Infarct healing is a dynamic process following acute myocardial infarction

46Citations
Citations of this article
63Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background: The role of infarct size on left ventricular (LV) remodeling in heart failure after an acute ST-segment elevation myocardial infarction (STEMI) is well recognized. Infarct size, as determined by cardiovascular magnetic resonance (CMR), decreases over time. The amount, rate, and duration of infarct healing are unknown. Methods: A total of 66 patients were prospectively enrolled after reperfusion for an acute STEMI. Patients underwent a CMR evaluation within 1 week, 4 months, and 14 months after STEMI. Results: Mean infarct sizes for the 66 patients at baseline (acute necrosis), early follow-up (early scar), and late follow-up (late scar) were 25 ± 17 g, 17 ± 12 g, and 15 ± 11 g, respectively. Patients were stratified in tertiles, based on infarct size, with the largest infarcts having the greatest absolute decrease in mass at early and late scar. The percent reduction of infarct mass was independent of initial infarct size. There was an 8 g or 32% decrease in infarct mass between acute necrosis and early scar (p ≥ 0.01) with a 2 g or 12% additional decrease in infarct mass between early and late scar (p ≥ 0.01). Conclusions: Infarct healing is a continuous process after reperfusion for STEMI, with greatest reduction in infarct size in the first few months. The dynamic nature of infarct healing through the first year after STEMI indicates that decisions based on infarct size, and interventions to reduce infarct size, must take into consideration the time frame of measurement. © 2012 Pokorney et al.; licensee BioMed Central Ltd.

Cite

CITATION STYLE

APA

Pokorney, S. D., Rodriguez, J. F., Ortiz, J. T., Lee, D. C., Bonow, R. O., & Wu, E. (2012). Infarct healing is a dynamic process following acute myocardial infarction. Journal of Cardiovascular Magnetic Resonance, 14(1). https://doi.org/10.1186/1532-429X-14-62

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free