The Present and Future
JACC State-of-the-Art Review
Medical Therapy for Long-Term Prevention of Atherothrombosis Following an Acute Coronary Syndrome: JACC State-of-the-Art Review

https://doi.org/10.1016/j.jacc.2018.09.052Get rights and content
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Abstract

Following an acute coronary syndrome (ACS), heightened predisposition to atherothrombotic events may persist for years. Advances in understanding the pathobiology that underlies this elevated risk furnish a mechanistic basis for devising long-term secondary prevention strategies. Recent progress in ACS pathophysiology has challenged the focus on single “vulnerable plaques” and shifted toward a more holistic consideration of the “vulnerable patient,” thus highlighting the primacy of medical therapy in secondary prevention. Despite current guideline-directed medical therapy, a consistent proportion of post-ACS patients experience recurrent atherothrombosis due to unaddressed “residual risk”: contemporary clinical trials underline the pivotal role of platelets, coagulation, cholesterol, and systemic inflammation and provide a perspective on a personalized, targeted approach. Emerging data sheds new light on heretofore unrecognized residual risk factors. This review aims to summarize evolving evidence relative to secondary prevention of atherothrombosis, with a focus on recent advances that promise to transform the management of the post-ACS patient.

Key Words

atherosclerosis
cholesterol
inflammation
post-MI stable coronary artery disease
residual risk
thrombosis

Abbreviations and Acronyms

ACS
acute coronary syndrome
CAD
coronary artery disease
CRP
C-reactive protein
DAPT
dual antiplatelet therapy
GDMT
guideline-directed medical therapy
LDL-C
low-density lipoprotein cholesterol
MACE
major adverse cardiac events
MI
myocardial infarction
PCI
percutaneous coronary intervention
RCT
randomized controlled trial

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Dr. Libby has served as an unpaid consultant for Amgen, AstraZeneca, Esperion Therapeutics, Ionis Pharmaceuticals, Sanofi-Regeneron, and XBiotech, Inc.; has served on the scientific advisory board of Corvidia Therapeutics, Olatec Therapeutics, and Medimmune; and has received laboratory funding from Novartis. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

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