Cardiac MRI

Changed by Mark Thurston, 23 Nov 2017

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Cardiac MRI consists of using MRI to study heart anatomy and pathology.

Advantages

MainThe main advantages of cardiac MRI in comparison with other techniques are:

  • a better definition of soft tissues
  • use of different types of sequences improves diagnostic accuracy
  • avoidno ionising radiation
    • nevertheless, there are some safety issues that must be considered. still require consideration

Limitations

The main limitation of MRI, in comparison with  compared to cardiac CT, is the poorer evaluation of the coronary arteries.

In addition, cardiac MRI employs some particular imaging planes.

Imaging

Dark blood Imaging

Dark blood imaging involves spin echo sequences. Its main advantage is a fast acquisition that minimizes respiratory and cardiac movement artefacts. It’s the main issue is a low signal/noise ratio and, therefore, a deficient spatial resolution. 

These can be T1, T2, or PD-weightedproton density weighted sequences:

  • T1 weighted sequences achieve better anatomic definition
  • T2 and DPPD weighted sequences reach better tissue characterization
White blood Imaging

White Blood Imagingblood imaging involves gradient echo sequences and steady-state free precession MRI (SSFP). In practice, the difference between both is SSFP is less vulnerable to T2* effect.

The main advantage of white blood imaging is its fast acquisition. It can obtain movement sequences and allows studying cardiac function and movement.

Flux quantification sequences

The most usual sequence of this group is phase contrast imaging. It encodes flux direction and speed, similarly to CSF flow studies.

Inversion Recovery sequences

These imaging techniques use additional 180º pulses to null signal from blood and other tissues, and, therefore, improving contrast.

The most used sequence is STIR.

Contrast-enhanced techniques

Perfusion imaging (also known as first-pass images)

These are T1 weighted, gradient-echo sequences. Image acquisition is performed 3 minutes after gadolinium contrast administration. If there is a hypoenhanced area, this implies a zone of myocardial infarction that is non-viable.

Viability study delayed (also known as myocardial enhancement study)

These are T1 weighted, gradient-echo sequences. Image acquisition is performed 10 minutes after gadolinium contrast administration. 

Focal myocardial fibrosis has a delayed gadolinium contrast wash out. So an hyperenhancement indicates a myocardial scar, thus an evolved myocardial infarction.

Usually, an extra inversion pulse is used to improve contrast between fibrosis and the surrounding myocardium.

  • -<p><strong>Cardiac MRI</strong> consists of using MRI to study heart anatomy and pathology.</p><h4>Advantages</h4><p>Main advantages of cardiac MRI in comparison with other techniques are:</p><ul>
  • -<li>a better definition of soft tissues</li>
  • +<p><strong>Cardiac MRI</strong> consists of using MRI to study heart anatomy and pathology.</p><h4>Advantages</h4><p>The main advantages of cardiac MRI in comparison with other techniques are:</p><ul>
  • +<li>better definition of soft tissues</li>
  • -<li>avoid ionising radiation<ul><li>nevertheless, there are some <a href="/articles/mri-safety">safety issues</a> that must be considered.</li></ul>
  • +<li>no ionising radiation<ul><li>some <a href="/articles/mri-safety">safety issues</a> still require consideration</li></ul>
  • -</ul><h4>Limitations</h4><p>The main limitation of MRI, in comparison with cardiac CT, is the poorer evaluation of the coronary arteries.</p><p>In addition, cardiac MRI employs some particular <a href="/cases/cardiac-mri-standard-imaging-planes-1">imaging planes</a>.</p><h4>Imaging</h4><h5>Dark blood Imaging</h5><p>Dark blood imaging involves <a href="/articles/spin-echo-sequences">spin echo sequences</a>. Its main advantage is a fast acquisition that minimizes respiratory and cardiac movement artefacts. It’s the main issue is a low signal/noise ratio and, therefore, a deficient spatial resolution. </p><p>These can be T1, T2 or PD-weighted sequences:</p><ul>
  • +</ul><h4>Limitations</h4><p>The main limitation of MRI, compared to <a title="Cardiac CT" href="/articles/cardiac-ct-1">cardiac CT</a>, is the poorer evaluation of the coronary arteries.</p><p>In addition, cardiac MRI employs some particular <a href="/cases/cardiac-mri-standard-imaging-planes-1">imaging planes</a>.</p><h4>Imaging</h4><h5>Dark blood Imaging</h5><p>Dark blood imaging involves <a href="/articles/spin-echo-sequences">spin echo sequences</a>. Its main advantage is a fast acquisition that minimizes respiratory and cardiac movement artefacts. It’s the main issue is a low signal/noise ratio and, therefore, a deficient spatial resolution. </p><p>These can be T1, T2, or proton density weighted sequences:</p><ul>
  • -<li>T2 and DP weighted sequences reach better tissue characterization</li>
  • -</ul><h5>White blood Imaging</h5><p>White Blood Imaging involves <a href="/articles/gradient-echo-sequences-1">gradient echo sequences</a> and <a href="/articles/steady-state-free-precession-mri-2">steady-state free precession MRI (SSFP)</a>. In practice, the difference between both is SSFP is less vulnerable to T2* effect.</p><p>The main advantage of white blood imaging is its fast acquisition. It can obtain movement sequences and allows studying cardiac function and movement.</p><h5>Flux quantification sequences</h5><p>The most usual sequence of this group is <a href="/articles/phase-contrast-imaging">phase contrast imaging</a>. It encodes flux direction and speed, similarly to <a href="/articles/csf-flow-studies">CSF flow studies</a>.</p><h5>Inversion Recovery sequences</h5><p>These imaging techniques use additional 180º pulses to null signal from blood and other tissues, and, therefore, improving contrast.</p><p>The most used sequence is <a href="/articles/short-tau-inversion-recovery">STIR</a>.</p><h4>Contrast-enhanced techniques</h4><h5>Perfusion imaging (also known as first-pass images)</h5><p>These are T1 weighted, gradient-echo sequences. Image acquisition is performed 3 minutes after gadolinium contrast administration. If there is a hypoenhanced area, this implies a zone of myocardial infarction that is non-viable.</p><h5>Viability study delayed (also known as myocardial enhancement study)</h5><p>These are T1 weighted, gradient-echo sequences. Image acquisition is performed 10 minutes after gadolinium contrast administration. </p><p>Focal myocardial fibrosis has a delayed gadolinium contrast wash out. So an hyperenhancement indicates a myocardial scar, thus an evolved myocardial infarction.</p><p>Usually, an extra inversion pulse is used to improve contrast between fibrosis and the surrounding myocardium.</p>
  • +<li>T2 and PD weighted sequences reach better tissue characterization</li>
  • +</ul><h5>White blood Imaging</h5><p>White blood imaging involves <a href="/articles/gradient-echo-sequences-1">gradient echo sequences</a> and <a href="/articles/steady-state-free-precession-mri-2">steady-state free precession MRI (SSFP)</a>. In practice, the difference between both is SSFP is less vulnerable to T2* effect.</p><p>The main advantage of white blood imaging is its fast acquisition. It can obtain movement sequences and allows studying cardiac function and movement.</p><h5>Flux quantification sequences</h5><p>The most usual sequence of this group is <a href="/articles/phase-contrast-imaging">phase contrast imaging</a>. It encodes flux direction and speed, similarly to <a href="/articles/csf-flow-studies">CSF flow studies</a>.</p><h5>Inversion Recovery sequences</h5><p>These imaging techniques use additional 180º pulses to null signal from blood and other tissues, and, therefore, improving contrast.</p><p>The most used sequence is <a href="/articles/short-tau-inversion-recovery">STIR</a>.</p><h4>Contrast-enhanced techniques</h4><h5>Perfusion imaging (also known as first-pass images)</h5><p>These are T1 weighted, gradient-echo sequences. Image acquisition is performed 3 minutes after gadolinium contrast administration. If there is a hypoenhanced area, this implies a zone of myocardial infarction that is non-viable.</p><h5>Viability study delayed (also known as myocardial enhancement study)</h5><p>These are T1 weighted, gradient-echo sequences. Image acquisition is performed 10 minutes after gadolinium contrast administration. </p><p>Focal myocardial fibrosis has a delayed gadolinium contrast wash out. So an hyperenhancement indicates a myocardial scar, thus an evolved myocardial infarction.</p><p>Usually, an extra inversion pulse is used to improve contrast between fibrosis and the surrounding myocardium.</p>

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