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J Am Coll Cardiol Img, 2009; 2:569-576, doi:10.1016/j.jcmg.2008.11.018
© 2009 by the American College of Cardiology Foundation
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Myocardium at Risk After Acute Infarction in Humans on Cardiac Magnetic Resonance

Quantitative Assessment During Follow-Up and Validation With Single-Photon Emission Computed Tomography

Marcus Carlsson, MD, PhD*, Joey F.A. Ubachs, MD*, Erik Hedström, MD, PhD*, Einar Heiberg, PhD*, Stefan Jovinge, MD, PhD{dagger}, Håkan Arheden, MD, PhD*,*

* Cardiac MR Group, Department of Clinical Physiology, Lund University Hospital, Lund, Sweden
{dagger} Department of Cardiology, Lund University Hospital, Lund, Sweden

* Reprint requests and correspondence: Dr. Håkan Arheden, Department of Clinical Physiology, Lund University Hospital, Lund SE-22185, Sweden (Email: hakan.arheden{at}med.lu.se).

Objectives: Our goal was to validate myocardium at risk on T2-weighted short tau inversion recovery (T2-STIR) cardiac magnetic resonance (CMR) over time, compared with that seen with perfusion single-photon emission computed tomography (SPECT) in patients with ST-segment elevation myocardial infarction, and to assess the amount of salvaged myocardium after 1 week.

Background: To assess reperfusion therapy, it is necessary to determine how much myocardium is salvaged by measuring the final infarct size in relation to the initial myocardium at risk of the left ventricle (LV).

Methods: Sixteen patients with first-time ST-segment elevation myocardial infarction received 99mTc tetrofosmin before primary percutaneous coronary intervention. SPECT was performed within 4 h and T2-STIR CMR within 1 day, 1 week, 6 weeks, and 6 months. At 1 week, patients were injected with a gadolinium-based contrast agent for quantification of infarct size.

Results: Myocardium at risk at occlusion on SPECT was 33 ± 10% of the LV. Myocardium at risk on T2-STIR did not differ from SPECT, at day 1 (29 ± 7%, p = 0.49) or week 1 (31 ± 6%, p = 0.16) but declined at week 6 (10 ± 12%, p = 0.0096 vs. 1 week) and month 6 (4 ± 11%, p = 0.0013 vs. 1 week). There was a correlation between myocardium at risk demonstrated by T2-STIR at week 1 and myocardium at risk by SPECT (r2 = 0.70, p < 0.001), and the difference between the methods on Bland-Altman analysis was not significant (–2.3 ± 5.7%, p = 0.16). Both modalities identified myocardium at risk in the same perfusion territory and in concordance with angiography. Final infarct size was 8 ± 7%, and salvage was 75 ± 19% of myocardium at risk.

Conclusions: This study demonstrates that T2-STIR performed up to 1 week after reperfusion can accurately determine myocardium at risk as it was before opening of the occluded artery. CMR can also quantify salvaged myocardium as myocardium at risk minus final infarct size.

Key Words: myocardium at risk • T2-STIR • CMR • salvaged myocardium

Abbreviations and Acronyms
  CMR = cardiac magnetic resonance
  DE = delayed enhanced
  LV = left ventricle/ventricular
  MI = myocardial infarction
  PCI = percutaneous coronary intervention
  SPECT = single-photon emission computed tomography
  STEMI = ST-segment elevation myocardial infarction
  T2-STIR = T2-weighted short tau inversion recovery


Related Article

A Closer Look on the Battlefield: The Salvaged Area at Risk as an Outcome Marker for Myocardial Reperfusion
Matthias G. Friedrich
J. Am. Coll. Cardiol. Img. 2009 2: 577-579. [Full Text] [PDF]



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Home page
J Am Coll Cardiol ImgHome page
M. G. Friedrich
A closer look on the battlefield the salvaged area at risk as an outcome marker for myocardial reperfusion.
J. Am. Coll. Cardiol. Img., May 1, 2009; 2(5): 577 - 579.
[Full Text] [PDF]



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