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Troponin criteria for myocardial infarction after percutaneous coronary intervention
Victor Novack1, Michael Pencina, David J Cohen
1Beth Israel Deaconess Medical Center, 330 Brookline Ave., Boston, MA 02215, USA.
Insights
Elevated cardiac biomarkers creatine kinase-MB fraction (CKMB) and troponin after percutaneous coronary intervention are linked to increased mortality. Higher troponin levels are needed to show similar mortality risk compared to CKMB.
Area of Science:
- Cardiology
- Biomarkers
- Interventional Cardiology
Background:
- The universal definition of myocardial infarction uses creatine kinase-MB fraction (CKMB) or troponin levels >3 times the 99th percentile.
- Troponin is preferred over CKMB for diagnosing myocardial infarction post-percutaneous coronary intervention (PCI).
Purpose of the Study:
- To analyze the association between post-PCI elevation of CKMB or troponin and 1-year mortality.
- To compare the diagnostic thresholds and mortality risks associated with CKMB and troponin elevations after PCI.
Main Methods:
- Analysis of 4930 patients undergoing elective coronary stent placement from the EVENT registry (July 2004-September 2007).
- Outcomes assessed included 1-year mortality in relation to postprocedure CKMB or troponin levels, normalized to local diagnostic criteria.
Main Results:
- Myocardial infarction was diagnosed in 7.2% of patients by CKMB criteria and 24.3% by troponin criteria (>3-fold elevation).
- Both CKMB and troponin elevations were associated with increased 1-year mortality (HR 1.38 and 1.35, respectively).
- A >3-fold CKMB increase showed a higher mortality hazard (aHR 2.5) than a >3-fold troponin increase (aHR 1.7); a >20-fold troponin elevation yielded similar mortality risk (aHR 2.6).
Conclusions:
- Post-PCI elevations in both troponin and CKMB are associated with higher 1-year mortality.
- Thresholds for similar mortality risk are significantly higher for troponin compared to CKMB after PCI.
Background:
The universal definition of myocardial infarction specifies creatine kinase-MB fraction (CKMB) or troponin values more than 3 times the 99th percentile of the upper reference limit as diagnostic after percutaneous coronary intervention, with a preference for the use of troponin.
Methods:
Outcomes of 4930 patients with elective coronary stent placement between July 1, 2004, and September 30, 2007, as part of the EVENT (Evaluation of Drug Eluting Stents and Ischemic Events) registry were analyzed to test the association between 1-year mortality and postprocedure elevation of either CKMB or troponin. All values were normalized to the individual clinical center myocardial infarction diagnostic levels.
Results:
Myocardial infarction occurred in 7.2% of patients by the CKMB criteria and in 24.3% of patients by the troponin criteria of greater than 3 times the diagnostic level. Both CKMB (hazard ratio [HR], 1.38; 95% CI, 1.22-1.55) and troponin (HR, 1.35; 95% CI, 1.18-1.54) as continuous values were associated with 1-year mortality. The mortality effect of a more than 3-fold increase was greater for CKMB (adjusted HR, 2.5; 95% CI, 1.5-4.1) than for troponin (adjusted HR, 1.7; 95% CI, 1.1-2.5). A troponin threshold more than 20 times the diagnostic level provided similar frequency (7.0%) and mortality risk (adjusted HR, 2.6; 95% CI, 1.6-4.3) as a 3-fold increase in CKMB. A regression spline model of the relationship between troponin and 1-year mortality demonstrated that the hazard of mortality increased from 1.02 at 3-fold to 1.67 at 20-fold troponin elevation.
Conclusion:
Troponin and CKMB elevations after percutaneous coronary intervention are associated with increased 1-year mortality rates, but thresholds for similar event frequency and mortality hazard are much higher for troponin than for CKMB.
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