Elsevier

Atherosclerosis

Volume 289, October 2019, Pages 118-125
Atherosclerosis

Review article
Atrial fibrillation with percutaneous coronary intervention: Navigating the minefield of antithrombotic therapies

https://doi.org/10.1016/j.atherosclerosis.2019.08.021Get rights and content

Highlights

  • This review provides insights into contemporary antithrombotic options for patients with atrial fibrillation undergoing percutaneous coronary intervention.

  • Nuances between key international guidelines regarding recommendations for these patients are discussed.

  • Evidence supports a dual antithrombotic pathway approach as the recommended therapy for the majority of these patients. If triple antithrombotic therapy is chosen, its duration should be kept as short as possible.

Abstract

This review aims to provide insights into contemporary therapeutic options for the treatment of patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) and compares current international guidelines. AF is a common cardiac arrhythmia and a major risk factor for stroke. The risk of stroke can be reduced with the use of oral anticoagulant (OAC) therapy. However, for patients with AF, PCI necessitates the use of combined antithrombotic therapies (OAC and antiplatelet therapies) to reduce thrombotic coronary complications. Optimal combinations and durations of OAC and/or antiplatelet therapy remains an area of clinical debate. Nuances exist within the current guidelines regarding duration and combination of antithrombotic therapy for AF patients requiring PCI. However, consensus was found across the following key points: (i) recent evidence supports a preferred role for a dual antithrombotic approach (OAC plus 1 antiplatelet); (ii) limited use of triple antithrombotic therapy is recommended across all guidelines for patients where the ischemic risk outweighs the risk of bleeding, with the duration to be kept as short as possible; and (iii) lifelong management using monotherapy with an OAC from 12 months post PCI is recommended for stable patients across all guidelines.

Introduction

Atrial fibrillation (AF) is a common cardiac arrhythmia with a higher prevalence in older populations and in patients with existing atherosclerotic disease. Approximately 20–30% of ischemic strokes are related to AF, associated with increased risk of heart failure, cardiovascular morbidity, and mortality [1]. Approximately 3 million patients undergo percutaneous coronary intervention (PCI) each year worldwide [2]. In randomized trials, dual antiplatelet therapy (DAPT; a P2Y12 receptor inhibitor plus aspirin) after PCI reduces the risk of future ischemic or atherothrombotic events, particularly stent-related thrombosis, recurrent myocardial infarction (MI), or cardiovascular death [2]. Clinical trials involving patients treated with newer-generation stents have shown 3–6 months' duration of DAPT to be as effective as 12 months’ therapy after elective PCI [[3], [4], [5], [6], [7], [8]], although in acute coronary syndrome (ACS) patients these results are inconclusive due to a lack of adequately powered trials [9]. In contrast, other studies observed a reduction in the risk of thromboembolic, major adverse cardiovascular and cerebrovascular events with DAPT beyond 1 year with an associated increased risk of bleeding [10,11]. For patients undergoing PCI, approximately 5–10% have concomitant AF or other indications for long-term oral anticoagulant (OAC) therapy [12]. The optimal antithrombotic management of patients undergoing PCI who also have AF has become a clinical conundrum related to the optimal duration and combination of therapies to reduce subsequent ischemic and thromboembolic risk without incurring unacceptably increased bleeding risk [12]. Moreover, the lack of consensus within current guidelines regarding duration and selection of combined therapy adds to this challenge [[13], [14], [15]]. This article will discuss the most recent contemporary therapeutic options for atrial fibrillation patients requiring PCI and compare current European, North American, and Canadian guidelines for the antithrombotic management.

Section snippets

Rationale for oral anticoagulation in patients with atrial fibrillation

For many years, vitamin K antagonists (VKAs; international normalized ratio 2.0 to 3.0) were the only OAC available for the prevention of strokes in patients with AF [16]. If a VKA was not used, aspirin could be prescribed [16]. However, the challenges with clinical application of VKAs are well defined, requiring regular monitoring, dose adjustments and interactions with numerous foods and drugs [1,17]. Clinical trials of non-VKA direct oral anticoagulants (NOACs) have demonstrated

Rationale for dual antiplatelet therapy in acute coronary syndrome/percutaneous coronary intervention

The basis for the use of DAPT after stenting compared to OAC came from the ISAR-SAFE trial (Intracoronary Stenting and Antithrombotic Regimen: Safety and efficacy of 6 months dual antiplatelet therapy after drug-eluting stenting), FANTASTIC study (Full ANTicoagulation versus ASpirin and TIClopidine), STARS study (Stent Anticoagulation Restenosis Study) and the MATTIS (multicenter aspirin and ticlopidine trial after intracoronary stenting) trial [[21], [22], [23], [24]]. However, because these

Rationale for and limitations of triple therapy

Given the rationale of DAPT for PCI/ACS and OAC for patients with AF, the default became ‘triple therapy’ with OAC and DAPT for patients with AF undergoing PCI. As such, triple therapy with a VKA plus DAPT after PCI was the standard of care despite an associated increase in bleeding risk and the lack of clinical trials to test efficacy [33,34]. Several RCTs have now evaluated the safety of traditional triple therapy (VKA plus clopidogrel plus aspirin) compared with a dual antithrombotic regimen

Comparison of current guidelines

Existing evidence from RCTs, registry data, and meta-analyses have supported the development of the latest guidelines for patients with AF undergoing PCI. Fig. 1 provides a comparison of the European, North American, and Canadian guidelines for the treatment of patients with AF undergoing PCI.

Patient A

  • 65-year-old male, retired teacher

  • 87 kg, 1.80 m, used to be a heavy smoker

  • History: Diagnosed with NVAF 5 years ago

  • Antithrombotic therapy: Rivaroxaban 20 mg od

  • Following investigation for chest pain with a positive myocardial perfusion imaging scan, he receives a second-generation drug-eluting stent in his mid-left anterior descending artery

Cardiologist recommends elective PCI following chest pains and CAD diagnosis.

Treatment options: The existing evidence and international guidelines suggest a

Conclusions

Nuances exist within the current guidelines regarding the duration of combined therapy and when to use dual antithrombotic therapy (OAC plus antiplatelet) versus triple therapy (OAC plus DAPT) in patients with AF undergoing PCI. However, consensus was found across the following key points: (i) recent evidence supports a role for a dual antithrombotic approach including a NOAC plus clopidogrel for up to 12 months after PCI in selected patients; (ii) the limited use of triple therapy is

Conflicts of interest

Dr Welsh reports grants and personal fees from AstraZeneca and Bayer, grants from Eli Lilly, and personal fees from Amgen, Pfizer/Bristol-Myers Squibb, and Boehringer Ingelheim. Dr Morais reports grants or personal fees (over the past 2 years) from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Menarini, Merck Sharp & Dohme, Novartis, and Servier. Dr Zeymer reports grants or personal fees from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Ferrer, Eli

Financial support

In part, this manuscript receiving funding support from Bayer AG.

Acknowledgements

The authors would like to acknowledge Dr. Cindy Jenner (Chameleon Communications International) for editorial assistance.

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