| Literature DB >> 35272796 |
Anton Camaj1, Valentin Fuster2, Gennaro Giustino3, Solomon W Bienstock4, David Sternheim2, Roxana Mehran5, George D Dangas6, Annapoorna Kini7, Samin K Sharma2, Jonathan Halperin2, Marc R Dweck8, Martin E Goldman9.
Abstract
The incidence of left ventricular (LV) thrombus following acute myocardial infarction has markedly declined in recent decades caused by advancements in reperfusion and antithrombotic therapies. Despite this, embolic events remain the most feared complication of LV thrombus necessitating systemic anticoagulation. Mechanistically, LV thrombus development depends on Virchow's triad (ie, endothelial injury from myocardial infarction, blood stasis from LV dysfunction, and hypercoagulability triggered by inflammation, with each of these elements representing potential therapeutic targets). Diagnostic modalities include transthoracic echocardiography with or without ultrasound-enhancing agents and cardiac magnetic resonance. Most LV thrombi develop within the first 2 weeks post-acute myocardial infarction, and the role of surveillance imaging appears limited. Vitamin K antagonists remain the mainstay of therapy because the efficacy of direct oral anticoagulants is less well established. Only meager data support the routine use of prophylactic anticoagulation, even in high-risk patients.Entities:
Keywords: acute myocardial infarction; anticoagulation; left ventricular thrombus
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Year: 2022 PMID: 35272796 DOI: 10.1016/j.jacc.2022.01.011
Source DB: PubMed Journal: J Am Coll Cardiol ISSN: 0735-1097 Impact factor: 24.094