Guidelines for Aspirin and Oral Anticoagulation in CAD and TIA
In patients with both CAD and TIA, lifelong aspirin 75-100 mg daily is recommended as the cornerstone of therapy, with oral anticoagulation (OAC) added only if there is a specific indication such as atrial fibrillation (AF), and when OAC is required, a direct oral anticoagulant (DOAC) is preferred over warfarin. 1
Antiplatelet Therapy for CAD with TIA (No AF or Other OAC Indication)
Primary Antithrombotic Strategy
- Aspirin 75-100 mg daily is recommended lifelong in patients with CAD (prior MI or revascularization) who have experienced a TIA 1
- Clopidogrel 75 mg daily is recommended as a safe and effective alternative to aspirin monotherapy in these patients 1
- Clopidogrel 75 mg daily may be considered in preference to aspirin specifically in patients with a history of ischemic stroke or TIA, though this is a weaker recommendation 1
Dual Antiplatelet Therapy (DAPT) Considerations
- After recent PCI-stenting in CAD patients, DAPT with aspirin 75-100 mg plus clopidogrel 75 mg daily for up to 6 months is recommended as the default strategy 1
- The combination of aspirin and clopidogrel is NOT routinely recommended for long-term secondary prevention in patients with TIA/stroke, as it increases hemorrhage risk without proportional benefit 1
- DAPT duration may be shortened to 1-3 months in patients at very high bleeding risk after PCI 1
Oral Anticoagulation When Indicated (e.g., AF)
Initiation and Selection of OAC
- When OAC is initiated in a patient with AF, a DOAC is recommended in preference to warfarin (VKA) 1
- Long-term OAC therapy is recommended in patients with AF and CHA2DS2-VASc score ≥2 in males and ≥3 in females 1
Timing of Anticoagulation After TIA
- For patients with TIA, anticoagulation can be started one day after the event 2
- For mild stroke, start after more than 3 days; for moderate stroke, after more than 6-8 days; for severe stroke, after more than 12-14 days 2
- Anticoagulation should not be started too early (less than 48 hours) after ischemic stroke as it may increase intracranial bleeding risk 2
Combination Therapy: OAC Plus Antiplatelet
After PCI in Patients Requiring OAC
The following stepwise approach is recommended: 1
Initial triple therapy (OAC + aspirin + clopidogrel):
- Low-dose aspirin once daily is added to OAC and clopidogrel immediately after PCI 1
Early cessation of aspirin (≤1 week) after uncomplicated PCI 1
Continuation of OAC plus clopidogrel:
Followed by OAC alone lifelong 1
Important Restrictions
- Ticagrelor or prasugrel are generally NOT recommended as part of triple antithrombotic therapy with aspirin and OAC 1
- A proton pump inhibitor is recommended in patients at increased risk of gastrointestinal bleeding for the duration of combined antithrombotic therapy 1
Special Considerations for CAD Patients
Rivaroxaban 2.5 mg Twice Daily Option
- In patients with stable CAD (including those with prior stroke/TIA), rivaroxaban 2.5 mg twice daily plus aspirin 75-100 mg once daily may be considered for reduction of major cardiovascular events 3
- This combination reduced the composite of stroke, MI, or cardiovascular death (HR 0.76,95% CI: 0.66-0.86) compared to aspirin alone 3
- This strategy is contraindicated in patients requiring dual antiplatelet therapy or full-dose oral anticoagulation 3
Patients with Acute MI and LV Thrombus
- Oral anticoagulation (INR 2.0-3.0) for at least 3 months and up to 1 year is reasonable 1
- Aspirin should be used concurrently in doses up to 162 mg/day (preferably enteric-coated) during oral anticoagulant therapy 1
Critical Pitfalls to Avoid
Contraindications to Dual Antiplatelet Therapy
- Active bleeding is an absolute contraindication to DAPT 4
- Severe untreated hypertension increases intracranial bleeding risk 4
- In cardioembolic TIA (especially with AF), long-term OAC is recommended instead of DAPT 1, 4
Drug Interactions
- Herbal medications (feverfew, garlic, ginkgo biloba, ginger, ginseng) may alter bleeding time and should be avoided with antithrombotic therapy 4
- St. John's wort may increase warfarin metabolism and interfere with anticoagulation 4