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dc.contributor.authorGaba, Prakriti
dc.contributor.authorBhatt, Deepak L
dc.contributor.authorSteg, Ph Gabriel
dc.contributor.authorMiller, Michael
dc.contributor.authorBrinton, Eliot A
dc.contributor.authorJacobson, Terry A
dc.contributor.authorKetchum, Steven B
dc.contributor.authorJuliano, Rebecca A
dc.contributor.authorJiao, Lixia
dc.contributor.authorDoyle, Ralph T
dc.contributor.authorGranowitz, Craig
dc.contributor.authorTardif, Jean-Claude
dc.contributor.authorGiugliano, Robert P
dc.contributor.authorMartens, Fabrice M A C
dc.contributor.authorGibson, C Michael
dc.contributor.authorBallantyne, Christie M
dc.date.accessioned2022-05-03T12:48:16Z
dc.date.available2022-05-03T12:48:16Z
dc.date.issued2022-05-03
dc.identifier.urihttp://hdl.handle.net/10713/18724
dc.description.abstractBACKGROUND: REDUCE-IT was a double-blind trial that randomized 8,179 statin-treated patients with controlled low-density lipoprotein cholesterol and moderately elevated triglycerides to icosapent ethyl (IPE) or placebo. There was a significant reduction in the primary endpoint, including death from cardiovascular (CV) causes. The specific impact of IPE among patients with prior myocardial infarction (MI) was unknown. OBJECTIVES: Our goal was to examine the benefit of IPE on ischemic events among patients with prior MI in REDUCE-IT. METHODS: We performed post hoc analyses of patients with prior MI. The primary endpoint was CV death, MI, stroke, coronary revascularization, or hospitalization for unstable angina. The key secondary endpoint was CV death, MI, or stroke. RESULTS: A total of 3,693 patients had a history of prior MI. The primary endpoint was reduced from 26.1% to 20.2% with IPE vs placebo; HR: 0.74 (95% CI: 0.65-0.85; P = 0.00001). The key secondary endpoint was reduced from 18.0% to 13.3%; HR: 0.71 (95% CI: 0.61-0.84; P = 0.00006). There was also a significant 35% relative risk reduction in total ischemic events (P = 0.0000001), a 34% reduction in MI (P = 0.00009), a 30% reduction in CV death (P = 0.01), and a 20% lower rate of all-cause mortality (P = 0.054), although there was a slight increase in atrial fibrillation. Sudden cardiac death and cardiac arrest were also significantly reduced by 40% and 56%, respectively. CONCLUSIONS: Patients with a history of prior MI in REDUCE-IT treated with IPE demonstrated large and significant relative and absolute risk reductions in ischemic events, including CV death. (A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High Risk Patients With Hypertriglyceridemia and on Statin. The Primary Objective is to Evaluate the Effect of 4 g/Day AMR101 for Preventing the Occurrence of a First Major Cardiovascular Event. [REDUCE-IT]; NCT01492361).en_US
dc.description.urihttps://doi.org/10.1016/j.jacc.2022.02.035en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofJournal of the American College of Cardiologyen_US
dc.rightsCopyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.en_US
dc.subjectclinical trialsen_US
dc.subjecticosapent ethylen_US
dc.subjectischemic eventsen_US
dc.subjectmyocardial infarctionen_US
dc.titlePrevention of Cardiovascular Events and Mortality With Icosapent Ethyl in Patients With Prior Myocardial Infarction.en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jacc.2022.02.035
dc.identifier.pmid35483753
dc.source.journaltitleJournal of the American College of Cardiology
dc.source.volume79
dc.source.issue17
dc.source.beginpage1660
dc.source.endpage1671
dc.source.countryUnited States


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