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Updated: Oct 25, 2025

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Long-term residual cardiovascular risk after acute coronary syndrome: antithrombotic treatment options
D R P P Chan Pin Yin1, J M Ten Berg2,3
1Department of Cardiology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Insights
Patients surviving acute coronary syndromes (ACS) face residual risk despite dual antiplatelet therapy (DAPT). Evaluating ischemic and bleeding risks at one year is crucial for guiding further antithrombotic treatment beyond DAPT.
Area of Science:
- Cardiology
- Thrombosis Research
- Clinical Medicine
Background:
- Residual thrombotic risk persists one year after acute coronary syndromes (ACS) despite secondary prevention.
- Dual antiplatelet therapy (DAPT) is standard for 12 months but carries bleeding risks.
- Prolonging DAPT beyond 12 months increases bleeding complications.
Purpose of the Study:
- To review residual thrombotic risk at one year post-ACS.
- To evaluate evidence for antithrombotic therapies beyond one year.
- To provide guidance on selecting patients for extended antithrombotic treatment.
Main Methods:
- Literature review of studies on antithrombotic therapies post-ACS.
- Analysis of clinical trial data regarding ischemic and bleeding events.
- Synthesis of evidence to create a practical patient selection guide.
Main Results:
- Assessing both ischemic and bleeding risks is critical for patients at one year post-ACS.
- Low-dose rivaroxaban plus aspirin demonstrates efficacy in reducing ischemic events.
- Risk stratification is essential for optimizing antithrombotic strategies.
Conclusions:
- Individualized risk assessment is key for managing patients post-ACS.
- Extended antithrombotic therapy options exist beyond standard DAPT.
- Careful patient selection can mitigate residual thrombotic risk while minimizing bleeding complications.
Abstract:
The residual risk of patients surviving until 1 year after acute coronary syndromes (ACS) is still high, despite secondary prevention. The cornerstone of treatment of patients with ACS is dual antiplatelet therapy (DAPT) consisting of low-dose aspirin and a P2Y12 inhibitor (clopidogrel, prasugrel or ticagrelor) for 12 months, or less in those patients at higher risk for bleeding. To reduce the residual risk beyond 1 year in those patients not at high bleeding risk who tolerated DAPT and did not suffer an (ischaemic or bleeding) event would intuitively mean to prolong DAPT. However, prolonged DAPT always comes at the cost of more bleeding. Therefore, assessing both ischaemic and bleeding risk in these patients at 1 year after ACS is crucial. In addition, another antithrombotic treatment consisting of low-dose rivaroxaban combined with low-dose aspirin has been shown to reduce ischaemic events. In this review, we describe residual thrombotic risk at 1 year after ACS, evaluate the evidence for antithrombotic options beyond 1 year and provide a practical guide to determine which patients would benefit the most from these therapies.
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