Table 3:

Myocardial infarction

Peri-procedural MI (≤72 h after the index procedure)
  •  New ischaemic symptoms (e.g. chest pain or shortness of breath), or new ischaemic signs (e.g. ventricular arrhythmias, new or worsening heart failure, new ST-segment changes, haemodynamic instability, new pathological Q-waves in at least two contiguous leads, imaging evidence of new loss of viable myocardium or new wall motion abnormality) AND

  •  Elevated cardiac biomarkers (preferable CK-MB) within 72 h after the index procedure, consisting of at least one sample post-procedure with a peak value exceeding 15× as the upper reference limit for troponin or 5× for CK-MB.a If cardiac biomarkers are increased at baseline (>99th percentile), a further increase in at least 50% post-procedure is required AND the peak value must exceed the previously stated limit

Spontaneous MI (>72 h after the index procedure) Any one of the following criteria
  •  Detection of rise and/or fall of cardiac biomarkers (preferably troponin) with at least one value above the 99th percentile URL, together with the evidence of myocardial ischaemia with at least one of the following:

  •  Symptoms of ischaemia

  •  ECG changes indicative of new ischaemia [new ST-T changes or new left bundle branch block (LBBB)]

  •  New pathological Q-waves in at least two contiguous leads

  •  Imaging evidence of a new loss of viable myocardium or new wall motion abnormality

  •  Sudden, unexpected cardiac death, involving cardiac arrest, often with symptoms suggestive of myocardial ischaemia, and accompanied by presumably new ST elevation, or new LBBB, and/or evidence of fresh thrombus by coronary angiography and/or at autopsy, but death occurring before blood samples could be obtained, or at a time before the appearance of cardiac biomarkers in the blood.

  •  Pathological findings of an acute myocardial infarction

Peri-procedural MI (≤72 h after the index procedure)
  •  New ischaemic symptoms (e.g. chest pain or shortness of breath), or new ischaemic signs (e.g. ventricular arrhythmias, new or worsening heart failure, new ST-segment changes, haemodynamic instability, new pathological Q-waves in at least two contiguous leads, imaging evidence of new loss of viable myocardium or new wall motion abnormality) AND

  •  Elevated cardiac biomarkers (preferable CK-MB) within 72 h after the index procedure, consisting of at least one sample post-procedure with a peak value exceeding 15× as the upper reference limit for troponin or 5× for CK-MB.a If cardiac biomarkers are increased at baseline (>99th percentile), a further increase in at least 50% post-procedure is required AND the peak value must exceed the previously stated limit

Spontaneous MI (>72 h after the index procedure) Any one of the following criteria
  •  Detection of rise and/or fall of cardiac biomarkers (preferably troponin) with at least one value above the 99th percentile URL, together with the evidence of myocardial ischaemia with at least one of the following:

  •  Symptoms of ischaemia

  •  ECG changes indicative of new ischaemia [new ST-T changes or new left bundle branch block (LBBB)]

  •  New pathological Q-waves in at least two contiguous leads

  •  Imaging evidence of a new loss of viable myocardium or new wall motion abnormality

  •  Sudden, unexpected cardiac death, involving cardiac arrest, often with symptoms suggestive of myocardial ischaemia, and accompanied by presumably new ST elevation, or new LBBB, and/or evidence of fresh thrombus by coronary angiography and/or at autopsy, but death occurring before blood samples could be obtained, or at a time before the appearance of cardiac biomarkers in the blood.

  •  Pathological findings of an acute myocardial infarction

aPreviously in the original VARC it was 10× and 5× for troponin and CK-MB, respectively.

Table 3:

Myocardial infarction

Peri-procedural MI (≤72 h after the index procedure)
  •  New ischaemic symptoms (e.g. chest pain or shortness of breath), or new ischaemic signs (e.g. ventricular arrhythmias, new or worsening heart failure, new ST-segment changes, haemodynamic instability, new pathological Q-waves in at least two contiguous leads, imaging evidence of new loss of viable myocardium or new wall motion abnormality) AND

  •  Elevated cardiac biomarkers (preferable CK-MB) within 72 h after the index procedure, consisting of at least one sample post-procedure with a peak value exceeding 15× as the upper reference limit for troponin or 5× for CK-MB.a If cardiac biomarkers are increased at baseline (>99th percentile), a further increase in at least 50% post-procedure is required AND the peak value must exceed the previously stated limit

Spontaneous MI (>72 h after the index procedure) Any one of the following criteria
  •  Detection of rise and/or fall of cardiac biomarkers (preferably troponin) with at least one value above the 99th percentile URL, together with the evidence of myocardial ischaemia with at least one of the following:

  •  Symptoms of ischaemia

  •  ECG changes indicative of new ischaemia [new ST-T changes or new left bundle branch block (LBBB)]

  •  New pathological Q-waves in at least two contiguous leads

  •  Imaging evidence of a new loss of viable myocardium or new wall motion abnormality

  •  Sudden, unexpected cardiac death, involving cardiac arrest, often with symptoms suggestive of myocardial ischaemia, and accompanied by presumably new ST elevation, or new LBBB, and/or evidence of fresh thrombus by coronary angiography and/or at autopsy, but death occurring before blood samples could be obtained, or at a time before the appearance of cardiac biomarkers in the blood.

  •  Pathological findings of an acute myocardial infarction

Peri-procedural MI (≤72 h after the index procedure)
  •  New ischaemic symptoms (e.g. chest pain or shortness of breath), or new ischaemic signs (e.g. ventricular arrhythmias, new or worsening heart failure, new ST-segment changes, haemodynamic instability, new pathological Q-waves in at least two contiguous leads, imaging evidence of new loss of viable myocardium or new wall motion abnormality) AND

  •  Elevated cardiac biomarkers (preferable CK-MB) within 72 h after the index procedure, consisting of at least one sample post-procedure with a peak value exceeding 15× as the upper reference limit for troponin or 5× for CK-MB.a If cardiac biomarkers are increased at baseline (>99th percentile), a further increase in at least 50% post-procedure is required AND the peak value must exceed the previously stated limit

Spontaneous MI (>72 h after the index procedure) Any one of the following criteria
  •  Detection of rise and/or fall of cardiac biomarkers (preferably troponin) with at least one value above the 99th percentile URL, together with the evidence of myocardial ischaemia with at least one of the following:

  •  Symptoms of ischaemia

  •  ECG changes indicative of new ischaemia [new ST-T changes or new left bundle branch block (LBBB)]

  •  New pathological Q-waves in at least two contiguous leads

  •  Imaging evidence of a new loss of viable myocardium or new wall motion abnormality

  •  Sudden, unexpected cardiac death, involving cardiac arrest, often with symptoms suggestive of myocardial ischaemia, and accompanied by presumably new ST elevation, or new LBBB, and/or evidence of fresh thrombus by coronary angiography and/or at autopsy, but death occurring before blood samples could be obtained, or at a time before the appearance of cardiac biomarkers in the blood.

  •  Pathological findings of an acute myocardial infarction

aPreviously in the original VARC it was 10× and 5× for troponin and CK-MB, respectively.

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