# Optimal Antithrombotic Regimens Across Atherosclerotic Vascular Beds: Toward Mechanism and Risk-Oriented Strategies

**Authors:** Pierre Sabouret, Domenico Mario Giamundo, Francesco Costa, Piera Capranzano, Luigi Spadafora, Stefano Cacciatore, Nelsa González Aguado, Marco Bernardi, Ahmed Ibrahim, Ali Abdelaziz, Giulia Alagna, Felice Gragnano, Paolo Calabrò, Giuseppe Andò

PMC · DOI: 10.3390/jcm15062325 · Journal of Clinical Medicine · 2026-03-18

## TL;DR

This review discusses how antithrombotic treatments should be tailored to individual patients based on their specific vascular conditions and risks.

## Contribution

The paper proposes a unifying framework for personalized antithrombotic strategies across diverse atherosclerotic conditions.

## Key findings

- Antithrombotic therapy varies significantly across different atherosclerotic vascular beds and clinical scenarios.
- Dual pathway inhibition with rivaroxaban and aspirin is recommended for high-risk chronic coronary and peripheral artery disease patients.
- Bleeding risk must be carefully balanced against antithrombotic benefit, especially in elderly or comorbid patients.

## Abstract

Arterial thrombosis emerges from the interplay between plaque disruption, platelet activation, and coagulation pathway amplification on a background of heterogeneous ischemic and bleeding risk. Optimal antithrombotic therapy therefore varies across clinical settings, from acute coronary syndromes (ACS) to chronic coronary syndromes (CCS), ischemic stroke, peripheral artery disease (PAD), and atrial fibrillation (AF) associated with atherosclerotic disease. Contemporary European and North American guidelines endorse an increasingly individualized approach, moving away from rigid “one-size-fits-all” dual antiplatelet therapy (DAPT) duration and intensity and incorporating dual pathway inhibition with low-dose rivaroxaban plus aspirin in selected high-risk CCS and PAD patients. In ischemic stroke, short-course DAPT is confined to minor events and transient ischemic attacks, whereas long-term monotherapy remains standard, and the coexistence of AF typically shifts the balance toward oral anticoagulation. Across all scenarios, antithrombotic benefit must be weighed against bleeding, especially in elderly, frail, or comorbid patients. Evidence gaps remain substantial, particularly in patients with overlapping vascular territories, AF plus atherosclerotic disease, and after ischemic stroke of complex or mixed mechanisms. This narrative review summarizes current evidence and guideline-based strategies in major atherosclerotic settings, proposes a unifying conceptual framework, and highlights key uncertainties and research directions for truly personalized antithrombotic care.

## Linked entities

- **Chemicals:** rivaroxaban (PubChem CID 6433119), aspirin (PubChem CID 2244)
- **Diseases:** acute coronary syndromes (MONDO:0005542), ischemic stroke (MONDO:1060198), atrial fibrillation (MONDO:0004981)

## Full-text entities

- **Diseases:** thrombosis (MESH:D013927), Atherosclerotic (MESH:D050197), bleeding (MESH:D006470), ischemic stroke (MESH:D002544), ischemic attacks (MESH:D002546), AF (MESH:D001281), ACS (MESH:D054058), PAD (MESH:D058729), ischemic and (MESH:D002545)
- **Chemicals:** rivaroxaban (MESH:D000069552), aspirin (MESH:D001241), Antithrombotic (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13026836/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026836/full.md

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Source: https://tomesphere.com/paper/PMC13026836