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Cited 19 time in webofscience Cited 25 time in scopus
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Cardiovascular and Bleeding Risks Associated With Nonsteroidal Anti-Inflammatory Drugs After Myocardial Infarction

Authors
Kang, Dong OhAn, Hyong ginPark, Geun UYum, YunjinPark, Eun JinPark, YoonjeeJang, Won YoungKim, Woo HyeunChoi, Jah YeonRoh, Seung YoungNa, Jin OhKim, Jin WonKim, Eung JuRha, Seung WoonPark, Chang GyuSeo, Hong SeogChoi, Cheol Ung
Issue Date
Aug-2020
Publisher
Elsevier BV
Keywords
antithrombotic therapy; celecoxib; meloxicam; myocardial infarction; nonsteroidal anti-inflammatory drugs; safety
Citation
Journal of the American College of Cardiology, v.76, no.5, pp 518 - 529
Pages
12
Indexed
SCIE
SCOPUS
Journal Title
Journal of the American College of Cardiology
Volume
76
Number
5
Start Page
518
End Page
529
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/822
DOI
10.1016/j.jacc.2020.06.017
ISSN
0735-1097
1558-3597
Abstract
BACKGROUND Limited data are available regarding the risk for adverse clinical events with concomitant nonsteroidal anti-inflammatory drug (NSAID) treatment after myocardial infarction (MI). OBJECTIVES The aim of this study was to investigate the risk for cardiovascular and bleeding events according to groups of antithrombotic medications and subtypes of NSAIDs in patients with MI. METHODS This was a nationwide cohort study to enroll a study population from the Health Insurance Review and Assessment Service database in Korea between 2009 and 2013. Patients were divided into groups on the basis of the prescribed antithrombotic medications. The primary and secondary outcomes were thromboembolic cardiovascular and clinically relevant bleeding events. The risk for adverse clinical events was assessed by ongoing NSAID treatment and subtypes of NSAIDs. RESULTS In total, 108,232 patients (mean age 64.2 +/- 12.8 years, 72.1% men, mean follow-up duration 2.3 +/- 1.8 years) with first diagnosed MI were enrolled. Concomitant NSAID treatment significantly increased the risk for cardiovascular events (hazard ratio [HR]: 6.96; 95% confidence interval [CI]: 6.24 to 6.77; p < 0.001) and bleeding events (HR: 4.08; 95% CI: 3.51 to 4.73; p < 0.001) compared with no NSAID treatment. Among NSAID subtypes, the risk for cardiovascular and bleeding events was lowest with the use of celecoxib (HR: 4.65; 95% CI: 3.17 to 6.82; p < 0.001, and 3.44; 95% CI: 2.20 to 5.39; p < 0.001, respectively) and meloxicam (HR: 3.03; 95% CI: 1.68 to 5.47; p < 0.001, and 2.80; 95% CI: 1.40 to 5.60; p < 0.001, respectively). CONCLUSIONS Concomitant NSAID treatment significantly increased the risk for cardiovascular and bleeding events after MI. Although NSAID treatment should be avoided after MI, celecoxib and meloxicam could be considered as alternative options in cases in which NSAID use is unavoidable. (c) 2020 by the American College of Cardiology Foundation.
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Choi, Jah Yeon
Guro Hospital (Department of Cardiology, Guro Hospital)
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