fibrillation (SPAF) I [10] study assessed aspirin, at 325 mg a day, compared to placebo and to warfarin in patients without prior stroke who had non-valvular atrial fibrillation (NVAF). There was a reduction in ischemic stroke with aspirin (3.6%/year) compared to placebo (6.3%/year) as well as in combined ischemic stroke and death (7.9%/year versus 11.8%/year). Warfarin was clearly superior to aspirin in stroke prevention in this study and in subsequent studies of NVAF. Bleeding risk was comparable in all groups. As per the American Heart Association (AHA) guidelines, aspirin is viewed as a reasonable alternative to anticoagulant therapy for those not eligible for an anticoagulant because of safety concerns as well as in case of refusal or lack of compliance with the anticoagulant [11].
A not uncommon scenario is the so-called “aspirin failure”, which identifies a patient presenting with ischemic stroke or TIA while presumably compliant with the prescribed aspirin. This often results in the patient being switched to an alternative antiplatelet agent, such as clopidogrel, and it is increasingly common to initiate dual antiplatelet therapy (DAPT) in the acute period. Aspirin resistance is an important concern in the vascular neurology community. One study reported that the prevalence of ASA resistance is 25% [12]. Another study reported that diabetes mellitus and high LDL cholesterol independently cause aspirin resistance by the upregulation of isoprostanes and subsequent activation of arachidonic acid. This finding was supported by high levels of 11-dehydrothromboxane B2, a breakdown product of thormboxane A2, in the urine of these subjects [13]. Additional contributing factors may include concurrent use of a proton-pump inhibitor reported to be associated with higher platelet aggregation and higher serum levels of thromboxane B2 [14]. Additionally of note, enteric-coated aspirin formulations were found to be associated with a reduced inhibition of thromboxane A2 related to reduced absorption, with the neutral pH, of the small intestine [15].

3.2. Clopidogrel

Clopidogrel is commonly used for vascular prophylaxis because of its established efficacy, reasonable side effect profile, and reasonable cost associated with its availability in generic form. It is a prodrug, which is metabolized to its active form by carboxylesterase-1. There is resultant irreversible platelet inhibition through binding to PGY12-ADP receptors on the platelet’s surface. This prevention of ADP binding to the PGY12 receptors results in activation of the glycoprotein GPII b/IIIa complex with the resultant inhibition of platelet aggregation [16].
The CAPRIE trial [17] compared aspirin, at 325 mg a day, to clopidogrel, at 75 mg a day, in 19,185 patients with either recent ischemic stroke, recent MI, or peripheral arterial disease. The relative risk reduction for a composite of either ischemic stroke, MI, or vascular death was 8.7% (p = 0.043) favoring clopidogrel over aspirin. Thus, the benefit was not necessarily to the degree that clopidogrel supplanted aspirin as the first choice for antiplatelet therapy, but it did identify this agent as an option for “aspirin failures”.
Like aspirin, clopidogrel enhances bleeding risk, and its enhanced efficacy in platelet inhibition warrants concern for invasive procedures, which could lead to a clinically significant bleeding complication. This translates into holding of the clopidogrel for 5 to 7 days, at least in the non-emergent clinical setting, prior to surgical procedures [18], and this includes procedures, such as the placement of a feeding gastrostomy and lumbar puncture, which are not uncommonly encountered in the neurological realm.
The peak of platelet inhibition of clopidogrel usually occurs in 3 to 5 days after initial administration of the standard 75 mg a day dose while a loading dose of 300 to 600 mg can show an effect at six hours [19][20]. Clopidogrel efficacy is predicated upon genetic-based responsiveness to its mechanism of action. The loss-of-function CYP2C19*2 allele is associated with decreased activation of clopidogrel, and its antiplatelet effect, as well as worse cardiovascular event outcome [21].

4. Presently Available Anticoagulants for Stroke Prevention

These anticoagulant agents include warfarin, rivaroxaban, apixaban, edoxaban, and dabigatran.

4.1. Warfarin

Warfarin inhibits the activity or synthesis of vitamin-K-dependent clotting factors including II, VII, IX, and X. Warfarin has been used for a number of years for protection against cardioembolic stroke and for protection against stroke associated with hypercoagulable conditions. It has been replaced by DOACs for many patients with NVAF but not for valvular-associated AF based upon results of the RE-ALIGN [22]. Persistent advantages of warfarin use, despite the inconvenience associated with drug–drug and food interactions with variable effect on the therapeutic dosing, are the ability to determine compliance by the determination of a therapeutic prothrombin time (PT) and international normalized ration (INR); adjustment of dosing for higher-risk clinical conditions; and the reversibility of the anticoagulant effect, when indicated for bleeding, which only recently became available for the DOACs. In addition, the ready availability of a PT/INR measurement in the emergency setting helps in determining potential eligibility for intravenous tissue plasminogen activator (TPA) for acute ischemic stroke, while patients on DOACs are routinely contraindicated for TPA unless it is well documented that they have not recently been receiving the medication.

4.2. Direct Oral Anticoagulants (DOACs)

Direct oral anticoagulants include rivaroxaban, apixaban, and edoxaban (which directly inhibit activated factor X) and dabigatran (which is a direct inhibitor of thrombin). Studies have shown that these DOACs have similar or superior efficacy in preventing thromboembolic strokes as well as a reduced or similar intracranial bleeding risk compared to warfarin. The major benefits of these DOACs over warfarin are [1] fixed dosing regimen, [2] no requirement of monitoring of PT/INR, [3] fewer drug–drug interactions, and [4] rapid and predictable onset of action [4][5][23]. Contraindication of DOACS are severe renal impairment and the required adjustment of dosing for moderate impairment or advanced age. Not unexpectedly, the major side effect concern of DOACs is excessive bleeding [5]. Available reversal agents for dabigatran and factor Xa inhibitors are idarucizumab (a monoclonal antibody) and andexanet alfa (engineered version of factor Xa), respectively [4].
The RE-LY (Randomized Evaluation of Long-Term Anticoagulation Therapy) study with dabigatran 110 or 150 mg twice daily compared to warfarin (INR 2-3) [22] showed that dabigatran is superior to warfarin, at the 150 mg twice a day dose, and non-inferior to warfarin at the 110 mg twice a day dose, in the reduction of stroke and systemic embolism in the patients with NVAF. Dabigatran had a similar rate to warfarin for major hemorrhage.
The AVERROES trials [24][25] and the ARISTOTLE-AF study [26] demonstrated that apixaban was superior to warfarin in reducing the risk of recurrence of stroke and systemic embolism without increasing the risk of major bleeding. However, among patients with prior stroke or TIA, there was no significant difference in reduction of stroke and systemic embolism between apixaban (2.5%) and warfarin (3.2%). The ROCKET-AF study showed that rivaroxaban 20 mg daily compared to warfarin (INR 2–3) showed that rivaroxaban is non-inferior to warfarin in reduction of stroke and systemic embolism in patients with non-valvular atrial fibrillation. In addition, the risk of major bleeding was comparatively less in the rivaroxaban group [27]. The ENGAGE-AF and -TIMI 48 studies demonstrated that edoxaban was non-inferior to warfarin in terms of reduction of recurrent strokes, systemic thromboembolism, major bleeding, and death [28][29].
The RIVER clinical trial in the patients with AF and bioprosthetic mitral valve showed that rivaroxaban was non-inferior to warfarin, with a slight tendency to decrease the prevention of stroke, death, and major bleeding at 12 months [30]. However, in the RE-ALIGN study of patients with AF and mechanical heart valves [31], the occurrence of stroke was 5% with dabigatran and 0% with warfarin. Major bleeding was also higher in the dabigatran group (dabigatran 4% vs. warfarin 2%). Presently, warfarin remains the agent of choice for protection against cardioembolism in patients with AF and mechanical heart valves as well as in those subjects with clinically significant mitral stenosis.
The timing for starting an anticoagulant is particularly important for chronic anticoagulant therapy in the patients with stroke and NVAF or VAF. Current guidelines recommend waiting for 4–14 days in a patient with hemorrhagic transformation or in patients with malignant ischemic stroke with AF. The presently available anticoagulant choices are summarized in Table 1.
Table 1. Anticoagulant choices, dosing, and comparative efficacy in non-valvular atrial fibrillation.
Agent Dosing Comparitive Efficacy to Warfarin
Digabatran 150 mg twice daily (75mg twice daily incase of renal impairment Superior
Apixaban 5 mg twice a day (2.5 mg twice a day for age ≥ 80, BMI <60 kg or serum creatinine >1.5 Superior
Rivaroxaban 20 mg a day (15 mg a day with renal impairment Non-inferior
Edoxaban 60 mg a day (do not use fro CrCL greater than 95ml/min because of an increased risk of ischemic stroke compared with warfarin in a NVAF trial) Non-inferior
Warfarin Targated INR of 2 to 3 Not applicable

4.3. Combination Therapy of DOAC and Aspirin in Stable Atherosclerotic Vascular Disease without Atrial Fibrillation

The COMPASS trial was a study in 27,395 patients with stable atherosclerotic vascular disease and reported that 2.5 mg rivaroxaban twice a day plus 100 mg of aspirin daily showed reduction of stroke, MI, and cardiovascular death compared to aspirin alone. Rivaroxaban 5 mg twice a day showed similar results to 2.5 mg rivaroxaban twice a day plus 100 mg of ASA daily but was associated with a higher rate of major bleeding [32]. Of note, this study excluded the patients with prior history of intracerebral hemorrhage, prior stroke within one month, and lacunar stroke. The major trials on anticoagulants for secondary prevention are depicted in Table 2.
Table 2. Major trials on antithrombotics.
Trial Name and References # of Patients Treatment Arms Primary End Points Results and p Value
CAST and ISC trial [7] 40,000 Aspirin 160 to 300 mg daily vs. placebo (control) Recurrence of ischemic stroke within 30 days Recurrence of ischemic stroke. Aspirin 1.6% vs. placebo 2.3%, p < 0.000001
SPAF; Stroke Prevention in Atrial Fibrillation [10] 1330 Aspirin 325 mg, warfarin, and placebo in patients with atrial fibrillation Recurrence of ischemic stroke and death Recurrence of ischemic stroke: aspirin 42% (p = 0.02), warfarin 67% (p = 0.01). Death: aspirin 32% (p = 0.02) and warfarin 58% (p = 0.01)
CAPRIE trial [17] 19,185 Aspirin 325 mg vs. clopidogrel 75 mg daily Recurrence of ischemic stroke Reduction of recurrence of ischemic stroke was 8.7% in favor of the clopidogrel group (p = 0.043)
MATCH trial [33] 7599 DAPT, aspirin 75 mg, and clopidogrel 75 mg vs. clopidogrel 75 mg daily Recurrence of ischemic stroke Reduction of recurrence of ischemic stroke: 6.4% (p = 0.244), no benefit of using DAPT
POINT trial [34] 4881 Aspirin 50 to 325 mg and clopidogrel 75 daily (first load with 600 mg) vs. aspirin 50 to 325 mg daily for 21 days of onset in minor ischemic stroke or higher-risk TIA Recurrence of ischemic stroke Recurrence of ischemic stroke is 5% in combined group vs. 6.5% in aspirin monotherapy group, p = 0.02
CHANCE [35] 5170 Aspirin 75 mg and clopidogrel 75 daily (first load with 300 mg) vs. placebo and aspirin 75 mg daily for 21 days of onset in minor ischemic stroke or higher-risk TIA Recurrence of ischemic stroke Recurrence of ischemic stroke is 8.2% in combined group vs. 11.75% in aspirin monotherapy group, p < 0.001
SAMMPRIS trial [36] 451 Aspirin 325 mg and clopidogrel 75 mg daily vs. medical therapy in combination with angioplasty and stenting in a patient with 70–99% intracranial stenosis for 90 days Recurrence of ischemic stroke and death Recurrence of ischemic stroke and death: medical management with angioplasty and stentin, 14.7% vs. medical management only 5.8%, (p = 0.002)
European Stroke Prevention Study 2 (ESPS 2) 37 6602 Aspirin 75 mg and dipyridamole 200 mg twice daily vs. aspirin 75 mg or dipyridamole 200 mg daily Recurrence of ischemic stroke and death Reduced the goal by 13.2% (p = 0.016) with aspirin alone, and 15.4% by higher dose of dipyridamole (p = 0.015), and 24.4% by the combination (p < 0.001)
SOCRATES trial [37] 13,199 Ticagrelor 90 mg twice daily (first loaded with 180 mg) vs. aspirin 100 mg daily (first loaded with 300 mg) in mild to moderate ischemic stroke and TIA for 90 days Recurrence of ischemic stroke Recurrence of ischemic stroke, ticagrelor 6.7% vs. aspirin 7.5%, p = 0.07. No benefit was noted.
THALES trial [38] 11,016 Ticagrelor 90 mg twice daily (first loaded with 180 mg) plus aspirin was compared to aspirin 75 to 100 mg daily (first loaded with 300 to 325 mg) in mild to moderate ischemic stroke and TIA Recurrence of ischemic stroke Recurrence of ischemic stroke; 5.0% for combination therapy compared to 6.3% for aspirin, p = 0.004
RE-ALIGN study [31] 252 Dabigatran vs. warfarin in patients with mechanical heart valve Recurrence of ischemic stroke and major bleeding Recurrent strokes: 5% with dabigatran and 0% with warfarin, and major bleeding 4% vs. 2%, respectively.
RE-LY study [22] 18,113 Warfarin vs. dabigatran 110 or 150 mg daily in patients with atrial fibrillation and stroke Recurrence of ischemic stroke or systemic embolization Warfarin 1.69% vs. dabigatran 1.53% (non-inferior to warfarin), p < 0.001 vs. dabigatran 150 mg, 1.11% (superior to warfarin), p < 0.001
AVERROES trials [25] 18,201 Apixaban 5 mg twice a day vs. warfarin in atrial fibrillation Recurrence of ischemic stroke or systemic embolization Apixaban, 1.27% vs. warfarin, 1.67%, p < 0.01 (superiority)
ROCKET-AF study [27] 14,264 Rivaroxaban 20 mg daily vs. warfarin in non-valvular atrial fibrillation Recurrence of ischemic stroke or systemic embolization Recurrence of stroke was 1.7% with rivaroxaban vs. 2.2% with warfarin, p < 0.001 (rivaroxaban is non-inferior to warfarin)
COMPASS trial [32] 27,395 Rivaroxaban 2.5 mg twice a day plus aspirin 75 mg and aspirin 75 mg daily in non-atrial fibrillation stroke Recurrence of ischemic stroke, MI, and cardiovascular death Primary outcome; stroke; 4.1% in combined group vs. 5.4% in aspirin alone group, p < 0.001, and death; 3.4% vs. 4.1%, p = 0.00254; however, major bleeding was 3.1% vs. 1.9%, respectively, p = 0.001

4.4. Embolic Stroke of Undetermined Source (ESUS)

Embolic stroke of undetermined source is an emerging area of clinical interest and research with particular emphasis on risk versus potential benefit. The RE-SPECT ESUS trial showed dabigatran is not superior to aspirin in secondary stroke prevention in such patients and demonstrated more non-major bleeding than aspirin [39]. The NAVIGATE ESUS trial, with rivaroxaban in comparison with aspirin, reported an unacceptable bleeding risk with rivaroxaban, and the study was prematurely terminated [40]. Thus, at the present time, at least until further study information is available, antiplatelet therapy remains the avenue of choice for ESUS [41].

4.5. Antithrombotic after Receiving Mechanical Thrombectomy in Acute Stage of Stroke

Periprocedural antiplatelet therapy and continuation of the therapy after mechanical thrombectomy (MT) shows better functional outcomes [42]. The current guideline recommends starting antiplatelets after 24 h of MT if repeat CTH shows no bleed. If MT confirms complete reperfusion, patient should be on ASA 81 mg daily or clopidogrel 75 mg daily depending on history of antithrombotic intake for secondary prevention of stroke. However, in case of no or incomplete perfusion, patient can be placed on dual antiplatelets with ASA and clopidogrel for 3 months followed by monotherapy. If patient has history of atrial fibrillation (a-fib) or newly diagnosed a-fib, oral anticoagulant such as apixaban or rivaroxaban should be the choice of treatment after MT with no bleed or malignant MCA stroke in repeat CT head. If any patient has hemorrhagic transformation from ischemic stroke in repeat CT head, antithrombotic or anticoagulant should be resumed after 4–14 days of stroke onset depending on the size of hemorrhage [43]. In case of concurrent internal carotid artery occlusion and when the patient needs to undergo carotid stenting along with mechanical thrombectomy, the choice of treatment should be periprocedural antiplatelets, and life-long continuation of that [44].

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Subjects: Clinical Neurology
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Shyamal Bir
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Entry Collection: Hypertension and Cardiovascular Diseases
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Update Date: 12 Jan 2022
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