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J Am Coll Cardiol, 2005; 45:544-552, doi:10.1016/j.jacc.2004.10.058
© 2005 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: CARDIAC IMAGING

Quantitative measurement of infarct size by contrast-enhanced magnetic resonance imaging early after acute myocardial infarction

Comparison with single-photon emission tomography using Tc99m-sestamibi

Tareq Ibrahim, MD*, Stephan G. Nekolla, PhD{dagger}, Mira Hörnke{dagger}, Hubertus P. Bülow, MD{dagger}, Josef Dirschinger, MD*, Albert Schömig, MD* and Markus Schwaiger, MD, FACC{dagger},*

* Deutsches Herzzentrum München and 1. Medizinische Klinik des Klinikums Rechts der Isar, Technische Universität München, Munich, Germany
{dagger} Nuklearmedizinische Klinik und Poliklinik der Technischen Universität München, Munich, Germany

Manuscript received December 14, 2003; revised manuscript received September 7, 2004, accepted October 12, 2004.

* Reprint requests and correspondence: Dr. Markus Schwaiger, Nuklearmedizinische Klinik der Technischen Universität München, Ismaningerstr. 22, D 81675 München, Germany (Email: m.schwaiger{at}lrz.tu-muenchen.de).

OBJECTIVES: The aim of this research was to evaluate kinetics and extent of myocardial contrast enhancement (CE) in comparison with single-photon emission computed tomography (SPECT) early after acute myocardial infarction (AMI).

BACKGROUND: Quantification of infarct size serves as a surrogate end point in evaluating new therapies of AMI. Contrast-enhanced magnetic resonance imaging (CeMRI) of the myocardium is a promising new method for identification of irreversible tissue injury.

METHODS: A total of 33 patients were examined by CeMRI and SPECT 7 ± 2 days after AMI and successful coronary intervention. After gadolinium-diethylenetraimine pentaacetic acid injection (0.2 mmol/kg), continuous short-axis slices of the left ventricle (LV) were acquired every 7 min up to 42 min using different inversion times (TI). Myocardial CE at each imaging time point was quantified and compared with corresponding SPECT perfusion defect.

RESULTS: All patients showed myocardial CE in the infarct region. A constant TI for CeMRI resulted in a decrease of signal intensity and extent of CE on late acquisitions. With TI adjustment, infarct image intensity peaked at 21 min with a contrast of 478% of remote myocardium and remained at this level up to 42 min after contrast injection (437%); CE extent was stable over time and agreed well with SPECT within an average difference of 3% of the LV myocardium, yielding the best correlation at 28 min (r = 0.86).

CONCLUSIONS: In patients after AMI and successful reperfusion, CE is stable over time and matches well with SPECT perfusion defect; CeMRI under standardized conditions can accurately assess myocardial infarct size in vivo and may be attractive for serving as a surrogate end point early after AMI.

Abbreviations and Acronyms
  AMI = acute myocardial infarction
  CE = contrast enhancement
  CeMRI = contrast-enhanced magnetic resonance imaging
  CK = creatine kinase
  EF = ejection fraction
  Gd-DTPA = gadolinium-diethylenetriamine pentaacetic acid
  LV = left ventricle/ventricular
  MI = myocardial infarction
  MRI = magnetic resonance imaging
  SPECT = single-photon emission computed tomography
  TI = inversion time




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