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CASE STUDIES

Assessing damaged myocardium using a novel black blood MDE sequence

By Giuseppe Muscogiuri, MD, PhD, FSCCT, radiologist, and Gianluca Pontone, MD, PhD, FESC, FEACVI, FSCCT, FISC, cardiologist and radiologist, Department of Cardiovascular Imaging, Centro Cardiologico Monzino, Milan, Italy

Cardiac MR enables both anatomical and functional assessment of the heart. Black blood (BB), T2 STIR and fat suppression are commonly used for the detection of areas at risk for infarction and scar. In some cases it is difficult to differentiate between scar and blood pool using late gadolinium enhancement (LGE) sequences. In particular, factors such as the volume of gadolinium-based contrast, clearance rate and the timing of the LGE acquisition contribute to the similar signal intensity of the blood pool and the area of infarct. To overcome this, usually we compare cine images and LGE images in the same cardiac phase of acquisition.

 

The availability of BB LGE sequences makes it easier to depict subendocardial infarction, as well as involvement of the papillary muscles with higher contrast-to-noise ratios. We evaluated GE Healthcare’s BB myocardial delayed enhancement (MDE)‡ sequence for research purposes in 73 patients with known or suspected coronary artery disease who underwent a cardiac MR exam.

Patient history

A 53-year-old patient weighing 52 kg (115 lbs.) for evaluation of acute myocardial infarction.

MR findings

Cardiac MR shows a subendocardial myocardial infarction with 50-100 percent of transmurality in inferoseptal, inferior segment of the middle-ventricle myocardium and apical septum (Figure 1A). The findings were confirmed on BB MDE images (Figure 1B).

 

 

Gallery Image 1
A
Gallery Image 2
B

Figure 1.

A 53-year-old patient with acute myocardial infarction on territory of right coronary artery. (A) Short axis shows subendocardial late gadolinium enhancement of inferior and inferoseptal myocardial segments. The findings were confirmed on (B) BB MDE images.

 

Discussion

The BB MDE sequence enabled us to depict the subendocardial enhancement and involvement of papillary muscles, and clearly distinguish the damaged myocardium from the blood pool activity. This capability may be especially useful in cases where the standard LGE sequence is non-diagnostic.

 

In particular, the possibility to have a dark blood in both ventricles with the BB MDE sequence is extremely promising. Overall, the image quality was good, providing excellent diagnostic capability.

 

 

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