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J Am Coll Cardiol Img, 2009; 2:969-979, doi:10.1016/j.jcmg.2009.03.017
© 2009 by the American College of Cardiology Foundation
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Contrast-Enhanced Anatomic Imaging as Compared to Contrast-Enhanced Tissue Characterization for Detection of Left Ventricular Thrombus

Jonathan W. Weinsaft, MD*,{dagger},*, Raymond J. Kim, MD{ddagger}, Michael Ross, MD*, Daniel Krauser, MD*, Shant Manoushagian, BA*, Troy M. LaBounty, MD*, Matthew D. Cham, MD*,{dagger}, James K. Min, MD*,{dagger}, Kirsten Healy, MD*, Yi Wang, PhD{dagger}, Michele Parker, MS, RN{ddagger}, Mary J. Roman, MD*, Richard B. Devereux, MD*

* Cardiology Division, Department of Medicine, Weill Cornell Medical College, New York, New York
{dagger} Department of Radiology, Weill Cornell Medical College, New York, New York
{ddagger} Duke Cardiovascular Magnetic Resonance Center, Durham, North Carolina

* Reprint requests and correspondence: Dr. Jonathan W. Weinsaft, Weill Cornell Medical College, 525 East 68th Street, New York, New York 10021 (Email: jww2001{at}med.cornell.edu).

Objectives: This study sought to compare contrast-enhanced anatomic imaging and contrast-enhanced tissue characterization (delayed-enhancement cardiac magnetic resonance [DE-CMR]) for left ventricular (LV) thrombus detection.

Background: Contrast echocardiography (echo) detects LV thrombus based on anatomic appearance, whereas DE-CMR imaging detects thrombus based on tissue characteristics. Although DE-CMR has been validated as an accurate technique for thrombus, its utility compared with contrast echo is unknown.

Methods: Multimodality imaging was performed in 121 patients at high risk for thrombus due to myocardial infarction or heart failure. Imaging included 3 anatomic imaging techniques for thrombus detection (contrast echo, noncontrast echo, cine-CMR) and a reference of DE-CMR tissue characterization. LV structural parameters were quantified to identify markers for thrombus and predictors of additive utility of contrast-enhanced thrombus imaging.

Results: Twenty-four patients had thrombus by DE-CMR. Patients with thrombus had larger infarcts (by DE-CMR), more aneurysms, and lower LV ejection fraction (by CMR and echo) than those without thrombus. Contrast echo nearly doubled sensitivity (61% vs. 33%, p < 0.05) and yielded improved accuracy (92% vs. 82%, p < 0.01) versus noncontrast echo. Patients who derived incremental diagnostic utility from DE-CMR had lower LV ejection fraction versus those in whom noncontrast echo alone accurately assessed thrombus (35 ± 9% vs. 42 ± 14%, p < 0.01), with a similar trend for patients who derived incremental benefit from contrast echo (p = 0.08). Contrast echo and cine-CMR closely agreed on the diagnosis of thrombus ({kappa} = 0.79, p < 0.001). Thrombus prevalence was lower by contrast echo than DE-CMR (p < 0.05). Thrombus detected by DE-CMR but not by contrast echo was more likely to be mural in shape or, when apical, small in volume (p < 0.05).

Conclusions: Echo contrast in high-risk patients markedly improves detection of LV thrombus, but does not detect a substantial number of thrombi identified by DE-CMR tissue characterization. Thrombi detected by DE-CMR but not by contrast echo are typically mural in shape or small in volume.

Key Words: thrombus • cardiac magnetic resonance • echocardiography

Abbreviations and Acronyms
  CMR = cardiac magnetic resonance
  DE = delayed-enhancement
  echo = echocardiography
  LV = left ventricular
  LVEF = left ventricular ejection fraction
  MVO = microvascular obstruction
  TI = inversion time






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