The prognostic role of troponin I elevation after elective percutaneous coronary intervention

Carla Auguadro1, Filippo Scalise, Mariella Manfredi

  • 1aCardiovascular Catheterization Laboratory, Policlinico di Monza bBiostatistics Unit, Policlinico di Monza cDepartment of Cardiology, Policlinico di Monza, Monza, Italy.

Insights

Minor troponin I elevations after percutaneous coronary intervention (PCI) predict major adverse cardiac events (MACE) in stable patients. This risk is amplified by older age and reduced ejection fraction, even in those with preserved heart function.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Biomarkers

Background:

  • The prognostic significance of minor troponin elevation post-PCI remains debated.
  • Stable coronary artery disease patients undergoing PCI are a key focus for risk stratification.

Purpose of the Study:

  • To evaluate the predictive value of isolated troponin I (TnI) elevation for adverse outcomes after elective PCI.
  • To identify independent predictors of major adverse cardiac events (MACE) in this patient cohort.

Main Methods:

  • Analysis of 1532 consecutive patients undergoing elective PCI, with 93.4% follow-up.
  • Assessment of outcomes including all-cause mortality, cardiac death, and rehospitalization for myocardial infarction or unstable angina.

Main Results:

  • Univariate analysis identified age ≥75, ejection fraction <50%, prior MI, and TnI ≥1.0 ng/mL as MACE predictors.
  • Multivariate analysis confirmed TnI elevation, older age, and reduced ejection fraction as independent MACE predictors.
  • TnI elevation also predicted MACE in patients with preserved ejection fraction, particularly when combined with older age.

Conclusions:

  • Isolated minor troponin I elevations post-elective PCI are independent predictors of MACE.
  • Older age and reduced ejection fraction are also significant independent predictors of MACE.
  • The combination of TnI elevation and older age confers the highest risk for MACE in stable patients post-PCI.
Abstract

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