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Introduction
 Acute myocardial infarction (MI) typically
occurs from a plaque rupture or erosion within a
coronary artery,known as the infarct-related
artery (IRA)
 In patients with NSTEMI compared with those with
ST-segment–elevation MI, identification of the
IRA can be challenging because patients are more
likely to present with either multivessel
coronary artery disease (CAD) or insignificant
CAD
Introduction
 The correct identification of the IRA in
acute MI has obvious importance for
coronary revascularization strategies
Background
 Determining the infarct-related artery
(IRA) in NSTEMI can be challenging
 Delayed-enhancement cardiac magnetic
resonance (DE-CMR) can accurately
identify small MIs
Objective
 To determine whether DE-CMR improves the
ability to identify the IRA in patients
with NSTEMI
Methods
 In this 3-center, prospective study,
authors enrolled 114 patients presenting
with their first MI
 Patients underwent DE-CMR followed by
coronary angiography
 The interventional cardiologist was
blinded to the DE-CMR results
Methods
 Later, coronary angiography and DE-CMR
images were reviewed independently and
blindly for identification of the IRA
 The pattern of DE-CMR hyperenhancement
was also used to determine whether there
was a nonischemic pathogenesis for
myocardial necrosis
Determining an IRA match or mismatch
between DE-CMR and CA
IRA: Infarct-related artery; DE-CMR: delayed-enhancement cardiac magnetic resonance; CA: coronary angiography
Baseline Characteristics of the Patients
Baseline Characteristics of the Patients
Results
 IRA was not identifiable by coronary
angiography in 37% of patients (n=42)
 In these,IRA or a new noncoronary artery
disease diagnosis was identified by DE-
CMR in 60% and 19% of patients,
respectively
 A different IRA or a noncoronary artery
disease diagnosis was identified by DE-
CMR in 14% and 13%, respectively
Results
 Overall, DE-CMR led to a new IRA
diagnosis in 31%, a diagnosis of
nonischemic pathogenesis in 15%, or
either in 46% (95% CI, 37%–55%) of
patients
 Of 55 patients undergoing
revascularization, 27% had
revascularization solely to nonculprit
coronary artery territories as determined
by DE-CMR
Summary of Results
Some Patient Examples
Frequency of IRA by DE-CMR and CA
based on severity of CAD
IRA: Infarct-related artery; DE-CMR: delayed-enhancement cardiac magnetic resonance; CA: coronary angiography; CAD: Coronary artery disease
Conclusions
 Identification of the IRA by coronary
angiography can be challenging in
patients with NSTEMI
 In nearly half, DE-CMR may lead to a new
IRA diagnosis or elucidate a non-ischemic
pathogenesis
 Revascularization solely of coronary
arteries that are believed to be non-
culprit arteries by DE-CMR is not
uncommon

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CMR in nstemi

  • 1.
  • 2. Introduction  Acute myocardial infarction (MI) typically occurs from a plaque rupture or erosion within a coronary artery,known as the infarct-related artery (IRA)  In patients with NSTEMI compared with those with ST-segment–elevation MI, identification of the IRA can be challenging because patients are more likely to present with either multivessel coronary artery disease (CAD) or insignificant CAD
  • 3. Introduction  The correct identification of the IRA in acute MI has obvious importance for coronary revascularization strategies
  • 4. Background  Determining the infarct-related artery (IRA) in NSTEMI can be challenging  Delayed-enhancement cardiac magnetic resonance (DE-CMR) can accurately identify small MIs
  • 5. Objective  To determine whether DE-CMR improves the ability to identify the IRA in patients with NSTEMI
  • 6. Methods  In this 3-center, prospective study, authors enrolled 114 patients presenting with their first MI  Patients underwent DE-CMR followed by coronary angiography  The interventional cardiologist was blinded to the DE-CMR results
  • 7. Methods  Later, coronary angiography and DE-CMR images were reviewed independently and blindly for identification of the IRA  The pattern of DE-CMR hyperenhancement was also used to determine whether there was a nonischemic pathogenesis for myocardial necrosis
  • 8. Determining an IRA match or mismatch between DE-CMR and CA IRA: Infarct-related artery; DE-CMR: delayed-enhancement cardiac magnetic resonance; CA: coronary angiography
  • 11. Results  IRA was not identifiable by coronary angiography in 37% of patients (n=42)  In these,IRA or a new noncoronary artery disease diagnosis was identified by DE- CMR in 60% and 19% of patients, respectively  A different IRA or a noncoronary artery disease diagnosis was identified by DE- CMR in 14% and 13%, respectively
  • 12. Results  Overall, DE-CMR led to a new IRA diagnosis in 31%, a diagnosis of nonischemic pathogenesis in 15%, or either in 46% (95% CI, 37%–55%) of patients  Of 55 patients undergoing revascularization, 27% had revascularization solely to nonculprit coronary artery territories as determined by DE-CMR
  • 15. Frequency of IRA by DE-CMR and CA based on severity of CAD IRA: Infarct-related artery; DE-CMR: delayed-enhancement cardiac magnetic resonance; CA: coronary angiography; CAD: Coronary artery disease
  • 16. Conclusions  Identification of the IRA by coronary angiography can be challenging in patients with NSTEMI  In nearly half, DE-CMR may lead to a new IRA diagnosis or elucidate a non-ischemic pathogenesis  Revascularization solely of coronary arteries that are believed to be non- culprit arteries by DE-CMR is not uncommon