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Prognostic role of coronary artery ectasia in patients with nonobstructive coronary artery disease
Filippo Luca Gurgoglione1, Giorgio Benatti2, Luigi Vignali2
1Division of Cardiology, University of Parma.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|February 2, 2024
Summary
Patients with coronary artery ectasia (CAE) and myocardial infarction with nonobstructive coronary arteries (MINOCA) face worse outcomes. MINOCA presentation in CAE patients predicts higher major adverse cardiovascular events (MACE), including nonfatal myocardial infarction.
Area of Science:
- Cardiology
- Vascular Medicine
- Diagnostic Imaging
Background:
- Coronary artery ectasia (CAE) is associated with adverse events in patients with ischemia/angina and nonobstructive coronary arteries (INOCA/ANOCA).
- The prognostic implications of CAE in patients presenting with myocardial infarction and nonobstructive coronary arteries (MINOCA) remain under-investigated.
Purpose of the Study:
- To compare clinical, angiographic, and prognostic features of patients with CAE presenting with MINOCA versus INOCA/ANOCA.
- To assess the association between MINOCA presentation and major adverse cardiovascular events (MACE) in patients with CAE.
Main Methods:
- Retrospective analysis of 97 patients with angiographic evidence of CAE.
- Patients were categorized into MINOCA and INOCA/ANOCA groups.
- Clinical data, quantitative angiographic information, and MACE incidence at follow-up were recorded.
Main Results:
- MINOCA presentation was linked to higher rates of inflammatory diseases, multivessel CAE, and Thrombolysis In Myocardial Infarction (TIMI) flow < 3.
- Patients with MINOCA experienced a significantly higher incidence of MACE (16.3% vs. 4.2%) and nonfatal myocardial infarction (10.2% vs. 0%) at median 38-month follow-up.
- MINOCA presentation and TIMI flow < 3 were independent predictors of MACE.
Conclusions:
- In patients with CAE and nonobstructive coronary artery disease, MINOCA presentation is associated with a worse prognosis.
- MINOCA presentation independently predicts an increased risk of MACE in this patient cohort.
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