TY - JOUR
T1 - Applying contemporary antithrombotic therapy in the secondary prevention of chronic atherosclerotic cardiovascular disease
AU - Welsh, Robert C.
AU - Peterson, Eric D.
AU - De Caterina, Raffaele
AU - Bode, Christoph
AU - Gersh, Bernard
AU - Eikelboom, John W.
N1 - Funding Information:
R. C. W. reports grants and personal fees from Astra Zeneca, Bayer, Boehringer-Ingelheim, Eli Lilly-Bristol-Myers Squibb, and Pfizer. E. D. P. reports grants and personal fees from Astra Zeneca and Janssen. R. De C. reports grants and personal fees from AstraZeneca, Boehringer-Ingelheim, Bayer, Bristol-Myers Squibb/Pfizer, Roche, Daiichi Sankyo, Lilly, Merck, and Novartis. C. B. has received grants and personal fees from Bayer. B. G. reports no conflicts for this work. J. W. E. reports grants and personal fees from Astra Zeneca, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb/Pfizer, Daiichi Sankyo, Janssen, Eli Lilly, GlaxoSmithKline, and Sanofi-Aventis.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/12
Y1 - 2019/12
N2 - For 4 decades, antithrombotic therapy with aspirin has been a cornerstone of secondary prevention for patients with chronic atherosclerotic cardiovascular disease (ASCVD). Unfortunately, despite the use of evidence-based therapies, patients with ASCVD continue to have recurrent major adverse cardiovascular events including death, myocardial infarction, and stroke—at a rate of approximately 2%-4% per year. To combat this continuing risk, several recent trials have evaluated the efficacy and safety of more intensive antithrombotic strategies through prolonged dual antiplatelet therapy (DAPT), combining a P2Y12 receptor antagonists and low-dose aspirin, or alternatively applying a dual pathway inhibition approach, combining low-dose non—vitamin K antagonist anticoagulant and low-dose aspirin. Both combination strategies have been shown to reduce recurrent ischemic events but at the cost of increased bleeding events. The clinical application of these antithrombotic strategies requires clinicians to assess and balance the risk of recurrent ischemic and bleeding events in an individual patient. Furthermore, clinicians may also need to adapt their antithrombotic strategies to achieve best patient outcomes, as ASCVD is a progressive disease and the risks of cardiovascular ischemic and bleeding events may shift over time. This state-of-the-art article reviews evidence from the trials and provides a practical approach to the application of DAPT and dual pathway antithrombotic therapy in the long-term management of patients with chronic ASCVD.
AB - For 4 decades, antithrombotic therapy with aspirin has been a cornerstone of secondary prevention for patients with chronic atherosclerotic cardiovascular disease (ASCVD). Unfortunately, despite the use of evidence-based therapies, patients with ASCVD continue to have recurrent major adverse cardiovascular events including death, myocardial infarction, and stroke—at a rate of approximately 2%-4% per year. To combat this continuing risk, several recent trials have evaluated the efficacy and safety of more intensive antithrombotic strategies through prolonged dual antiplatelet therapy (DAPT), combining a P2Y12 receptor antagonists and low-dose aspirin, or alternatively applying a dual pathway inhibition approach, combining low-dose non—vitamin K antagonist anticoagulant and low-dose aspirin. Both combination strategies have been shown to reduce recurrent ischemic events but at the cost of increased bleeding events. The clinical application of these antithrombotic strategies requires clinicians to assess and balance the risk of recurrent ischemic and bleeding events in an individual patient. Furthermore, clinicians may also need to adapt their antithrombotic strategies to achieve best patient outcomes, as ASCVD is a progressive disease and the risks of cardiovascular ischemic and bleeding events may shift over time. This state-of-the-art article reviews evidence from the trials and provides a practical approach to the application of DAPT and dual pathway antithrombotic therapy in the long-term management of patients with chronic ASCVD.
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U2 - 10.1016/j.ahj.2019.09.006
DO - 10.1016/j.ahj.2019.09.006
M3 - Review article
C2 - 31715433
AN - SCOPUS:85074687618
SN - 0002-8703
VL - 218
SP - 100
EP - 109
JO - American Heart Journal
JF - American Heart Journal
ER -