Coronary cyclic flow variations following primary angioplasty is associated with poor short-term prognosis

Mariano Albertal1, Fernando Cura, Mitchell W Krucoff

  • 1Department of Interventional Cardiology and Endovascular Therapeutics, Instituto Cardiovascular de Buenos Aires, Buenos Aires, Argentina. malbertal@fibertel.com.ar

Insights

Coronary cyclic flow variations (CCFV) after percutaneous coronary intervention (PCI) in ST-segment Elevation Myocardial Infarction (STEMI) patients indicate a higher risk of mortality and major adverse cardiac events within 30 days. This finding suggests CCFV can predict poor outcomes post-PCI.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Biomedical Engineering

Background:

  • Coronary cyclic flow variations (CCFV) are a platelet-related phenomenon observed after reperfusion.
  • While CCFV predicts complications after thrombolytic therapy, its significance after percutaneous coronary intervention (PCI) remains unevaluated.

Purpose of the Study:

  • To assess the impact of CCFV on major adverse cardiac events (MACE) in ST-segment Elevation Myocardial Infarction (STEMI) patients undergoing primary PCI.
  • To determine if CCFV is an independent predictor of adverse outcomes following PCI.

Main Methods:

  • A cohort of 131 STEMI patients undergoing PCI were monitored for 24 hours.
  • CCFV was defined as >= 3 ST-segment transitions (>= 150 microV).
  • Multivariate logistic regression analyzed the association between CCFV and 30-day MACE, adjusting for clinical and angiographic factors.

Main Results:

  • 14.6% of patients developed CCFV.
  • The CCFV group exhibited significantly higher 30-day mortality (21.4% vs. 3.8%) and MACE rates (42.9% vs. 10.7%).
  • CCFV was an independent predictor of 30-day MACE (adjusted RR 5.09; p=0.0016).

Conclusions:

  • The presence of CCFV after primary PCI in STEMI patients is associated with significantly increased short-term mortality and MACE.
  • CCFV may serve as an early indicator of inadequate myocardial perfusion and predict adverse outcomes post-PCI.
Abstract

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